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Del(10)1H
Radiation induced Allele Detail
Summary
Symbol: Del(10)1H
Name: deletion, Chr 10, Harwell 1
MGI ID: MGI:1856365
Synonyms: Del(10)Sl121H, KitlSl-12H, SCF, steel 12 Harwell
Gene: Del(10)1H  Location: unknown  Genetic Position: Chr10, cytoband D1
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
  Del(10)1H involves 1 genes/genome features (Kitl) View all
 
Mutation detailsThis X-ray-induced deletion encompasses about 10% of Chr 10, including the Kitl locus (J:5931). Southern analyses of genomic DNA indicate that there is a 13 kb deletion of sequence present in wild-type DNA and presence of a 7 kb fragment that is not present in wild-type DNA (J:10750). (J:5931, J:10750)
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 Del(10)1H Mutation:  0 strains or lines available
References
Original:  J:18279 Cattanach BM, et al., A new steel allele with pre-implantation homozygous lethality. Mouse News Lett. 1988;80:156-57
All:  6 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
05/28/2024
MGI 6.13
The Jackson Laboratory