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 |
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Ranking
ClinVar | |
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0 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | GOLGA8R |
HGNC | HGNC:44405 HGNC |
Ensembl | ENSG00000232653 Ensembl |
AllianceGenome | HGNC:44405 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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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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