Nop2/sun rna methyltransferase family, member 5

Preferred Label : Nop2/sun rna methyltransferase family, member 5;

Symbol : NSUN5;

CISMeF acronym : NSUN5;

Type : Gene;

Alternative titles and symbols : Nop2/sun domain family, member 5; Williams-beuren syndrome critical region 20; Rcm1, s. cerevisiae, homolog of; WBSCR20; WBSCR20A; RCM1;

Ensembl ID : ENSG00000130305;

Prefixed ID : *615732;

Details

Origin ID

615732;

UMLS CUI

C1538492;

Automatic exact mappings (from CISMeF team)
- NOP2/Sun RNA methyltransferase 5 [HGNC gene]
- TNNI3 wt Allele [NCIt concept]
- restrictive cardiomyopathy 1 [DO Concept]
HGNC gene
- NOP2/Sun RNA methyltransferase 5 [HGNC gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NOP2/Sun RNA methyltransferase 5 [HGNC gene]

Keyword's position in hierarchy(ies) :

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