TBC1D24

Summary

TBC1D24 is a gene^[1]. TBC1D24 ranks in the top 2% of gene entities by monthly Wikipedia readership (5 views/month).^[2]

Key Facts

• TBC1D24's instance of is recorded as gene^[3].
• TBC1D24 is a type of protein-coding gene^[4].
• TBC1D24's HomoloGene ID is recorded as 27469^[5].
• TBC1D24's genomic start is recorded as 2475051^[6].
• TBC1D24's genomic start is recorded as 2525147^[7].
• TBC1D24's genomic end is recorded as 2509560^[8].
• TBC1D24's genomic end is recorded as 2555735^[9].
• TBC1D24's ortholog is recorded as Tbc1d24^[10].
• TBC1D24's ortholog is recorded as Tbc1d24^[11].
• TBC1D24's ortholog is recorded as sky^[12].
• TBC1D24's ortholog is recorded as tbc1d24^[13].
• TBC1D24's ortholog is recorded as tbc-7^[14].
• TBC1D24's encodes is recorded as TBC1 domain family member 24^[15].
• TBC1D24's found in taxon is recorded as Homo sapiens^[16].
• TBC1D24's chromosome is recorded as human chromosome 16^[17].
• TBC1D24's genetic association is recorded as familial infantile myoclonic epilepsy^[18].
• TBC1D24's genetic association is recorded as autosomal dominant nonsyndromic deafness 65^[19].
• TBC1D24's genetic association is recorded as autosomal recessive nonsyndromic deafness 86^[20].
• TBC1D24's genetic association is recorded as rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome^[21].
• TBC1D24's genetic association is recorded as progressive myoclonic epilepsy with dystonia^[22].
• TBC1D24's strand orientation is recorded as forward strand^[23].
• TBC1D24's exact match is recorded as http://identifiers.org/ncbigene/57465^[24].
• TBC1D24's cytogenetic location is recorded as 16p13.3^[25].
• TBC1D24's expressed in is recorded as parotid gland^[26].
• TBC1D24's expressed in is recorded as Brodmann area 23^[27].

Why It Matters

TBC1D24 ranks in the top 2% of gene entities by monthly Wikipedia readership (5 views/month).^[2] TBC1D24 is known by 10 alternative names across languages and contexts.^[28]