TBC1D24 Chromosome 16

TBC1 domain family member 24
159 variants 159 Health Risk

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What This Gene Does
This gene encodes a protein with a conserved domain, referred to as the TBC domain, characteristic of proteins which interact with GTPases. TBC domain proteins may serve as GTPase-activating proteins for a particular group of GTPases, the Rab (Ras-related proteins in brain) small GTPases which are involved in the regulation of membrane trafficking. Mutations in this gene are associated with familial infantile myoclonic epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2011]
Gene Info
Gene Group
TLDc domain containing
Locus Type
gene with protein product
Location
16p13.3
Ensembl
ENSG00000162065
Associated Conditions (41)
Parkinsonian disorder
Developmental and epileptic encephalopathy
16
Autosomal dominant nonsyndromic hearing loss 65
1
Autosomal dominant epilepsy
Caused by mutation in the TBC1 domain family
member 24
DOORS syndrome
Inborn genetic diseases
Familial infantile myoclonic epilepsy
Autosomal recessive nonsyndromic hearing loss 86
TBC1D24-related disorder
Sarcoma
Uterine carcinosarcoma
Nonpapillary renal cell carcinoma
Self-limited epilepsy with centrotemporal spikes
6 conditions
Familial cancer of breast
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
+21 more conditions
Key Variants
RS1057519629
Conflicting classifications of pathogenicity
Parkinsonian disorder, Developmental and epileptic encephalopathy, 16
Health Risk
RS1057519630
Conflicting classifications of pathogenicity
Parkinsonian disorder, Autosomal dominant epilepsy, Developmental and epileptic encephalopathy
Health Risk
RS1060502501
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
Health Risk
RS1131691552
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
Health Risk
RS1243475474
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy, 1
Health Risk
RS1314368308
Conflicting classifications of pathogenicity
Familial infantile myoclonic epilepsy, Familial infantile myoclonic epilepsy
Health Risk
RS1364280797
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
Health Risk
RS141399869
Conflicting classifications of pathogenicity
DOORS syndrome, Developmental and epileptic encephalopathy, 16
Health Risk
RS1435411888
Conflicting classifications of pathogenicity
Inborn genetic diseases, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
Health Risk
RS1468286638
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
Health Risk
RS188739853
Conflicting classifications of pathogenicity
Familial infantile myoclonic epilepsy, Inborn genetic diseases, TBC1D24-related disorder
Health Risk
RS199852092
Conflicting classifications of pathogenicity
Familial infantile myoclonic epilepsy, Familial infantile myoclonic epilepsy
Health Risk
All Variants (159)
RSID Category Clinical Significance Conditions
RS1057519629 Health Risk Conflicting classifications of pathogenicity Parkinsonian disorder, Developmental and epileptic encephalopathy, 16
RS1057519630 Health Risk Conflicting classifications of pathogenicity Parkinsonian disorder, Autosomal dominant epilepsy, Developmental and epileptic encephalopathy
RS1060502501 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS1131691552 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS1243475474 Health Risk Conflicting classifications of pathogenicity Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy, 1
RS1314368308 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Familial infantile myoclonic epilepsy
RS1364280797 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS141399869 Health Risk Conflicting classifications of pathogenicity DOORS syndrome, Developmental and epileptic encephalopathy, 16
RS1435411888 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS1468286638 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS188739853 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, TBC1D24-related disorder
RS199852092 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Familial infantile myoclonic epilepsy
RS200226466 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, TBC1D24-related disorder
RS200641000 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Developmental and epileptic encephalopathy, 1
RS200926225 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 16, Inborn genetic diseases
RS201174513 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS201618854 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS201649140 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, TBC1D24-related disorder
RS202162520 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Self-limited epilepsy with centrotemporal spikes, Inborn genetic diseases
RS2065741660 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 1, Autosomal dominant nonsyndromic hearing loss 65
RS2065786997 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS267607104 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS267607105 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, DOORS syndrome
RS367966267 Health Risk Conflicting classifications of pathogenicity Autosomal recessive nonsyndromic hearing loss 86, TBC1D24-related disorder, Autosomal recessive nonsyndromic hearing loss 86
RS369172908 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS369958726 Health Risk Conflicting classifications of pathogenicity Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy, 1
RS370244846 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, Developmental and epileptic encephalopathy
RS370427146 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 1
RS370869383 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Developmental and epileptic encephalopathy, 1
RS371213803 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Developmental and epileptic encephalopathy, 1
RS372317366 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Developmental and epileptic encephalopathy, 1
RS373862230 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS373914077 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 1
RS377448015 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 1
RS377697825 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, Developmental and epileptic encephalopathy
RS3810796 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS483352866 Health Risk Conflicting classifications of pathogenicity Autosomal recessive nonsyndromic hearing loss 86, Autosomal dominant nonsyndromic hearing loss 65, DOORS syndrome
RS540861763 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Familial infantile myoclonic epilepsy
RS545689324 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS553497128 Health Risk Conflicting classifications of pathogenicity TBC1D24-related disorder, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS565299079 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 1
RS574768683 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, 6 conditions, Developmental and epileptic encephalopathy
RS575173753 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS61731477 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, TBC1D24-related disorder, Developmental and epileptic encephalopathy
RS61731478 Health Risk Conflicting classifications of pathogenicity Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy, 1
RS747821285 Health Risk Conflicting classifications of pathogenicity DOORS syndrome, Developmental and epileptic encephalopathy, 1
RS749163517 Health Risk Conflicting classifications of pathogenicity Familial infantile myoclonic epilepsy, Inborn genetic diseases, Autosomal dominant nonsyndromic hearing loss 65
RS749232409 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy
RS749626631 Health Risk Conflicting classifications of pathogenicity Familial cancer of breast, Developmental and epileptic encephalopathy, 1
RS749994791 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 16, 1
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