HYDIN Back

hydrocephalus inducing homolog (mouse)

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NCBI Description of HYDIN
This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1.

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

HYDIN is highly significantly mutated in
(none)
HYDIN is significantly mutated in
(none)
HYDIN is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for HYDIN