CEP152

GENE INFORMATION

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Gene name

CEP152 (HGNC Symbol)

Synonyms

KIAA0912, MCPH4, SCKL5

Description

Centrosomal protein 152kDa (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

Chromosome

15

Cytoband

q21.1

Chromosome location (bp)

48712928 - 48811146

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000103995 (version 78.38)

Entrez gene

22995

UniProt

O94986 (UniProt - Evidence at protein level)

neXtProt

NX_O94986

Antibodypedia

CEP152 antibodies
 

PROTEIN VIEW

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CEP152-001
 
CEP152-003
 
CEP152-004
 
CEP152-007
 
 
 
 
 

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)

CEP152-001 ENSP00000370337
ENST00000380950
O94986
Show all »
Show » Show » 1710 195.6 No 0
CEP152-003 ENSP00000321000
ENST00000325747
O94986
Show all »
Show » Show » 1275 147.3 No 0
CEP152-004 ENSP00000382271
ENST00000399334
O94986
Show all »
Show » Show » 1654 189.1 No 0
CEP152-007 ENSP00000453914
ENST00000558591
H0YN91
Show all »
Show » Show » 68 7.8 No 0