GOLGA8N golgin A8 family member N

Information
Symbol
GOLGA8N
Type
protein-coding
Description
golgin A8 family member N
Entrez Gene ID
643699
Genome
hg19
Position
chr15:32,885,657-32,899,438
Genome
hg38
Position
chr15:32,593,456-32,607,237
HGNC
HGNC:44405 HGNC
Ensembl
ENSG00000232653 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
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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
SYNONYM GOLGA8R
HGNC HGNC:44405 HGNC
Ensembl ENSG00000232653 Ensembl
AllianceGenome HGNC:44405
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000569659.6 hg38 chr15 32,593,456 32,607,310 13,855
ENST00000448387.7 hg38 chr15 32,593,456 32,607,237 13,782
ENST00000448387.7 hg19 chr15 32,885,657 32,899,438 13,782
ENST00000569659.6 hg19 chr15 32,885,657 32,899,511 13,855
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