PRG2 proteoglycan 2, pro eosinophil major basic protein
Information
- Symbol
- PRG2
- Type
- protein-coding
- Description
- proteoglycan 2, pro eosinophil major basic protein
- Entrez Gene ID
- 5553
- Genome
- hg19
- Position
- chr11:57,154,253-57,158,123
- Genome
- hg38
- Position
- chr11:57,386,780-57,390,650
- MIM
- 605601 OMIM
- HGNC
- HGNC:9362 HGNC
- Ensembl
- ENSG00000186652 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | BMPG |
SYNONYM | MBP |
SYNONYM | MBP1 |
SYNONYM | proMBP |
MIM | 605601 OMIM |
HGNC | HGNC:9362 HGNC |
Ensembl | ENSG00000186652 Ensembl |
AllianceGenome | HGNC:9362 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000311862.10 | hg38 | chr11 | 57,386,780 | 57,390,650 | 3,871 |
ENST00000533605.5 | hg38 | chr11 | 57,386,815 | 57,390,637 | 3,823 |
ENST00000525955.1 | hg38 | chr11 | 57,386,943 | 57,390,636 | 3,694 |
ENST00000311862.10 | hg19 | chr11 | 57,154,253 | 57,158,123 | 3,871 |
ENST00000533605.5 | hg19 | chr11 | 57,154,288 | 57,158,110 | 3,823 |
ENST00000525955.1 | hg19 | chr11 | 57,154,416 | 57,158,109 | 3,694 |
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