CEP68 centrosomal protein 68

Information
Symbol
CEP68
Type
protein-coding
Description
centrosomal protein 68
Entrez Gene ID
23177
Genome
hg19
Position
chr2:65,283,550-65,314,138
Genome
hg38
Position
chr2:65,056,416-65,087,004
MIM
616889 OMIM
HGNC
HGNC:29076 HGNC
Ensembl
ENSG00000011523 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 24
Uncertain significance 0 126
Ranking
ClinVar
0
0
2
162
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM KIAA0582
MIM 616889 OMIM
HGNC HGNC:29076 HGNC
Ensembl ENSG00000011523 Ensembl
AllianceGenome HGNC:29076
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000377990.7 hg38 chr2 65,056,416 65,087,004 30,589
ENST00000703983.1 hg38 chr2 65,056,354 65,086,957 30,604
ENST00000703985.1 hg38 chr2 65,056,362 65,081,574 25,213
ENST00000704388.1 hg38 chr2 65,056,410 65,080,525 24,116
ENST00000704387.1 hg38 chr2 65,056,407 65,080,517 24,111
ENST00000260569.4 hg38 chr2 65,056,465 65,087,004 30,540
ENST00000704570.1 hg38 chr2 65,056,372 65,086,999 30,628
ENST00000704447.1 hg38 chr2 65,056,432 65,075,243 18,812
ENST00000704449.1 hg38 chr2 65,056,407 65,075,243 18,837
ENST00000704450.1 hg38 chr2 65,056,407 65,075,245 18,839
ENST00000475851.2 hg38 chr2 65,056,366 65,086,971 30,606
ENST00000704479.1 hg38 chr2 65,056,383 65,075,245 18,863
ENST00000704487.1 hg38 chr2 65,056,395 65,083,795 27,401
ENST00000704486.1 hg38 chr2 65,056,410 65,086,957 30,548
ENST00000704481.1 hg38 chr2 65,056,401 65,086,971 30,571
ENST00000703983.1 hg19 chr2 65,283,488 65,314,091 30,604
ENST00000703985.1 hg19 chr2 65,283,496 65,308,708 25,213
ENST00000377990.7 hg19 chr2 65,283,550 65,314,138 30,589
ENST00000260569.4 hg19 chr2 65,283,599 65,314,138 30,540
ENST00000475851.2 hg19 chr2 65,283,500 65,314,105 30,606
ENST00000704387.1 hg19 chr2 65,283,541 65,307,651 24,111
ENST00000704388.1 hg19 chr2 65,283,544 65,307,659 24,116
ENST00000704447.1 hg19 chr2 65,283,566 65,302,377 18,812
ENST00000704449.1 hg19 chr2 65,283,541 65,302,377 18,837
ENST00000704450.1 hg19 chr2 65,283,541 65,302,379 18,839
ENST00000704479.1 hg19 chr2 65,283,517 65,302,379 18,863
ENST00000704481.1 hg19 chr2 65,283,535 65,314,105 30,571
ENST00000704486.1 hg19 chr2 65,283,544 65,314,091 30,548
ENST00000704487.1 hg19 chr2 65,283,529 65,310,929 27,401
ENST00000704570.1 hg19 chr2 65,283,506 65,314,133 30,628
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