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Hydinhy3
Spontaneous Allele Detail
Nomenclature
Symbol: Hydinhy3
Name: HYDIN, axonemal central pair apparatus protein; hydrocephalus 3
MGI ID: MGI:1856913
Synonyms: hy-3
Gene: Hydin  Location: Chr8:110266977-110610253 bp, + strand  Genetic Position: Chr8, 57.5 cM
Hydinhy3/Hydinhy3

Show the 6 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Not Specified
 
Mutation detailsMatings between mice carrying a transgenic insertion allele in this gene and hy3 mice demonstrated that these two mutations fail to complement each other, and suggests that these two mutations are allelic and very likely result from disrupted function of the same gene or set of genes. (J:83437)
Inheritance:    Recessive
Phenotypes
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View phenotypes 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: 2 strains available      Cell Lines: 0 lines available
Carrying any Hydin Mutation:  6 strains or lines available
Notes
Phenotypic Similarity to Human Syndrome: Hydrocephalus in homozygous mice (J:5426)

References
Original:  J:13035 Gruneberg H, Two new mutant genes in the house mouse. J Genet. 1943;45:22-28
All:  8 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/18/2015
MGI 6.0
The Jackson Laboratory