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].
| Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
|---|---|---|---|---|---|
| HYDIN, axonemal central pair apparatus protein | MIM:610812 | Ensembl:ENSG00000157423 | HGNC:HGNC:19368 | PA134866950 | 16q22.2 |
GO terms in HYDIN
| 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 |
Gene expression in normal tissue: HYDIN
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in HYDIN
| Database | Pathway ID | Pathway Des. |
|---|
Gene in drug-gene network: Network Plot
Gene-drug targets distribution
Gene Structure: PDB
Models in HYDIN
CLASSFICATION
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