PPBP pro-platelet basic protein
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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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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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 |
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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 |
Type | ID |
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SYNONYM | B-TG1 |
SYNONYM | Beta-TG |
SYNONYM | CTAP-III |
SYNONYM | CTAP3 |
SYNONYM | CTAPIII |
SYNONYM | CXCL7 |
SYNONYM | LA-PF4 |
SYNONYM | LDGF |
SYNONYM | MDGF |
SYNONYM | NAP-2 |
SYNONYM | PBP |
SYNONYM | SCYB7 |
SYNONYM | TC1 |
SYNONYM | TC2 |
SYNONYM | TGB |
SYNONYM | TGB1 |
SYNONYM | THBGB |
SYNONYM | THBGB1 |
MIM | 121010 OMIM |
HGNC | HGNC:9240 HGNC |
Ensembl | ENSG00000163736 Ensembl |
AllianceGenome | HGNC:9240 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000296028.4 | hg38 | chr4 | 73,986,439 | 73,988,190 | 1,752 |
ENST00000296028.4 | hg19 | chr4 | 74,852,156 | 74,853,907 | 1,752 |
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