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Search results 101 to 124 out of 124 for Kcnj13

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Type Details Score
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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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: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: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: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: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
30009826 | J:280225
 
First Author: Roman D
Year: 2018
Journal: Exp Eye Res
Title: Conditional loss of Kcnj13 in the retinal pigment epithelium causes photoreceptor degeneration.
Volume: 176
Pages: 219-226
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Allele
Kcnj13<em2Smoc> | MGI:7290663
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 2, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em2Mrd> | MGI:5775280
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 2, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em3Mrd> | MGI:5775281
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 3, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em4Mrd> | MGI:5775283
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 4, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em5Mrd> | MGI:5775295
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 5, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em6Mrd> | MGI:5775298
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 6, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em1Mrd> | MGI:5775213
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 1, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Kcnj13<em7Mrd> | MGI:5775299
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 7, Graeme Mardon
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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DO Term
DOID:0110118 | Leber congenital amaurosis 16
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Strain
MGI:7623414 | C57BL/6JSmoc-Kcnj13<em2Smoc>/Smoc
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
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Allele
Kcnj13<em1Smoc> | MGI:7290662
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Conditional ready, No functional change
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DO Term
DOID:0111570 | snowflake vitreoretinal degeneration
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Strain
MGI:6475637 | C57BL/6JSmoc-Kcnj13<em1Smoc>/Smoc
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
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Publication
28878288 | J:256546
First Author: Shahi PK
Year: 2017
Journal: Sci Rep
Title: Abnormal Electroretinogram after Kir7.1 Channel Suppression Suggests Role in Retinal Electrophysiology.
Volume: 7
Issue: 1
Pages: 10651
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Publication
29740340 | J:325433
 
First Author: Cornejo I
Year: 2018
Journal: Front Physiol
Title: Tissue Distribution of Kir7.1 Inwardly Rectifying K+ Channel Probed in a Knock-in Mouse Expressing a Haemagglutinin-Tagged Protein.
Volume: 9
Pages: 428
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