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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YBR081C | SPT7 | SGDID:S000000285 | SMARCA4 BAF190A BRG1 SNF2B SNF2L4 |
Transcription activator BRG1 (EC 3.6.4.-) (ATP-dependent helicase SMARCA4) (BRG1-associated factor 190A) (BAF190A) (Mitotic growth and transcription activator) (Protein BRG-1) (Protein brahma homolog 1) (SNF2-beta) (SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 4) |
3.6.4.- | Homo sapiens | Juvenile Type Testicular Granulosa Cell Tumor,Ventricular Septal Defect,Spinal Meningioma,Heart Disease,Ovarian Small Cell Carcinoma,Spinal Canal And Spinal Cord Meningioma,Charge Syndrome,Lymphosarcoma,Hypertrichosis,Atrial Heart Septal Defect,Smarca4-Deficient Sarcoma Of Thorax,Cerebral Palsy,Homozygous Familial Hypercholesterolemia,Atypical Teratoid Rhabdoid Tumor,Amyotrophic Lateral Sclerosis 1,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Developmental And Epileptic Encephalopathy 14,Infratentorial Cancer,Alpha Thalassemia-X-Linked Intellectual Disability Syndrome,Small-Cell Carcinoma Of The Ovary Of Hypercalcemic Type,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Oculopharyngeal Muscular Dystrophy,Ovarian Clear Cell Adenocarcinoma,Testicular Granulosa Cell Tumor,Clear Cell Adenofibroma,Cockayne Syndrome,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Breast Cancer,Microphthalmia,Rhabdoid Tumor Predisposition Syndrome 2,Familial Hypercholesterolemia,Hepatocellular Carcinoma,Endometrioid Ovary Carcinoma,Microcephaly,Neurilemmomatosis,Rhabdomyosarcoma,Clark-Baraitser Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Cleft Palate, Isolated,Gastric Cancer,Disease Of Mental Health,Choroid Plexus Cancer,Alpha-Thalassemia,Rhabdoid Cancer,Kidney Rhabdoid Cancer,Chromosome 16p13.3 Deletion Syndrome, Proximal,Retinoblastoma,Orofacial Cleft 8,Childhood Medulloblastoma,Adiaspiromycosis,Basan Syndrome,Neural Tube Defects,Strabismus,Coffin-Siris Syndrome 1,Floating-Harbor Syndrome,Schimke Immunoosseous Dysplasia,Small Cell Carcinoma,Tumor Predisposition Syndrome,Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations,Acute Promyelocytic Leukemia,Hypercholesterolemia, Familial, 1,Non-Syndromic Intellectual Disability,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Coffin-Siris Syndrome 4,Congenital Disorder Of Glycosylation, Type Ig,Autism Spectrum Disorder,Cartilage-Hair Hypoplasia,Kabuki Syndrome 1,Uv-Sensitive Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Medulloblastoma,Neuroblastoma 1,Lung Cancer,Epilepsy, Familial Temporal Lobe, 1,Hyperoxaluria, Primary, Type I |
6hr2_e | P51532 | ENSG00000127616 | SMARCA4 | 98.60 | 3.90E-12 | 5.20E-16 | 107.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | ATAD2 L16 PRO2000 |
ATPase family AAA domain-containing protein 2 (EC 3.6.1.-) (AAA nuclear coregulator cancer-associated protein) (ANCCA) |
3.6.1.- | Homo sapiens | Breast Cancer,Gastric Cancer,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly |
5f36_a | Q6PL18 | ENSG00000156802 | ATAD2 | 98.50 | 3.00E-11 | 3.70E-15 | 105.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | Kat2b Pcaf |
Histone acetyltransferase KAT2B (EC 2.3.1.48) (Histone acetyltransferase PCAF) (Histone acetylase PCAF) (Lysine acetyltransferase 2B) (P300/CBP-associated factor) (P/CAF) (Spermidine acetyltransferase KAT2B) (EC 2.3.1.57) |
2.3.1.48,2.3.1.57, | Mus musculus | 5ml0_a | Q9JHD1 | 98.70 | 3.20E-12 | 4.30E-16 | 104.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YBR081C | SPT7 | SGDID:S000000285 | BRD3 KIAA0043 RING3L |
Bromodomain-containing protein 3 (RING3-like protein) |
Homo sapiens | Leukemia, Acute Myeloid,Salivary Gland Disease,Intestinal Botulism,Foodborne Botulism,Wound Botulism,Infant Botulism,Salivary Gland Carcinoma,Nut Midline Carcinoma |
2e7n_a | Q15059 | ENSG00000169925 | BRD3 | 98.60 | 4.10E-12 | 5.50E-16 | 106.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | PF3D7_1475600 |
PF3D7_1475600 |
Plasmodium falciparum | 5vs7_a | Q8IK82 | 98.70 | 1.30E-12 | 1.70E-16 | 109.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | 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 | 98.60 | 6.10E-12 | 8.20E-16 | 113.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | LDBPK_363130 |
LDBPK_363130 |
Leishmania donovani | 5c4q_a | E9BU22 | 98.70 | 1.20E-12 | 1.60E-16 | 112.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BRD2 KIAA9001 RING3 |
Bromodomain-containing protein 2 (O27.1.1) (Really interesting new gene 3 protein) |
Homo sapiens | Epilepsy,Leukemia, Acute Myeloid,Benign Epilepsy With Centrotemporal Spikes,Diamond-Blackfan Anemia 3,Adolescence-Adult Electroclinical Syndrome,Photosensitive Epilepsy,Nut Midline Carcinoma,Epilepsy, Myoclonic Juvenile,Epilepsy, Idiopathic Generalized |
2dvq_a | P25440 | ENSG00000204256 | BRD2 | 98.80 | 9.50E-13 | 1.20E-16 | 111.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | cgd4_650 |
cgd4_650 |
Cryptosporidium parvum | 6mf9_b | Q5CQH9 | 98.70 | 2.70E-12 | 3.30E-16 | 118.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | CECR2 KIAA1740 |
Cat eye syndrome critical region protein 2 |
Homo sapiens | Cat Eye Syndrome,Coloboma Of Macula,Neural Tube Defects |
3nxb_a | Q9BXF3 | ENSG00000099954 | CECR2 | 98.70 | 1.10E-12 | 1.50E-16 | 110.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | TRIM28 KAP1 RNF96 TIF1B |
Transcription intermediary factor 1-beta (TIF1-beta) (E3 SUMO-protein ligase TRIM28) (EC 2.3.2.27) (KRAB-associated protein 1) (KAP-1) (KRAB-interacting protein 1) (KRIP-1) (Nuclear corepressor KAP-1) (RING finger protein 96) (RING-type E3 ubiquitin transferase TIF1-beta) (Tripartite motif-containing protein 28) |
2.3.2.27 | Homo sapiens | Wilms Tumor 5,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Breast Medullary Carcinoma,Colorectal Cancer,Wilms Tumor 1,Transient Neonatal Diabetes Mellitus,Hyperoxaluria, Primary, Type I |
2ro1_a | Q13263 | ENSG00000130726 | TRIM28 | 98.40 | 5.60E-11 | 7.40E-15 | 107.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | PF3D7_0823300 |
PF3D7_0823300 |
2.3.1.48 | Plasmodium falciparum | 4qns_b | Q8IB67 | 98.70 | 1.20E-12 | 1.70E-16 | 107.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YBR081C | SPT7 | SGDID:S000000285 | BAZ2B KIAA1476 |
Bromodomain adjacent to zinc finger domain protein 2B (hWALp4) |
Homo sapiens | Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome |
4qc3_a | Q9UIF8 | ENSG00000226266 | BAZ2B | 98.70 | 2.80E-12 | 3.80E-16 | 104.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | TbgDal_XI11310 |
TbgDal_XI11310 |
Trypanosoma brucei | 5c8g_a | D0A8L1 | 98.90 | 1.80E-13 | 2.40E-17 | 119.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BDF1 CAALFM_C500200CA CaO19.8593 CaO19.978 |
Bromodomain-containing factor 1 |
Candida albicans | 5n13_a | Q5A4W8 | 98.60 | 3.90E-12 | 5.20E-16 | 105.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | KAT2A GCN5 GCN5L2 |
Histone acetyltransferase KAT2A (EC 2.3.1.48) (General control of amino acid synthesis protein 5-like 2) (Histone acetyltransferase GCN5) (hGCN5) (Histone glutaryltransferase KAT2A) (EC 2.3.1.-) (Histone succinyltransferase KAT2A) (EC 2.3.1.-) (Lysine acetyltransferase 2A) (STAF97) |
2.3.1.48 | Homo sapiens | Amyotrophic Lateral Sclerosis 1,Spinocerebellar Ataxia 7,Chromosome 16p13.3 Deletion Syndrome, Proximal |
1f68_a | Q92830 | ENSG00000108773 | KAT2A | 98.80 | 9.70E-13 | 1.30E-16 | 107.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | TAF1 BA2R CCG1 CCGS TAF2A |
Transcription initiation factor TFIID subunit 1 (EC 2.3.1.48) (EC 2.7.11.1) (Cell cycle gene 1 protein) (TBP-associated factor 250 kDa) (p250) (Transcription initiation factor TFIID 250 kDa subunit) (TAF(II)250) (TAFII-250) (TAFII250) |
2.3.1.48,2.7.11.1, | Homo sapiens | Parkinsonism,Movement Disease,Blepharospasm,Dystonia,Parkinson Disease, Late-Onset,Disease Of Mental Health,Retinoblastoma,Dystonia, Dopa-Responsive,Dystonia 12,Mental Retardation, X-Linked, Syndromic 33,Alternating Hemiplegia Of Childhood,Focal Dystonia,Multifocal Dystonia,Segmental Dystonia,Hemidystonia,Huntington Disease,Syndromic Intellectual Disability,Lymphatic Malformation 5,Rett Syndrome,Dystonia 3, Torsion, X-Linked,Hereditary Lymphedema Ii |
5i29_a | P21675 | ENSG00000147133 | TAF1 | 98.90 | 3.10E-13 | 3.90E-17 | 120.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | 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 |
5bt3_a | Q09472 | ENSG00000100393 | EP300 | 98.50 | 1.50E-11 | 2.00E-15 | 103.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | Pbrm1 Baf180 Pb1 |
Protein polybromo-1 (BRG1-associated factor 180) (BAF180) |
Mus musculus | 2yqd_a | Q8BSQ9 | 98.70 | 1.40E-12 | 1.90E-16 | 109.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BAZ1A ACF1 WCRF180 HSPC317 |
Bromodomain adjacent to zinc finger domain protein 1A (ATP-dependent chromatin-remodeling protein) (ATP-utilizing chromatin assembly and remodeling factor 1) (hACF1) (CHRAC subunit ACF1) (Williams syndrome transcription factor-related chromatin-remodeling factor 180) (WCRF180) (hWALp1) |
Homo sapiens | Charge Syndrome,Robinow Syndrome, Autosomal Recessive 1,Chromosome 14q11-Q22 Deletion Syndrome,Vacterl Association,Schimke Immunoosseous Dysplasia,Vater/Vacterl Association,Baraitser-Winter Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability |
5uiy_a | Q9NRL2 | ENSG00000198604 | BAZ1A | 98.70 | 1.30E-12 | 1.70E-16 | 110.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | cgd2_2690 |
cgd2_2690 |
Cryptosporidium parvum | 6cw0_a | A3FQ86 | 98.60 | 4.00E-12 | 5.40E-16 | 104.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | Tb10.6k15.2370 |
Tb10.6k15.2370 |
Trypanosoma brucei | 5ko4_b | Q38AE9 | 98.60 | 6.00E-12 | 8.10E-16 | 103.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | PHIP DCAF14 WDR11 |
PH-interacting protein (PHIP) (DDB1- and CUL4-associated factor 14) (IRS-1 PH domain-binding protein) (WD repeat-containing protein 11) |
Homo sapiens | Melanoma,Phimosis,Chung-Jansen Syndrome,Syndromic Intellectual Disability,Autosomal Dominant Non-Syndromic Intellectual Disability |
5enc_a | Q8WWQ0 | ENSG00000146247 | PHIP | 98.70 | 2.60E-12 | 3.40E-16 | 111.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | BRD4 HUNK1 |
Bromodomain-containing protein 4 (Protein HUNK1) |
Homo sapiens | Cornelia De Lange Syndrome,Lymphoepithelioma-Like Thymic Carcinoma,Leukemia, Acute Myeloid,Ureteral Obstruction,T-Cell Acute Lymphoblastic Leukemia,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Cornelia De Lange Syndrome 1,Ewing Sarcoma,Acute Promyelocytic Leukemia,Kbg Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Medulloblastoma |
2mjv_b | O60885 | ENSG00000141867 | BRD4 | 98.50 | 1.70E-11 | 2.20E-15 | 106.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | BRPF1 BR140 |
Peregrin (Bromodomain and PHD finger-containing protein 1) (Protein Br140) |
Homo sapiens | Intellectual Developmental Disorder With Dysmorphic Facies And Ptosis,Eyelid Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Ohdo Syndrome, Sbbys Variant,Adult Medulloblastoma,Syndromic Intellectual Disability,Ohdo Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Ptosis |
2rs9_b | P55201 | ENSG00000156983 | BRPF1 | 98.70 | 3.10E-12 | 4.10E-16 | 108.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | TAF8 TAFII43 TBN |
Transcription initiation factor TFIID subunit 8 (Protein taube nuss) (TBP-associated factor 43 kDa) (TBP-associated factor 8) (Transcription initiation factor TFIID 43 kDa subunit) (TAFII-43) (TAFII43) (hTAFII43) |
Homo sapiens | Sjogren-Larsson Syndrome,Microcephaly,Ureterolithiasis,Corpus Callosum, Partial Agenesis Of, X-Linked |
4wv4_b | Q7Z7C8 | ENSG00000137413 | TAF8 | 98.60 | 7.10E-12 | 8.70E-16 | 105.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | BRD7 BP75 CELTIX1 |
Bromodomain-containing protein 7 (75 kDa bromodomain protein) (Protein CELTIX-1) |
Homo sapiens | Granular Cell Carcinoma,Malignant Granular Cell Myoblastoma,Endometrial Adenosquamous Carcinoma,Hepatocellular Carcinoma,Neurilemmomatosis,Rhabdoid Cancer,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly,Autosomal Dominant Non-Syndromic Intellectual Disability |
2i7k_a | Q9NPI1 | ENSG00000166164 | BRD7 | 98.60 | 7.20E-12 | 9.40E-16 | 105.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | C4B63_57g96 |
C4B63_57g96 |
Trypanosoma cruzi | 6nim_b | A0A2V2V5V1 | 98.60 | 4.10E-12 | 5.30E-16 | 107.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | ZMYND11 BRAM1 BS69 |
Zinc finger MYND domain-containing protein 11 (Adenovirus 5 E1A-binding protein) (Bone morphogenetic protein receptor-associated molecule 1) (Protein BS69) |
Homo sapiens | Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly,Mental Retardation, Autosomal Dominant 30,Paragangliomas 5,Fibrodysplasia Ossificans Progressiva,Autism Spectrum Disorder,Ptosis,Autosomal Dominant Non-Syndromic Intellectual Disability |
4ns5_a | Q15326 | ENSG00000015171 | ZMYND11 | 98.00 | 2.00E-09 | 2.40E-13 | 103.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | TAF1L |
Transcription initiation factor TFIID subunit 1-like (TAF(II)210) (TBP-associated factor 1-like) (TBP-associated factor 210 kDa) (Transcription initiation factor TFIID 210 kDa subunit) |
Homo sapiens | Movement Disease,Blepharospasm,Parkinson Disease, Late-Onset,Dystonia, Dopa-Responsive,Dystonia 12,Focal Dystonia,Multifocal Dystonia,Segmental Dystonia,Hemidystonia,Lymphatic Malformation 5,Dystonia 3, Torsion, X-Linked,Hereditary Lymphedema Ii |
3hmh_a | Q8IZX4 | ENSG00000122728 | TAF1L | 98.80 | 9.30E-13 | 1.10E-16 | 120.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | Transcription initiation factor TFIID subunit |
Transcription initiation factor TFIID subunit |
Oryctolagus cuniculus | 6df4_a | U3KMH2 | 99.00 | 3.70E-14 | 4.30E-18 | 132.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | LDBPK_363520 |
LDBPK_363520 |
Leishmania donovani | 5fea_a | E9BU61 | 98.80 | 9.70E-13 | 1.20E-16 | 115.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | SMARCA2 BAF190B BRM SNF2A SNF2L2 |
Probable global transcription activator SNF2L2 (EC 3.6.4.-) (ATP-dependent helicase SMARCA2) (BRG1-associated factor 190B) (BAF190B) (Protein brahma homolog) (hBRM) (SNF2-alpha) (SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 2) |
3.6.4.- | Homo sapiens | Juvenile Type Testicular Granulosa Cell Tumor,Chiari Malformation,Charge Syndrome,Adenoid Cystic Carcinoma,Cornelia De Lange Syndrome,Smarca4-Deficient Sarcoma Of Thorax,Nicolaides-Baraitser Syndrome,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Developmental And Epileptic Encephalopathy 14,Alpha Thalassemia-X-Linked Intellectual Disability Syndrome,Pituitary Stalk Interruption Syndrome,Psychotic Disorder,Testicular Granulosa Cell Tumor,Brain Cancer,Blepharophimosis,Cockayne Syndrome,Primary Hyperoxaluria,Hepatocellular Carcinoma,Microcephaly,Neurilemmomatosis,Clark-Baraitser Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Schizophrenia 7,Xeroderma Pigmentosum, Variant Type,Disease Of Mental Health,Alpha-Thalassemia,Rhabdoid Cancer,Chromosome 16p13.3 Deletion Syndrome, Proximal,Retinoblastoma,Adiaspiromycosis,Basan Syndrome,Schizophrenia,Odontochondrodysplasia,Brachydactyly,Coffin-Siris Syndrome 1,Floating-Harbor Syndrome,Schimke Immunoosseous Dysplasia,Small Cell Carcinoma,Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations,Non-Syndromic Intellectual Disability,Ohdo Syndrome,Cartilage-Hair Hypoplasia,Uv-Sensitive Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Epilepsy, Familial Temporal Lobe, 1 |
2dat_a | P51531 | ENSG00000080503 | SMARCA2 | 98.60 | 3.80E-12 | 4.90E-16 | 108.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | cgd3_3190 |
cgd3_3190 |
Cryptosporidium parvum | 4ldf_a | Q5CUE2 | 98.80 | 6.40E-13 | 8.50E-17 | 111.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BRD9 UNQ3040/PRO9856 |
Bromodomain-containing protein 9 (Rhabdomyosarcoma antigen MU-RMS-40.8) |
Homo sapiens | Chronic Dacryoadenitis,Hereditary Melanoma,Rhabdoid Cancer,Nut Midline Carcinoma |
5i7y_a | Q9H8M2 | ENSG00000028310 | BRD9 | 98.70 | 1.70E-12 | 2.40E-16 | 104.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | 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 |
6g8r_b | Q13342 | ENSG00000079263 | SP140 | 98.50 | 2.20E-11 | 2.90E-15 | 111.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | PF3D7_1033700 |
PF3D7_1033700 |
Plasmodium falciparum | 5ulc_x | Q8IJ72 | 98.80 | 7.50E-13 | 8.90E-17 | 122.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BAZ2A KIAA0314 TIP5 |
Bromodomain adjacent to zinc finger domain protein 2A (Transcription termination factor I-interacting protein 5) (TTF-I-interacting protein 5) (Tip5) (hWALp3) |
Homo sapiens | Inflammatory Spondylopathy,Deficiency Anemia,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly |
4qbm_a | Q9UIF9 | ENSG00000076108 | BAZ2A | 98.70 | 1.20E-12 | 1.60E-16 | 106.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | LDBPK_091320 |
LDBPK_091320 |
Leishmania donovani | 5tck_a | E9BA17 | 98.40 | 6.70E-11 | 7.30E-15 | 111.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | cgd4_1340 |
cgd4_1340 |
Cryptosporidium parvum | 5u9n_a | Q5CQB7 | 98.40 | 8.20E-11 | 8.70E-15 | 110.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | KAT2B PCAF |
Histone acetyltransferase KAT2B (EC 2.3.1.48) (Histone acetyltransferase PCAF) (Histone acetylase PCAF) (Lysine acetyltransferase 2B) (P300/CBP-associated factor) (P/CAF) (Spermidine acetyltransferase KAT2B) (EC 2.3.1.57) |
2.3.1.48,2.3.1.57, | Homo sapiens | Hemangioma Of Spleen,Spinocerebellar Ataxia 7,Microphthalmia,Prostate Cancer,Chromosome 16p13.3 Deletion Syndrome, Proximal,Holt-Oram Syndrome |
1zs5_a | Q92831 | ENSG00000114166 | KAT2B | 98.70 | 1.70E-12 | 2.20E-16 | 109.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | 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 | 98.50 | 2.00E-11 | 2.70E-15 | 109.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | 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 |
2ri7_a | Q12830 | ENSG00000171634 | BPTF | 98.30 | 9.50E-11 | 1.40E-14 | 101.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | PF3D7_0110500 |
PF3D7_0110500 |
Plasmodium falciparum | 4py6_a | Q8I240 | 98.60 | 1.10E-11 | 1.30E-15 | 111.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | BRWD1 C21orf107 WDR9 |
Bromodomain and WD repeat-containing protein 1 (WD repeat-containing protein 9) |
Homo sapiens | Chordoid Meningioma,Premature Menopause,Down Syndrome,Meningioma, Familial,Premature Ovarian Failure 1 |
3q2e_a | Q9NSI6 | ENSG00000185658 | BRWD1 | 98.70 | 2.10E-12 | 2.80E-16 | 109.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | TbgDal_X9100 |
TbgDal_X9100 |
Trypanosoma brucei | 5czg_a | D0A3H5 | 98.70 | 1.10E-12 | 1.50E-16 | 109.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | Tb10.6k15.3240 |
Tb10.6k15.3240 |
Trypanosoma brucei | 2n9g_a | Q38AM1 | 98.70 | 1.20E-12 | 1.60E-16 | 108.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | CREBBP CBP |
CREB-binding protein (Histone lysine acetyltransferase CREBBP) (EC 2.3.1.48) (Protein-lysine acetyltransferase CREBBP) (EC 2.3.1.-) |
2.3.1.48 | Homo sapiens | Adult Hepatocellular Carcinoma,Skin Melanoma,Chromosomal Disease,Dystonia 9,Squamous Cell Carcinoma,Hypertrichosis,Chronic Myelomonocytic Leukemia,Adenoid Cystic Carcinoma,Spasticity,Atrial Heart Septal Defect,Cornelia De Lange Syndrome,Melanoma,Leukemia, Chronic Myeloid,Plasma Cell Neoplasm,Corpus Callosum, Agenesis Of,Amyotrophic Lateral Sclerosis 1,Interatrial Communication,T-Cell Lymphoblastic Leukemia/Lymphoma,Rare Genetic Intellectual Disability,Pectus Carinatum,Motor Neuron Disease,Leukemia,Neonatal Leukemia,Acute Leukemia,Menke-Hennekam Syndrome,Leukemia, Acute Myeloid,Familial Isolated Trichomegaly,Basal Cell Carcinoma,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Machado-Joseph Disease,Human T-Cell Leukemia Virus Type 1,Human T-Cell Leukemia Virus Type 2,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Acute Myeloid Leukemia With T(8;16)(P11;P13) Translocation,Hair Follicle Neoplasm,Myeloid Leukemia,Meningoencephalitis,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Gliosarcoma,Giant Cell Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Tethered Spinal Cord Syndrome,Microcephaly,Hypoxia,Chromosome 16p13.3 Duplication Syndrome,Central Nervous System Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Prostate Cancer,Disease Of Mental Health,Cervical Cancer,Dentatorubral-Pallidoluysian Atrophy,Chromosome 16p13.3 Deletion Syndrome, Proximal,Retinoblastoma,Gastric Adenocarcinoma,Rubinstein-Taybi Syndrome 1,Lung Squamous Cell Carcinoma,Bladder Urothelial Carcinoma,Beckwith-Wiedemann Syndrome,Menke-Hennekam Syndrome 1,Intraocular Pressure Quantitative Trait Locus,Floating-Harbor Syndrome,Myelodysplastic Syndrome,Thumb Deformity,Diffuse Large B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Hirschsprung Disease 1,Huntington Disease,Wilms Tumor 1,Meningioma, Familial,Phonagnosia,Kabuki Syndrome 1,Scoliosis,Leukemia, Acute Monocytic,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Otopalatodigital Syndrome, Type I,Hennekam Syndrome,Chromosomal Deletion Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Medulloblastoma,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Autism |
5i86_b | Q92793 | ENSG00000005339 | CREBBP | 98.60 | 7.50E-12 | 1.00E-15 | 104.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | 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 |
5fg6_a | O95696 | ENSG00000100425 | BRD1 | 98.60 | 4.90E-12 | 6.50E-16 | 108.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | RSC4 YKR008W YK107 |
Chromatin structure-remodeling complex subunit RSC4 (RSC complex subunit RSC4) (Remodel the structure of chromatin complex subunit 4) |
Saccharomyces cerevisiae | 2r0s_a | Q02206 | 98.30 | 9.50E-11 | 1.10E-14 | 117.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | PBRM1 BAF180 PB1 |
Protein polybromo-1 (hPB1) (BRG1-associated factor 180) (BAF180) (Polybromo-1D) |
Homo sapiens | Spinal Meningioma,Epithelioid Sarcoma,Spinal Canal And Spinal Cord Meningioma,Chromophil Adenoma Of The Kidney,Chordoma,Clear Cell Papillary Renal Cell Carcinoma,Collecting Duct Carcinoma,Clear Cell Renal Cell Carcinoma,Chromophobe Renal Cell Carcinoma,Intrahepatic Cholangiocarcinoma,Kidney Cancer,Clear Cell Adenofibroma,Neurilemmomatosis,Deafness, Autosomal Recessive 51,Contractural Arachnodactyly, Congenital,Rhabdoid Cancer,Renal Cell Carcinoma, Papillary, 1,Distal Arthrogryposis,Renal Cell Carcinoma, Nonpapillary,Uterine Corpus Endometrial Carcinoma,Autosomal Dominant Non-Syndromic Intellectual Disability,Melanoma, Uveal |
2ktb_b | Q86U86 | ENSG00000163939 | PBRM1 | 98.60 | 6.40E-12 | 8.50E-16 | 106.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR081C | SPT7 | SGDID:S000000285 | ASH1L KIAA1420 KMT2H |
Histone-lysine N-methyltransferase ASH1L (EC 2.1.1.359) (EC 2.1.1.367) (ASH1-like protein) (huASH1) (Absent small and homeotic disks protein 1 homolog) (Lysine N-methyltransferase 2H) |
2.1.1.359 | Homo sapiens | Facioscapulohumeral Muscular Dystrophy 1,Sotos Syndrome 1,Pulpitis,Mental Retardation, Autosomal Dominant 52,Autism Spectrum Disorder,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism |
3mqm_b | Q9NR48 | ENSG00000116539 | ASH1L | 98.50 | 1.90E-11 | 2.40E-15 | 104.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YBR081C | SPT7 | SGDID:S000000285 | C4B63_1g51 |
C4B63_1g51 |
Trypanosoma cruzi | 6ney_a | A0A2V2W6E9 | 98.50 | 3.10E-11 | 3.80E-15 | 106.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | Tb11.01.5000 |
Tb11.01.5000 |
Trypanosoma brucei | 5k29_b | Q382J7 | 98.40 | 4.00E-11 | 5.10E-15 | 103.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | Zmynd11 |
Zinc finger MYND domain-containing protein 11 |
Mus musculus | 4n4g_a | Q8R5C8 | 98.20 | 2.40E-10 | 2.80E-14 | 112.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YBR081C | SPT7 | SGDID:S000000285 | TRIM24 RNF82 TIF1 TIF1A |
Transcription intermediary factor 1-alpha (TIF1-alpha) (EC 2.3.2.27) (E3 ubiquitin-protein ligase TRIM24) (RING finger protein 82) (RING-type E3 ubiquitin transferase TIF1-alpha) (Tripartite motif-containing protein 24) |
2.3.2.27 | Homo sapiens | Cerebellar Agenesis,Differentiated Thyroid Carcinoma,Breast Cancer,8p11 Myeloproliferative Syndrome,Adult Dermatomyositis,Childhood Type Dermatomyositis,Lung Squamous Cell Carcinoma |
2yyn_b | O15164 | ENSG00000122779 | TRIM24 | 98.60 | 5.00E-12 | 6.40E-16 | 110.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |