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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YNL116W DMA2 / SGDID:S000005060
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
YNL116W DMA2 SGDID:S000005060
garA Rv1827 MTCY1A11.16c
Glycogen accumulation regulator GarA
Mycobacterium tuberculosis
2kfu_a P9WJA9 97.30 1.70E-07 1.80E-11 80.90 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
DHX16 DBP2 DDX16 KIAA0577 PRP2
Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 (EC 3.6.4.13) (ATP-dependent RNA helicase #3) (DEAH-box protein 16)
3.6.4.13 Homo sapiens
Seizure Disorder,Neuromuscular Disease,Corpus Callosum, Agenesis Of,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Neuromuscular Oculoauditory Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome
5z56_x O60231 ENSG00000204560 DHX16 97.00 1.00E-06 8.50E-11 89.50 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Tb927.7.2480
Tb927.7.2480
Trypanosoma brucei
2n84_a Q57XM6 97.50 6.30E-08 6.40E-12 85.40 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
MKI67
Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67)
Homo sapiens
Skin Melanoma,Cervical Intraepithelial Neoplasia,Neuroendocrine Tumor,Endometrial Cancer,Squamous Cell Carcinoma,Clear Cell Meningioma,Malignant Fibrous Histiocytoma,Endometrial Hyperplasia,Desmoid Tumor,Adenoma,Myxofibrosarcoma,Parathyroid Carcinoma,Adenosarcoma,Mucoepidermoid Carcinoma,Benign Meningioma,B-Cell Lymphoma,Oral Leukoplakia,Sinonasal Undifferentiated Carcinoma,Embryonal Sarcoma,Keratocystic Odontogenic Tumor,Brain Ependymoma,Congenital Mesoblastic Nephroma,Polymorphous Low-Grade Adenocarcinoma,Cavernous Hemangioma,Pulmonary Vein Stenosis,Leiomyoma,Basal Cell Carcinoma,Necrotizing Sialometaplasia,Transitional Cell Carcinoma,Bladder Cancer,Soft Tissue Sarcoma,Spitz Nevus,Leukoplakia,Breast Ductal Carcinoma,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Ameloblastic Carcinoma,Keratoacanthoma,Inverted Papilloma,Spinal Cord Melanoma,Central Neurocytoma,Bowen'S Disease,Breast Disease,Prostate Cancer,Papillary Thyroid Microcarcinoma,Epithelioid Trophoblastic Tumor,Adrenal Cortical Carcinoma,Breast Fibroadenoma,Bladder Adenocarcinoma,Cervical Squamous Cell Carcinoma,Sarcoma, Synovial,Barrett Esophagus,Gastrointestinal Stromal Tumor,Inflammatory Myofibroblastic Tumor,Renal Cell Carcinoma, Nonpapillary,Meningioma, Familial,Ductal Carcinoma In Situ,Lung Cancer
2aff_a P46013 ENSG00000148773 MKI67 96.60 5.30E-06 5.90E-10 65.60 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Kif13a
Kinesin-like protein KIF13A
Mus musculus
5djo_b Q9EQW7 96.50 9.60E-06 1.00E-09 69.80 0 0 1 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
ICP0_EHV1B
E3 ubiquitin-protein ligase ICP0 (EC 2.3.2.27) (RING-type E3 ubiquitin transferase ICP0)
2.3.2.27 Equine herpesvirus 1
1chc_a P28990 96.80 2.80E-06 2.60E-10 65.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
SLMAP KIAA1601 SLAP UNQ1847/PRO3577
Sarcolemmal membrane-associated protein (Sarcolemmal-associated protein)
Homo sapiens
Heart Conduction Disease,Cerebral Cavernous Malformations 3,Brugada Syndrome,Lung Cancer
6ar0_a Q14BN4 ENSG00000163681 SLMAP 96.40 1.10E-05 1.10E-09 68.20 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
RAD53 MEC2 SAD1 SPK1 YPL153C P2588
Serine/threonine-protein kinase RAD53 (EC 2.7.12.1) (CHEK2 homolog) (Serine-protein kinase 1)
2.7.12.1 Saccharomyces cerevisiae
1fhq_a P22216 96.80 2.80E-06 2.80E-10 73.60 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
TIFA T2BP
TRAF-interacting protein with FHA domain-containing protein A (Putative MAPK-activating protein PM14) (Putative NF-kappa-B-activating protein 20) (TRAF2-binding protein)
Homo sapiens
Hepatocellular Carcinoma
4zgi_a Q96CG3 ENSG00000145365 TIFA 96.40 1.20E-05 1.20E-09 67.60 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
KIF1A ATSV C2orf20
Kinesin-like protein KIF1A (Axonal transporter of synaptic vesicles) (Microtubule-based motor KIF1A) (Unc-104- and KIF1A-related protein) (hUnc-104)
Homo sapiens
Paraplegia,Hemophagocytic Lymphohistiocytosis, Familial, 1,Autonomic Neuropathy,Spasticity,Axonal Neuropathy,Neuropathy, Hereditary Sensory And Autonomic, Type V,Hereditary Spastic Paraplegia 30,Charcot-Marie-Tooth Disease, Axonal, Type 2q,Autosomal Recessive Hereditary Sensory And Autonomic Neuropathy,Hereditary Spastic Paraplegia,Motor Peripheral Neuropathy,Dandy-Walker Syndrome,Neuropathy, Hereditary Sensory And Autonomic, Type Iib,Spastic Paraparesis,Dystonia,Diaphragmatic Eventration,Peho-Like Syndrome,Neuropathy,Charcot-Marie-Tooth Disease,Tukel Syndrome,Goldberg-Shprintzen Syndrome,Epiphyseal Dysplasia, Multiple, 4,Disease Of Mental Health,Spastic Paraplegia 57, Autosomal Recessive,Spastic Paraplegia 30, Autosomal Dominant,Spastic Paraplegia 10, Autosomal Dominant,Spastic Paraplegia 4, Autosomal Dominant,Hereditary Sensory Neuropathy,Neuropathy, Hereditary Sensory, Type Iic,Nescav Syndrome,Masa Syndrome,Spastic Ataxia 2,Spastic Ataxia,Autism Spectrum Disorder,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Laryngomalacia,Autosomal Dominant Non-Syndromic Intellectual Disability,Charcot-Marie-Tooth Disease, Axonal, Type 2k,Microcephaly With Or Without Chorioretinopathy, Lymphedema, Or Mental Retardation,Autism,Joubert Syndrome 1,Peho Syndrome
4ejq_c Q12756 ENSG00000130294 KIF1A 96.40 1.40E-05 1.40E-09 67.40 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
CT_664
CT_664
Chlamydia trachomatis
3gqs_a O84671 96.80 1.80E-06 2.10E-10 66.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
SNIP1
Smad nuclear-interacting protein 1 (FHA domain-containing protein SNIP1)
Homo sapiens
Epilepsy,Benign Epilepsy With Centrotemporal Spikes,Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism
6ff7_0 Q8TAD8 ENSG00000163877 SNIP1 97.00 1.00E-06 8.30E-11 89.60 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
VPS64 FAR9 YDR200C YD9346.10C
Vacuolar protein sorting-associated protein 64 (Factor arrest protein 9)
Saccharomyces cerevisiae
6a8w_a Q03944 97.10 6.80E-07 6.80E-11 76.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Rv1747
ABC transporter ATP-binding/permease protein Rv1747 (EC 7.-.-.-)
Mycobacterium tuberculosis
6cah_a O65934 96.30 1.50E-05 1.60E-09 61.70 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
odhI Cgl1441 cg1630
Oxoglutarate dehydrogenase inhibitor
Corynebacterium glutamicum
2kb4_a Q8NQJ3 97.20 4.10E-07 4.30E-11 76.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
fhaA TB39.8 Rv0020c
FHA domain-containing protein FhaA
Mycobacterium tuberculosis
2lc1_a P71590 96.40 9.60E-06 1.10E-09 61.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Pnkp
Bifunctional polynucleotide phosphatase/kinase (DNA 5'-kinase/3'-phosphatase) (Polynucleotide kinase-3'-phosphatase) [Includes: Polynucleotide 3'-phosphatase (EC 3.1.3.32) (2'(3')-polynucleotidase); Polynucleotide 5'-hydroxyl-kinase (EC 2.7.1.78)]
2.7.1.78,3.1.3.32, Mus musculus
1yj5_c Q9JLV6 96.60 5.40E-06 5.60E-10 69.50 0 0 1 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
garA MSMEG_3647 MSMEI_3561
Glycogen accumulation regulator GarA
Mycolicibacterium smegmatis
6i2q_b A0QYG2 96.40 9.50E-06 1.10E-09 63.20 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Saci_1210
Saci_1210
Sulfolobus acidocaldarius
5a8i_a Q4J9H4 97.40 8.80E-08 9.00E-12 86.90 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
MEK1 MRE4 YOR351C O6357
Meiosis-specific serine/threonine-protein kinase MEK1 (EC 2.7.11.1)
2.7.11.1 Saccharomyces cerevisiae
5yyx_a P24719 96.30 1.50E-05 1.50E-09 66.50 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
SLC4A1AP HLC3
Kanadaptin (Human lung cancer oncogene 3 protein) (HLC-3) (Kidney anion exchanger adapter protein) (Solute carrier family 4 anion exchanger member 1 adapter protein)
Homo sapiens
Laminopathy,Bare Lymphocyte Syndrome, Type I,Glycerol Kinase Deficiency
4h87_b Q9BWU0 ENSG00000163798 SLC4A1AP 96.40 1.30E-05 1.40E-09 64.80 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
MDC1 KIAA0170 NFBD1
Mediator of DNA damage checkpoint protein 1 (Nuclear factor with BRCT domains 1)
Homo sapiens
Cerebellar Disease,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Riddle Syndrome,Lig4 Syndrome,Renal Cell Carcinoma, Nonpapillary,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Primary Autosomal Recessive Microcephaly
3umz_a Q14676 ENSG00000137337 MDC1 96.30 1.50E-05 1.70E-09 61.50 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
CHEK2 CDS1 CHK2 RAD53
Serine/threonine-protein kinase Chk2 (EC 2.7.11.1) (CHK2 checkpoint homolog) (Cds1 homolog) (Hucds1) (hCds1) (Checkpoint kinase 2)
2.7.11.1 Homo sapiens
Squamous Cell Carcinoma,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Adenoid Cystic Carcinoma,Cowden Syndrome,Cervical Adenoma Malignum,Leiomyosarcoma,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Diffuse Midline Glioma, H3 K27m-Mutant,Essential Thrombocythemia,Congenital Heart Defects, Multiple Types, 3,Familial Colorectal Cancer,Leukemia,Inherited Cancer-Predisposing Syndrome,Wilms Tumor 5,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Li-Fraumeni Syndrome 1,Telangiectasis,Basal Cell Carcinoma,Lung Leiomyosarcoma,Prostate Leiomyosarcoma,Cerebellar Disease,Bile Duct Cystadenoma,T-Cell Prolymphocytic Leukemia,Nk-Cell Enteropathy,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Li-Fraumeni Syndrome 2,Premature Menopause,Rhabdomyosarcoma,Xeroderma Pigmentosum, Variant Type,Sarcoma,Fanconi Anemia, Complementation Group A,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Thrombocytopenia,Lynch Syndrome,Esophageal Cancer,Seckel Syndrome,Myelodysplastic Syndrome,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Wilms Tumor 1,Autosomal Recessive Cerebellar Ataxia,Lymphoma,Nijmegen Breakage Syndrome,Colitis,Li-Fraumeni Syndrome,Premature Ovarian Failure 1,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Osteogenic Sarcoma
1gxc_g O96017 ENSG00000183765 CHEK2 96.30 1.70E-05 1.60E-09 68.50 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
DDL At3g20550 K10D20.9
FHA domain-containing protein DDL (Protein DAWDLE)
Arabidopsis thaliana
3vpy_a Q8W4D8 97.00 1.20E-06 1.20E-10 75.00 0 0 0 0 0 0 1 0
YNL116W DMA2 SGDID:S000005060
PML1 YLR016C L1591
Pre-mRNA leakage protein 1
Saccharomyces cerevisiae
3els_a Q07930 97.10 7.20E-07 6.90E-11 78.40 0 0 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
RNF8 KIAA0646
E3 ubiquitin-protein ligase RNF8 (hRNF8) (EC 2.3.2.27) (RING finger protein 8) (RING-type E3 ubiquitin transferase RNF8)
2.3.2.27 Homo sapiens
Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Riddle Syndrome
2csw_a O76064 ENSG00000112130 RNF8 96.60 5.80E-06 6.20E-10 68.90 1 1 0 0 0 0 0 0
YNL116W DMA2 SGDID:S000005060
Ppp1r8 Nipp1
Nuclear inhibitor of protein phosphatase 1 (NIPP-1) (Protein phosphatase 1 regulatory inhibitor subunit 8)
Mus musculus
2jpe_a Q8R3G1 96.90 1.30E-06 1.30E-10 72.60 0 0 1 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab