Rpgrip1-like - CISMeF

Preferred Label : Rpgrip1-like;

Symbol : RPGRIP1L;

CISMeF acronym : RPGRIP1L;

Type : Gene;

Alternative titles and symbols : Nephrocystin 8; NPHP8; KIAA1005;

Ensembl ID : ENSG00000103494;

Prefixed ID : *610937;

Details

Origin ID

610937;

UMLS CUI

C2242767;

Automatic exact mappings (from CISMeF team)
- RPGRIP1 like [ORDO Gene]
- RPGRIP1 like [HGNC gene]
HGNC gene
- RPGRIP1 like [HGNC gene]
NCIt concept(s)
- Protein Fantom [NCIt concept]
- RPGRIP1L Gene [NCIt concept]
- RPGRIP1L wt Allele [NCIt concept]
ORDO concept(s)
- RPGRIP1 like [ORDO Gene]
Phenotypes related
- Coach syndrome 3 [OMIM Phenotype]
- Joubert syndrome 7 [OMIM Phenotype]
- Meckel syndrome, type 5 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RPGRIP1 like [HGNC gene]

Keyword's position in hierarchy(ies) :

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