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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YJR119C | JHD2 | SGDID:S000003880 | JMJ14 JMJ4 PKDM7B At4g20400 F9F13.50 |
Probable lysine-specific demethylase JMJ14 (EC 1.14.11.-) (Jumonji domain-containing protein 14) (Jumonji domain-containing protein 4) (Lysine-specific histone demethylase JMJ14) (Protein JUMONJI 14) |
1.14.11.- | Arabidopsis thaliana | 5ykn_a | Q8GUI6 | 100.00 | 1.20E-53 | 9.40E-58 | 485.60 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YJR119C | JHD2 | SGDID:S000003880 | KDM6A UTX |
Lysine-specific demethylase 6A (EC 1.14.11.68) (Histone demethylase UTX) (Ubiquitously-transcribed TPR protein on the X chromosome) (Ubiquitously-transcribed X chromosome tetratricopeptide repeat protein) ([histone H3]-trimethyl-L-lysine(27) demethylase 6A) |
1.14.11.68 | Homo sapiens | Charge Syndrome,Chronic Myelomonocytic Leukemia,Kleefstra Syndrome,Leukemia, Acute Myeloid,T-Cell Acute Lymphoblastic Leukemia,Microphthalmia,Adhesions Of Uterus,Weaver Syndrome,Sotos Syndrome 1,Turner Syndrome,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Bartholin'S Gland Carcinoma,Kabuki Syndrome 2,Form Agnosia,Kabuki Syndrome 1,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Scoliosis,Autosomal Dominant Non-Syndromic Intellectual Disability,Medulloblastoma |
6ful_a | O15550 | ENSG00000147050 | KDM6A | 99.90 | 5.90E-31 | 4.60E-35 | 297.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | Kdm6b Jmjd3 Kiaa0346 |
Lysine-specific demethylase 6B (EC 1.14.11.68) (JmjC domain-containing protein 3) (Jumonji domain-containing protein 3) ([histone H3]-trimethyl-L-lysine(27) demethylase 6B) |
1.14.11.68 | Mus musculus | 4eyu_a | Q5NCY0 | 99.90 | 5.90E-29 | 4.80E-33 | 278.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YJR119C | JHD2 | SGDID:S000003880 | ARID1A BAF250 BAF250A C1orf4 OSA1 SMARCF1 |
AT-rich interactive domain-containing protein 1A (ARID domain-containing protein 1A) (B120) (BRG1-associated factor 250) (BAF250) (BRG1-associated factor 250a) (BAF250A) (Osa homolog 1) (hOSA1) (SWI-like protein) (SWI/SNF complex protein p270) (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin subfamily F member 1) (hELD) |
Homo sapiens | Uterine Body Mixed Cancer,Ovarian Carcinosarcoma,Ovarian Small Cell Carcinoma,Endometrial Cancer,Endometriosis Of Ovary,Hypertrichosis,Seizure Disorder,Endometrial Hyperplasia,Uterine Corpus Cancer,Clear Cell Renal Cell Carcinoma,Clear Cell Adenocarcinoma,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Cholangiolocellular Carcinoma,Intrahepatic Cholangiocarcinoma,Adenofibroma,Periventricular Leukomalacia,Ovarian Clear Cell Adenocarcinoma,Small Intestine Cancer,Brain Cancer,Clear Cell Adenofibroma,Ovarian Cancer,Female Reproductive Endometrioid Cancer,Colorectal Cancer,Endometrial Serous Adenocarcinoma,Serous Cystadenocarcinoma,Hepatocellular Carcinoma,Endometrioid Ovary Carcinoma,Fallopian Tube Endometrioid Adenocarcinoma,Microcephaly,Neurilemmomatosis,Clark-Baraitser Syndrome,Fanconi Anemia, Complementation Group A,Gastric Cancer,Ovarian Cystadenocarcinoma,Mixed Cell Type Cancer,Rhabdoid Cancer,Ovary Adenocarcinoma,Lung Squamous Cell Carcinoma,Coffin-Siris Syndrome 1,Non-Syndromic Intellectual Disability,Ovarian Clear Cell Carcinoma,Uterine Corpus Endometrial Carcinoma,Coffin-Siris Syndrome 2,Autosomal Dominant Non-Syndromic Intellectual Disability,Medulloblastoma,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay |
1ryu_a | O14497 | ENSG00000117713 | ARID1A | 99.50 | 5.40E-18 | 4.40E-22 | 152.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJR119C | JHD2 | SGDID:S000003880 | 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 |
2wwu_a | Q9UPP1 | ENSG00000172943 | PHF8 | 99.40 | 1.20E-17 | 9.50E-22 | 179.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | RPH1 YER169W |
DNA damage-responsive transcriptional repressor RPH1 |
Saccharomyces cerevisiae | 3opt_a | P39956 | 100.00 | 3.40E-39 | 2.60E-43 | 348.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJR119C | JHD2 | SGDID:S000003880 | ARID5B DESRT MRF2 |
AT-rich interactive domain-containing protein 5B (ARID domain-containing protein 5B) (MRF1-like protein) (Modulator recognition factor 2) (MRF-2) |
Homo sapiens | Childhood Acute Lymphocytic Leukemia,Childhood B-Cell Acute Lymphoblastic Leukemia,Adenoid Cystic Carcinoma,B-Lymphoblastic Leukemia/Lymphoma With Etv6-Runx1,Childhood Leukemia,Leukemia, Acute Lymphoblastic |
1ig6_a | Q14865 | 99.30 | 4.20E-16 | 3.20E-20 | 136.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YJR119C | JHD2 | SGDID:S000003880 | 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 | 99.90 | 7.90E-31 | 6.20E-35 | 296.30 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
YJR119C | JHD2 | SGDID:S000003880 | SWI1 ADR6 GAM3 YPL016W LPA1 |
SWI/SNF chromatin-remodeling complex subunit SWI1 (Regulatory protein GAM3) (SWI/SNF complex subunit SWI1) (Transcription regulatory protein ADR6) (Transcription regulatory protein SWI1) |
Saccharomyces cerevisiae | 2li6_a | P09547 | 99.30 | 1.30E-16 | 1.10E-20 | 142.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJR119C | JHD2 | SGDID:S000003880 | ARID1B BAF250B DAN15 KIAA1235 OSA2 |
AT-rich interactive domain-containing protein 1B (ARID domain-containing protein 1B) (BRG1-associated factor 250b) (BAF250B) (BRG1-binding protein hELD/OSA1) (Osa homolog 2) (hOsa2) (p250R) |
Homo sapiens | Spinal Meningioma,Uterine Body Mixed Cancer,Apert Syndrome,Spinal Canal And Spinal Cord Meningioma,Saethre-Chotzen Syndrome,Pfeiffer Syndrome,Hypertrichosis,Speech Disorder,Cornelia De Lange Syndrome,Constipation,Nicolaides-Baraitser Syndrome,Corpus Callosum, Agenesis Of,Chromosome 6q24-Q25 Deletion Syndrome,Rare Genetic Intellectual Disability,Pituitary Stalk Interruption Syndrome,Familial Isolated Trichomegaly,Arid1b-Related Disorder,Capillary Hemangioma,Hypermobile Ehlers-Danlos Syndrome,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Trichohepatoenteric Syndrome 1,Blepharophimosis,Hepatocellular Carcinoma,Endometrioid Ovary Carcinoma,Microcephaly,Neurilemmomatosis,Dysphagia,Muenke Syndrome,Clark-Baraitser Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Jackson-Weiss Syndrome,Crouzon Syndrome,Rhabdoid Cancer,Wiedemann-Steiner Syndrome,Nail Disorder, Nonsyndromic Congenital, 9,Coffin-Siris Syndrome 1,Torticollis,Trichomegaly,Glass Syndrome,Cervical Dystonia,Non-Syndromic Intellectual Disability,Ovarian Clear Cell Carcinoma,Trichohepatoenteric Syndrome 2,Autism Spectrum Disorder,Autosomal Dominant Non-Syndromic Intellectual Disability,Medulloblastoma,Autism |
2cxy_a | Q8NFD5 | ENSG00000049618 | ARID1B | 99.40 | 2.10E-17 | 1.70E-21 | 149.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJR119C | JHD2 | SGDID:S000003880 | 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 |
3pua_a | O75151 | ENSG00000197724 | PHF2 | 99.30 | 1.30E-16 | 1.00E-20 | 172.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | KDM4D JHDM3D JMJD2D |
Lysine-specific demethylase 4D (EC 1.14.11.66) (JmjC domain-containing histone demethylation protein 3D) (Jumonji domain-containing protein 2D) ([histone H3]-trimethyl-L-lysine(9) demethylase 4D) |
1.14.11.66 | Homo sapiens | Osteogenesis Imperfecta, Type Xiii,Primary Hypertrophic Osteoarthropathy,Osteogenesis Imperfecta, Type Xviii,Osteogenesis Imperfecta, Type Xvi,Gastrointestinal Stromal Tumor,Osteogenesis Imperfecta, Type Xvii |
5plv_a | Q6B0I6 | ENSG00000186280 | KDM4D | 100.00 | 3.80E-39 | 2.90E-43 | 347.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | UTY KDM6C |
Histone demethylase UTY (EC 1.14.11.68) (Ubiquitously-transcribed TPR protein on the Y chromosome) (Ubiquitously-transcribed Y chromosome tetratricopeptide repeat protein) ([histone H3]-trimethyl-L-lysine(27) demethylase UTY) |
1.14.11.68 | Homo sapiens | 4uf0_a | O14607 | ENSG00000183878 | UTY | 99.90 | 1.70E-30 | 1.30E-34 | 290.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJR119C | JHD2 | SGDID:S000003880 | JMJ703 Os05g0196500 LOC_Os05g10770 P0617H07.8 |
Lysine-specific demethylase JMJ703 (EC 1.14.11.-) (Jumonji domain-containing protein 703) (Lysine-specific histone demethylase JMJ703) (Protein JUMONJI 703) |
1.14.11.- | Oryza sativa | 4igq_a | Q53WJ1 | 100.00 | 5.00E-45 | 3.90E-49 | 393.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YJR119C | JHD2 | SGDID:S000003880 | MQD22.4 MQD22_4 At5g46910 |
MQD22.4 MQD22_4 At5g46910 |
Arabidopsis thaliana | 6ip0_a | F4KIX0 | 100.00 | 6.20E-50 | 4.80E-54 | 448.50 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YJR119C | JHD2 | SGDID:S000003880 | 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 |
5fyz_a | Q9UGL1 | ENSG00000117139 | KDM5B | 100.00 | 2.10E-55 | 1.60E-59 | 492.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | 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 |
5v9p_a | P29375 | ENSG00000073614 | KDM5A | 100.00 | 1.10E-84 | 8.30E-89 | 772.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YJR119C | JHD2 | SGDID:S000003880 | ARID3A DRIL1 DRIL3 DRX E2FBP1 |
AT-rich interactive domain-containing protein 3A (ARID domain-containing protein 3A) (B-cell regulator of IgH transcription) (Bright) (Dead ringer-like protein 1) (E2F-binding protein 1) |
Homo sapiens | Flinders Island Spotted Fever |
2kk0_a | Q99856 | ENSG00000116017 | ARID3A | 99.50 | 1.20E-18 | 9.30E-23 | 162.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJR119C | JHD2 | SGDID:S000003880 | KDM4A JHDM3A JMJD2 JMJD2A KIAA0677 |
Lysine-specific demethylase 4A (EC 1.14.11.66) (EC 1.14.11.69) (JmjC domain-containing histone demethylation protein 3A) (Jumonji domain-containing protein 2A) ([histone H3]-trimethyl-L-lysine(36) demethylase 4A) ([histone H3]-trimethyl-L-lysine(9) demethylase 4A) |
1.14.11.66,1.14.11.69, | Homo sapiens | Familial Isolated Hypoparathyroidism,Primary Hyperoxaluria,Meier-Gorlin Syndrome 1 |
2gp3_a | O75164 | ENSG00000066135 | KDM4A | 100.00 | 1.50E-39 | 1.10E-43 | 348.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |