Wingless-type mmtv integration site family, member 10b

Preferred Label : Wingless-type mmtv integration site family, member 10b;

Symbol : WNT10B;

CISMeF acronym : WNT10B;

Type : Gene;

Ensembl ID : ENSG00000169884;

Prefixed ID : *601906;

Details

Origin ID

601906;

UMLS CUI

C1421511;

Automatic exact mappings (from CISMeF team)
- Protein Wnt-10b [NCIt concept]
- WNT10B Gene [NCIt concept]
- Wnt family member 10B [ORDO Gene]
- Wnt family member 10B [HGNC gene]
HGNC gene
- Wnt family member 10B [HGNC gene]
NCIt concept(s)
- Protein Wnt-10b [NCIt concept]
- WNT10B Gene [NCIt concept]
- WNT10B wt Allele [NCIt concept]
ORDO concept(s)
- Wnt family member 10B [ORDO Gene]
Phenotypes related
- Split-hand/foot malformation 6 [OMIM Phenotype]
- Tooth agenesis, selective, 8 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT10B Gene [NCIt concept]
- Wnt family member 10B [HGNC gene]

Keyword's position in hierarchy(ies) :

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