HYDIN


Summary: 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. [provided by RefSeq, Jan 2013].

NameOMIM IDEnsembl IDHGNC IDPHARMGKB IDMap Location
HYDIN, axonemal central pair apparatus proteinMIM:610812Ensembl:ENSG00000157423HGNC:HGNC:19368PA13486695016q22.2

GO terms in HYDIN


Term TypeEvidence TypeGO Term IDGO Des.
CCIEAGO:1990718axonemal central pair projection
BPIEAGO:0002064epithelial cell development
BPIEAGO:0003341cilium movement
BPIEAGO:0021591ventricular system development
BPIEAGO:0060438trachea development
BPIEAGO:1904158axonemal central apparatus assembly

Gene expression in normal tissue: HYDIN

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in HYDIN


DatabasePathway IDPathway Des.

Gene-Drug: Aster Plot


Drug IDDrug NameModel Num.
iGMDRD30917AAG1
iGMDRD264Bryostatin 11

Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in HYDIN

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