InnateDB Protein
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IDBP-57584.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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CEP63
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Protein Name
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centrosomal protein 63kDa
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000336524
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InnateDB Gene
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IDBG-57578 (CEP63)
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Protein Structure
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Function |
Required for normal spindle assembly. Plays a key role in mother-centriole-dependent centriole duplication, through centrosomal recruitment of CEP152. Also recruits CDK1 to centrosomes. Plays a role in DNA damage response. Following DNA damage, such as double-strand breaks (DSBs), is removed from centrosomes; this leads to the inactivation of spindle assembly and delay in mitotic progression. {ECO:0000269PubMed:21406398, ECO:0000269PubMed:21983783}.
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Subcellular Localization |
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Note=Colocalizes with CEP152 in a discrete ring around the proximal end of the parental centriole. At this site, a cohesive structure is predicted to engage parental centrioles and procentrioles.
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Disease Associations |
Seckel syndrome 6 (SCKL6) [MIM:614728]: A rare autosomal recessive disorder characterized by proportionate dwarfism of prenatal onset associated with low birth weight, growth retardation, severe microcephaly with a bird-headed like appearance, and mental retardation. {ECO:0000269PubMed:21983783}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 31 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
31
[view]
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Protein-Protein |
31
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
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PFAM |
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q96MT8
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PhosphoSite |
PhosphoSite-Q96MT8
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TrEMBL |
D6RAY6
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UniProt Splice Variant |
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Entrez Gene |
80254
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UniGene |
Hs.443301
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RefSeq |
XP_005247852
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HUGO |
HGNC:25815
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OMIM |
614724
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CCDS |
CCDS3086
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HPRD |
07826
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IMGT |
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EMBL |
AC010207
AC026117
AC109912
AC139764
AK023448
AK023738
AK056465
BC014050
BC068997
BK005503
CH471052
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GenPept |
AAH14050
AAH68997
BAB14578
BAB14662
BAB71192
DAA05503
EAW79136
EAW79137
EAW79138
EAW79139
EAW79140
EAW79141
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