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T22H
Radiation induced Allele Detail
Summary
Symbol: T22H
Name: brachyury, T-box transcription factor T; brachyury 22 Harwell
MGI ID: MGI:1857529
Synonyms: Del(17)T22H, Del(17)T22H11H
Gene: T  Location: Chr17:8653255-8661328 bp, + strand  Genetic Position: Chr17, 4.92 cM
Alliance: T22H page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
  T22H involves 1 genes/genome features (T) View all
 
Mutation detailsG-banded mitotic chromosome preparations show significant shortening of band 17A3. This allele comprises a deletion with a proximal breakpoint distal to D17Mit245 and a distal breakpoint proximal to D17Mit156. Loci D17Mit19 and 164, D17Tu1, and T are known to be deleted. (J:62654, J:62655)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any T Mutation:  59 strains or lines available
References
Original:  J:11036 Howard CA, et al., Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes. Genetics. 1990 Dec;126(4):1103-14
All:  5 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
10/29/2024
MGI 6.24
The Jackson Laboratory