GORASP2 golgi reassembly stacking protein 2
Information
- Symbol
- GORASP2
- Type
- protein-coding
- Description
- golgi reassembly stacking protein 2
- Entrez Gene ID
- 26003
- Genome
- hg19
- Position
- chr2:171,785,763-171,823,640
- Genome
- hg38
- Position
- chr2:170,929,253-170,967,130
- MIM
- 608693 OMIM
- HGNC
- HGNC:17500 HGNC
- Ensembl
- ENSG00000115806 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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60 |
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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
[No Data.]
Locus Zoom
Variants
Search Word
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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 |
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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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Target data | : |
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 |
---|---|
SYNONYM | GOLPH6 |
SYNONYM | GRASP55 |
SYNONYM | GRS2 |
SYNONYM | p59 |
MIM | 608693 OMIM |
HGNC | HGNC:17500 HGNC |
Ensembl | ENSG00000115806 Ensembl |
AllianceGenome | HGNC:17500 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000234160.5 | hg38 | chr2 | 170,929,253 | 170,967,130 | 37,878 |
ENST00000234160.5 | hg19 | chr2 | 171,785,763 | 171,823,640 | 37,878 |
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