About   Help   FAQ
Hgstn
Spontaneous Allele Detail
Summary
Symbol: Hgstn
Name: HGF-regulated tyrosine kinase substrate; teetering
MGI ID: MGI:1857076
Gene: Hgs  Location: Chr11:120358461-120374805 bp, + strand  Genetic Position: Chr11, 84.16 cM
Alliance: Hgstn page
Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsA spontaneous A-to-G point mutation results in the amino acid substitution of methionine with valine at position 89 (p.M89V). (J:221937)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 51 assay results
In Structures Affected by this Mutation: 21 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 Hgs Mutation:  38 strains or lines available
References
Original:  J:13411 Lane PW, et al., Teetering (tn). Mouse News Lett. 1962;27:38
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory