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Glra1cincinnati
Spontaneous Allele Detail
Summary
Symbol: Glra1cincinnati
Name: glycine receptor, alpha 1 subunit; cincinnati
MGI ID: MGI:3802579
Synonyms: Glra1dup5
Gene: Glra1  Location: Chr11:55405065-55499024 bp, - strand  Genetic Position: Chr11, 33.12 cM
Alliance: Glra1cincinnati page
Mutation
origin
Strain of Origin:  B6.129S6-Acadltm1Uab/Mmmh
Mutation
description
Allele Type:    Spontaneous
Mutation:    Duplication
  Glra1cincinnati involves 1 genes/genome features (Glra1) View all
 
Mutation detailsA tandem duplication containing the last 279 bp of intron 4, all 83 bp of exon 5 and the first 175 bp of intron 5 created a premature stop codon at the junction between the two copies of exon 5 (F187X). The predicted protein product lacks the 262 residues from the C-terminus of the 449 residuefull-length protein. (J:137595)
Inheritance:    Recessive
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 Glra1 Mutation:  30 strains or lines available
References
Original:  J:137595 Holland KD, et al., De novo exon duplication in a new allele of mouse Glra1 (spasmodic). Genetics. 2006 Dec;174(4):2245-7
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