Mks transition zone complex subunit 1

Preferred Label : Mks transition zone complex subunit 1;

Symbol : MKS1;

CISMeF acronym : MKS1;

Type : Gene;

Alternative titles and symbols : Bbs13 gene; BBS13; FLJ20345; Mks1 gene;

Ensembl ID : ENSG00000011143;

Prefixed ID : *609883;

Details

Origin ID

609883;

UMLS CUI

C1417186;

Automatic exact mappings (from CISMeF team)
- Bardet-Biedl syndrome 13 [DO Concept]
- MKS transition zone complex subunit 1 [ORDO Gene]
- MKS transition zone complex subunit 1 [HGNC gene]
- Meckel syndrome 1 [DO Concept]
HGNC gene
- MKS transition zone complex subunit 1 [HGNC gene]
ORDO concept(s)
- MKS transition zone complex subunit 1 [ORDO Gene]
Phenotypes related
- Bardet-biedl syndrome 13 [OMIM Phenotype]
- Joubert syndrome 28 [OMIM Phenotype]
- Meckel syndrome, type 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MKS transition zone complex subunit 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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