Protein-coding gene in the species Homo sapiens
PHF8 Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4DO0, 3K3O, 2WWU, 3K3N, 3KV4,%%s2WWU, 3K3N, 3K3O, 3KV4, 4DO0
Identifiers Aliases PHF8 , JHDM1F, MRXSSD, ZNF422, PHD finger protein 8, KDM7BExternal IDs OMIM: 300560; MGI: 2444341; HomoloGene: 49405; GeneCards: PHF8; OMA:PHF8 - orthologs Gene location (Human) Chr. X chromosome (human)[1] Band Xp11.22 Start 53,936,676 bp[1] End 54,048,958 bp[1]
Gene location (Mouse) Chr. X chromosome (mouse)[2] Band X|X F3 Start 150,303,668 bp[2] End 150,416,855 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right testis sural nerve left testis testicle tendon of biceps brachii Achilles tendon epithelium of colon right lobe of liver gonad right uterine tube
Top expressed in zygote primary oocyte otic vesicle saccule blood secondary oocyte otic placode Gonadal ridge granulocyte medial ganglionic eminence
More reference expression data
BioGPS
Gene ontology Molecular function
2-oxoglutarate-dependent dioxygenase activity
iron ion binding
histone H3-methyl-lysine-9 demethylase activity
histone H4-methyl-lysine-20 demethylase activity
chromatin binding
dioxygenase activity
metal ion binding
methylated histone binding
protein binding
histone H3-methyl-lysine-36 demethylase activity
oxidoreductase activity
histone H3-tri/di-methyl-lysine-27 demethylase activity
histone demethylase activity
zinc ion binding
Cellular component
nuclear membrane
nucleoplasm
nucleolus
nucleus
Biological process
regulation of transcription, DNA-templated
histone H3-K27 demethylation
histone H3-K9 demethylation
histone H4-K20 demethylation
transcription, DNA-templated
positive regulation of transcription, DNA-templated
brain development
negative regulation of ribosomal DNA heterochromatin assembly
histone H3-K36 demethylation
cell cycle
positive regulation of transcription by RNA polymerase I
G1/S transition of mitotic cell cycle
chromatin organization
Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez Ensembl UniProt RefSeq (mRNA) NM_001184896 NM_001184897 NM_001184898 NM_015107
RefSeq (protein) NP_001171825 NP_001171826 NP_001171827 NP_055922
Location (UCSC) Chr X: 53.94 – 54.05 Mb Chr X: 150.3 – 150.42 Mb PubMed search [3] [4]
Wikidata View/Edit Human View/Edit Mouse
PHD finger protein 8 is a protein that in humans is encoded by the PHF8 gene.[5]
^ a b c GRCh38: Ensembl release 89: ENSG00000172943 – Ensembl, May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000041229 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Entrez Gene: PHF8 PHD finger protein 8".
Last Update: 2024-05-05T14:09:40Z
PHD finger protein 8 is a protein that in humans is encoded by the PHF8 gene. PHF8 belongs to the family of ferrous iron and alpha-ketoglutarate-dependent...
Word Count : 971
Last Update: 2024-04-14T22:13:37Z
PHF8 . The research found that PHF8 encodes for a histone lysine demethylase, and is involved in epigenetic regulation. The catalytic activity of PHF8 ...
Word Count : 10403
Last Update: 2024-06-14T19:37:35Z
X-linked intellectual disability (OMIM: 300263) as caused by mutations in the PHF8 gene (OMIM: 300560). In the rarest of cases, abnormalities with the X or...
Word Count : 10131
Last Update: 2024-04-03T16:02:24Z
Sickle cell anemia 11p15 P Siderius X-linked mental retardation syndrome PHF8 X-Linked Recessive Sideroblastic anemia ABCB7, SLC25A38, GLRX5 recessive...
Word Count : 969
Last Update: 2024-05-09T15:43:25Z
300354; CUL4B Mental retardation syndrome, X-linked, Siderius type; 300263; PHF8 Mental retardation, autosomal dominant 1; 156200; MBD5 Mental retardation...
Word Count : 18877