NME/NM23 family member 8

Preferred Label : NME/NM23 family member 8;

Approved symbol HGNC : NME8;

Name synonyms HGNC : sperm-specific thioredoxin 2;

Alias symbols HGNC : SPTRX2; CILD6; NM23-H8; DNAI8;

Chromosome HGNC : 7p14.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000086288;

Details

Origin ID

HGNC:16473;

UMLS CUI

C1424308;

Automatic exact mappings (from CISMeF team)
- NME/NM23 family member 8 [ORDO Gene]
- Nme/nm23 family, member 8 [OMIM gene]
OMIM gene
- Nme/nm23 family, member 8 [OMIM gene]
Orphanet gene
- NME/NM23 family member 8 [ORDO Gene]
See also inter- (CISMeF)
- Ciliary dyskinesia, primary, 6 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Nme/nm23 family, member 8 [OMIM gene]

Keyword's position in hierarchy(ies) :

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