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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
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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:  40 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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory