| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YER169W | RPH1 | SGDID:S000000971 | JmjC |
JmjC domain, hydroxylase |
pfam Domain | PF02373 | 99.20 | 1.90E-15 | 1.90E-19 | 131.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YER169W | RPH1 | SGDID:S000000971 | MQD22.4 MQD22_4 At5g46910 |
MQD22.4 MQD22_4 At5g46910 |
Arabidopsis thaliana | 6ip0_a | F4KIX0 | 100.00 | 1.10E-50 | 9.80E-55 | 459.80 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
| YER169W | RPH1 | SGDID:S000000971 | 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 | 99.70 | 1.20E-21 | 1.10E-25 | 218.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER169W | RPH1 | SGDID:S000000971 | 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 | 99.70 | 1.80E-21 | 1.60E-25 | 220.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YER169W | RPH1 | SGDID:S000000971 | 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 | 2.10E-56 | 1.80E-60 | 487.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YER169W | RPH1 | SGDID:S000000971 | 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 | 3.90E-47 | 3.40E-51 | 452.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YER169W | RPH1 | SGDID:S000000971 | RPH1 YER169W |
DNA damage-responsive transcriptional repressor RPH1 |
Saccharomyces cerevisiae | 3opt_a | P39956 | 100.00 | 1.10E-64 | 9.90E-69 | 557.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YER169W | RPH1 | SGDID:S000000971 | 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 | 1.10E-51 | 9.30E-56 | 451.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YER169W | RPH1 | SGDID:S000000971 | 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 | 99.60 | 1.30E-20 | 1.20E-24 | 210.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
| YER169W | RPH1 | SGDID:S000000971 | 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 | 5.50E-56 | 4.70E-60 | 486.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YER169W | RPH1 | SGDID:S000000971 | 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-51 | 1.60E-55 | 473.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YER169W | RPH1 | SGDID:S000000971 | 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 | 1.10E-51 | 9.40E-56 | 467.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |