TBC1D24
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 16[13]
- Cytogenetic location
- 16p13.3[20]
- Expressed in
- parotid gland, Brodmann area 23, middle temporal gyrus, corpus epididymis, cerebellar vermis, renal medulla, superior frontal gyrus, entorhinal cortex, Brodmann area 46, cerebellar hemisphere[21][22][23][24][25][26][27][28][29][30]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- familial infantile myoclonic epilepsy, autosomal dominant nonsyndromic deafness 65, autosomal recessive nonsyndromic deafness 86, rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome, progressive myoclonic epilepsy with dystonia[14][15][16][17][18]
- HomoloGene ID
- 27469[3]
- Strand orientation
- forward strand[19]
🏷️ Also known as
en TLDC6
en DEE16
en DFNA65
en DFNB86
en DOORS
en EIEE16
en EPRPDC
en FIME
en TBC1D24
en TBC1 domain family member 24
ar TBC١D٢٤
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000162065
- Ensembl transcript ID
- ENST00000630263, ENST00000562105, ENST00000564879, ENST00000566853, ENST00000567020, ENST00000569874, ENST00000627285, ENST00000636980, ENST00000646147, ENST00000643767
- Entrez Gene ID
- 57465
- Exact match
- identifiers.org
- Freebase ID
- /m/011x4_cj
- HGNC ID
- 29203
- HGNC gene symbol
- TBC1D24
- OMIM ID
- 613577
- RefSeq RNA ID
- NM_020705, NM_001199107, XM_017023493, XM_017023494, XM_017023495, XM_047434388
- UMLS CUI
- C1823245
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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