|
|
| 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 image(s) involving this allele.
|
 |
|
Mutation
origin |
|
Strain of Origin:
|
Not Specified
|
|
Mutation
description |
|
Allele
Type: | |
Spontaneous |
|
Mutation: | |
Undefined |
| |
|
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 for all genotypes (concatenated display).
|
|
Disease models
|
|
| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
|
| References |
|
Original: |
J:13035
Gruneberg H,
"Two new mutant genes in the house mouse."
J Genet 1943;45():22-28
|
|
All: |
8 reference(s)
|
|
Analysis Tools
