CHTOP wt Allele

Preferred Label : CHTOP wt Allele;

NCIt synonyms : FL-SRAG; SRAG-5; Chromosome 1 Open Reading Frame 77 Gene; Chromatin Target of PRMT1 wt Allele; Friend of Prmt1 Gene; C1orf77; DKFZP547E1010; HT031; PP7704; SRAG; FOP; SRAG-3;

NCIt definition : Human CHTOP wild-type allele is located in the vicinity of 1q21.3 and is approximately 12 kb in length. This allele, which encodes chromatin target of PRMT1 protein, plays a role in transcriptional regulation, nuclear export of mature mRNA and histone methylation.;

NCI Metathesaurus CUI : CL1778854;

GenBank Accession Number : NM_015607;

Details

Origin ID

C186564;

UMLS CUI

C5575509;

Automatic exact mappings (from CISMeF team)
- Chromatin target of prmt1 [OMIM gene]
- Fibroblast growth factor receptor 1 oncogene partner [OMIM gene]
- Fibrodysplasia ossificans progressiva [ORDO Disease]
- Fibrodysplasia ossificans progressiva [ICD-11 Subcategory]
- Fibrodysplasia ossificans progressiva [OMIM Phenotype]
OMIM relation
- Chromatin target of prmt1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 1q21.3 [NCIt concept]
gene_plays_role_in_process
- Histone Methylation [NCIt concept]
- Ligand Binding [NCIt concept]
- RNA Binding [NCIt concept]
- Transcriptional Regulation [NCIt concept]
- mRNA Export [NCIt concept]

Keyword's position in hierarchy(ies) :

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