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| Nomenclature |
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Symbol:
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Nme5tm1Lex
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Name:
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NME/NM23 family member 5;
targeted mutation 1, Lexicon Genetics
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MGI ID: |
MGI:5429195 |
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Gene:
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Nme5
Location:
Chr18:34562634-34579115 bp, - strand
Genetic Position: Chr18,
18.69 cM, cytoband B3
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:185566
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Parent Cell Line:
| Lex-2 (ES Cell) |
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Strain of Origin:
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129S5/SvEvBrd
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Intragenic deletion |
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Deletion of coding exon 1. (J:185566)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Nme5 Mutation:
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1 strain or line available |
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| References |
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Original: |
J:185566
Vogel P et al.,
"Congenital hydrocephalus in genetically engineered mice."
Vet Pathol 2012 Jan;49(1):166-81
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All: |
1 reference(s)
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Analysis Tools
