WDR62

GENE INFORMATION

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Gene name

WDR62 (HGNC Symbol)

Synonyms

C19orf14, DKFZP434J046, FLJ33298, MCPH2

Description

WD repeat domain 62 (HGNC Symbol)

Entrez gene summary

This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]

Chromosome

19

Cytoband

q13.12

Chromosome location (bp)

36054881 - 36105106

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000075702 (version 78.38)

Entrez gene

284403

UniProt

O43379 (UniProt - Evidence at protein level)

neXtProt

NX_O43379

Antibodypedia

WDR62 antibodies
 

PROTEIN VIEW

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WDR62-001
 
WDR62-006
 
WDR62-007
 
 
 
 
 

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)

WDR62-001 ENSP00000384792
ENST00000401500
O43379
Show all »
Show » Show » 1523 166.5 No 0
WDR62-006 ENSP00000270301
ENST00000270301
O43379
Show all »
Show » Show » 1518 166 No 0
WDR62-007 ENSP00000413475
ENST00000427823
H7C3R4
Show all »
Show » Show » 318 34.7 No 0