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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 details
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
08/12/2014
MGI 5.19
The Jackson Laboratory