The CEP63 gene homepage

General information
Gene symbol CEP63
Gene name centrosomal protein 63kDa
Chromosome 3
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NG_032870.1
Transcript reference NM_001042383.1, NM_001042384.1, NM_001042400.1, NM_025180.3
Associated with diseases ID, SCKL, SCKL-6
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 149
Unique public DNA variants reported 15
Individuals with public variants 35
Hidden variants 53
Date created October 29, 2013
Date last updated September 28, 2016
Version CEP63:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:25815
Entrez Gene 80254
PubMed articles CEP63
OMIM - Gene 614724
OMIM - Diseases SCKL (Seckel syndrome (SCKL))
SCKL-6 (Seckel syndrome, type 6 (SCKL-6))
HGMD CEP63
GeneCards CEP63
GeneTests CEP63


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001566 3 transcript variant 1 NM_025180.3 NP_079456.2 149
00001567 3 transcript variant 2 NM_001042400.1 NP_001035859.1 132
00001565 3 transcript variant 3 NM_001042383.1 NP_001035842.1 92
00016300 3 Manually created transcript. (removed from reference sequence) NM_001042384.1 - 59


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