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Hydinhyrh
Spontaneous Allele Detail
Nomenclature
Symbol: Hydinhyrh
Name: HYDIN, axonemal central pair apparatus protein; hydrocephalus with rhinitis
MGI ID: MGI:3801608
Gene: Hydin  Location: Chr8:110266977-110610253 bp, + strand  Genetic Position: Chr8, 57.5 cM
Mutation
origin
Strain of Origin:  B10.RIII-H2r H2-T18b/(71NS)SnJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis spontaneous C-to-T transition at position 110,575,054 (GRCm38) results in a change from arginine to a premature stop codon at residue 3806 (p.R3806*).
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
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 Hydin Mutation:  9 strains or lines available
References
Original:  J:137815 Dionne L, et al., A Hydrocephalus Mutation with Rhinitis on Mouse Chromosome Eight. MGI Direct Data Submission. 2008;
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
07/07/2020
MGI 6.15
The Jackson Laboratory