PMIS2 PMIS2 transmembrane protein
Information
- Symbol
- PMIS2
- Type
- protein-coding
- Description
- PMIS2 transmembrane protein
- Entrez Gene ID
- 111216276
- Genome
- hg19
- Position
- chr19:36,077,075-36,078,198
- Genome
- hg38
- Position
- chr19:35,586,173-35,587,296
- HGNC
- HGNC:53649 HGNC
- Ensembl
- ENSG00000283758 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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0 |
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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 |
Search Word
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 |
Type | ID |
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SYNONYM | IFITMD9 |
HGNC | HGNC:53649 HGNC |
Ensembl | ENSG00000283758 Ensembl |
AllianceGenome | HGNC:53649 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000646476.1 | hg38 | chr19 | 35,586,161 | 35,587,206 | 1,046 |
ENST00000640449.2 | hg38 | chr19 | 35,586,173 | 35,587,296 | 1,124 |
ENST00000646476.1 | hg19 | chr19 | 36,077,063 | 36,078,108 | 1,046 |
ENST00000640449.2 | hg19 | chr19 | 36,077,075 | 36,078,198 | 1,124 |
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