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Sh3tc2m1J
Spontaneous Allele Detail
Nomenclature
Symbol: Sh3tc2m1J
Name: SH3 domain and tetratricopeptide repeats 2; mutation 1, The Jackson Laboratory
MGI ID: MGI:5444299
Gene: Sh3tc2  Location: Chr18:61952928-62015719 bp, + strand  Genetic Position: Chr18, 34.78 cM
Mutation
origin
Strain of Origin:  B6.129P2-Cnr2tm1Dgen/J
Mutation
description
Allele Type:    Spontaneous (Not Applicable)
Mutation:    Single point mutation
 
Mutation detailsThe mutation is identified as a C-to-T substitution at coding nucleotide 211 (c.211C>T) in exon 3 of 17 exons. The mutation alters the corresponding amino acid from glutamine to a stop codon at position 71 (p.Q71*).
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Sh3tc2 Mutation:  41 strains or lines available
References
Original:  J:229591 Burgess RW, A spontaneous allele of Sh3tc2. MGI Direct Data Submission. 2016;
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
04/06/2021
MGI 6.16
The Jackson Laboratory