PHOSPHO2 phosphatase, orphan 2
Information
- Symbol
- PHOSPHO2
- Type
- protein-coding
- Description
- phosphatase, orphan 2
- Entrez Gene ID
- 493911
- Genome
- hg19
- Position
- chr2:170,550,979-170,558,218
- Genome
- hg38
- Position
- chr2:169,694,469-169,701,708
- HGNC
- HGNC:28316 HGNC
- Ensembl
- ENSG00000144362 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000616481.4 | hg38 | chr2 | 169,694,454 | 169,701,706 | 7,253 |
ENST00000616524.4 | hg38 | chr2 | 169,694,454 | 169,701,706 | 7,253 |
ENST00000617738.4 | hg38 | chr2 | 169,694,454 | 169,701,706 | 7,253 |
ENST00000359744.8 | hg38 | chr2 | 169,694,469 | 169,701,708 | 7,240 |
ENST00000616481.4 | hg19 | chr2 | 170,550,964 | 170,558,216 | 7,253 |
ENST00000616524.4 | hg19 | chr2 | 170,550,964 | 170,558,216 | 7,253 |
ENST00000617738.4 | hg19 | chr2 | 170,550,964 | 170,558,216 | 7,253 |
ENST00000359744.8 | hg19 | chr2 | 170,550,979 | 170,558,218 | 7,240 |
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