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Protein-coding gene in the species Homo sapiens
channel-like protein 1 is a protein that in humans is encoded by the TMC1 gene. TMC1 contains six transmembrane domains with both the C and N termini on
TMC1
Medical condition
KCNQ4, MYO15A, MYO6, MYO7A, OTOF, PCDH15, POU3F4, SLC26A4, STRC, TECTA, TMC1, TMIE, TMPRSS3, USH1C, and WFS1 genes cause nonsyndromic deafness, with weaker
Nonsyndromic_deafness
Method used by several animal species to determine location using sound
in echolocation frequency among dolphins. Tmc1 and Pjvk are proteins related to hearing sensitivity: Tmc1 is associated with hair cell development and
Animal_echolocation
Partial or total inability to hear
Researchers reported in 2015 that genetically deaf mice which were treated with TMC1 gene therapy recovered some of their hearing. In 2017, additional studies
Hearing_loss
Human chromosome
testis expressed 10 TGFBR1: transforming growth factor beta, receptor type I TMC1: transmembrane channel-like 1 TMEM215: encoding protein Transmembrane protein
Chromosome_9
Protein-coding gene in the species Homo sapiens
components of the mechanoelectrical transduction (MET) channel, including TMC1. While the mechanism by which TOMT contributes to MET currents and auditory
LRTOMT
Group of transport proteins
residues (aas) in length and exhibit 7 to 10 transmembrane segments (TMSs). Tmc1 and Tmc2 (TC#s 1.A.17.4.6 and 1.A.17.4.1, respectively) may play a role in
Calcium-dependent chloride channel
Calcium-dependent_chloride_channel
Protein-coding gene in the species Homo sapiens
2002). "Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function". Nat Genet. 30 (3): 277–84. doi:10
TMC2
Q969X1 16802 TMBIM4 HGNC:24257; Q9HC24 16803 TMBIM6 HGNC:11723; P55061 16804 TMC1 HGNC:16513; Q8TDI8 16805 TMC2 HGNC:16527; Q8TDI7 16806 TMC3 HGNC:22995; Q7Z5M5
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
autosomal dominant 2B; 612644; GJB3 Deafness, autosomal dominant 36; 606705; TMC1 Deafness, autosomal dominant 36, with dentinogenesis; 605594; DSPP Deafness
List_of_OMIM_disorder_codes
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