KRI1 KRI1 homolog
Information
- Symbol
- KRI1
- Type
- protein-coding
- Description
- KRI1 homolog
- Entrez Gene ID
- 65095
- Genome
- hg19
- Position
- chr19:10,663,761-10,676,686
- Genome
- hg38
- Position
- chr19:10,553,085-10,566,010
- HGNC
- HGNC:25769 HGNC
- Ensembl
- ENSG00000129347 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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106 |
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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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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000652042.1 | hg38 | chr19 | 10,553,085 | 10,566,026 | 12,942 |
ENST00000312962.12 | hg38 | chr19 | 10,553,085 | 10,566,010 | 12,926 |
ENST00000312962.12 | hg19 | chr19 | 10,663,761 | 10,676,686 | 12,926 |
ENST00000652042.1 | hg19 | chr19 | 10,663,761 | 10,676,702 | 12,942 |
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