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].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

GO terms in HYDIN


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Term Type
Evidence Type
GO Term ID
GO Des.
CC IEA GO:1990718 axonemal central pair projection
BP IEA GO:0002064 epithelial cell development
BP IEA GO:0003341 cilium movement
BP IEA GO:0021591 ventricular system development
BP IEA GO:0060438 trachea development
BP IEA GO:1904158 axonemal central apparatus assembly
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Gene expression in normal tissue: HYDIN

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in HYDIN


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Database
Pathway ID
Pathway Des.
No matching records found

Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD309 17AAG 1
iGMDRD264 Bryostatin 1 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in HYDIN

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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