PHF8

4DO0, 3K3O, 2WWU, 3K3N, 3KV4,%%s2WWU, 3K3N, 3K3O, 3KV4, 4DO0

PHF8
PHF8
Structures disponibles
PDBRecherche d'orthologue : PDBe RCSB
Identifiants
AliasPHF8
IDs externesOMIM: 300560 MGI: 2444341 HomoloGene: 49405 GeneCards: PHF8
Nomenclature EC1.14.11.65
Wikidata
Voir/Editer HumainVoir/Editer Souris

Le PHF8 est un gène du chromosome X humain aussi appelé KDM7B ou JHDM1F ou MRXSSD ou ZNF422[5].

Maladies liées

  • Déficience intellectuelle liée à l'X type Siderius[6]

Notes et références

  1. a b et c GRCh38: Ensembl release 89: ENSG00000172943 - Ensembl, May 2017
  2. a b et c GRCm38: Ensembl release 89: ENSMUSG00000041229 - Ensembl, May 2017
  3. « Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
  4. « Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
  5. « PHF8 PHD finger protein 8 [Homo sapiens (human)] - Gene - NCBI », sur www.ncbi.nlm.nih.gov (consulté le )
  6. « Orphanet: Déficience intellectuelle liée à l'X type Siderius », sur www.orpha.net (consulté le )

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