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| Nomenclature |
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Symbol:
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EbpTd
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Name:
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phenylalkylamine Ca2+ antagonist (emopamil) binding protein;
tattered
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MGI ID: |
MGI:1857832 |
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Gene:
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Ebp
Location:
ChrX:8185329-8193512 bp, - strand
Genetic Position: ChrX,
3.7 cM
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Mutation
origin |
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Strain of Origin:
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Not Specified
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Single point mutation |
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Mutation details: G to A transition at position 454, resulting in an amino acid substitution of arginine for glycine at position 107. This residue is predicted to reside in the cytoplasmic loop between transmembrane domains 2 and 3. (J:55860)
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Inheritance: | |
Semidominant |
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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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| References |
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Original: |
J:13907
Cattanach BM,
"A new X-linked mutation, Td"
Mouse News Lett 1982;66():61-2
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All: |
7 reference(s)
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Analysis Tools
