TMC1 Chromosome 9

Transmembrane channel like 1
138 variants 138 Health Risk

Upload your DNA to see your personal genotypes for variants in TMC1.

What This Gene Does
This gene is considered a member of a gene family predicted to encode transmembrane proteins. The specific function of this gene is unknown; however, it is known to be required for normal function of cochlear hair cells. Mutations in this gene have been associated with progressive postlingual hearing loss and profound prelingual deafness. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Transmembrane channel like family
Locus Type
gene with protein product
Location
9q21.13
Ensembl
ENSG00000165091
Associated Conditions (16)
Autosomal dominant nonsyndromic hearing loss 36
Autosomal recessive nonsyndromic hearing loss 7
Inborn genetic diseases
Sensorineural hearing loss disorder
Nonsyndromic genetic hearing loss
Hearing impairment
Hearing loss
autosomal recessive
Rare genetic deafness
TMC1-related disorder
Monogenic hearing loss
Deafness
Delayed speech and language development
Moderate intellectual disability
Bilateral sensorineural hearing impairment
Ear malformation
Key Variants
RS1057515622
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
Health Risk
RS111033497
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
Health Risk
RS11143384
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
Health Risk
RS113342704
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36, Inborn genetic diseases
Health Risk
RS1181901214
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 7, Sensorineural hearing loss disorder, Autosomal recessive nonsyndromic hearing loss 7
Health Risk
RS121908074
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 7, Nonsyndromic genetic hearing loss, Autosomal recessive nonsyndromic hearing loss 7
Health Risk
RS1391895910
Conflicting classifications of pathogenicity
Health Risk
RS139985214
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
Health Risk
RS140388347
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140398130
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
Health Risk
RS142073640
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
Health Risk
RS1439351996
Conflicting classifications of pathogenicity
Hearing impairment, Hearing impairment
Health Risk
All Variants (138)
RSID Category Clinical Significance Conditions
RS368084452 Health Risk Pathogenic Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
RS727503483 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7
RS727504554 Health Risk Pathogenic Rare genetic deafness, Rare genetic deafness
RS730880359 Health Risk Pathogenic Rare genetic deafness, Rare genetic deafness
RS745767539 Health Risk Pathogenic
RS747645067 Health Risk Pathogenic Delayed speech and language development, Moderate intellectual disability, Bilateral sensorineural hearing impairment
RS750724544 Health Risk Pathogenic
RS752678337 Health Risk Pathogenic
RS753687760 Health Risk Pathogenic Nonsyndromic genetic hearing loss, Nonsyndromic genetic hearing loss
RS757327146 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Hearing loss, autosomal recessive
RS765657443 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7
RS775428246 Health Risk Pathogenic Rare genetic deafness, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
RS776267308 Health Risk Pathogenic
RS776689179 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7
RS777777359 Health Risk Pathogenic Hearing loss, autosomal recessive, Autosomal dominant nonsyndromic hearing loss 36
RS786201027 Health Risk Pathogenic Autosomal dominant nonsyndromic hearing loss 36, Autosomal dominant nonsyndromic hearing loss 36
RS876657727 Health Risk Pathogenic Rare genetic deafness, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
RS876657729 Health Risk Pathogenic Rare genetic deafness, Rare genetic deafness
RS878853229 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
RS878853230 Health Risk Pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7
RS964315149 Health Risk Pathogenic
RS1172357346 Health Risk Pathogenic/Likely pathogenic
RS121908072 Health Risk Pathogenic/Likely pathogenic Autosomal dominant nonsyndromic hearing loss 36, Rare genetic deafness, Autosomal dominant nonsyndromic hearing loss 36
RS121908076 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 7, Hearing loss, autosomal recessive
RS1263141648 Health Risk Pathogenic/Likely pathogenic
RS138527651 Health Risk Pathogenic/Likely pathogenic Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
RS1448901281 Health Risk Pathogenic/Likely pathogenic Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
RS1564554255 Health Risk Pathogenic/Likely pathogenic Deafness, Hearing loss, autosomal recessive
RS1564556995 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 7, Hearing loss, autosomal recessive
RS1588067173 Health Risk Pathogenic/Likely pathogenic Rare genetic deafness, Rare genetic deafness
RS2132189585 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7
RS370898981 Health Risk Pathogenic/Likely pathogenic Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
RS563322370 Health Risk Pathogenic/Likely pathogenic Autosomal dominant nonsyndromic hearing loss 36, Autosomal recessive nonsyndromic hearing loss 7, TMC1-related disorder
RS758288878 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 7, Autosomal recessive nonsyndromic hearing loss 7
RS761261855 Health Risk Pathogenic/Likely pathogenic Deafness, Hearing loss, autosomal recessive
RS772640673 Health Risk Pathogenic/Likely pathogenic Nonsyndromic genetic hearing loss, Autosomal recessive nonsyndromic hearing loss 7, Autosomal dominant nonsyndromic hearing loss 36
RS773851192 Health Risk Pathogenic/Likely pathogenic Deafness, Hearing loss, autosomal recessive
RS876657728 Health Risk Pathogenic/Likely pathogenic Rare genetic deafness, Rare genetic deafness
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