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

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YMR176W ECM5 / SGDID:S000004788
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
YMR176W ECM5 SGDID:S000004788
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 2.60E-55 2.30E-59 508.60 0 0 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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
2lm1_a Q9VMJ7 99.50 3.70E-18 3.60E-22 161.60 0 0 0 0 1 0 0 0
YMR176W ECM5 SGDID:S000004788
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 1.50E-71 1.40E-75 667.00 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 99.50 1.40E-18 1.30E-22 208.40 0 0 0 0 0 1 0 0
YMR176W ECM5 SGDID:S000004788
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 99.60 1.00E-19 9.50E-24 183.60 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 99.50 8.40E-19 8.00E-23 171.70 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 1.90E-70 1.70E-74 668.30 0 0 0 0 0 0 1 0
YMR176W ECM5 SGDID:S000004788
Kdm5b Jarid1b Kiaa4034 Plu1
Lysine-specific demethylase 5B (EC 1.14.11.67) (Histone demethylase JARID1B) (Jumonji/ARID domain-containing protein 1B) (PLU-1) ([histone H3]-trimethyl-L-lysine(4) demethylase 5B)
1.14.11.67 Mus musculus
2eqy_a Q80Y84 99.20 3.70E-15 3.50E-19 145.10 0 0 1 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 1.70E-47 1.50E-51 443.30 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
Jarid2 Jmj
Protein Jumonji (Jumonji/ARID domain-containing protein 2)
Mus musculus
2rq5_a Q62315 99.30 2.60E-16 2.50E-20 152.20 0 0 1 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 100.00 4.60E-34 4.50E-38 339.50 0 0 1 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 99.40 9.70E-18 8.30E-22 161.40 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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
2oeh_a Q14865 ENSG00000150347 ARID5B 99.10 1.20E-14 1.10E-18 137.20 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
KDM5C DXS1272E JARID1C SMCX XE169
Lysine-specific demethylase 5C (EC 1.14.11.67) (Histone demethylase JARID1C) (Jumonji/ARID domain-containing protein 1C) (Protein SmcX) (Protein Xe169) ([histone H3]-trimethyl-L-lysine(4) demethylase 5C)
1.14.11.67 Homo sapiens
Plasma Cell Neoplasm,Kleefstra Syndrome,Clear Cell Renal Cell Carcinoma,Rare Genetic Intellectual Disability,Iqsec2,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Alpha-Thalassemia,Chromosome 16p13.3 Deletion Syndrome, Proximal,Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type,Renal Cell Carcinoma, Papillary, 1,Smith-Magenis Syndrome,Non-Syndromic X-Linked Intellectual Disability,Renal Cell Carcinoma, Nonpapillary,Autism Spectrum Disorder,Kabuki Syndrome 1,Autosomal Dominant Non-Syndromic Intellectual Disability,Myeloma, Multiple,Syndromic X-Linked Intellectual Disability Siderius Type
2jrz_a P41229 ENSG00000126012 KDM5C 99.20 1.90E-15 1.80E-19 145.50 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
RPH1 YER169W
DNA damage-responsive transcriptional repressor RPH1
Saccharomyces cerevisiae
3opt_a P39956 100.00 1.30E-46 1.20E-50 437.10 0 0 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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
2jxj_a P29375 ENSG00000073614 KDM5A 99.10 5.50E-15 5.40E-19 136.50 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 99.40 3.10E-17 2.90E-21 157.90 0 0 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 2.80E-47 2.50E-51 439.30 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 100.00 2.40E-35 2.20E-39 356.10 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 100.00 4.20E-36 4.00E-40 357.30 0 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
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 3.50E-19 3.30E-23 173.10 1 1 0 0 0 0 0 0
YMR176W ECM5 SGDID:S000004788
MQD22.4 MQD22_4 At5g46910
MQD22.4 MQD22_4 At5g46910
Arabidopsis thaliana
6ip0_a F4KIX0 100.00 2.10E-62 1.90E-66 588.80 0 0 0 0 0 0 1 0

Weizmann Institute of Science | Maya Schuldiner Lab