PIGW phosphatidylinositol glycan anchor biosynthesis class W
Information
- Symbol
- PIGW
- Type
- protein-coding
- Description
- phosphatidylinositol glycan anchor biosynthesis class W
- Entrez Gene ID
- 284098
- Genome
- hg19
- Position
- chr17:34,890,814-34,895,152
- Genome
- hg38
- Position
- chr17:36,534,987-36,539,303
- MIM
- 610275 OMIM
- HGNC
- HGNC:23213 HGNC
- Ensembl
- ENSG00000277161 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 10 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 15 |
Likely benign | 0 | 170 |
Conflicting classifications of pathogenicity | 0 | 12 |
not provided | 1 | 0 |
Uncertain significance | 0 | 358 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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44 |
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499 |
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8 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | Gwt1 |
SYNONYM | HPMRS5 |
MIM | 610275 OMIM |
HGNC | HGNC:23213 HGNC |
Ensembl | ENSG00000277161 Ensembl |
AllianceGenome | HGNC:23213 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000620233.1 | hg38 | chr17 | 36,535,555 | 36,539,310 | 3,756 |
ENST00000614443.2 | hg38 | chr17 | 36,534,987 | 36,539,303 | 4,317 |
ENST00000614443.2 | hg19 | chr17 | 34,890,814 | 34,895,152 | 4,339 |
ENST00000620233.1 | hg19 | chr17 | 34,891,403 | 34,895,159 | 3,757 |
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