TBC1 domain family member 24 isoform X1 [Homo sapiens]

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Investigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss. [Sci Rep. 2024]
Investigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss.
Lei P, Zhu Q, Dong W. Sci Rep. 2024 Feb 27; 14(1):4734. Epub 2024 Feb 27.
TBC1D24-related familial infantile multifocal myoclonus: Description of a new Chinese pedigree with a 20 year follow up. [Epilepsy Res. 2022]
TBC1D24-related familial infantile multifocal myoclonus: Description of a new Chinese pedigree with a 20 year follow up.
Shao Q, Shi X, Ma B, Zeng J, Zheng A, Xie W. Epilepsy Res. 2022 May; 182:106923. Epub 2022 Apr 8.
TBC1D24 emerges as an important contributor to progressive postlingual dominant hearing loss. [Sci Rep. 2021]
TBC1D24 emerges as an important contributor to progressive postlingual dominant hearing loss.
Oziębło D, Leja ML, Lazniewski M, Sarosiak A, Tacikowska G, Kochanek K, Plewczynski D, Skarżyński H, Ołdak M. Sci Rep. 2021 May 13; 11(1):10300. Epub 2021 May 13.

RefSeq genomic sequence
See the genomic reference sequence for the TBC1D24 gene (NG_028170.1).
RefSeq mRNA
See reference mRNA sequence for the TBC1D24 gene (XM_017023493.2).

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Protein