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Search results 1 to 100 out of 239 for Pcdh15

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Hits by Strain

Hits by Category

Type Details Score
Gene
65217 | PCDH15
Type: gene
Organism: human
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Gene
609280 | PCDH15
Type: gene
Organism: dog, domestic
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Gene
100140108 | PCDH15
Type: gene
Organism: cattle
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Gene
423644 | PCDH15
Type: gene
Organism: chicken
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Gene
702413 | PCDH15
Type: gene
Organism: macaque, rhesus
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Gene
100494111 | pcdh15
Type: gene
Organism: frog, western clawed
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Gene
690865 | Pcdh15
Type: gene
Organism: rat
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Gene
450468 | PCDH15
Type: gene
Organism: chimpanzee
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Protein Coding Gene
MGI:1891428 | Pcdh15
Type: protein_coding_gene
Organism: mouse, laboratory
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GXD Expression
GXD Expression
 
Probe: MGI:6723844
Assay Type: Immunohistochemistry
Annotation Date: 2021-07-16
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906128
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6723937
Age: postnatal day 12
Image: 6 Pcdh15 tm1a/+
Specimen Label: 6 Pcdh15 tm1a/+
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
Probe: MGI:6723844
Assay Type: Immunohistochemistry
Annotation Date: 2021-07-16
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906128
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6723937
Age: postnatal day 12
Image: 6 Pcdh15 tm1a/tm1a
Note: No difference expression from heterozygous control.
Specimen Label: 6 Pcdh15 tm1a/tm1a
Detected: true
Specimen Num: 2
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Publication
30057206 | J:328653
First Author: Dionne G
Year: 2018
Journal: Neuron
Title: Mechanotransduction by PCDH15 Relies on a Novel cis-Dimeric Architecture.
Volume: 99
Issue: 3
Pages: 480-492.e5
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Publication
- | J:198553
     
First Author: Beutler B
Year: 2013
Journal: MGI Direct Data Submission
Title: Direct data submission for a Pcdh15 allele
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Publication
16799054 | J:112247
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
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Publication
19816713 | J:320724
First Author: Huertas-Vazquez A
Year: 2010
Journal: Hum Genet
Title: A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.
Volume: 127
Issue: 1
Pages: 83-9
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Publication
- | J:209275
     
First Author: Petit C
Year: 2014
Journal: MGI Direct Data Submission
Title: Direct Data Submission for Pcdh15 floxed allele from Ugds
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Publication
11487575 | J:71203
First Author: Alagramam KN
Year: 2001
Journal: Hum Mol Genet
Title: Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
Volume: 10
Issue: 16
Pages: 1709-18
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Publication
11429292 | J:70588
First Author: Murcia CL
Year: 2001
Journal: Mech Dev
Title: Expression of Pcdh15 in the inner ear, nervous system and various epithelia of the developing embryo.
Volume: 105
Issue: 1-2
Pages: 163-6
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Publication
21427143 | J:171627
First Author: Webb SW
Year: 2011
Journal: Development
Title: Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain.
Volume: 138
Issue: 8
Pages: 1607-17
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Publication
23035094 | J:190930
First Author: Zallocchi M
Year: 2012
Journal: J Neurosci
Title: Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.
Volume: 32
Issue: 40
Pages: 13841-59
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Publication
- | J:283661
     
First Author: Pepermans E
Year: 2020
Journal: MGI Direct Data Submission
Title: Direct data submission of two Pcdh15 floxed alleles from Unite de Genetique des Deficits Sensoriels
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Publication
14570705 | J:124774
First Author: Ahmed ZM
Year: 2003
Journal: Hum Mol Genet
Title: PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Volume: 12
Issue: 24
Pages: 3215-23
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Publication
10978835 | J:66637
First Author: Alagramam KN
Year: 2000
Journal: Hear Res
Title: Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer.
Volume: 148
Issue: 1-2
Pages: 181-91
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Publication
15952048 | J:148677
First Author: Alagramam KN
Year: 2005
Journal: J Assoc Res Otolaryngol
Title: Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.
Volume: 6
Issue: 2
Pages: 106-18
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Publication
12939319 | J:85211
First Author: Ball SL
Year: 2003
Journal: Invest Ophthalmol Vis Sci
Title: Assessment of retinal structure and function in Ames waltzer mice.
Volume: 44
Issue: 9
Pages: 3986-92
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Publication
16408167 | J:148675
First Author: Pawlowski KS
Year: 2006
Journal: J Assoc Res Otolaryngol
Title: Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development.
Volume: 7
Issue: 2
Pages: 83-94
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Publication
11138007 | J:66738
First Author: Alagramam KN
Year: 2001
Journal: Nat Genet
Title: The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
Volume: 27
Issue: 1
Pages: 99-102
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Publication
23467356 | J:196281
First Author: Geng R
Year: 2013
Journal: J Neurosci
Title: Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells.
Volume: 33
Issue: 10
Pages: 4395-404
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Publication
15811708 | J:97048
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
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Publication
24940003 | J:244761
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
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Publication
15537665 | J:95655
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
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Publication
25114259 | J:214830
First Author: Maeda R
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2.
Volume: 111
Issue: 35
Pages: 12907-12
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Publication
- | J:28688
 
First Author: Cook S
Year: 1993
Journal: Mouse Genome
Title: Re-mutation to Ames waltzer
Volume: 91
Pages: 554
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Publication
- | J:140625
     
First Author: Blasius AL
Year: 2008
Journal: MGI Direct Data Submission
Title: Record for "squirm" updated August 12, 2008
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Publication
23135401 | J:192825
First Author: Sotomayor M
Year: 2012
Journal: Nature
Title: Structure of a force-conveying cadherin bond essential for inner-ear mechanotransduction.
Volume: 492
Issue: 7427
Pages: 128-32
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Publication
20097680 | J:158344
First Author: Chance MR
Year: 2010
Journal: Hum Mol Genet
Title: Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.
Volume: 19
Issue: 8
Pages: 1515-27
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Publication
11124469 | J:106625
First Author: Raphael Y
Year: 2001
Journal: Hear Res
Title: Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice.
Volume: 151
Issue: 1-2
Pages: 237-249
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Publication
10430593 | J:56493
First Author: Alagramam KN
Year: 1999
Journal: Genetics
Title: A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.
Volume: 152
Issue: 4
Pages: 1691-9
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Publication
12782354 | J:84779
First Author: Hampton LL
Year: 2003
Journal: Hear Res
Title: A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.
Volume: 180
Issue: 1-2
Pages: 67-75
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Publication
35830793 | J:342094
First Author: Liu L
Year: 2022
Journal: Cell Rep
Title: Template-independent genome editing in the Pcdh15(av-3j) mouse, a model of human DFNB23 nonsyndromic deafness.
Volume: 40
Issue: 2
Pages: 111061
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Publication
34751129 | J:342718
   
First Author: Sethna S
Year: 2021
Journal: Elife
Title: Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome.
Volume: 10
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Publication
16887306 | J:111661
First Author: Zheng QY
Year: 2006
Journal: Hear Res
Title: A new spontaneous mutation in the mouse protocadherin 15 gene.
Volume: 219
Issue: 1-2
Pages: 110-20
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Publication
24405699 | J:220571
First Author: Ye R
Year: 2014
Journal: Genes Brain Behav
Title: Quantitative trait loci mapping and gene network analysis implicate protocadherin-15 as a determinant of brain serotonin transporter expression.
Volume: 13
Issue: 3
Pages: 261-75
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Publication
20498078 | J:245265
First Author: Elledge HM
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Structure of the N terminus of cadherin 23 reveals a new adhesion mechanism for a subset of cadherin superfamily members.
Volume: 107
Issue: 23
Pages: 10708-12
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Publication
35637313 | J:325092
First Author: Zhen Y
Year: 2022
Journal: Commun Biol
Title: Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways.
Volume: 5
Issue: 1
Pages: 511
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Publication
24044941 | J:220658
 
First Author: Torres AA
Year: 2013
Journal: Mutat Res
Title: The circling mutant Pcdh15roda is a new mouse model for hearing loss.
Volume: 751-752
Pages: 29-35
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Publication
16481439 | J:105750
First Author: Senften M
Year: 2006
Journal: J Neurosci
Title: Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.
Volume: 26
Issue: 7
Pages: 2060-71
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Publication
29069081 | J:248825
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
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Publication
23217710 | J:193334
First Author: Xiong W
Year: 2012
Journal: Cell
Title: TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells.
Volume: 151
Issue: 6
Pages: 1283-95
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Publication
17805295 | J:125331
First Author: Kazmierczak P
Year: 2007
Journal: Nature
Title: Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.
Volume: 449
Issue: 7158
Pages: 87-91
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Publication
21532990 | J:172400
First Author: Alagramam KN
Year: 2011
Journal: PLoS One
Title: Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells.
Volume: 6
Issue: 4
Pages: e19183
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Publication
22363448 | J:219988
First Author: Zallocchi M
Year: 2012
Journal: PLoS One
Title: Role for a novel Usher protein complex in hair cell synaptic maturation.
Volume: 7
Issue: 2
Pages: e30573
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Publication
22381527 | J:183898
First Author: Zheng QY
Year: 2012
Journal: Hum Mol Genet
Title: Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
Volume: 21
Issue: 11
Pages: 2588-98
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Publication
33009420 | J:299425
First Author: Michel V
Year: 2020
Journal: Sci Rep
Title: Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells.
Volume: 10
Issue: 1
Pages: 16430
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Publication
30061390 | J:266273
First Author: Honda A
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia.
Volume: 115
Issue: 33
Pages: 8388-8393
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Publication
15928608 | J:99757
 
First Author: Reiners J
Year: 2005
Journal: Mol Vis
Title: Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).
Volume: 11
Pages: 347-55
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Publication
23144817 | J:195357
First Author: Roeseler DA
Year: 2012
Journal: PLoS One
Title: Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2.
Volume: 7
Issue: 11
Pages: e47366
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Publication
22318628 | J:182748
First Author: Chacon-Heszele MF
Year: 2012
Journal: Development
Title: Regulation of cochlear convergent extension by the vertebrate planar cell polarity pathway is dependent on p120-catenin.
Volume: 139
Issue: 5
Pages: 968-78
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Publication
37011103 | J:346281
First Author: Krey JF
Year: 2023
Journal: PLoS Biol
Title: Control of stereocilia length during development of hair bundles.
Volume: 21
Issue: 4
Pages: e3001964
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Protein Coding Gene
MGP_CAROLIEiJ_G0015432 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0017347 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0017324 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0017285 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0017284 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0017108 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_1891428 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0017742 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0016678 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0017080 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0017185 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0017178 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0017258 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0017206 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0017781 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0016462 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0016742 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0030848 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0016245 | -
Type: protein_coding_gene
Organism: Mus spretus
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Publication
5093631 | J:5225
First Author: Osako S
Year: 1971
Journal: Acta Otolaryngol
Title: Electron microscopic studies of capillary permeability in normal and ames waltzer deaf mice.
Volume: 71
Issue: 5
Pages: 365-76
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Publication
- | J:14990
 
First Author: Schaible RH
Year: 1956
Journal: Mouse News Lett
Title: av
Volume: 15
Pages: 29
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Publication
- | J:81272
     
First Author: Gagnon LH
Year: 2003
Journal: MGI Direct Data Submission
Title: A new allele of protocadherin 15 (Pcdh15) named Ames waltzer 4 Jackson. Mouse Mutant Resources Web Site, The Jackson Laboratory, Bar Harbor, Maine
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Publication
- | J:203622
     
First Author: Daniel C
Year: 2014
Journal: MGI Direct Data Submission
Title: Direct data submission for mcduck
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Publication
- | J:236676
     
First Author: Ludwig S
Year: 2016
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for sphere
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Publication
- | J:255213
     
First Author: Prince L
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for tortilla
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759725
Stage: TS25
Assay Id: MGI:4867262
Age: embryonic day 17.0
Specimen Label: E17
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759726
Stage: TS26
Assay Id: MGI:4867262
Age: embryonic day 18.0
Specimen Label: E18
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759727
Stage: TS27
Assay Id: MGI:4867262
Age: postnatal day 0
Specimen Label: P0
Detected: true
Specimen Num: 3
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759727
Stage: TS27
Assay Id: MGI:4867262
Age: postnatal day 2
Specimen Label: P2
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867262
Age: postnatal day 4
Specimen Label: P4
Detected: true
Specimen Num: 5
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867262
Age: postnatal day 6
Specimen Label: P6
Detected: true
Specimen Num: 6
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GXD Expression
GXD Expression
     
Probe: MGI:4867243
Assay Type: RT-PCR
Annotation Date: 2011-01-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:4867262
Age: postnatal day 8
Specimen Label: P8
Detected: true
Specimen Num: 7
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GXD Expression
GXD Expression
   
Probe: MGI:7595522
Assay Type: RT-PCR
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759724
Stage: TS24
Assay Id: MGI:7595530
Age: embryonic day 16.0
Image: 4
Specimen Label: E16
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
   
Probe: MGI:7595522
Assay Type: RT-PCR
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759727
Stage: TS27
Assay Id: MGI:7595530
Age: postnatal day 0
Image: 4
Specimen Label: P0
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
   
Probe: MGI:7595522
Assay Type: RT-PCR
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:7595530
Age: postnatal day 4
Image: 4
Specimen Label: P4
Detected: true
Specimen Num: 3
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:7595522
Assay Type: RT-PCR
Annotation Date: 2024-02-20
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1759728
Stage: TS28
Assay Id: MGI:7595530
Age: postnatal day 7
Image: 4
Specimen Label: P7
Detected: true
Specimen Num: 4
•
•
•
•
•
GXD Expression
GXD Expression
 
Probe: MGI:3843332
Assay Type: RNA in situ
Annotation Date: 2009-05-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1760624
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:3843481
Age: embryonic day 16.0
Image: 2E
Specimen Label: 2E
Detected: true
Specimen Num: 18
•
•
•
•
•
GXD Expression
GXD Expression
 
Probe: MGI:3843332
Assay Type: RNA in situ
Annotation Date: 2009-05-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737320
Pattern: Regionally restricted
Stage: TS20
Assay Id: MGI:3843481
Age: embryonic day 12.0
Note: Expression is in metanephric vesicles and developing glomeruli.
Specimen Label: Not shown E12
Detected: true
Specimen Num: 1
•
•
•
•
•
GXD Expression
GXD Expression
 
Probe: MGI:3843332
Assay Type: RNA in situ
Annotation Date: 2009-05-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1760024
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:3843481
Age: embryonic day 16.0
Image: 1A
Specimen Label: 1A
Detected: true
Specimen Num: 4
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:3843332
Assay Type: RNA in situ
Annotation Date: 2009-05-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1760020
Pattern: Not Specified
Stage: TS20
Assay Id: MGI:3843481
Age: embryonic day 12.0
Specimen Label: Not shown E12
Detected: true
Specimen Num: 1
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:3843332
Assay Type: RNA in situ
Annotation Date: 2009-05-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1760022
Pattern: Not Specified
Stage: TS22
Assay Id: MGI:3843481
Age: embryonic day 14.0
Specimen Label: Not shown E14
Detected: true
Specimen Num: 2
•
•
•
•
•




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