PATE4 prostate and testis expressed 4
Information
- Symbol
- PATE4
- Type
- protein-coding
- Description
- prostate and testis expressed 4
- Entrez Gene ID
- 399968
- Genome
- hg19
- Position
- chr11:125,703,211-125,709,967
- Genome
- hg38
- Position
- chr11:125,833,316-125,840,072
- HGNC
- HGNC:35427 HGNC
- Ensembl
- ENSG00000237353 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
8 |
 |
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 | |||||||||||
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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 | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | PATE-B |
| HGNC | HGNC:35427 HGNC |
| Ensembl | ENSG00000237353 Ensembl |
| AllianceGenome | HGNC:35427 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000457514.3 | hg38 | chr11 | 125,833,316 | 125,840,072 | 6,757 |
| ENST00000534411.5 | hg38 | chr11 | 125,833,316 | 125,839,100 | 5,785 |
| ENST00000534411.5 | hg19 | chr11 | 125,703,211 | 125,708,995 | 5,785 |
| ENST00000457514.3 | hg19 | chr11 | 125,703,211 | 125,709,967 | 6,757 |
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