GIN1 gypsy retrotransposon integrase 1
Information
- Symbol
- GIN1
- Type
- protein-coding
- Description
- gypsy retrotransposon integrase 1
- Entrez Gene ID
- 54826
- Genome
- hg19
- Position
- chr5:102,421,704-102,455,842
- Genome
- hg38
- Position
- chr5:103,086,000-103,120,138
- HGNC
- HGNC:25959 HGNC
- Ensembl
- ENSG00000145723 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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62 |
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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
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 |
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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 |
Search Word
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 |
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SYNONYM | GIN-1 |
SYNONYM | TGIN1 |
SYNONYM | ZH2C2 |
HGNC | HGNC:25959 HGNC |
Ensembl | ENSG00000145723 Ensembl |
AllianceGenome | HGNC:25959 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000508629.5 | hg38 | chr5 | 103,087,813 | 103,120,097 | 32,285 |
ENST00000399004.7 | hg38 | chr5 | 103,086,000 | 103,120,138 | 34,139 |
ENST00000399004.7 | hg19 | chr5 | 102,421,704 | 102,455,842 | 34,139 |
ENST00000508629.5 | hg19 | chr5 | 102,423,517 | 102,455,801 | 32,285 |
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