PLAUR plasminogen activator, urokinase receptor
Information
- Symbol
- PLAUR
- Type
- protein-coding
- Description
- plasminogen activator, urokinase receptor
- Entrez Gene ID
- 5329
- Genome
- hg19
- Position
- chr19:44,152,731-44,174,321
- Genome
- hg38
- Position
- chr19:43,648,579-43,670,169
- MIM
- 173391 OMIM
- HGNC
- HGNC:9053 HGNC
- Ensembl
- ENSG00000011422 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 20 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
6 |
 |
54 |
 |
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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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 | CD87 |
| SYNONYM | U-PAR |
| SYNONYM | UPAR |
| SYNONYM | URKR |
| MIM | 173391 OMIM |
| HGNC | HGNC:9053 HGNC |
| Ensembl | ENSG00000011422 Ensembl |
| AllianceGenome | HGNC:9053 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000340093.8 | hg38 | chr19 | 43,648,579 | 43,670,169 | 21,591 |
| ENST00000339082.7 | hg38 | chr19 | 43,646,095 | 43,670,166 | 24,072 |
| ENST00000221264.8 | hg38 | chr19 | 43,648,580 | 43,670,547 | 21,968 |
| ENST00000601723.5 | hg38 | chr19 | 43,648,579 | 43,670,153 | 21,575 |
| ENST00000339082.7 | hg19 | chr19 | 44,150,247 | 44,174,318 | 24,072 |
| ENST00000601723.5 | hg19 | chr19 | 44,152,731 | 44,174,305 | 21,575 |
| ENST00000340093.8 | hg19 | chr19 | 44,152,731 | 44,174,321 | 21,591 |
| ENST00000221264.8 | hg19 | chr19 | 44,152,732 | 44,174,699 | 21,968 |
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