GOLGA5 golgin A5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
not provided | 8 | 0 |
Uncertain significance | 1 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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74 |
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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
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Target data | : |
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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 |
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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 |
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MGeND data only
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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 | GOLIM5 |
SYNONYM | RFG5 |
SYNONYM | ret-II |
MIM | 606918 OMIM |
HGNC | HGNC:4428 HGNC |
Ensembl | ENSG00000066455 Ensembl |
AllianceGenome | HGNC:4428 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000163416.7 | hg38 | chr14 | 92,794,305 | 92,839,947 | 45,643 |
ENST00000163416.7 | hg19 | chr14 | 93,260,650 | 93,306,292 | 45,643 |
Key | Value |
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strand | + |
start | 93,260,575 |
Gene Symbol | GOLGA5 |
Entrez GeneId | 9,950 |
Chr Band | 14q |
end | 93,306,305 |
chr | chr14 |
Name | golgi autoantigen, golgin subfamily a, 5 (PTC5) |
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