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Search results 301 to 363 out of 363 for Tmc1

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Type Details Score
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication      
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication
First Author: Yu X
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Deafness mutation D572N of TMC1 destabilizes TMC1 expression by disrupting LHFPL5 binding.
Volume: 117
Issue: 47
Pages: 29894-29903
Allele  
Name: transmembrane channel-like gene family 1; endonuclease-mediated mutation 2, Robert Fettiplace
Allele Type: Endonuclease-mediated
Allele  
Name: transmembrane channel-like gene family 1; endonuclease-mediated mutation 5, Robert Fettiplace
Allele Type: Endonuclease-mediated
Allele
Name: transmembrane channel-like gene family 1; endonuclease-mediated mutation 1, Robert Fettiplace
Allele Type: Endonuclease-mediated
Attribute String: Humanized sequence
Allele  
Name: transmembrane channel-like gene family 1; endonuclease-mediated mutation 4, Robert Fettiplace
Allele Type: Endonuclease-mediated
Allele  
Name: Tmc1 modifier 1; C3HeB/FeJ
Allele Type: QTL
Allele  
Name: Tmc1 modifier 1; C57BL/6J
Allele Type: QTL
Allele  
Name: Tmc1 modifier 3; DBA/2J
Allele Type: QTL
Allele  
Name: Tmc1 modifier 3; C3HeB/FeJ
Allele Type: QTL
Allele  
Name: Tmc1 modifier 2; C3HeB/FeJ
Allele Type: QTL
Allele  
Name: Tmc1 modifier 2; DBA/2J
Allele Type: QTL
Allele  
Name: Tmc1 modifier 4; C3HeB/FeJ
Allele Type: QTL
Allele  
Name: Tmc1 modifier 4; DBA/2J
Allele Type: QTL
Allele  
Name: transmembrane channel-like gene family 1; endonuclease-mediated mutation 3, Robert Fettiplace
Allele Type: Endonuclease-mediated
Allele  
Name: transmembrane channel-like gene family 1; deafness
Allele Type: Spontaneous
Allele  
Name: transmembrane channel-like gene family 1; Martin Hrabe de Angelis beethoven
Allele Type: Chemically induced (ENU)
Allele  
Name: transmembrane channel-like gene family 1; stitch
Allele Type: Chemically induced (ENU)
Allele  
Name: transmembrane channel-like gene family 1; baringo
Allele Type: Chemically induced (ENU)
Allele  
Name: transmembrane channel-like gene family 1; nice
Allele Type: Chemically induced (ENU)
Genotype
Symbol: Tmc1/Tmc1<+> Tmc1m1/?
Background: involves: C3HeB/FeJ * C57BL/6J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1<+> Tmc1m2/?
Background: involves: C3HeB/FeJ * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1<+> Tmc1m3/?
Background: involves: C3HeB/FeJ * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1<+> Tmc1m4/?
Background: involves: C3HeB/FeJ * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1
Background: involves: C57BL/6
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1
Background: involves: C57BL/6
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1
Background: involves: C57BL/6
Zygosity: hm
Has Mutant Allele: true
DO Term
DO Term
Genotype
Symbol: Tmc1/Tmc1<+>
Background: C3HeB/FeJ-Tmc1/Ieg
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1
Background: STOCK Grhl3/J
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Tmc1/Tmc1
Background: involves: STOCK Grhl3 * M. m. molossinus
Zygosity: hm
Has Mutant Allele: true
Publication
First Author: Qiu X
Year: 2023
Journal: Cell Rep
Title: The tetraspan LHFPL5 is critical to establish maximal force sensitivity of the mechanotransduction channel of cochlear hair cells.
Volume: 42
Issue: 3
Pages: 112245
Publication
First Author: Haywood-Watson RJ 2nd
Year: 2006
Journal: Invest Ophthalmol Vis Sci
Title: Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
Volume: 47
Issue: 7
Pages: 3074-84
Publication
First Author: Pepermans E
Year: 2014
Journal: EMBO Mol Med
Title: The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.
Volume: 6
Issue: 7
Pages: 984-92
Publication
First Author: Zheng QY
Year: 2005
Journal: Hum Mol Genet
Title: Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
Volume: 14
Issue: 1
Pages: 103-11
Publication
First Author: Washington JL 3rd
Year: 2005
Journal: Hear Res
Title: Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
Volume: 202
Issue: 1-2
Pages: 161-9
Protein Domain
Type: Family
Description: Protocadherin-15 (Pcdh15) belongs to the epsilon subfamily of nonclustered protocadherins. It is a component of the tip-links, the extracellular filaments that connect the tips of stereocilia and gate hair cell mechano-electrical transduction channels in the inner ear []. Pcdh15 interacts with transmembrane channel-like proteins TMC1 and TMC2, which have been implicated in mechanotransduction in mammalian hair cells []. Mutations in genes coding for Pcdh15 cause deafness in both mice and humans [, ]. Pcdh15 plays an important role in hair-bundle morphogenesis [].The cadherin family consists of a large group of cell adhesion proteins. It can be classified into three subfamilies: classical cadherins, desmosomal cadherins and protocadherins (PCDHs). Based on the genomic structure, the PCDH family can be divided into two groups, clustered PCDHs and non-clustered PCDHs. Non-clustered PCDHs can be further classified into three subgroups: delta1 (PCDH1, PCDH7, PCDH9, PCDH11 and PCDH20), delta2 (PCDH8, PCDH10, PCDH12, PCDH17, PCDH18 and PCDH19) and epsilon (PCDH15, PCDH16, PCDH21 and MUCDHL). Non-clustered PCDHs are expressed predominantly in the nervous system and have spatiotemporally diverse expression patterns [].
Publication  
First Author: Yeh WH
Year: 2020
Journal: Sci Transl Med
Title: In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness.
Volume: 12
Issue: 546
Publication
First Author: Boucher S
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.
Volume: 117
Issue: 49
Pages: 31278-31289
Publication  
First Author: An Y
Year: 2024
Journal: Front Pharmacol
Title: The transmembrane channel-like 6 (TMC6) in primary sensory neurons involving thermal sensation via modulating M channels.
Volume: 15
Pages: 1330167
Publication
First Author: Johnson KR
Year: 2015
Journal: Mamm Genome
Title: A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice.
Volume: 26
Issue: 7-8
Pages: 338-47
Publication
First Author: Mahendrasingam S
Year: 2017
Journal: PLoS One
Title: Spatiotemporal changes in the distribution of LHFPL5 in mice cochlear hair bundles during development and in the absence of PCDH15.
Volume: 12
Issue: 10
Pages: e0185285
Protein
Organism: Mus musculus/domesticus
Length: 1943  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1783  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1865  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1333  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 1714  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1675  
Fragment?: false
Publication
First Author: Kim SY
Year: 2011
Journal: Cell Adh Migr
Title: Non-clustered protocadherin.
Volume: 5
Issue: 2
Pages: 97-105