PRRT4 proline rich transmembrane protein 4
Information
- Symbol
- PRRT4
- Type
- protein-coding
- Description
- proline rich transmembrane protein 4
- Entrez Gene ID
- 401399
- Genome
- hg19
- Position
- chr7:127,990,379-128,001,744
- Genome
- hg38
- Position
- chr7:128,350,325-128,361,690
- HGNC
- HGNC:37280 HGNC
- Ensembl
- ENSG00000224940 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 126 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
128 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000489835.6 | hg38 | chr7 | 128,350,325 | 128,361,604 | 11,280 |
| ENST00000535159.5 | hg38 | chr7 | 128,350,856 | 128,361,685 | 10,830 |
| ENST00000446477.7 | hg38 | chr7 | 128,350,325 | 128,361,690 | 11,366 |
| ENST00000489835.6 | hg19 | chr7 | 127,990,379 | 128,001,658 | 11,280 |
| ENST00000446477.7 | hg19 | chr7 | 127,990,379 | 128,001,744 | 11,366 |
| ENST00000535159.5 | hg19 | chr7 | 127,990,910 | 128,001,739 | 10,830 |
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