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Foxc1ch
Spontaneous Allele Detail
Nomenclature
Symbol: Foxc1ch
Name: forkhead box C1; congenital hydrocephalus
MGI ID: MGI:1856705
Synonyms: ch, mf1ch
Gene: Foxc1  Location: Chr13:31806691-31810643 bp, + strand  Genetic Position: Chr13, 13.52 cM
Foxc1ch/Foxc1ch

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  CBA x STOCK Tyrc f
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 23 assay results
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 Foxc1 Mutation:  1 strain or line available
References
Original:  J:75733 Gruneberg H, Congenital hydrocephalus in the mouse, a case of spurious pleiotropism. J Genet. 1943;45(1):1-21
All:  17 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
10/08/2014
MGI 5.20
The Jackson Laboratory