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EbpTd
Radiation induced Allele Detail
Nomenclature
Symbol: EbpTd
Name: phenylalkylamine Ca2+ antagonist (emopamil) binding protein; tattered
MGI ID: MGI:1857832
Gene: Ebp  Location: ChrX:8185329-8193512 bp, - strand  Genetic Position: ChrX, 3.7 cM
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Radiation induced
Mutation:    Single point mutation
 
Mutation detailsG 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)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 3 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Ebp Mutation:  14 strains or lines available
References
Original:  J:13907 Cattanach BM, A new X-linked mutation, Td. Mouse News Lett. 1982;66:61-2
All:  7 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/12/2018
MGI 6.12
The Jackson Laboratory