Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80254
Gene name Gene Name - the full gene name approved by the HGNC.
Centrosomal protein 63
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CEP63
Synonyms (NCBI Gene) Gene synonyms aliases
SCKL6
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein with six coiled-coil domains. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. Several alternatively spliced transcript variants
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs142766824 C>G,T Conflicting-interpretations-of-pathogenicity Missense variant, non coding transcript variant, coding sequence variant
rs746387482 ->TTAA Likely-pathogenic 5 prime UTR variant, coding sequence variant, non coding transcript variant, inframe indel, stop gained
rs752207334 G>A,T Pathogenic Splice acceptor variant
rs763001827 C>T Pathogenic, uncertain-significance Non coding transcript variant, missense variant, coding sequence variant, 5 prime UTR variant, stop gained
rs1164567042 G>A,T Pathogenic 5 prime UTR variant, coding sequence variant, non coding transcript variant, stop gained, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT000831 hsa-miR-15a-5p Microarray 18362358
MIRT000830 hsa-miR-16-5p Microarray 18362358
MIRT659578 hsa-miR-585-5p HITS-CLIP 23824327
MIRT659577 hsa-miR-5682 HITS-CLIP 23824327
MIRT659576 hsa-miR-374b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000077 Process DNA damage checkpoint signaling ISS
GO:0000922 Component Spindle pole ISS
GO:0005515 Function Protein binding IPI 12812986, 17043677, 20360068, 21516116, 22458338, 24240477, 25416956, 25910212, 26297806, 26496610, 26638075, 26871637, 27107012, 30021884, 31413325, 31515488, 32296183, 32402286, 32814053, 33961781, 35709258
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614724 25815 ENSG00000182923
Protein
UniProt ID Q96MT8
Protein name Centrosomal protein of 63 kDa (Cep63)
Protein function Required for normal spindle assembly (PubMed:21406398, PubMed:21983783, PubMed:26297806, PubMed:35793002). Plays a key role in mother-centriole-dependent centriole duplication; the function seems also to involve CEP152, CDK5RAP2 and WDR62 throug
PDB 6CSU , 6CSV , 7W91
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17045 CEP63 18 280 Centrosomal protein of 63 kDa Coiled-coil
Sequence
MEALLEGIQNRGHGGGFLTSCEAELQELMKQIDIMVAHKKSEWEGRTHALETCLKIREQE
LKSLRSQLDVTHKEVGMLHQQVEEHEKIKQEMTMEYKQELKKLHEELCILKRSYEKLQKK
QMREFRGNTKNHREDRSEIERLTAKIEEFRQKSLDWEKQRLIYQQQVSSLEAQRKALAEQ
SEIIQAQLVNRKQKLESVELSSQSEIQHLSSKLERANDTICANELEIERLTMRVNDLVGT
SMTVLQEQQQKEEKLRESEKLLEALQEEKRELKAALQSQE
NLIHEARIQKEKLQEKVKAT
NTQHAVEAIRPREESLAEKKYTSQGQGDLDSVLSQLNFTHTSEDLLQAEVTCLEGSLESV
SATCKQLSQELMEKYEELKRMEAHNNEYKAEIKKLKEQILQGEQSYSSALEGMKMEISHL
TQELHQRDITIASTKGSSSDMEKRLRAEMQKAEDKAVEHKEILDQLESLKLENRHLSEMV
MKLELGLHEAKEISLADLQENYIEALNKLVSENQQLQKDLMNTKSQLEISTQMCKKQNDR
IFKPTHSRTTEFKNTEFKPTHGQHRHDGIKTEHYKTDLHSPRGQASDSINPMSRVLSPLS
PQISPCSSTRSLTSYSLCKTHSLPSALDTNEANFSDTMSESMNDQEEFISSCSLPVSPLG
SIATRFLEEEELRSHHILERLDAHIEELKRESEKTVRQFTALK
Sequence length 703
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Regulation of PLK1 Activity at G2/M Transition
Loss of Nlp from mitotic centrosomes
Recruitment of mitotic centrosome proteins and complexes
Loss of proteins required for interphase microtubule organization from the centrosome
Recruitment of NuMA to mitotic centrosomes
Anchoring of the basal body to the plasma membrane
AURKA Activation by TPX2
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Seckel Syndrome seckel syndrome 6 rs1164567042, rs746387482 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
developmental dyslexia Developmental dyslexia N/A N/A ClinVar
Microcephaly autosomal recessive primary microcephaly N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Autosomal Recessive Primary Microcephaly Associate 21983783, 26297806, 34068194
Dyslexia Associate 26400686
Microcephaly Associate 21983783, 26297806, 34068194
Neurologic Manifestations Associate 34068194