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hhy
Gene Detail
 Symbol
Name
ID
hhy
hemorrhagic hydrocephalus
MGI:3505572
Feature Type heritable phenotypic marker
Genetic Map
Chromosome 12
Syntenic

Mapping data(1)
Sequence Map
Chr12:105342095-113896905 bp
From MGI annotation of GRCm38

  8554811 bp   ±  kb flank

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Mouse Genome Browser
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Spontaneous(1)
 
Homozygous mutant mice display hydrocephalus, intracranial hemorrhage due to ventricular dilatation, and heterotopia in the subcortical regions. Hydroencephaly usually becomes evident before 15 weeks of age and affected animals die within several days after notice.
 
References (Earliest) J:93608 Kuwamura M, et al., Hemorrhagic hydrocephalus (hhy): a novel mutation on mouse chromosome 12. Brain Res Dev Brain Res. 2004 Aug 18;152(1):69-72
(Latest) J:180189 Mori N, et al., Ccdc85c encoding a protein at apical junctions of radial glia is disrupted in hemorrhagic hydrocephalus (hhy) mice. Am J Pathol. 2012 Jan;180(1):314-27
All references(2)

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
09/09/2014
MGI 5.19
The Jackson Laboratory