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| Nomenclature |
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Symbol:
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Bhlhe22tm2.1Meg
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Name:
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basic helix-loop-helix family, member e22;
targeted mutation 2.1, Michael E Greenberg
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MGI ID: |
MGI:4440744 |
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Synonyms: |
Bhlhb5fl |
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Gene:
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Bhlhe22
Location:
Chr3:18054174-18057517 bp, + strand
Genetic Position: Chr3,
4.98 cM, cytoband A2
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:158273
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129/Sv
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Mutation
description |
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Allele
Type: | |
Targeted (Floxed/Frt) |
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Mutation: | |
Insertion |
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LoxP sites flank the single coding exon of this gene. (J:158273)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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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 Bhlhe22 Mutation:
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0 strains or lines available |
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| References |
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Original: |
J:158273
Ross SE et al.,
"Loss of inhibitory interneurons in the dorsal spinal cord and elevated itch in Bhlhb5 mutant mice."
Neuron 2010 Mar 25;65(6):886-98
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All: |
2 reference(s)
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Analysis Tools
