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].
Loading, please wait...
Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
---|---|---|---|---|---|
OMIM IDMIM:610812 Ensembl IDEnsembl:ENSG00000157423 HGNC IDHGNC:HGNC:19368 PHARMGKB IDPA134866950 Map Location16q22.2 |
GO terms in HYDIN
Loading, please wait...
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 |
Showing 1 to 6 of 6 rows
Gene expression in normal tissue: HYDIN
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in HYDIN
Loading, please wait...
Database | Pathway ID | Pathway Des. |
---|---|---|
No matching records found |
Gene-Drug: Aster Plot
Gene in drug-gene network: Network Plot

Gene-drug targets distribution
Gene Structure: PDB
Models in HYDIN
Loading, please wait...
Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
---|---|---|---|---|---|---|---|---|
No matching records found |