Skip to main content Skip to navigation Skip to search
Open toolbar

Accessibility

Disclaimer
Accessibility arrangements
Home

Main menu

  • Home
  • Download
  • Information
  • Contact

Mobile Main Menu

  • Home
  • Download
  • Information
  • Contact
AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

Breadcrumb

  1. Home
YGR232W NAS6 / SGDID:S000003464
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YGR232W NAS6 SGDID:S000003464
ASPG
ASPG
3.5.1.1 Cavia porcellus
5dnc_b H0W0T5 99.40 1.10E-17 5.70E-22 110.30 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
NAS6 YGR232W G8564
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6)
Saccharomyces cerevisiae
1wg0_a P50086 99.90 1.00E-26 4.60E-31 138.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
KLLA0_C04147g
KLLA0_C04147g
Kluyveromyces lactis
5h2a_a Q6CUK7 99.60 2.00E-20 8.90E-25 113.30 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Espn
Espin (Ectoplasmic specialization protein)
Mus musculus
5et1_b Q9ET47 99.70 1.70E-21 7.40E-26 122.20 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
AKR2A AFT AKR2 At4g35450 F15J1.20
Ankyrin repeat domain-containing protein 2A (AtAKR2)
Arabidopsis thaliana
4tum_c Q9SAR5 98.60 3.20E-11 1.40E-15 64.20 0 0 0 0 0 0 1 0
YGR232W NAS6 SGDID:S000003464
85/88 kDa calcium-independent phospholipase A2 (CaI-PLA2) (EC 3.1.1.4) (2-lysophosphatidylcholine acylhydrolase) (EC 3.1.1.5) (Group VI phospholipase A2) (GVI PLA2) (Intracellular membrane-associated calcium-independent phospholipase A2 beta) (iPLA2-beta) (PLA2G6) (Palmitoyl-CoA hydrolase) (EC 3.1.2.2) (Patatin-like phospholipase domain-containing protein 9) (PNPLA9)
Cricetulus griseus
6aun_a A0A384E119 99.70 2.10E-21 9.90E-26 132.90 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
SWI6 YLR182W L9470.8
Regulatory protein SWI6 (Cell-cycle box factor subunit SWI6) (MBF subunit P90) (Trans-acting activator of HO endonuclease gene)
Saccharomyces cerevisiae
1sw6_b P09959 99.20 3.80E-15 1.70E-19 92.50 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPC3 TRP3
Short transient receptor potential channel 3 (TrpC3) (Transient receptor protein 3) (TRP-3) (hTrp-3) (hTrp3)
Homo sapiens
T Cell And Nk Cell Immunodeficiency,Immunodeficiency 10,Progressive Familial Heart Block,Familial Episodic Pain Syndrome,Cerebellar Ataxia Type 42,Cerebellar Ataxia Type 41,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Malignant Hypertension,Spinocerebellar Ataxia 14,Spinocerebellar Ataxia 41,Williams-Beuren Syndrome,Hereditary Ataxia,Hypertension, Essential,Mucolipidosis Iv
5zbg_b Q13507 ENSG00000138741 TRPC3 98.60 1.60E-11 8.00E-16 85.40 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpv3
Transient receptor potential cation channel subfamily V member 3 (TrpV3)
Mus musculus
4n5q_b Q8K424 98.80 2.40E-12 1.10E-16 76.80 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
qdtf
qdtf
Providencia alcalifaciens
4xd1_a F8RC03 98.70 7.70E-12 3.80E-16 80.00 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
CDKN2C CDKN6
Cyclin-dependent kinase 4 inhibitor C (Cyclin-dependent kinase 6 inhibitor) (p18-INK4c) (p18-INK6)
Homo sapiens
Plasma Cell Neoplasm,Retinal Cancer,Parathyroid Adenoma,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Breast Cancer,Multiple Endocrine Neoplasia,Oligodendroglioma,Pheochromocytoma,Retinoblastoma,Chromophobe Adenoma,Multiple Endocrine Neoplasia, Type Iv,Lymphoma, Non-Hodgkin, Familial,Multiple Endocrine Neoplasia, Type I,Meningioma, Familial,Lymphoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Lung Cancer
1bu9_a P42773 98.90 8.10E-13 3.60E-17 73.70 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Nfkbib Ikbb
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta)
Mus musculus
1k3z_d Q60778 99.80 2.80E-24 1.20E-28 130.80 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ANKRD27 PP12899
Ankyrin repeat domain-containing protein 27 (VPS9 domain-containing protein)
Homo sapiens
Parastremmatic Dwarfism,Hermansky-Pudlak Syndrome,Pontiac Fever
4b93_b Q96NW4 ENSG00000105186 ANKRD27 99.60 2.60E-20 1.20E-24 112.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Shank3 Prosap2
SH3 and multiple ankyrin repeat domains protein 3 (Shank3) (Proline-rich synapse-associated protein 2) (ProSAP2) (SPANK-2)
Rattus norvegicus
5g4x_a Q9JLU4 99.70 6.10E-23 2.80E-27 128.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
CDKN2A CDKN2 MTS1
Cyclin-dependent kinase inhibitor 2A (Cyclin-dependent kinase 4 inhibitor A) (CDK4I) (Multiple tumor suppressor 1) (MTS-1) (p16-INK4a) (p16-INK4) (p16INK4A)
Homo sapiens
Melanoma-Astrocytoma Syndrome,Spitzoid Melanoma,Melanoma In Congenital Melanocytic Nevus,Adult Hepatocellular Carcinoma,Breast Papillomatosis,Pancreatic Adenocarcinoma,Supratentorial Cancer,Mesothelioma, Malignant,Skin Melanoma,Cervical Intraepithelial Neoplasia,Gliomatosis Cerebri,Heart Disease,Uterine Carcinosarcoma,Endometrial Cancer,Tonsillar Fossa Cancer,Peritoneum Cancer,Cervix Uteri Carcinoma In Situ,Acanthoma,Squamous Cell Carcinoma,Follicular Dendritic Cell Sarcoma,Ocular Melanoma,Childhood Acute Lymphocytic Leukemia,Childhood B-Cell Acute Lymphoblastic Leukemia,Retinitis Pigmentosa,Peritoneal Mesothelioma,Malignant Exocrine Pancreas Neoplasm,Pancreas Sarcoma,Lung Cancer Susceptibility 3,Uterus Carcinoma In Situ,Penile Cancer,Acral Lentiginous Melanoma,Penile Benign Neoplasm,Adenoid Cystic Carcinoma,Carcinosarcoma,Coronary Restenosis,Chordoma,Bone Cancer,Vulva Basal Cell Carcinoma,Suppression Of Tumorigenicity 12,Melanoma,Desmoid Tumor,Epidermolytic Acanthoma,Osteogenesis Imperfecta, Type Xiii,Muir-Torre Syndrome,Diabetes Mellitus,Chondromyxoid Fibroma,Dedifferentiated Liposarcoma,Adenoma,Malignant Peritoneal Mesothelioma,Papillary Squamous Carcinoma,Cholecystitis,Leiomyosarcoma,Vaginal Cancer,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,Collecting Duct Carcinoma,Alzheimer Disease,Plasma Cell Leukemia,Ovarian Seromucinous Carcinoma,Primary Cutaneous B-Cell Lymphoma,Vulvar Disease,Sarcomatoid Mesothelioma,Urinary Bladder Inverted Papilloma,Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type,Vulvar Seborrheic Keratosis,Myocardial Infarction,Vulva Squamous Cell Carcinoma,Pleomorphic Adenoma,Mucoepidermoid Carcinoma,Ischemic Fasciitis,Borst-Jadassohn Intraepidermal Carcinoma,Cervical Basaloid Squamous Cell Carcinoma,Neurofibroma,B-Cell Lymphoma,Bile Duct Cancer,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Oral Cancer,Laryngeal Small Cell Carcinoma,Plasmablastic Lymphoma,Ocular Cancer,Human Cytomegalovirus Infection,Inverted Transitional Papilloma,Intracranial Meningioma,Retinal Cancer,Familial Retinoblastoma,Anal Canal Carcinoma,Posterior Fossa Ependymoma,Male Urethral Cancer,Lymphohistiocytoid Mesothelioma,Cervix Disease,Malignant Pleural Mesothelioma,Retroperitoneum Carcinoma,Endocervical Carcinoma,Vulvar Eccrine Porocarcinoma,Neurofibromatosis, Type I,Leukemia,Cholangiolocellular Carcinoma,Vulva Cancer,Adenosquamous Carcinoma,Neuroblastoma,Vulvar Intraepithelial Neoplasia,Pilocytic Astrocytoma,Gliofibroma,Cervical Adenoid Cystic Carcinoma,Proliferative Verrucous Leukoplakia,Childhood Leukemia,Middle Ear Carcinoma,Glomus Tumor,Esophagus Adenocarcinoma,Laryngeal Disease,Inherited Cancer-Predisposing Syndrome,Nasal Cavity Adenocarcinoma,Barrett'S Adenocarcinoma,Adenocarcinoma In Situ,Malignant Spiradenoma,Large Congenital Melanocytic Nevus,Glioma,Supraglottis Neoplasm,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Noonan Syndrome 1,Vaginal Tubulovillous Adenoma,Anal Canal Paget'S Disease,Basal Cell Carcinoma,Penile Urethral Cancer,Atypical Polypoid Adenomyoma,Inflammatory Liposarcoma,Leukemia, Acute Lymphoblastic,Hereditary Melanoma,Cervicitis,Early Invasive Cervical Adenocarcinoma,Low-Grade Astrocytoma,Adult Malignant Schwannoma,Larynx Cancer,Laryngeal Benign Neoplasm,Rectal Disease,Adenomyoma,Papilloma,Bizarre Leiomyoma,Kidney Cancer,Ovarian Brenner Tumor,Plexiform Neurofibroma,Perivascular Epithelioid Cell Tumor,Atypical Neurofibroma,Benign Mesothelioma,Pleural Cancer,Cystic Teratoma,Transitional Cell Carcinoma,Thyroid Lymphoma,Phimosis,Dysplastic Nevus Syndrome,Nodular Malignant Melanoma,Bladder Cancer,Bladder Clear Cell Adenocarcinoma,Urethra Clear Cell Adenocarcinoma,Megaesophagus,Spitz Nevus,Precursor T-Cell Acute Lymphoblastic Leukemia,Hypopharynx Cancer,Bile Duct Adenoma,Lung Adenoma,Endometrial Adenocarcinoma,Laryngeal Squamous Cell Carcinoma,Prostate Squamous Cell Carcinoma,Oropharynx Cancer,Cervix Carcinoma,Soft Palate Cancer,Oral Cavity Cancer,Keratinizing Squamous Cell Carcinoma,Basaloid Squamous Cell Carcinoma,Anal Squamous Cell Carcinoma,Middle Ear Squamous Cell Carcinoma,Endometrial Squamous Cell Carcinoma,Fallopian Tube Squamous Cell Carcinoma,Lip And Oral Cavity Cancer,Ovarian Cancer,Supraglottis Cancer,Burkitt Lymphoma,Lung Giant Cell Carcinoma,Adenocarcinoma,In Situ Carcinoma,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Mucinous Adenocarcinoma,Maxillary Sinus Benign Neoplasm,Pancreatic Adenosquamous Carcinoma,Trachea Carcinoma In Situ,Breast Cancer,Glioblastoma,Tonsil Cancer,Squamous Cell Carcinoma, Head And Neck,Actinic Keratosis,Hereditary Breast Ovarian Cancer Syndrome,Well-Differentiated Liposarcoma,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Pleomorphic Liposarcoma,Giant Cell Glioblastoma,Mediastinum Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Familial Hypercholesterolemia,Histiocytic Sarcoma,Epstein-Barr Virus-Associated Gastric Carcinoma,Gallbladder Cancer,Squamous Cell Papilloma,Hepatocellular Carcinoma,Anus Disease,Ameloblastic Carcinoma,Tenosynovial Giant Cell Tumor,Nasal Cavity Cancer,Nasal Cavity Lymphoma,Fallopian Tube Endometrioid Adenocarcinoma,Skin Squamous Cell Carcinoma,Malignant Spindle Cell Melanoma,Inverted Papilloma,Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Neurilemmomatosis,Anus Cancer,Pheochromocytoma,Central Nervous System Lymphoma,Rhabdomyosarcoma,Intracranial Aneurysm,Tongue Disease,Bowenoid Papulosis,Atrophic Vulva,Teratoma,Vulvar Dystrophy,Fibrosarcoma Of Bone,Localized Osteosarcoma,Anogenital Venereal Wart,Leukemia, Acute Lymphoblastic 3,Bone Osteosarcoma,Liposarcoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Neurofibrosarcoma,Pancreatic Ductal Carcinoma,Cervical Cancer,Chronic Cervicitis,Cecal Benign Neoplasm,Ovarian Cystadenocarcinoma,Penile Disease,Infiltrating Angiolipoma,Central Nervous System Cancer,Rhabdoid Cancer,Lung Benign Neoplasm,Integumentary System Disease,Keratosis,Retinoblastoma,Cervical Adenocarcinoma,Endometrial Mucinous Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Verrucous Carcinoma,Bladder Squamous Cell Carcinoma,Cervical Squamous Cell Carcinoma,Esophagus Verrucous Carcinoma,Childhood Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Sensory System Disease,Merkel Cell Carcinoma,Endometrial Transitional Cell Carcinoma,Bladder Urothelial Carcinoma,Keratosis, Seborrheic,Renal Cell Carcinoma, Papillary, 1,Small Cell Cancer Of The Lung,Adult T-Cell Leukemia,Esophageal Cancer,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Tetralogy Of Fallot,Barrett Esophagus,Myelodysplastic Syndrome,Small Cell Carcinoma,Tumor Predisposition Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Melanoma-Pancreatic Cancer Syndrome,Gastrointestinal Stromal Tumor,Colorectal Adenoma,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Gallbladder Adenoma,Bone Squamous Cell Carcinoma,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Cecum Adenoma,Tonsil Squamous Cell Carcinoma,Mucosal Melanoma,Parotid Gland Adenoid Cystic Carcinoma,Endocervical Adenocarcinoma,Nasopharyngeal Carcinoma,Wolf-Hirschhorn Syndrome,Meningioma, Familial,Lymphoma,Lipoprotein Quantitative Trait Locus,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Cell Type Benign Neoplasm,Male Reproductive Organ Benign Neoplasm,Pharynx Cancer,Persistent Hyperplastic Primary Vitreous,Li-Fraumeni Syndrome,Dermatofibrosarcoma Protuberans,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Melanoma, Cutaneous Malignant 1,Recessive Dystrophic Epidermolysis Bullosa,Melanoma, Cutaneous Malignant 2,Melanoma, Uveal,Retinitis Pigmentosa 11,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer
1bi7_b P42771 99.70 1.90E-21 9.30E-26 103.10 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TNKS PARP5A PARPL TIN1 TINF1 TNKS1
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Poly [ADP-ribose] polymerase 5A) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TNKS-1) (TRF1-interacting ankyrin-related ADP-ribose polymerase) (Tankyrase I) (Tankyrase-1) (TANK1)
2.4.2.30 Homo sapiens
Cornelia De Lange Syndrome,Lung Acinar Adenocarcinoma,Amyotrophic Lateral Sclerosis 1,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Meningioma, Familial,Arthrogryposis, Renal Dysfunction, And Cholestasis 1
5jhq_d O95271 ENSG00000173273 TNKS 99.70 3.20E-21 1.40E-25 125.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
RNASEL RNS4
2-5A-dependent ribonuclease (2-5A-dependent RNase) (EC 3.1.26.-) (Ribonuclease 4) (Ribonuclease L) (RNase L)
3.1.26.- Homo sapiens
Viral Infectious Disease,Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,Rasopathy,Dengue Disease,Prostate Cancer, Hereditary, 1,West Nile Encephalitis,West Nile Fever,Noonan Syndrome 1,Chronic Fatigue Syndrome,Herpes Simplex,West Nile Virus Infection,Vaccinia,Prostate Cancer,Lynch Syndrome,La Crosse Encephalitis,Noonan Syndrome 2,Paralytic Poliomyelitis,Aicardi-Goutieres Syndrome,Immune Deficiency Disease,Microphthalmia With Limb Anomalies
1wdy_a Q05823 ENSG00000135828 RNASEL 99.70 8.50E-23 3.70E-27 124.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
EF_0377
EF_0377
Enterococcus faecalis
3hra_a Q838Q8 99.60 4.50E-20 2.00E-24 106.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
fdtF
fdtF
Salmonella enterica
5uin_a U3GK13 98.60 2.40E-11 1.20E-15 77.50 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Kank1
Kank1
Mus musculus
5yay_a E9Q238 99.40 9.70E-17 4.50E-21 96.30 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
SWH1 OSH1 YAR042W YAR044W
Oxysterol-binding protein homolog 1
Saccharomyces cerevisiae
5h28_a P35845 99.40 4.80E-17 2.10E-21 97.80 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
legAS4 lpg1718
legAS4 lpg1718
Legionella pneumophila
5czy_a Q5ZUS4 99.40 2.00E-17 9.60E-22 107.80 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpv6
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2)
Mus musculus
2rfa_a Q91WD2 99.60 1.90E-19 8.30E-24 106.40 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
EHMT1 EUHMTASE1 GLP KIAA1876 KMT1D
Histone-lysine N-methyltransferase EHMT1 (EC 2.1.1.-) (Euchromatic histone-lysine N-methyltransferase 1) (Eu-HMTase1) (G9a-like protein 1) (GLP) (GLP1) (Histone H3-K9 methyltransferase 5) (H3-K9-HMTase 5) (Lysine N-methyltransferase 1D)
2.1.1.- Homo sapiens
Kleefstra Syndrome,Deafness, Autosomal Dominant 47,Hypoplastic Left Heart Syndrome,Polymicrogyria,Kleefstra Syndrome Due To A Point Mutation,Pontocerebellar Hypoplasia, Type 2a,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kleefstra Syndrome 1,Chromosome 16p13.3 Deletion Syndrome, Proximal,Pitt-Hopkins Syndrome,Schizophrenia,Ogden Syndrome,Autism Spectrum Disorder,Kabuki Syndrome 1,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome,Autism,Christianson Syndrome
6by9_a Q9H9B1 ENSG00000181090 EHMT1 99.70 3.10E-22 1.40E-26 124.50 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
PSMD10
26S proteasome non-ATPase regulatory subunit 10 (26S proteasome regulatory subunit p28) (Gankyrin) (p28(GANK))
Homo sapiens
Dedifferentiated Liposarcoma,Hepatocellular Carcinoma,Retinoblastoma
1uoh_a O75832 ENSG00000101843 PSMD10 99.80 4.40E-25 2.00E-29 130.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Notch1 Motch
Neurogenic locus notch homolog protein 1 (Notch 1) (Motch A) (mT14) (p300) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)]
Mus musculus
1ymp_a Q01705 98.80 1.40E-12 6.20E-17 69.90 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Tnks Tnks1
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TRF1-interacting ankyrin-related ADP-ribose polymerase 1) (Tankyrase I) (Tankyrase-1) (TANK1)
2.4.2.30 Mus musculus
6cf6_a Q6PFX9 99.80 2.20E-24 9.70E-29 135.00 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPC6 TRP6
Short transient receptor potential channel 6 (TrpC6) (Transient receptor protein 6) (TRP-6)
Homo sapiens
Nephrotic Syndrome,T Cell And Nk Cell Immunodeficiency,Progressive Familial Heart Block,End Stage Renal Disease,Hypertrophic Pyloric Stenosis,Pyloric Stenosis,Genetic Steroid-Resistant Nephrotic Syndrome,Glutamate-Cysteine Ligase Deficiency,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Familial Nephrotic Syndrome,Focal Segmental Glomerulosclerosis,Kidney Disease,Malignant Hypertension,Lipoid Nephrosis,Alport Syndrome,Focal Segmental Glomerulosclerosis 1,Pulmonary Hypertension,Focal Segmental Glomerulosclerosis 2,Hypothalamic Neoplasm,Diencephalic Neoplasm,Frasier Syndrome,Denys-Drash Syndrome,Hypertension, Essential,Membranous Nephropathy,Mucolipidosis Iv
5yx9_b Q9Y210 ENSG00000137672 TRPC6 99.50 1.80E-18 8.90E-23 120.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020
Drosophila melanogaster
5vkq_d E0A9E1 99.70 6.20E-22 2.90E-26 145.50 0 0 0 0 1 0 0 0
YGR232W NAS6 SGDID:S000003464
BCL3 BCL4 D19S37
B-cell lymphoma 3 protein (BCL-3) (Proto-oncogene BCL3)
Homo sapiens
B-Cell Lymphoma,Leukemia,Lymphoma, Non-Hodgkin, Familial,Lymphoma,Leukemia, Chronic Lymphocytic
1k1a_a P20749 ENSG00000069399 BCL3 99.80 5.80E-26 2.60E-30 135.30 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
AKT1 At2g26650 F18A8.2
Potassium channel AKT1
Arabidopsis thaliana
5aar_a Q38998 99.30 1.40E-16 5.90E-21 90.60 0 0 0 0 0 0 1 0
YGR232W NAS6 SGDID:S000003464
ASB11
Ankyrin repeat and SOCS box protein 11 (ASB-11)
Homo sapiens
Lacrimal Duct Obstruction
4uuc_a Q8WXH4 ENSG00000165192 ASB11 99.80 5.00E-24 2.20E-28 125.50 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
RFXANK ANKRA1 RFXB
DNA-binding protein RFXANK (Ankyrin repeat family A protein 1) (Regulatory factor X subunit B) (RFX-B) (Regulatory factor X-associated ankyrin-containing protein)
Homo sapiens
Severe Combined Immunodeficiency,Tibial Neuropathy,Tarsal Tunnel Syndrome,Combined Immunodeficiency,Discharging Ear,Purine Nucleoside Phosphorylase Deficiency,Alcoholic Gastritis,Acquired Thrombocytopenia,Omenn Syndrome,Retinitis Pigmentosa 48,Bare Lymphocyte Syndrome, Type I,Immune Deficiency Disease,Bare Lymphocyte Syndrome, Type Ii,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Bjornstad Syndrome
3uxg_a O14593 ENSG00000064490 RFXANK 99.30 9.20E-16 4.10E-20 86.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
NFKB2 LYT10
Nuclear factor NF-kappa-B p100 subunit (DNA-binding factor KBF2) (H2TF1) (Lymphocyte translocation chromosome 10 protein) (Nuclear factor of kappa light polypeptide gene enhancer in B-cells 2) (Oncogene Lyt-10) (Lyt10) [Cleaved into: Nuclear factor NF-kappa-B p52 subunit]
Homo sapiens
Immunodeficiency 10,B Cell Deficiency,Ectodermal Dysplasia,B-Cell Non-Hodgkin Lymphoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Asbestos-Related Lung Carcinoma,Combined Immunodeficiency,Legionellosis,Osteopetrosis,Neuroaspergillosis,Immunodeficiency, Common Variable, 10,Splenic Marginal Zone Lymphoma,Lymphoma,Acth Deficiency, Isolated,Incontinentia Pigmenti,Immunodeficiency, Common Variable, 1
4ot9_a Q00653 ENSG00000077150 NFKB2 99.70 3.50E-21 1.60E-25 121.10 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
K1L
K1L
Vaccinia virus
3kea_b Q6IV60 99.50 7.10E-18 3.20E-22 102.70 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPV6 ECAC2
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (CaT-like) (CaT-L) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2)
Homo sapiens
Metatropic Dysplasia,Pseudohypoaldosteronism,Hypervitaminosis D,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Pendred Syndrome,Hyperparathyroidism,Bone Mineral Density Quantitative Trait Locus 15,Aromatase Deficiency,Prostate Cancer,Hyperparathyroidism, Transient Neonatal,Scapuloperoneal Spinal Muscular Atrophy,Hyperparathyroidism, Neonatal Severe,Spondyloepiphyseal Dysplasia, Maroteaux Type,Spondylometaphyseal Dysplasia, Kozlowski Type,Brachyolmia,Autosomal Recessive Disease,Estrogen-Receptor Negative Breast Cancer,Mucolipidosis Iv
6e2f_c Q9H1D0 ENSG00000165125 TRPV6 99.60 2.20E-20 1.10E-24 126.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpv2 Sac2b Vrl1
Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Stretch-activated channel 2B) (Vanilloid receptor-like protein 1) (VRL-1)
Rattus norvegicus
2etb_a Q9WUD2 99.10 2.30E-14 1.00E-18 85.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ABAYE2397
ABAYE2397
Acinetobacter baumannii
5d66_a B0VB33 99.70 1.30E-21 5.80E-26 112.90 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
lin-12 R107.8
Protein lin-12 (Abnormal cell lineage protein 12) (Notch-like protein lin-12)
Caenorhabditis elegans
2fo1_e P14585 99.70 2.90E-22 1.30E-26 126.60 0 0 0 0 0 1 0 0
YGR232W NAS6 SGDID:S000003464
KANK1 ANKRD15 KANK KIAA0172
KN motif and ankyrin repeat domain-containing protein 1 (Ankyrin repeat domain-containing protein 15) (Kidney ankyrin repeat-containing protein)
Homo sapiens
Metanephric Adenoma,Chromosome 9p Deletion Syndrome,Nephrotic Syndrome,Cerebral Palsy,Inherited Congenital Spastic Tetraplegia,Cerebral Palsy, Spastic Quadriplegic, 2,Myeloproliferative Neoplasm,Quadriplegia,Renal Adenoma,Tukel Syndrome,Spastic Quadriplegia,Spastic Cerebral Palsy,Brain Glioma,Autosomal Dominant Non-Syndromic Intellectual Disability
5ybu_a Q14678 ENSG00000107104 KANK1 99.60 5.50E-20 2.50E-24 110.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ASAP3 DDEFL1 UPLC1
Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3 (Development and differentiation-enhancing factor-like 1) (Protein up-regulated in liver cancer 1)
Homo sapiens
2b0o_e Q8TDY4 ENSG00000088280 ASAP3 98.50 3.10E-11 1.40E-15 74.00 0 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPV2
TRPV2
Oryctolagus cuniculus
6bwj_a G1SNM3 99.10 1.60E-14 7.40E-19 99.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
NOTCH1 TAN1
Neurogenic locus notch homolog protein 1 (Notch 1) (hN1) (Translocation-associated notch protein TAN-1) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)]
Homo sapiens
Ventricular Septal Defect,Heart Septal Defect,Heart Disease,Richter'S Syndrome,Squamous Cell Carcinoma,Severe Combined Immunodeficiency,Lymphoblastic Lymphoma,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Ossifying Fibroma,Adenoid Cystic Carcinoma,Double Outlet Right Ventricle,Hajdu-Cheney Syndrome,Bone Cancer,Atrial Heart Septal Defect,Invasive Bladder Transitional Cell Carcinoma,Prion Disease,Connective Tissue Disease,Uterine Adnexa Cancer,Kleefstra Syndrome,Tongue Carcinoma,Orofacial Cleft 4,Clear Cell Renal Cell Carcinoma,Aortic Dissection,Alzheimer Disease,Rasopathy,Nodular Regenerative Hyperplasia,Mucoepidermoid Carcinoma,T-Cell Non-Hodgkin Lymphoma,Holoprosencephaly,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Biliary Tract Disease,Infratentorial Cancer,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Leukemia,Colon Adenocarcinoma,Neuroblastoma,Hypoplastic Left Heart Syndrome,Lacrimal Gland Adenoid Cystic Carcinoma,Shone Complex,Acute Leukemia,Intrahepatic Cholangiocarcinoma,Leukemia, Acute Myeloid,Bone Marrow Cancer,Basal Cell Carcinoma,Hematologic Cancer,Hemangioma,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Basal Cell Nevus Syndrome,Aortic Disease,Aortic Valve Disease 1,Focal Segmental Glomerulosclerosis,Brain Cancer,Precursor T-Cell Acute Lymphoblastic Leukemia,Lung Adenoma,Oropharynx Cancer,Aplastic Anemia,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Tonsil Cancer,Exudative Vitreoretinopathy 5,Microphthalmia,Malignant Astrocytoma,Adult Liposarcoma,Breast Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Aneurysm,Hydrocephalus,Tongue Disease,Cerebral Degeneration,Spondylocostal Dysostosis 3, Autosomal Recessive,Alagille Syndrome 1,Skin Carcinoma,Hemophagocytic Lymphohistiocytosis, Familial, 2,Gastric Cancer,Friedreich Ataxia,Prostate Cancer,Disease Of Mental Health,Cervical Cancer,Aortic Aneurysm,Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1,Orofacial Cleft 8,Scalp-Ear-Nipple Syndrome,Lung Squamous Cell Carcinoma,Adenoiditis,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Adams-Oliver Syndrome 5,Loeys-Dietz Syndrome,Hypoplastic Left Heart Syndrome 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Heart, Malformation Of,Tongue Squamous Cell Carcinoma,Acute Promyelocytic Leukemia,Bone Squamous Cell Carcinoma,Aortic Aneurysm, Familial Thoracic 1,Endosteal Hyperostosis, Autosomal Dominant,Wilms Tumor 1,Mental Retardation, Autosomal Dominant 40,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Brain Glioma,Patent Ductus Arteriosus 1,Adams-Oliver Syndrome,Wilson-Turner X-Linked Mental Retardation Syndrome,Dowling-Degos Disease,Leukemia, Chronic Lymphocytic,Marfan Syndrome,Left Ventricular Noncompaction,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Oliver Syndrome,Pancreatic Cancer
2f8y_a P46531 ENSG00000148400 NOTCH1 99.70 2.40E-22 1.00E-26 118.10 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
KANK2 ANKRD25 KIAA1518 MXRA3 SIP
KN motif and ankyrin repeat domain-containing protein 2 (Ankyrin repeat domain-containing protein 25) (Matrix-remodeling-associated protein 3) (SRC-1-interacting protein) (SIP) (SRC-interacting protein) (SRC1-interacting protein)
Homo sapiens
Nephrotic Syndrome,Pseudoainhum,Familial Woolly Hair Syndrome,Succinic Semialdehyde Dehydrogenase Deficiency,Focal Segmental Glomerulosclerosis,Ectodermal Dysplasia 4, Hair/Nail Type,Striate Palmoplantar Keratoderma,Nephrotic Syndrome, Type 16,Palmoplantar Keratoderma And Woolly Hair,Woolly Hair, Autosomal Dominant,Gamma-Amino Butyric Acid Metabolism Disorder,Multiple Pterygium Syndrome, Escobar Variant
4hbd_a Q63ZY3 ENSG00000197256 KANK2 99.60 6.90E-20 3.20E-24 111.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TV1425 TVG1472127
Putative ankyrin repeat protein TV1425
Thermoplasma volcanium
2rfm_b Q978J0 99.50 2.70E-18 1.20E-22 98.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpc4 Trrp4
Short transient receptor potential channel 4 (TrpC4) (Capacitative calcium entry channel Trp4) (Receptor-activated cation channel TRP4)
Mus musculus
5z96_a Q9QUQ5 98.90 4.80E-13 2.30E-17 92.00 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPV4
Transient receptor potential cation channel subfamily V member 4 (TrpV4) (Vanilloid receptor-related osmotically activated channel) (VR-OAC)
Gallus gallus
3jxj_a A0A1D5PXA5 99.00 6.50E-14 2.90E-18 84.00 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ALDOA
Fructose-bisphosphate aldolase A (EC 4.1.2.13) (Muscle-type aldolase)
4.1.2.13 Oryctolagus cuniculus
6mwq_d P00883 99.70 1.10E-22 5.40E-27 131.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ILK ILK1 ILK2
Integrin-linked protein kinase (EC 2.7.11.1) (59 kDa serine/threonine-protein kinase) (Beta-integrin-linked kinase) (ILK-1) (ILK-2) (p59ILK)
2.7.11.1 Homo sapiens
Polycystic Kidney Disease,Thyroid Gland Anaplastic Carcinoma,Hypertrophic Cardiomyopathy,Dilated Cardiomyopathy,Hypermobile Ehlers-Danlos Syndrome,Focal Segmental Glomerulosclerosis,Brain Cancer,Ovarian Cancer,Colorectal Cancer,Prostate Cancer,Hyperphosphatemia,Exudative Vitreoretinopathy,Renal Fibrosis,Lung Cancer,Pancreatic Cancer
2kbx_a Q13418 ENSG00000166333 ILK 99.00 1.80E-13 8.00E-18 76.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ZDHHC17 HIP14 HIP3 HYPH KIAA0946 HSPC294
Palmitoyltransferase ZDHHC17 (EC 2.3.1.225) (Acyltransferase ZDHHC17) (EC 2.3.1.-) (DHHC domain-containing cysteine-rich protein 17) (DHHC17) (Huntingtin yeast partner H) (Huntingtin-interacting protein 14) (HIP-14) (Huntingtin-interacting protein 3) (HIP-3) (Huntingtin-interacting protein H) (Putative MAPK-activating protein PM11) (Putative NF-kappa-B-activating protein 205) (Zinc finger DHHC domain-containing protein 17)
2.3.1.225 Homo sapiens
Huntington Disease,Hypoparathyroidism, X-Linked
3eu9_a Q8IUH5 ENSG00000186908 ZDHHC17 99.80 3.70E-25 1.70E-29 131.60 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
trpc4b trpc4a
trpc4b trpc4a
Danio rerio
6g1k_b U3N7D8 98.90 5.60E-13 2.80E-17 93.20 0 0 0 1 0 0 0 0
YGR232W NAS6 SGDID:S000003464
trpv4
trpv4
Xenopus tropicalis
6c8f_a F7BWY7 99.20 2.90E-15 1.40E-19 101.70 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
spa
Immunoglobulin G-binding protein A (IgG-binding protein A) (Staphylococcal protein A) (SpA)
Staphylococcus aureus
5cbn_a P38507 98.90 6.60E-13 3.00E-17 74.90 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
legA12 lpg0483
legA12 lpg0483
Legionella pneumophila
5vrq_a Q5ZY89 99.40 9.40E-17 4.50E-21 102.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ASB9
Ankyrin repeat and SOCS box protein 9 (ASB-9)
Homo sapiens
Uterine Corpus Endometrial Carcinoma
3d9h_a Q96DX5 ENSG00000102048 ASB9 99.70 1.50E-22 7.10E-27 123.40 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ANKRA2 ANKRA
Ankyrin repeat family A protein 2 (RFXANK-like protein 2)
Homo sapiens
Donnai-Barrow Syndrome,Three M Syndrome 1,Branchiooculofacial Syndrome
3so8_a Q9H9E1 ENSG00000164331 ANKRA2 99.20 2.80E-15 1.30E-19 83.50 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
GLS GLS1 KIAA0838
Glutaminase kidney isoform, mitochondrial (GLS) (EC 3.5.1.2) (K-glutaminase) (L-glutamine amidohydrolase) [Cleaved into: Glutaminase kidney isoform, mitochondrial 68 kDa chain; Glutaminase kidney isoform, mitochondrial 65 kDa chain]
3.5.1.2 Homo sapiens
Autosomal Dominant Polycystic Kidney Disease,Amyotrophic Lateral Sclerosis 1,Leukemia, Acute Lymphoblastic,Cataract,Liver Cirrhosis,Hepatic Encephalopathy,Spastic Ataxia-Dysarthria Due To Glutaminase Deficiency,Contractural Arachnodactyly, Congenital,Schizophrenia,Developmental And Epileptic Encephalopathy 71,Infantile Cataract, Skin Abnormalities, Glutamate Excess, And Impaired Intellectual Development,Global Developmental Delay, Progressive Ataxia, And Elevated Glutamine,Distal Arthrogryposis,Autosomal Recessive Disease,Tracheoesophageal Fistula With Or Without Esophageal Atresia,Metabolic Acidosis
5uqe_d O94925 ENSG00000115419 GLS 99.10 1.30E-14 6.40E-19 95.00 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
AVO2 YMR068W YM9916.07
Target of rapamycin complex 2 subunit AVO2 (TORC2 subunit AVO2) (Adheres voraciously to TOR2 protein 2)
Saccharomyces cerevisiae
6emk_h Q04749 99.60 6.10E-20 3.10E-24 116.70 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Asap2 Ddef2 Gm1523 Gm592
Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 (Development and differentiation-enhancing factor 2) (Paxillin-associated protein with ARF GAP activity 3) (PAG3) (Pyk2 C-terminus-associated protein) (PAP)
Mus musculus
1dcq_a Q7SIG6 98.90 7.10E-13 3.20E-17 80.40 0 0 1 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TRPV2 VRL
Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Vanilloid receptor-like protein 1) (VRL-1)
Homo sapiens
Dentin Sensitivity,Inflammatory Bowel Disease 28,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Dilated Cardiomyopathy,Facial Dermatosis,Scapuloperoneal Spinal Muscular Atrophy,Brachyolmia
2f37_b Q9Y5S1 ENSG00000187688 TRPV2 99.50 6.10E-18 2.70E-22 100.90 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
LMJF_29_1100
LMJF_29_1100
Leishmania major
3ljn_a E9ADW8 99.80 5.00E-23 2.30E-27 129.60 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
NFKBIA IKBA MAD3 NFKBI
NF-kappa-B inhibitor alpha (I-kappa-B-alpha) (IkB-alpha) (IkappaBalpha) (Major histocompatibility complex enhancer-binding protein MAD3)
Homo sapiens
Vascular Disease,Stomach Carcinoma In Situ,Bone Cancer,Leukemia, Chronic Myeloid,Diabetes Mellitus,Hepatitis B,Mycobacterium Malmoense,Ectodermal Dysplasia,B-Cell Lymphoma,Osteomyelitis, Sterile Multifocal, With Periostitis And Pustulosis,T-Cell Lymphoblastic Leukemia/Lymphoma,Carbuncle,Shigellosis,Periostitis,Hypohidrotic Ectodermal Dysplasia With Immunodeficiency,Newcastle Disease,Legionellosis,Ovarian Cancer,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Crohn'S Disease,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Giant Cell Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Tropical Spastic Paraparesis,Chromosome 14q11-Q22 Deletion Syndrome,Cardiomyopathy, Dilated, 1gg,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Adult T-Cell Leukemia,Inflammatory Bowel Disease,Immune Deficiency Disease,Myelodysplastic Syndrome,Intellectual Developmental Disorder, X-Linked 108,Ectodermal Dysplasia And Immunodeficiency 2,Mantle Cell Lymphoma,Nasopharyngeal Carcinoma,Psoriatic Arthritis,Leukemia, Chronic Lymphocytic,Systemic Lupus Erythematosus,Myeloma, Multiple,Lung Cancer,Helicobacter Pylori Infection,Asthma,Pancreatic Cancer
1nfi_e P25963 ENSG00000100906 NFKBIA 99.40 1.20E-17 5.10E-22 97.30 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
legA1 lpg2416
legA1 lpg2416
Legionella pneumophila
2aja_b Q5ZSV0 99.50 2.10E-18 9.70E-23 109.20 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
PPP1R12A MBS MYPT1
Protein phosphatase 1 regulatory subunit 12A (130 kDa myosin-binding subunit of smooth muscle myosin phosphatase) (Myosin phosphatase-targeting subunit 1) (Myosin phosphatase target subunit 1) (PP1M subunit M110) (Protein phosphatase myosin-binding subunit)
Gallus gallus
1s70_b Q90623 99.70 1.20E-21 5.50E-26 120.20 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpv1 Vr1 Vr1l
Transient receptor potential cation channel subfamily V member 1 (TrpV1) (Capsaicin receptor) (Osm-9-like TRP channel 1) (OTRPC1) (Vanilloid receptor 1) (Vanilloid receptor type 1-like)
Rattus norvegicus
2pnn_a O35433 99.20 2.00E-15 8.70E-20 91.20 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ANK2 ANKB
Ankyrin-2 (ANK-2) (Ankyrin-B) (Brain ankyrin) (Non-erythroid ankyrin)
Homo sapiens
Timothy Syndrome,Heart Disease,Hypertrophic Cardiomyopathy,Familial Long Qt Syndrome,Legionnaire Disease,Long Qt Syndrome 12,Dilated Cardiomyopathy,Jervell And Lange-Nielsen Syndrome 1,Hereditary Spherocytosis,Long Qt Syndrome,Heart Conduction Disease,Progressive Familial Heart Block, Type Ia,Sick Sinus Syndrome,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Developmental And Epileptic Encephalopathy 5,Long Qt Syndrome 13,Disease Of Mental Health,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Long Qt Syndrome 9,Long Qt Syndrome 10,Long Qt Syndrome 11,Coffin-Siris Syndrome 1,Brugada Syndrome 3,Familial Atrial Fibrillation,Sinoatrial Node Disease,Long Qt Syndrome 1,Intrinsic Cardiomyopathy,Autism Spectrum Disorder,Atrial Fibrillation,Cardiac Arrest,Autism,Catecholaminergic Polymorphic Ventricular Tachycardia,Spinocerebellar Ataxia 5,Cardiac Arrhythmia, Ankyrin-B-Related
4rly_a Q01484 ENSG00000145362 ANK2 99.70 1.80E-22 7.90E-27 125.30 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Bd3460
Bd3460
Bdellovibrio bacteriovorus
5cec_b Q6MHS9 99.50 9.30E-19 4.20E-23 103.30 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
TNKS2 PARP5B TANK2 TNKL
Poly [ADP-ribose] polymerase tankyrase-2 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 6) (ARTD6) (Poly [ADP-ribose] polymerase 5B) (Protein poly-ADP-ribosyltransferase tankyrase-2) (EC 2.4.2.-) (TNKS-2) (TRF1-interacting ankyrin-related ADP-ribose polymerase 2) (Tankyrase II) (Tankyrase-2) (TANK2) (Tankyrase-like protein) (Tankyrase-related protein)
2.4.2.30 Homo sapiens
Familial Isolated Hypoparathyroidism,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Arthrogryposis, Renal Dysfunction, And Cholestasis 1
4z68_a Q9H2K2 ENSG00000107854 TNKS2 98.90 3.50E-13 1.60E-17 74.30 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Trpv5 Ecac1
Transient receptor potential cation channel subfamily V member 5 (TrpV5) (Epithelial calcium channel 1) (ECaC1) (Osm-9-like TRP channel 3) (OTRPC3)
Oryctolagus cuniculus
6o1u_d Q9XSM3 99.40 1.80E-17 8.90E-22 112.90 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
Lebu_0176
Lebu_0176
Leptotrichia buccalis
3t8k_a C7NDE2 99.00 1.20E-13 5.20E-18 78.70 0 0 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ANK1 ANK
Ankyrin-1 (ANK-1) (Ankyrin-R) (Erythrocyte ankyrin)
Homo sapiens
Migraine With Or Without Aura 1,Hereditary Elliptocytosis,Glutamate-Cysteine Ligase Deficiency,Familial Episodic Pain Syndrome,8p11.2 Deletion Syndrome,Hereditary Spherocytosis,Ehrlichiosis,Facial Dermatosis,Hemolytic Anemia,Congenital Hemolytic Anemia,Developmental And Epileptic Encephalopathy 5,Myopathy, Distal, 3,Disease Of Mental Health,Kallmann Syndrome,Malaria,Spherocytosis, Type 1,Brugada Syndrome,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema,Spinocerebellar Ataxia 5
1n11_a P16157 ENSG00000029534 ANK1 99.70 4.50E-22 2.00E-26 128.20 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
ACAP2 CENTB2 KIAA0041
Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 (Centaurin-beta-2) (Cnt-b2)
Homo sapiens
Tethered Spinal Cord Syndrome
6if3_a Q15057 ENSG00000114331 ACAP2 98.90 4.80E-13 2.20E-17 75.40 1 1 0 0 0 0 0 0
YGR232W NAS6 SGDID:S000003464
PPP1R13L IASPP NKIP1 PPP1R13BL RAI
RelA-associated inhibitor (Inhibitor of ASPP protein) (Protein iASPP) (NFkB-interacting protein 1) (PPP1R13B-like protein)
Homo sapiens
Basal Cell Carcinoma,Dilated Cardiomyopathy,Noonan Syndrome With Multiple Lentigines
2vge_a Q8WUF5 ENSG00000104881 PPP1R13L 99.30 4.30E-16 2.00E-20 91.90 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab