PPAN-P2RY11 PPAN-P2RY11 readthrough
Information
- Symbol
- PPAN-P2RY11
- Type
- protein-coding
- Description
- PPAN-P2RY11 readthrough
- Entrez Gene ID
- 692312
- Genome
- hg19
- Position
- chr19:10,217,071-10,225,414
- Genome
- hg38
- Position
- chr19:10,106,395-10,114,738
- HGNC
- HGNC:33526 HGNC
- Ensembl
- ENSG00000243207 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 22 |
| Likely benign | 0 | 50 |
| association | 0 | 4 |
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
8 |
 |
78 |
 |
4 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 | BXDC3 |
| SYNONYM | P2RY11 |
| SYNONYM | P2Y11 |
| SYNONYM | PPAN |
| SYNONYM | SSF1 |
| SYNONYM | Ssf-1 |
| HGNC | HGNC:33526 HGNC |
| Ensembl | ENSG00000243207 Ensembl |
| AllianceGenome | HGNC:33526 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000428358.5 | hg38 | chr19 | 10,106,223 | 10,114,780 | 8,558 |
| ENST00000393796.4 | hg38 | chr19 | 10,106,395 | 10,114,738 | 8,344 |
| ENST00000428358.5 | hg19 | chr19 | 10,216,899 | 10,225,456 | 8,558 |
| ENST00000393796.4 | hg19 | chr19 | 10,217,071 | 10,225,414 | 8,344 |
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