Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23177
Gene name Gene Name - the full gene name approved by the HGNC.
Centrosomal protein 68
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CEP68
Synonyms (NCBI Gene) Gene synonyms aliases
KIAA0582
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p14
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020387 hsa-miR-29c-3p Sequencing 20371350
MIRT645117 hsa-miR-3606-3p HITS-CLIP 23824327
MIRT645116 hsa-miR-513a-3p HITS-CLIP 23824327
MIRT645115 hsa-miR-513c-3p HITS-CLIP 23824327
MIRT640721 hsa-miR-548av-5p 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:0005515 Function Protein binding IPI 25416956, 25503564
GO:0005654 Component Nucleoplasm IDA
GO:0005813 Component Centrosome IDA 18042621, 21399614, 31974111
GO:0005829 Component Cytosol IDA
GO:0007098 Process Centrosome cycle IMP 18042621
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616889 29076 ENSG00000011523
Protein
UniProt ID Q76N32
Protein name Centrosomal protein of 68 kDa (Cep68)
Protein function Involved in maintenance of centrosome cohesion, probably as part of a linker structure which prevents centrosome splitting (PubMed:18042621). Required for localization of CDK5RAP2 to the centrosome during interphase (PubMed:24554434, PubMed:2550
Family and domains
Sequence
MALGEEKAEAEASEDTKAQSYGRGSCRERELDIPGPMSGEQPPRLEAEGGLISPVWGAEG
IPAPTCWIGTDPGGPSRAHQPQASDANREPVAERSEPALSGLPPATMGSGDLLLSGESQV
EKTKLSSSEEFPQTLSLPRTTTICSGHDADTEDDPSLADLPQALDLSQQPHSSGLSCLSQ
WKSVLSPGSAAQPSSCSISASSTGSSLQGHQERAEPRGGSLAKVSSSLEPVVPQEPSSVV
GLGPRPQWSPQPVFSGGDASGLGRRRLSFQAEYWACVLPDSLPPSPDRHSPLWNPNKEYE
DLLDYTYPLRPGPQLPKHLDSRVPADPVLQDSGVDLDSFSVSPASTLKSPTNVSPNCPPA
EATALPFSGPREPSLKQWPSRVPQKQGGMGLASWSQLASTPRAPGSRDARWERREPALRG
AKDRLTIGKHLDMGSPQLRTRDRGWPSPRPEREKRTSQSARRPTCTESRWKSEEEVESDD
EYLALPARLTQVSSLVSYLGSISTLVTLPTGDIKGQSPLEVSDSDGPASFPSSSSQSQLP
PGAALQGSGDPEGQNPCFLRSFVRAHDSAGEGSLGSSQALGVSSGLLKTRPSLPARLDRW
PFSDPDVEGQLPRKGGEQGKESLVQCVKTFCCQLEELICWLYNVADVTDHGTAARSNLTS
LKSSLQLYRQFKKDIDEHQSLTESVLQKGEILLQCLLENTPVLEDVLGRIAKQSGELESH
ADRLYDSILASLDMLAGCTLIPDKKPMAAMEHPCEGV
Sequence length 757
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
29892015, 30061737, 28416818
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
29632382
Unknown
Disease term Disease name Evidence References Source
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation 29892015, 30061737 ClinVar
Diabetes Diabetes GWAS
Atrial Fibrillation Atrial Fibrillation GWAS
Hypertension Hypertension GWAS
Associations from Text Mining
Disease Name Relationship Type References
Angioedema Associate 24618698
Asthma Associate 21072201
Asthma Aspirin Induced Associate 21072201
Atrial Fibrillation Associate 29545482
Hypersensitivity Associate 24618698
Respiratory Tract Diseases Associate 24618698
Retinitis Pigmentosa Associate 15215745
Status Asthmaticus Associate 24618698
Urticaria Associate 24618698