Transmembrane protein 67

Preferred Label : Transmembrane protein 67;

Symbol : TMEM67;

CISMeF acronym : TMEM67;

Type : Gene;

Alternative titles and symbols : Mks3 gene; MECKELIN;

Ensembl ID : ENSG00000164953;

Prefixed ID : *609884;

Details

Origin ID

609884;

UMLS CUI

C1823331;

Automatic exact mappings (from CISMeF team)
- transmembrane protein 67 [ORDO Gene]
- transmembrane protein 67 [HGNC gene]
HGNC gene
- transmembrane protein 67 [HGNC gene]
ORDO concept(s)
- transmembrane protein 67 [ORDO Gene]
Phenotypes related
- Bardet-biedl syndrome 14 [OMIM Phenotype]
- Coach syndrome 1 [OMIM Phenotype]
- Joubert syndrome 6 [OMIM Phenotype]
- Meckel syndrome, type 3 [OMIM Phenotype]
- Nephronophthisis 11 [OMIM Phenotype]
- Rhyns syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- transmembrane protein 67 [HGNC gene]

Keyword's position in hierarchy(ies) :

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