HYDIN

GENE INFORMATION

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Gene name

HYDIN (HGNC Symbol)

Synonyms

CILD5, DKFZp434D0513, KIAA1864, PPP1R31

Description

HYDIN, axonemal central pair apparatus protein (HGNC Symbol)

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]

Chromosome

16

Cytoband

q22.2

Chromosome location (bp)

70807378 - 71230722

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000157423 (version 78.38)

Entrez gene

54768

UniProt

Q4G0P3 (UniProt - Evidence at protein level)

neXtProt

NX_Q4G0P3

Antibodypedia

HYDIN antibodies
 

PROTEIN VIEW

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HYDIN-001
 
HYDIN-002
 
HYDIN-003
 
HYDIN-004
 
HYDIN-005
 
HYDIN-008
 
HYDIN-014
 
HYDIN-015
 
HYDIN-019
 
HYDIN-022
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HYDIN-001 ENSP00000377197
ENST00000393567
Q4G0P3
Show all »
Show » Show » 5121 575.9 No 0
HYDIN-002 ENSP00000314736
ENST00000321489
Q4G0P3
Show all »
Show » Show » 1017 114.2 No 0
HYDIN-003 ENSP00000444970
ENST00000538248
Q4G0P3
Show all »
Show » Show » 950 106.3 No 0
HYDIN-004 ENSP00000437341
ENST00000541601
Q4G0P3
Show all »
Show » Show » 940 105.3 No 0
HYDIN-005 ENSP00000288168
ENST00000288168
F8WD03
Show all »
Show » 725 81.6 No 0
HYDIN-008 ENSP00000437598
ENST00000538382
Show » Show » 204 23.5 No 0
HYDIN-014 ENSP00000440202
ENST00000545267
F5GXK3
Show all »
Show » 36 4 No 0
HYDIN-015 ENSP00000443525
ENST00000539973
F5H8I6
Show all »
Show » 39 4.3 No 0
HYDIN-019 ENSP00000446122
ENST00000542890
Show » 127 14.1 No 0
HYDIN-022 ENSP00000479502
ENST00000546297
Show » 82 9.1 No 0