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Sequence Detail
ID/Version
Q8R4P5 Q7TQB2 Q9D435 (UniProt | EBI) Last sequence update: 2002-06-01
Last annotation update: 2014-07-09
Sequence
description
from provider
RecName: Full=Transmembrane channel-like protein 1;AltName: Full=Beethoven protein;AltName: Full=Deafness protein;AltName: Full=Transmembrane cochlear-expressed protein 1;
Provider SWISS-PROT
Sequence
Polypeptide 757 aa
For this sequence
Source
Organism mouse
See UniProt | EBI for source
Annotated genes and markers Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.
Type Symbol Name GO Terms Expression
Assays
Orthologs Phenotypic
Alleles
Gene Tmc1 transmembrane channel-like gene family 1 18 4 5 15
Sequence references in MGI J:75103 Vreugde S, et al., Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat Genet. 2002 Mar;30(3):257-8
J:75142 Kurima K, et al., Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nat Genet. 2002 Mar;30(3):277-84
J:84240 Keresztes G, et al., TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins. BMC Genomics. 2003 Jun 17;4(1):24
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/19/2014
MGI 5.19
The Jackson Laboratory