Tbc1 domain family, member 24

Preferred Label : Tbc1 domain family, member 24;

Symbol : TBC1D24;

CISMeF acronym : TBC1D24;

Type : Gene;

Alternative titles and symbols : Skywalker, drosophila, homolog of; KIAA1171; SKY;

Ensembl ID : ENSG00000162065;

Prefixed ID : *613577;

Details

Origin ID

613577;

UMLS CUI

C1823245;

Automatic exact mappings (from CISMeF team)
- Spectral Karyotyping [NCIt concept]
- TBC1 domain family member 24 [ORDO Gene]
- TBC1 domain family member 24 [HGNC gene]
HGNC gene
- TBC1 domain family member 24 [HGNC gene]
ORDO concept(s)
- TBC1 domain family member 24 [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 65 [OMIM Phenotype]
- Deafness, autosomal recessive 86 [OMIM Phenotype]
- Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome [OMIM Phenotype]
- Developmental and epileptic encephalopathy 16 [OMIM Phenotype]
- Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp [OMIM Phenotype]
- Myoclonic epilepsy, familial infantile [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TBC1 domain family member 24 [HGNC gene]

Keyword's position in hierarchy(ies) :

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