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Gene : CEP152 Homo sapiens

Name  ? centrosomal protein 152 Cytological Location  15q21.1
Brief Description  centrosomal protein 152
Description  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]
  • synonyms:
  • asterless,
  • MCPH4,
  • SCKL5,
  • NM_014985,
  • KIAA0912,
  • SCKL5,
  • centrosomal protein 152kDa,
  • uc001zwy.4,
  • HGNC:29298,
  • MCPH9,
  • CEP152,
  • MCPH9,
  • AB020719,
  • OTTHUMG00000172219
  • identifiers:
  • 22995,
  • ENSG00000103995,
  • CEP152

Genome feature

Region: gene ? Length: 149371  
Location: 15:48662534-48811904 reverse strand Cyto location: 15q21.1

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SN Ps

5 Cross References

18 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results