EHMT1 wt Allele

Preferred Label : EHMT1 wt Allele;

NCIt synonyms : RP11-188C12.1; Eu-HMTase1; KMT1D; EGLP; FLJ12879; FP13812; EUHMTASE1; Euchromatic Histone-Lysine N-Methyltransferase 1 wt Allele; DKFZp667M072; KIAA1876; bA188C12.1;

NCIt definition : Human EHMT1 wild-type allele is located in the vicinity of 9q34.3 and is approximately 139 kb in length. This allele, which encodes histone-lysine N-methyltransferase, H3 lysine-9 specific 5 protein, plays a role in the modulation of histone methylation. Mutation of the gene is associated with chromosome 9q subtelomeric deletion syndrome.;

GenBank Accession Number : AY083210;

Details

Origin ID

C75327;

UMLS CUI

C2699842;

OMIM relation
- Euchromatic histone methyltransferase 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 9q34.3 [NCIt concept]
gene_is_element_in_pathway
- Lysine Degradation Pathway [NCIt concept]
gene_plays_role_in_process
- Chromatin Remodeling [NCIt concept]
- Gene Expression [NCIt concept]
- Histone Methylation [NCIt concept]
- Methylation [NCIt concept]

Keyword's position in hierarchy(ies) :

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