Version 5.4
| Homo sapiens Gene: HYDIN | |||||||||||||||||||
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| Summary | |||||||||||||||||||
| InnateDB Gene | IDBG-40648.7 | ||||||||||||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
| Gene Symbol | HYDIN | ||||||||||||||||||
| Gene Name | HYDIN, axonemal central pair apparatus protein | ||||||||||||||||||
| Synonyms | |||||||||||||||||||
| Species | Homo sapiens | ||||||||||||||||||
| Ensembl Gene | ENSG00000157423 | ||||||||||||||||||
| Encoded Proteins |
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
HYDIN, axonemal central pair apparatus protein
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
hydrocephalus inducing homolog (mouse)
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| Protein Structure | |||||||||||||||||||
| Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
| Entrez Gene | |||||||||||||||||||
| 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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| Gene Information | |||||||||||||||||||
| Type | Protein coding | ||||||||||||||||||
| Genomic Location | Chromosome 16:70807378-71230722 | ||||||||||||||||||
| Strand | Reverse strand | ||||||||||||||||||
| Band | q22.2 | ||||||||||||||||||
| Transcripts | |||||||||||||||||||
| Interactions | |||||||||||||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
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| Gene Ontology | |||||||||||||||||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||||||||||||||||
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Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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| Cross-References | |||||||||||||||||||
| SwissProt | |||||||||||||||||||
| TrEMBL | J3QL79 | ||||||||||||||||||
| UniProt Splice Variant | |||||||||||||||||||
| Entrez Gene | 54768 | ||||||||||||||||||
| UniGene | Hs.461229 Hs.741984 Hs.742081 Hs.742190 Hs.742278 Hs.742447 Hs.742453 Hs.742456 Hs.742457 Hs.743479 Hs.743703 | ||||||||||||||||||
| RefSeq | NM_001198542 NM_001198543 NM_001270974 NM_017558 XM_005276093 XM_006721206 | ||||||||||||||||||
| HUGO | HGNC:19368 | ||||||||||||||||||
| OMIM | 610812 | ||||||||||||||||||
| CCDS | CCDS10897 CCDS56004 CCDS56005 CCDS59269 | ||||||||||||||||||
| HPRD | 11042 | ||||||||||||||||||
| IMGT | |||||||||||||||||||
| EMBL | AC027281 AC099495 AC138625 | ||||||||||||||||||
| GenPept | |||||||||||||||||||
| RNA Seq Atlas | 101930373 54768 | ||||||||||||||||||