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

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YPL181W CTI6 / SGDID:S000006102
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
YPL181W CTI6 SGDID:S000006102
jmjd-1.2 F29B9.2
Lysine-specific demethylase 7 homolog (ceKDM7A) (EC 1.14.11.-) (JmjC domain-containing protein 1.2) (PHD finger protein 8 homolog) (PHF8 homolog)
1.14.11.- Caenorhabditis elegans
3n9m_a Q9GYI0 95.70 9.30E-05 1.00E-08 71.20 0 0 0 0 0 1 0 0
YPL181W CTI6 SGDID:S000006102
Ing4
Inhibitor of growth protein 4 (p29ING4)
Mus musculus
1weu_a Q8C0D7 96.10 2.60E-05 3.20E-09 56.50 0 0 1 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KMT2E MLL5
Inactive histone-lysine N-methyltransferase 2E (Inactive lysine N-methyltransferase 2E) (Myeloid/lymphoid or mixed-lineage leukemia protein 5)
Homo sapiens
Epilepsy,Non-Specific Syndromic Intellectual Disability,Kleefstra Syndrome 2,Disease Of Mental Health,O'Donnell-Luria-Rodan Syndrome,Cerebroretinal Microangiopathy With Calcifications And Cysts 1,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Autism
2lv9_a Q8IZD2 ENSG00000005483 KMT2E 96.60 4.60E-06 5.50E-10 62.20 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KMT2C HALR KIAA1506 MLL3
Histone-lysine N-methyltransferase 2C (Lysine N-methyltransferase 2C) (EC 2.1.1.354) (Homologous to ALR protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 3)
2.1.1.354 Homo sapiens
Plasma Cell Neoplasm,Kleefstra Syndrome,Leukemia,Leukemia, Acute Myeloid,Kleefstra Syndrome Due To A Point Mutation,Cystic Kidney Disease,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Kleefstra Syndrome 2,Disease Of Mental Health,Kleefstra Syndrome 1,Autism Spectrum Disorder,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Cardiomyopathy, Infantile Histiocytoid
6mlc_a Q8NEZ4 ENSG00000055609 KMT2C 95.20 0.00022 2.60E-08 51.90 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
ING5
Inhibitor of growth protein 5 (p28ING5)
Homo sapiens
Atrophy Of Testis,Ohdo Syndrome, Sbbys Variant,Kleefstra Syndrome 1,Ohdo Syndrome
3c6w_a Q8WYH8 ENSG00000168395 ING5 95.20 0.0002 2.70E-08 45.40 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
PHF21A BHC80 KIAA1696 BM-006
PHD finger protein 21A (BHC80a) (BRAF35-HDAC complex protein BHC80)
Homo sapiens
Epilepsy,Potocki-Shaffer Syndrome,Kleefstra Syndrome,Meier-Gorlin Syndrome 1,Weaver Syndrome,Syndromic Intellectual Disability,Intellectual Developmental Disorder With Behavioral Abnormalities And Craniofacial Dysmorphism With Or Without Seizures,Autism Spectrum Disorder,Kabuki Syndrome 1,Kbg Syndrome,Parietal Foramina,Autism
2yql_a Q96BD5 ENSG00000135365 PHF21A 95.00 0.00027 4.00E-08 42.10 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
UHRF1 ICBP90 NP95 RNF106
E3 ubiquitin-protein ligase UHRF1 (EC 2.3.2.27) (Inverted CCAAT box-binding protein of 90 kDa) (Nuclear protein 95) (Nuclear zinc finger protein Np95) (HuNp95) (hNp95) (RING finger protein 106) (RING-type E3 ubiquitin transferase UHRF1) (Transcription factor ICBP90) (Ubiquitin-like PHD and RING finger domain-containing protein 1) (hUHRF1) (Ubiquitin-like-containing PHD and RING finger domains protein 1)
2.3.2.27 Homo sapiens
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Breast Cancer,Colorectal Cancer,Oligospermia,Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant,Retinoblastoma,Neuropathy, Hereditary Sensory, Type Ie,Oculoauricular Syndrome,Cartilage-Hair Hypoplasia
3zvz_b Q96T88 ENSG00000276043 UHRF1 95.50 9.80E-05 1.50E-08 43.30 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
DIDO1 C20orf158 DATF1 KIAA0333
Death-inducer obliterator 1 (DIO-1) (hDido1) (Death-associated transcription factor 1) (DATF-1)
Homo sapiens
2m3h_a Q9BTC0 ENSG00000101191 DIDO1 96.20 1.70E-05 2.50E-09 47.80 0 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
PHF20 C20orf104 GLEA2 HCA58 NZF TZP
PHD finger protein 20 (Glioma-expressed antigen 2) (Hepatocellular carcinoma-associated antigen 58) (Novel zinc finger protein) (Transcription factor TZP)
Homo sapiens
Hepatocellular Carcinoma,Glycogen Storage Disease Iv
5tab_a Q9BVI0 ENSG00000025293 PHF20 96.50 5.70E-06 8.30E-10 49.80 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
Ing2 Ing1l
Inhibitor of growth protein 2 (Inhibitor of growth 1-like protein) (p33ING2)
Mus musculus
2g6q_a Q9ESK4 95.40 0.00014 1.90E-08 46.60 0 0 1 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
AL1 At5g05610 MOP10.15
PHD finger protein ALFIN-LIKE 1 (Protein AL1)
Arabidopsis thaliana
5y20_a Q9FFF5 95.30 0.00013 2.10E-08 40.90 0 0 0 0 0 0 1 0
YPL181W CTI6 SGDID:S000006102
PHF13
PHD finger protein 13 (Survival time-associated PHD finger protein in ovarian cancer 1) (SPOC1)
Homo sapiens
Ovarian Cancer,Pick Disease Of Brain,Chromosome 1p36 Deletion Syndrome,Ovarian Cancer 1
3o70_a Q86YI8 ENSG00000116273 PHF13 96.60 4.60E-06 6.00E-10 56.10 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
ASH2L ASH2L1
Set1/Ash2 histone methyltransferase complex subunit ASH2 (ASH2-like protein)
Homo sapiens
Kleefstra Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kabuki Syndrome 1
3rsn_a Q9UBL3 ENSG00000129691 ASH2L 96.20 2.40E-05 2.60E-09 65.30 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KDM5B JARID1B PLU1 RBBP2H1
Lysine-specific demethylase 5B (EC 1.14.11.67) (Cancer/testis antigen 31) (CT31) (Histone demethylase JARID1B) (Jumonji/ARID domain-containing protein 1B) (PLU-1) (Retinoblastoma-binding protein 2 homolog 1) (RBP2-H1) ([histone H3]-trimethyl-L-lysine(4) demethylase 5B)
1.14.11.67 Homo sapiens
Skin Melanoma,Melanoma,Breast Cancer,Mental Retardation, Autosomal Recessive 65,Retinoblastoma,Autism Spectrum Disorder,Autosomal Dominant Non-Syndromic Intellectual Disability,Autosomal Recessive Non-Syndromic Intellectual Disability,Autism
2ma5_a Q9UGL1 ENSG00000117139 KDM5B 96.10 2.10E-05 3.00E-09 49.10 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
ING4 My036
Inhibitor of growth protein 4 (p29ING4)
Homo sapiens
2pnx_c Q9UNL4 ENSG00000111653 ING4 95.40 0.00013 1.80E-08 45.10 0 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
TRIM33 KIAA1113 RFG7 TIF1G
E3 ubiquitin-protein ligase TRIM33 (EC 2.3.2.27) (Ectodermin homolog) (RET-fused gene 7 protein) (Protein Rfg7) (RING-type E3 ubiquitin transferase TRIM33) (Transcription intermediary factor 1-gamma) (TIF1-gamma) (Tripartite motif-containing protein 33)
2.3.2.27 Homo sapiens
Muscular Disease,Chronic Myelomonocytic Leukemia,Muscle Tissue Disease,Orbital Plasma Cell Granuloma,Antisynthetase Syndrome,Myositis,Differentiated Thyroid Carcinoma,Chronic Orbital Inflammation,Adult Dermatomyositis,Childhood Type Dermatomyositis
5mr8_a Q9UPN9 ENSG00000197323 TRIM33 95.00 0.00029 3.90E-08 54.70 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
PHF8 KIAA1111 ZNF422
Histone lysine demethylase PHF8 (EC 1.14.11.27) (EC 1.14.11.65) (PHD finger protein 8) ([histone H3]-dimethyl-L-lysine(36) demethylase PHF8) ([histone H3]-dimethyl-L-lysine(9) demethylase PHF8)
1.14.11.27,1.14.11.65, Homo sapiens
Cleft Lip,Cleft Lip/Palate,X-Linked Intellectual Disability, Siderius Type,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Van Der Woude Syndrome 1,Disease Of Mental Health,Orofacial Cleft,Non-Syndromic X-Linked Intellectual Disability,Borjeson-Forssman-Lehmann Syndrome,Acute Promyelocytic Leukemia,Kabuki Syndrome 1,Syndromic X-Linked Intellectual Disability,Autism,Syndromic X-Linked Intellectual Disability Siderius Type
3kv4_a Q9UPP1 ENSG00000172943 PHF8 96.60 5.00E-06 6.10E-10 76.30 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
pygo gam CG11518
Protein pygopus (Protein gammy legs)
Drosophila melanogaster
3zpv_k Q9V9W8 96.30 1.40E-05 2.00E-09 50.90 0 0 0 0 1 0 0 0
YPL181W CTI6 SGDID:S000006102
pps Dmel\CG6525 FBgn0082831 PPS SPP Spp spp CG6525 Dmel_CG6525
pps Dmel\CG6525 FBgn0082831 PPS SPP Spp spp CG6525 Dmel_CG6525
3.6.-.- Drosophila melanogaster
5wlf_a Q9VG78 95.90 3.50E-05 5.20E-09 47.10 0 0 0 0 1 0 0 0
YPL181W CTI6 SGDID:S000006102
lid CG9088
Lysine-specific demethylase lid (EC 1.14.11.67) (Histone demethylase lid) (Jumonji/ARID domain-containing protein lid) (Protein little imaginal disks) (Retinoblastoma-binding protein 2 homolog) ([histone H3]-trimethyl-L-lysine(4) demethylase lid)
1.14.11.67 Drosophila melanogaster
2miq_a Q9VMJ7 96.40 1.10E-05 1.40E-09 57.50 0 0 0 0 1 0 0 0
YPL181W CTI6 SGDID:S000006102
PYGO1
Pygopus homolog 1
Homo sapiens
Desmoid Disease, Hereditary
2vpb_a Q9Y3Y4 ENSG00000171016 PYGO1 96.30 1.30E-05 1.80E-09 51.90 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
YNG1 YOR064C YOR29-15
Protein YNG1 (ING1 homolog 1)
Saccharomyces cerevisiae
2jmj_a Q08465 96.10 2.60E-05 3.00E-09 57.70 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
EBS At4g22140 F1N20.240
Chromatin remodeling protein EBS (Protein EARLY BOLTING IN SHORT DAYS)
Arabidopsis thaliana
5z8l_a F4JL28 96.60 5.00E-06 6.20E-10 69.70 0 0 0 0 0 0 1 0
YPL181W CTI6 SGDID:S000006102
100775247 GLYMA_18G285900
100775247 GLYMA_18G285900
Glycine max
5vab_a I1N521 95.00 0.00024 3.70E-08 41.50 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KMT2D ALR MLL2 MLL4
Histone-lysine N-methyltransferase 2D (Lysine N-methyltransferase 2D) (EC 2.1.1.354) (ALL1-related protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 2)
2.1.1.354 Homo sapiens
Charge Syndrome,Plasma Cell Neoplasm,Cold Agglutinin Disease,Kleefstra Syndrome,Cavernous Sinus Meningioma,Rasopathy,Holoprosencephaly,Hypoplastic Left Heart Syndrome,Leukemia, Acute Myeloid,Dandy-Walker Syndrome,Rubinstein Taybi Like Syndrome,Breast Malignant Phyllodes Tumor,Microphthalmia,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Complement Component C1s Deficiency,Chromosome 16p13.3 Deletion Syndrome, Proximal,Mental Retardation, Autosomal Dominant 26,Childhood Medulloblastoma,Lung Squamous Cell Carcinoma,Smith-Magenis Syndrome,Spinocerebellar Ataxia 2,Tetralogy Of Fallot,Peripheral T-Cell Lymphoma,Congenital Disorder Of Glycosylation, Type Ig,Autism Spectrum Disorder,Lymphoma,Kabuki Syndrome 1,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Scoliosis,Autosomal Dominant Non-Syndromic Intellectual Disability,Myeloma, Multiple,Medulloblastoma,Isolated Growth Hormone Deficiency Type Iii,Postaxial Acrofacial Dysostosis
6o7g_b O14686 ENSG00000167548 KMT2D 96.50 5.20E-06 7.40E-10 52.80 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
PHF2 CENP-35 KIAA0662
Lysine-specific demethylase PHF2 (EC 1.14.11.-) (GRC5) (PHD finger protein 2)
1.14.11.- Homo sapiens
Dissociative Disorder,Culler-Jones Syndrome
3kqi_a O75151 ENSG00000197724 PHF2 95.90 4.30E-05 6.40E-09 48.60 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
BRD1 BRL BRPF2
Bromodomain-containing protein 1 (BR140-like protein) (Bromodomain and PHD finger-containing protein 2)
Homo sapiens
Tuberculum Sellae Meningioma,Griscelli Syndrome, Type 3,Ohdo Syndrome, Sbbys Variant,Sella Turcica Neoplasm,Schizophrenia,Ohdo Syndrome
2l43_a O95696 ENSG00000100425 BRD1 96.20 1.90E-05 2.40E-09 55.30 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
SP100
Nuclear autoantigen Sp-100 (Nuclear dot-associated Sp100 protein) (Speckled 100 kDa)
Homo sapiens
Viral Infectious Disease,Chronic Cholangitis,Cholangitis,Autoimmune Cholangitis,Primary Biliary Cholangitis,Herpes Simplex,Cholangitis, Primary Sclerosing,Acute Promyelocytic Leukemia,Autoimmune Disease Of Gastrointestinal Tract,Crest Syndrome,Bjornstad Syndrome
5pwf_a P23497 ENSG00000067066 SP100 95.60 8.90E-05 1.20E-08 57.10 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KDM5A JARID1A RBBP2 RBP2
Lysine-specific demethylase 5A (EC 1.14.11.67) (Histone demethylase JARID1A) (Jumonji/ARID domain-containing protein 1A) (Retinoblastoma-binding protein 2) (RBBP-2) ([histone H3]-trimethyl-L-lysine(4) demethylase 5A)
1.14.11.67 Homo sapiens
Leukemia, Acute Myeloid,Acute Megakaryoblastic Leukemia Without Down Syndrome,Acute Megakaryocytic Leukemia,Meier-Gorlin Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Retinoblastoma,Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type,Childhood Acute Myeloid Leukemia
2kgi_a P29375 ENSG00000073614 KDM5A 95.90 3.60E-05 5.20E-09 46.10 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
SET3 YKR029C
SET domain-containing protein 3
Saccharomyces cerevisiae
5tdr_a P36124 96.90 1.40E-06 1.90E-10 56.80 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
YNG2 EAF4 NBN1 YHR090C
Chromatin modification-related protein YNG2 (ESA1-associated factor 4) (ING1 homolog 2)
Saccharomyces cerevisiae
2mum_a P38806 95.00 0.00026 3.80E-08 41.50 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1
Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.354) (ALL-1) (CXXC-type zinc finger protein 7) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)]
2.1.1.354 Homo sapiens
Childhood Acute Lymphocytic Leukemia,Lymphoblastic Lymphoma,Hypertrichosis,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Cornelia De Lange Syndrome,Leukemia, Chronic Myeloid,Acute Myeloid Leukemia With T(9;11)(P22;Q23),B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Rare Genetic Intellectual Disability,Myeloproliferative Neoplasm,Leukemia,Pancytopenia,Mixed Phenotype Acute Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With 11q23 Abnormalities,Intravascular Large B-Cell Lymphoma,Familial Isolated Trichomegaly,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Ring Chromosome 21,Acute Megakaryoblastic Leukemia Without Down Syndrome,Rubinstein Taybi Like Syndrome,Central Nervous System Leukemia,Monocytic Leukemia,Ring Chromosome,Myeloid Sarcoma,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Acute Monoblastic Leukemia,Colon Leiomyoma,Cytogenetically Normal Acute Myeloid Leukemia,Microcephaly,Hypoxia,Chronic Granulomatous Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Leukemia, Acute Lymphoblastic 3,Disease Of Mental Health,Cornelia De Lange Syndrome 1,Lymphoma, Non-Hodgkin, Familial,Wiedemann-Steiner Syndrome,Myelodysplastic Syndrome,Hairy Elbows,Acute Promyelocytic Leukemia,Wilms Tumor 1,Kabuki Syndrome 1,Kbg Syndrome,Leukemia, Acute Monocytic,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism
2kyu_a Q03164 ENSG00000118058 KMT2A 96.30 1.20E-05 1.70E-09 51.20 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
POPTR_004G159900
POPTR_004G159900
Populus trichocarpa
5znp_a B9H0V2 96.60 4.90E-06 6.00E-10 69.00 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
EP300 P300
Histone acetyltransferase p300 (p300 HAT) (EC 2.3.1.48) (E1A-associated protein p300) (Histone butyryltransferase p300) (EC 2.3.1.-) (Histone crotonyltransferase p300) (EC 2.3.1.-) (Protein 2-hydroxyisobutyryltransferase p300) (EC 2.3.1.-) (Protein lactyltransferas p300) (EC 2.3.1.-) (Protein propionyltransferase p300) (EC 2.3.1.-)
2.3.1.48 Homo sapiens
Flying Phobia,Chromosomal Disease,Uterine Carcinosarcoma,Charge Syndrome,Squamous Cell Carcinoma,Retinitis Pigmentosa,Cornelia De Lange Syndrome,Cockayne Syndrome A,T-Cell Lymphoblastic Leukemia/Lymphoma,Amelogenesis Imperfecta,Rare Genetic Intellectual Disability,Menke-Hennekam Syndrome,Leukemia, Acute Myeloid,Familial Isolated Hypoparathyroidism,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Human T-Cell Leukemia Virus Type 1,Human T-Cell Leukemia Virus Type 2,Monocytic Leukemia,Cockayne Syndrome,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Microphthalmia,Colorectal Cancer,Microcephaly,Hypoxia,Polydactyly, Postaxial, Type A1,Alacrima, Achalasia, And Mental Retardation Syndrome,Sarcoma,Fibrosarcoma,Prostate Cancer,Disease Of Mental Health,Rubinstein-Taybi Syndrome 2,Cervical Cancer,Chromosome 3pter-P25 Deletion Syndrome,Chromosome 16p13.3 Deletion Syndrome, Proximal,Retinoblastoma,Type 2 Diabetes Mellitus,Rubinstein-Taybi Syndrome 1,Lynch Syndrome,Lung Squamous Cell Carcinoma,Albinism, Ocular, With Late-Onset Sensorineural Deafness,Bladder Urothelial Carcinoma,Neural Tube Defects,Menke-Hennekam Syndrome 2,Esophageal Cancer,Thumb Deformity,Early Infantile Epileptic Encephalopathy,Diffuse Large B-Cell Lymphoma,Gastrointestinal Stromal Tumor,Holt-Oram Syndrome,Huntington Disease,Congenital Disorder Of Glycosylation, Type Ig,Kabuki Syndrome 1,Leukemia, Acute Monocytic,Amelogenesis Imperfecta, Type Ig,Autosomal Dominant Non-Syndromic Intellectual Disability,Otopalatodigital Syndrome, Type I,Hennekam Syndrome,Chromosomal Deletion Syndrome,Nut Midline Carcinoma,Medulloblastoma,Leigh Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability 19,Lung Cancer,Pancreatic Cancer
6gyt_a Q09472 ENSG00000100393 EP300 95.80 6.00E-05 7.90E-09 58.00 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
BPTF FAC1 FALZ
Nucleosome-remodeling factor subunit BPTF (Bromodomain and PHD finger-containing transcription factor) (Fetal Alz-50 clone 1 protein) (Fetal Alzheimer antigen)
Homo sapiens
Seizure Disorder,Alzheimer Disease,Non-Specific Syndromic Intellectual Disability,17q24.2 Microdeletion Syndrome,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Neurodevelopmental Disorder With Dysmorphic Facies And Distal Limb Anomalies,Disease Of Mental Health,Legius Syndrome,Autism
2fui_a Q12830 ENSG00000171634 BPTF 96.10 2.20E-05 3.40E-09 47.60 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
SP140 LYSP100
Nuclear body protein SP140 (Lymphoid-restricted homolog of Sp100) (LYSp100) (Nuclear autoantigen Sp-140) (Speckled 140 kDa)
Homo sapiens
Hepatic Veno-Occlusive Disease,Crohn'S Disease,Multiple Sclerosis,Hepatic Venoocclusive Disease With Immunodeficiency,Acute Promyelocytic Leukemia
2md7_b Q13342 ENSG00000079263 SP140 95.40 0.00012 1.80E-08 44.60 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
SHPRH KIAA2023
E3 ubiquitin-protein ligase SHPRH (EC 2.3.2.27) (EC 3.6.4.-) (RING-type E3 ubiquitin transferase SHPRH) (SNF2, histone-linker, PHD and RING finger domain-containing helicase)
2.3.2.27 Homo sapiens
Xeroderma Pigmentosum, Variant Type
2m85_a Q149N8 ENSG00000146414 SHPRH 96.60 4.90E-06 6.70E-10 55.20 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
Pcl CG5109
Polycomb protein Pcl (Polycomblike protein)
Drosophila melanogaster
5oqd_c Q24459 96.30 1.40E-05 1.50E-09 68.50 0 0 0 0 1 0 0 0
YPL181W CTI6 SGDID:S000006102
Taf3
Transcription initiation factor TFIID subunit 3 (140 kDa TATA box-binding protein-associated factor) (TBP-associated factor 3) (Transcription initiation factor TFIID 140 kDa subunit) (TAF(II)140) (TAF140) (TAFII-140) (TAFII140)
Mus musculus
2k17_a Q5HZG4 95.30 0.00016 2.30E-08 46.20 0 0 1 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
TAF3
Transcription initiation factor TFIID subunit 3 (140 kDa TATA box-binding protein-associated factor) (TBP-associated factor 3) (Transcription initiation factor TFIID 140 kDa subunit) (TAF(II)140) (TAF140) (TAFII-140) (TAFII140)
Homo sapiens
Lateral Meningocele Syndrome
5wxh_a Q5VWG9 ENSG00000165632 TAF3 95.60 8.00E-05 1.20E-08 44.80 1 1 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
SIZ1 Os05g0125000 LOC_Os05g03430 OSJNBb0079L11.3
E3 SUMO-protein ligase SIZ1 (EC 2.3.2.-) (E3 SUMO-protein transferase SIZ1)
2.3.2.- Oryza sativa
2rsd_a Q6L4L4 96.50 7.10E-06 9.40E-10 54.70 0 0 0 0 0 0 0 0
YPL181W CTI6 SGDID:S000006102
BCL9L DLNB11
B-cell CLL/lymphoma 9-like protein (B-cell lymphoma 9-like protein) (BCL9-like protein) (Protein BCL9-2)
Homo sapiens
Acinar Cell Cystadenocarcinoma
2xb1_c Q86UU0 ENSG00000186174 BCL9L 96.30 1.60E-05 2.00E-09 57.60 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab