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Search results 101 to 185 out of 185 for Krt71

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Type Details Score
Publication
- | J:24189
 
First Author: Harris B
Year: 1994
Journal: Mouse Genome
Title: The map location of grey coat (grc) is confirmed on Chromosome 5
Volume: 92
Pages: 672
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Publication
- | J:50994
     
First Author: Harris BS
Year: 1998
Journal: MGI Direct Data Submission
Title: The Jackson Laboratory Mouse Mutant Resource 1998 Mutation Reports
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Publication
30638933 | J:290212
First Author: Noto M
Year: 2019
Journal: Biochem Biophys Res Commun
Title: Sox13 is a novel early marker for hair follicle development.
Volume: 509
Issue: 4
Pages: 862-868
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Publication
2289471 | J:11008
First Author: Noebels JL
Year: 1990
Journal: Epilepsy Res
Title: Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.
Volume: 7
Issue: 2
Pages: 129-35
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Publication
2272507 | J:10942
First Author: Davisson MT
Year: 1990
Journal: Genet Res
Title: The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15.
Volume: 56
Issue: 2-3
Pages: 167-78
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Publication
12399393 | J:79964
First Author: Poirier C
Year: 2002
Journal: Genetics
Title: Hague (Hag). A new mouse hair mutation with an unstable semidominant allele.
Volume: 162
Issue: 2
Pages: 831-40
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Publication
20962855 | J:173143
First Author: Dai D
Year: 2011
Journal: J Invest Dermatol
Title: Fuz controls the morphogenesis and differentiation of hair follicles through the formation of primary cilia.
Volume: 131
Issue: 2
Pages: 302-10
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Publication
19470461 | J:150086
First Author: Kiso M
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice.
Volume: 106
Issue: 23
Pages: 9292-7
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Publication
22144916 | J:179810
First Author: Blanco S
Year: 2011
Journal: PLoS Genet
Title: The RNA-methyltransferase Misu (NSun2) poises epidermal stem cells to differentiate.
Volume: 7
Issue: 12
Pages: e1002403
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Publication
7738386 | J:25255
First Author: Hogan ME
Year: 1995
Journal: J Invest Dermatol
Title: Defects of pelage hairs in 20 mouse mutations.
Volume: 104
Issue: 5 Suppl
Pages: 31S-32S
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Publication
23201579 | J:193107
First Author: Jin C
Year: 2013
Journal: Dev Biol
Title: Deciphering gene expression program of MAP3K1 in mouse eyelid morphogenesis.
Volume: 374
Issue: 1
Pages: 96-107
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Publication
23271346 | J:192592
First Author: Sotiropoulou PA
Year: 2013
Journal: Genes Dev
Title: BRCA1 deficiency in skin epidermis leads to selective loss of hair follicle stem cells and their progeny.
Volume: 27
Issue: 1
Pages: 39-51
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Publication
25546423 | J:228844
First Author: Leilei Y
Year: 2014
Journal: PLoS One
Title: iRhom2 mutation leads to aberrant hair follicle differentiation in mice.
Volume: 9
Issue: 12
Pages: e115114
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Publication
22935613 | J:205544
First Author: Dai D
Year: 2013
Journal: Cell Death Differ
Title: Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia.
Volume: 20
Issue: 1
Pages: 130-8
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Publication
16831889 | J:109436
First Author: Schweizer J
Year: 2006
Journal: J Cell Biol
Title: New consensus nomenclature for mammalian keratins.
Volume: 174
Issue: 2
Pages: 169-74
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Publication
- | J:30359
       
First Author: Sundberg JP (ed.)
Year: 1994
Title: Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
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Publication
- | J:30778
First Author: Sweet HO
Year: 1995
Journal: Mouse Genome
Title: Remutations at The Jackson Laboratory (Update to Mouse Genome 1993; 91:862-5 - J16313)
Volume: 93
Issue: 4
Pages: 1030-4
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Publication
16510873 | J:105811
First Author: Wu X
Year: 2006
Journal: Genes Dev
Title: Cdc42 controls progenitor cell differentiation and beta-catenin turnover in skin.
Volume: 20
Issue: 5
Pages: 571-85
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Publication
25917818 | J:222308
First Author: Fairfield H
Year: 2015
Journal: Genome Res
Title: Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
Volume: 25
Issue: 7
Pages: 948-57
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Publication
- | J:342607
       
First Author: Birgit Meldal and Sandra Orchard (1). (1) European Bioinformatics Institute (EBI), Hinxton, Cambridgeshire, United Kingdom
Year: 2023
Title: Manual transfer of experimentally-verified manual GO annotation data to homologous complexes by curator judgment of sequence, composition and function similarity
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Publication
- | J:157064
     
First Author: University of California, Davis
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the University of California, Davis
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Publication
- | J:345476
       
First Author: Haiming Tang, Dustin Ebert, Matthias Blum, Robert Finn, Paul Thomas
Year: 2023
Title: TreeGrafter-generated GO annotations
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Publication
- | J:94790
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Mouse Synonym Curation
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Publication
- | J:265051
     
First Author: MGI and IMPC
Year: 2018
Journal: Database Release
Title: MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC)
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Publication
- | J:57656
     
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
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Publication
- | J:148605
     
First Author: Wellcome Trust Sanger Institute
Year: 2009
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute
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Publication
11217851 | J:65060
First Author: Kawai J
Year: 2001
Journal: Nature
Title: Functional annotation of a full-length mouse cDNA collection.
Volume: 409
Issue: 6821
Pages: 685-90
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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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Publication
21677750 | J:173534
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
- | J:60000
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
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Publication
- | J:342587
       
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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Publication
- | J:68900
     
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
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Publication
12466851 | J:80000
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
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Publication
- | J:164563
       
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
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Publication
21267068 | J:153498
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
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Publication
- | J:157972
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
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Publication
- | J:75000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
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Publication
- | J:57747
     
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
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Publication
- | J:161428
       
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
- | J:144086
     
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
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Publication
- | J:144087
     
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
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Allele
Krt71<Ca-2H> | MGI:5299232
 
Name: keratin 71; caracul 2 Harwell
Allele Type: Radiation induced
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Genotype
Genotype
Symbol: Krt71/Krt71
Background: involves: 101/H
Zygosity: hm
Has Mutant Allele: true
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Allele
Krt71<Ca-19J> | MGI:5586972
Name: keratin 71; caracul 19 Jackson
Allele Type: Spontaneous
Attribute String: Not Specified
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Genotype
Genotype
Symbol: Krt71/Krt71<+>
Background: BALB/cJ-Krt71/GrsrJ
Zygosity: ht
Has Mutant Allele: true
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DO Term
DOID:0110710 | hypotrichosis 13
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Allele
Bstk | MGI:5308660
 
Name: Belly streak
Allele Type: Radiation induced
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Genotype
Genotype
Symbol: Bstk/Bstk<+>
Background: involves: C3H/HeH
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Bstk/Bstk
Background: involves: C3H/HeH
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Krt71/Krt71
Background: involves: 101/H
Zygosity: ht
Has Mutant Allele: true
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Publication
21083932 | J:166446
 
First Author: Kim BK
Year: 2010
Journal: BMC Genomics
Title: Gene expression profile of the skin in the 'hairpoor' (HrHp) mice by microarray analysis.
Volume: 11
Pages: 640
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Allele
Scn8a<med-J> | MGI:1856079
 
Name: sodium channel, voltage-gated, type VIII, alpha; motor end plate disease Jackson
Allele Type: Spontaneous
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Publication
12706885 | J:83212
 
First Author: Buchner DA
Year: 2003
Journal: Gene
Title: TSRC1, a widely expressed gene containing seven thrombospondin type I repeats.
Volume: 307
Pages: 23-30
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Publication
12920299 | J:84898
First Author: Buchner DA
Year: 2003
Journal: Science
Title: SCNM1, a putative RNA splicing factor that modifies disease severity in mice.
Volume: 301
Issue: 5635
Pages: 967-9
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Publication
8663325 | J:34154
First Author: Kohrman DC
Year: 1996
Journal: J Biol Chem
Title: Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.
Volume: 271
Issue: 29
Pages: 17576-81
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Strain
MGI:2161825 | B6C3Fe a/a-Krt71<Ca> Scn8a<med-J>/J
Attribute String: mutant strain
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Strain
MGI:2164555 | C57BL/6J-Scn8a<med-J>
Attribute String: mutant strain
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Publication
289327 | J:6191
 
First Author: Sidman RL
Year: 1979
Journal: Ann N Y Acad Sci
Title: Inherited muscle and nerve diseases in mice: a tabulation with commentary.
Volume: 317
Pages: 497-505
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Publication
26252017 | J:242789
First Author: Pal D
Year: 2015
Journal: PLoS One
Title: Reduced Nav1.6 Sodium Channel Activity in Mice Increases In Vivo Sensitivity to Volatile Anesthetics.
Volume: 10
Issue: 8
Pages: e0134960
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Publication
13679025 | J:85319
First Author: Buchner DA
Year: 2003
Journal: Genomics
Title: High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spot.
Volume: 82
Issue: 4
Pages: 452-9
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Publication
17999925 | J:130137
 
First Author: Sun Y
Year: 2007
Journal: Brain Res
Title: Comparison of gamma-aminobutyrate receptors in the medial vestibular nucleus of control and Scn8a mutant mice.
Volume: 1186
Pages: 188-93
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Publication
12204355 | J:108906
First Author: Koay G
Year: 2002
Journal: Hear Res
Title: Behavioral audiograms of homozygous med(J) mutant mice with sodium channel deficiency and unaffected controls.
Volume: 171
Issue: 1-2
Pages: 111-118
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Publication
14769375 | J:87267
First Author: Hamann M
Year: 2003
Journal: Exp Neurol
Title: Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia.
Volume: 184
Issue: 2
Pages: 830-8
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Publication
18791226 | J:141236
First Author: Howell VM
Year: 2008
Journal: Genetics
Title: A targeted deleterious allele of the splicing factor SCNM1 in the mouse.
Volume: 180
Issue: 3
Pages: 1419-27
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Publication
12374766 | J:79617
First Author: Kearney JA
Year: 2002
Journal: Hum Mol Genet
Title: Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).
Volume: 11
Issue: 22
Pages: 2765-75
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Publication
10564739 | J:58473
First Author: Chen K
Year: 1999
Journal: Brain Res
Title: Reduced spontaneous activity in the dorsal cochlear nucleus of Scn8a mutant mice.
Volume: 847
Issue: 1
Pages: 85-9
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Publication
7049455 | J:6824
First Author: Papiernik M
Year: 1982
Journal: Clin Exp Immunol
Title: Impairment of T lymphocyte functions in mice with motor end-plate disease.
Volume: 48
Issue: 2
Pages: 429-36
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Publication
9949206 | J:53340
First Author: Sprunger LK
Year: 1999
Journal: Hum Mol Genet
Title: Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3.
Volume: 8
Issue: 3
Pages: 471-9
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Publication
- | J:64101
 
First Author: Lane PW
Year: 1976
Journal: Mouse News Lett
Title: Scn8amed-J - motor end-plate disease-Jackson
Volume: 54
Pages: 40
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Genotype
Genotype
Symbol: Scn8a/Scn8a Scnm1/Scnm1
Background: involves: C57BL/6J
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a Scnm1/Scnm1
Background: involves: C57BL/6 * FVB * SJL * STOCK Krt71
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a Scnm1/Scnm1
Background: involves: C57BL/6 * STOCK Krt71
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a Scnm1/Scnm1
Background: involves: C57BL/6J * STOCK Krt71
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a
Background: involves: STOCK Krt71
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a Scnm1/Scnm1<+>
Background: involves: C3HeB/FeJ * C57BL/6J
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Scn8a/Scn8a
Background: involves: C3H
Zygosity: hm
Has Mutant Allele: true
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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