Hydin<hy3> Spontaneous Allele Detail MGI Mouse (MGI:1856913)

Hydin^hy3
Spontaneous Allele Detail

Summary

Symbol:	Hydin^hy3
Name:	HYDIN, axonemal central pair apparatus protein; hydrocephalus 3
MGI ID:	MGI:1856913
Synonyms:	hy-3
Gene:	Hydin Location: Chr8:110993609-111336885 bp, + strand Genetic Position: Chr8, 57.5 cM
Alliance:	Hydin^hy3 page

Hydin^hy3/Hydin^hy3

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: Matings 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

View phenotypes and curated references for all genotypes (concatenated display).

Disease models

Expression

In Structures Affected by this Mutation:

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:	228 strains or lines available

References

Original:	J:13035 Gruneberg H, Two new mutant genes in the house mouse. J Genet. 1943;45(1):22-28
All:	9 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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