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Stomtm1Wcm
Targeted Allele Detail
Summary
Symbol: Stomtm1Wcm
Name: stomatin; targeted mutation 1, William C Mentzer
MGI ID: MGI:2182798
Gene: Stom  Location: Chr2:35203998-35226988 bp, - strand  Genetic Position: Chr2, 23.53 cM, cytoband B-C1
Alliance: Stomtm1Wcm page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:54046
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA 637 base pair region, containing the putative promoter and the translational start codon, was replaced with a human growth hormone polyA-signal and a neomycin selection cassette. Encoded protein was undetected by immunoblotting of red blood cell samples obtained from homozygous mutant mice. (J:54046)
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 Stom Mutation:  24 strains or lines available
References
Original:  J:54046 Zhu Y, et al., Stomatocytosis is absent in stomatin-deficient murine red blood cells. Blood. 1999 Apr 1;93(7):2404-10
All:  2 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
11/12/2024
MGI 6.24
The Jackson Laboratory