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Glra1spd
Spontaneous Allele Detail
Summary
Symbol: Glra1spd
Name: glycine receptor, alpha 1 subunit; spasmodic
MGI ID: MGI:1856362
Synonyms: Glra1spd -, spd
Gene: Glra1  Location: Chr11:55405065-55499024 bp, - strand  Genetic Position: Chr11, 33.12 cM
Alliance: Glra1spd page
Mutation
origin
Strain of Origin:  A/HeJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis allele is the result of a missense mutation comprising a G-toT transversion producing an alanine-to-serine substitution at position 80 in the N-terminal domain of the encoded protein (p.A80S). (J:18524, J:20373)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 3 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 Glra1 Mutation:  30 strains or lines available
References
Original:  J:9027 Lane PW, et al., Spasmodic, a mutation on chromosome 11 in the mouse. J Hered. 1987 Nov-Dec;78(6):353-6
All:  16 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
03/19/2024
MGI 6.23
The Jackson Laboratory