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KDM6A and HSD17B10
Data Source:
BioGRID
(affinity chromatography technology)
KDM6A
HSD17B10
Description
lysine demethylase 6A
hydroxysteroid 17-beta dehydrogenase 10
Image
GO Annotations
Cellular Component
Nucleus
Nucleoplasm
Histone Methyltransferase Complex
MLL3/4 Complex
Cytoplasm
Mitochondrion
Mitochondrial Matrix
Plasma Membrane
Mitochondrial Ribonuclease P Complex
Mitochondrial Nucleoid
Molecular Function
RNA Polymerase II Cis-regulatory Region Sequence-specific DNA Binding
Protein Binding
Chromatin DNA Binding
Metal Ion Binding
Dioxygenase Activity
Histone Demethylase Activity (H3-K27 Specific)
TRNA Binding
RNA Binding
3-hydroxyacyl-CoA Dehydrogenase Activity
Protein Binding
Cholate 7-alpha-dehydrogenase Activity
Testosterone Dehydrogenase [NAD(P)] Activity
17-beta-hydroxysteroid Dehydrogenase (NAD+) Activity
3-hydroxy-2-methylbutyryl-CoA Dehydrogenase Activity
Testosterone Dehydrogenase (NAD+) Activity
Androstan-3-alpha,17-beta-diol Dehydrogenase Activity
Chenodeoxycholate 7-alpha-dehydrogenase (NAD+) Activity
Isoursodeoxycholate 7-beta-dehydrogenase (NAD+) Activity
Ursodeoxycholate 7-beta-dehydrogenase (NAD+) Activity
Biological Process
Chromatin Remodeling
Heart Development
Regulation Of Gene Expression
Histone H3-K4 Methylation
Histone H3-K27 Demethylation
Isoleucine Catabolic Process
Lipid Metabolic Process
Fatty Acid Beta-oxidation
Bile Acid Biosynthetic Process
Mitochondrion Organization
C21-steroid Hormone Metabolic Process
Androgen Metabolic Process
Estrogen Metabolic Process
Branched-chain Amino Acid Catabolic Process
Protein Homotetramerization
Brexanolone Metabolic Process
Mitochondrial TRNA Methylation
Mitochondrial TRNA Processing
Mitochondrial TRNA 5'-end Processing
Mitochondrial TRNA 3'-end Processing
Pathways
HDMs demethylate histones
Activation of anterior HOX genes in hindbrain development during early embryogenesis
tRNA processing in the mitochondrion
tRNA modification in the mitochondrion
Branched-chain amino acid catabolism
rRNA processing in the mitochondrion
Drugs
NADH
1-Azepan-1-Yl-2-Phenyl-2-(4-Thioxo-1,4-Dihydro-Pyrazolo[3,4-D]Pyrimidin-5-Yl)Ethanone Adduct
Omega-3-carboxylic acids
Diseases
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency; HSD10 deficiency
Non-syndromic X-linked mental retardation
Syndromic X-linked mental retardation, including: Turner type (MRXST); Siderius type (MRXSSD) ; Cabezas type (MRXC); Raymond type (MRXSR); Type10 (MRXS10); Type14 (MRXS14); Mental retardation with isolated growth hormone deficiency (MRGH)
GWAS
Bipolar disorder (
31043756
)
Body mass index (
28892062
)
Interacting Genes
11 interacting genes:
GSC2
H3-4
H3C1
H3C14
MEOX2
MTDH
NKX2-5
SMAD9
SRF
TBX5
TLE1
32 interacting genes:
ALDH3B1
ALDOA
APP
ATP5F1A
CDC42
CHD3
CPS1
CS
ETFDH
FAF1
GLUD1
GLUL
HADHA
HADHB
HMGCL
HMGCS2
HTRA2
MDH1
OGDH
PDHA1
PDHB
PDHX
PRKN
PTEN
PYGL
TOMM20
TOMM22
TOMM40
TRAF3IP2
TRAF5
TRAF6
UBE2D1
Entrez ID
7403
3028
HPRD ID
02131
02223
Ensembl ID
ENSG00000147050
ENSG00000072506
Uniprot IDs
A0A087X0R0
A0A6Q8PFK0
B4E0L8
B7ZKN1
B7ZKN5
B7ZKN6
E1U0S6
F5H5V6
F5H6S1
F8W8R6
O15550
Q59HG3
Q86TD1
A0A0S2Z410
Q99714
PDB IDs
3AVR
3AVS
6FUK
6FUL
1F67
1SO8
1U7T
2O23
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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