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Ttc7hea
Spontaneous Allele Detail
Summary
Symbol: Ttc7hea
Name: tetratricopeptide repeat domain 7; hereditary erythroblastic anemia
MGI ID: MGI:1856896
Gene: Ttc7  Location: Chr17:87590328-87689197 bp, + strand  Genetic Position: Chr17, 57.12 cM, cytoband E4
Alliance: Ttc7hea page
Mutation
origin
Strain of Origin:  CFO
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
    Exons 1-14 are deleted (out of 20 exons). (J:97094)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Ttc7 Mutation:  43 strains or lines available
Notes
Arose in the inbred CFO strain derived from outbred CF-1 mice.

References
Original:  J:7515 Shimizu K, et al., Hereditary erythroblastic anaemia in the laboratory mouse. Lab Anim. 1983 Jul;17(3):198-202
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory