GOLGA6L7 golgin A6 family like 7
Information
- Symbol
- GOLGA6L7
- Type
- protein-coding
- Description
- golgin A6 family like 7
- Entrez Gene ID
- 728310
- Genome
- hg19
- Position
- chr15:29,086,978-29,093,790
- Genome
- hg38
- Position
- chr15:28,841,832-28,848,644
- HGNC
- HGNC:37442 HGNC
- Ensembl
- ENSG00000261649 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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2 |
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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
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | GOLGA6L7P |
HGNC | HGNC:37442 HGNC |
Ensembl | ENSG00000261649 Ensembl |
AllianceGenome | HGNC:37442 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000567390.7 | hg38 | chr15 | 28,841,832 | 28,848,644 | 6,813 |
ENST00000567390.7 | hg19 | chr15 | 29,086,978 | 29,093,790 | 6,813 |
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