TBCK Chromosome 4

TBC1 domain containing kinase
89 variants 89 Health Risk

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What This Gene Does
This gene encodes a protein that contains a protein kinase domain, a Rhodanase-like domain and the Tre-2/Bub2/Cdc16 (TBC) domain. The encoded protein is thought to play a role in actin organization, cell growth and cell proliferation by regulating the mammalian target of the rapamycin (mTOR) signaling pathway. This protein may also be involved in the transcriptional regulation of the components of the mTOR complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
Gene Info
Gene Group
FERRY complex subunits
Locus Type
gene with protein product
Location
4q24
Ensembl
ENSG00000145348
Associated Conditions (14)
Hypotonia
infantile
with psychomotor retardation and characteristic facies 3
Inborn genetic diseases
TBCK-related disorder
Neurodevelopmental disorder
6 conditions
Abnormality of the nervous system
Colon adenocarcinoma
Syndromic Infantile Encephalopathy
Intellectual disability
Global developmental delay
with psychomotor retardation and characteristic facies 1
Ovarian serous cystadenocarcinoma
Key Variants
RS1213724402
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS149002761
Conflicting classifications of pathogenicity
Inborn genetic diseases, Hypotonia, infantile
Health Risk
RS1579198426
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS1579198447
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS1740799305
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS2150065916
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS2478444503
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS34840340
Conflicting classifications of pathogenicity
Inborn genetic diseases, TBCK-related disorder, Inborn genetic diseases
Health Risk
RS369077117
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS370050799
Conflicting classifications of pathogenicity
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
Health Risk
RS374168890
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS61733982
Conflicting classifications of pathogenicity
TBCK-related disorder, TBCK-related disorder
Health Risk
All Variants (89)
RSID Category Clinical Significance Conditions
RS1213724402 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS149002761 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Hypotonia, infantile
RS1579198426 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1579198447 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1740799305 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS2150065916 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS2478444503 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS34840340 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, TBCK-related disorder, Inborn genetic diseases
RS369077117 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS370050799 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS374168890 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS61733982 Health Risk Conflicting classifications of pathogenicity TBCK-related disorder, TBCK-related disorder
RS760715215 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS769293834 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS775570874 Health Risk Conflicting classifications of pathogenicity Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS962500324 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Hypotonia, infantile
RS1004103406 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1174436721 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1311326943 Health Risk Likely pathogenic
RS1560929669 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1579257340 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1579342363 Health Risk Likely pathogenic
RS1759036277 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1759337270 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS2150010400 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS2467608578 Health Risk Likely pathogenic TBCK-related disorder, TBCK-related disorder
RS2477001736 Health Risk Likely pathogenic
RS2477024261 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS2477382277 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS559351051 Health Risk Likely pathogenic
RS749416609 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS758167759 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS758791315 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS778000956 Health Risk Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS778219583 Health Risk Likely pathogenic
RS925343986 Health Risk Likely pathogenic Inborn genetic diseases, Hypotonia, infantile
RS1131691329 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1268456443 Health Risk Pathogenic
RS1296819597 Health Risk Pathogenic
RS1303851095 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1560755661 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1560880946 Health Risk Pathogenic
RS1579391376 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1579395680 Health Risk Pathogenic Neurodevelopmental disorder, Hypotonia, infantile
RS1750958862 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1750962854 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
RS1750971659 Health Risk Pathogenic Inborn genetic diseases, Hypotonia, infantile
RS1759331986 Health Risk Pathogenic
RS1759333124 Health Risk Pathogenic
RS1767828321 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
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