| Gene Symbol | CEP152 |
| Entrez Gene ID | 22995 |
| Full Name | centrosomal protein 152 |
| Synonyms | MCPH4,MCPH9,SCKL5 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| 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]. |
| Disorder MIM: | |
| Disorder Html: | Microcephaly 9, primary, autosomal recessive, 614852 (3); Seckel syndrome 5, 613823 (3) |
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