C21orf59

GENE INFORMATION

? »

Gene name

C21orf59 (HGNC Symbol)

Synonyms

C21orf48, CILD26, FBB18, FLJ20467

Description

Chromosome 21 open reading frame 59 (HGNC Symbol)

Entrez gene summary

This gene a protein plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]

Chromosome

21

Cytoband

q22.11

Chromosome location (bp)

32592079 - 32612866

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000159079 (version 78.38)

Entrez gene

56683

UniProt

P57076 (UniProt - Evidence at protein level)

neXtProt

NX_P57076

Antibodypedia

C21orf59 antibodies
 

PROTEIN VIEW

? »
 
 
 
C21orf59-001
 
C21orf59-002
 
C21orf59-004
 
C21orf59-005
 
C21orf59-006
 
C21orf59-007
 
 
 
 
 

PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

C21orf59-001 ENSP00000290155
ENST00000290155
P57076
Show all »
Show » Show » 290 33.2 No 0
C21orf59-002 ENSP00000371989
ENST00000382549
D3DSE6
Show all »
Show » 245 27.6 No 0
C21orf59-004 ENSP00000407362
ENST00000425336
Show » 117 13.3 No 0
C21orf59-005 ENSP00000411306
ENST00000431599
Show » 79 8.5 No 0
C21orf59-006 ENSP00000411467
ENST00000440966
C9J818
Show all »
Show » 258 29.4 No 0
C21orf59-007 ENSP00000393104
ENST00000458138
C9JX57
Show all »
Show » 184 20.7 No 0