HCFC1 wt Allele

Preferred Label : HCFC1 wt Allele;

NCIt synonyms : VP16-Accessory Protein Gene; Host Cell Factor C1 (VP16-Accessory Protein) Gene; MGC70925; MRX3; CFF; Protein Phosphatase 1, Regulatory Subunit 89 Gene; XLID3; HFC1; HCF-1; VCAF; PPP1R89; Mental Retardation, X-Linked 3 Gene; Host Cell Factor C1 wt Allele; HCF1; MAHCX; HCF;

NCIt definition : Human HCFC1 wild-type allele is located in the vicinity of Xq28 and is approximately 25 kb in length. This allele, which encodes host cell factor 1 protein, plays a role in histone modification, transcriptional regulation, and herpes simplex virus gene transcription. Mutation of the gene is associated with cblX type methylmalonic aciduria and homocysteineima and X-linked mental redardation 3.;

NCI Metathesaurus CUI : CL1794075;

GenBank Accession Number : NM_005334;

Details

Origin ID

C188797;

UMLS CUI

C5702620;

Automatic exact mappings (from CISMeF team)
- mental retardation, X-Linked 3 [MeSH Supplementary Concept]
OMIM relation
- Host cell factor c1 [OMIM gene]
See also inter- (CISMeF)
- Methylmalonic aciduria and homocystinuria, cblx type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
Validated automatic mappings to NTBT
- Host cell factor c1 [OMIM gene]
- host cell factor C1 [ORDO Gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- Xq28 [NCIt concept]
gene_plays_role_in_process
- Cell Cycle Regulation Process [NCIt concept]
- Chromatin Remodeling [NCIt concept]
- Histone Modification [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

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