PRMT1 wt Allele

Preferred Label : PRMT1 wt Allele;

NCIt synonyms : HMT1 HnRNP Methyltransferase-Like 2 (S. cerevisiae) Gene; ANM1; HMT1-Like 2; IR1B4; HCP1; Protein Arginine Methyltransferase 1 wt Allele; HMT1 (HnRNP Methyltransferase, S. cerevisiae)-Like 2 Gene; HRMT1L2;

NCIt definition : Human PRMT1 wild-type allele is located in the vicinity of 19q13.33 and is approximately 13 kb in length. This allele, which encodes protein arginine N-methyltransferase 1 protein, is involved in the methylation of histone H4 and chromatin.;

NCI Metathesaurus CUI : CL522225;

GenBank Accession Number : D66904;

Details

Origin ID

C134686;

UMLS CUI

C4521507;

Automatic exact mappings (from CISMeF team)
- HRMT1L2 [MeSH concept]
- PRMT2 protein, human [MeSH Supplementary Concept]
- Phosphodiesterase 7a [OMIM gene]
- Protein arginine methyltransferase 1 [OMIM gene]
- Solute carrier family 46 (folate transporter), member 1 [OMIM gene]
- centromere protein F [ORDO Gene]
- solute carrier family 46 member 1 [ORDO Gene]
OMIM relation
- Protein arginine methyltransferase 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 19q13.33 [NCIt concept]
gene_is_element_in_pathway
- BTG Cell Cycle Regulation Pathway [NCIt concept]
- Gene Expression Regulation by Vitamin D Receptor Pathway [NCIt concept]
- p53 Effector Pathway [NCIt concept]
gene_plays_role_in_process
- Chromatin Remodeling [NCIt concept]
- Methylation [NCIt concept]
- Protein Methylation [NCIt concept]

Keyword's position in hierarchy(ies) :

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