GOLGA8K golgin A8 family member K

Information
Symbol
GOLGA8K
Type
protein-coding
Description
golgin A8 family member K
Entrez Gene ID
653125
Genome
hg19
Position
chr15:32,681,800-32,695,493
Genome
hg38
Position
chr15:32,389,599-32,403,292
HGNC
HGNC:38652 HGNC
Ensembl
ENSG00000249931 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 16
Ranking
ClinVar
0
0
0
16
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 :
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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
HGNC HGNC:38652 HGNC
Ensembl ENSG00000249931 Ensembl
AllianceGenome HGNC:38652
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000512626.3 hg38 chr15 32,389,599 32,403,292 13,694
ENST00000512626.3 hg19 chr15 32,681,800 32,695,493 13,694
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