PRAME PRAME nuclear receptor transcriptional regulator
Information
- Symbol
- PRAME
- Type
- protein-coding
- Description
- PRAME nuclear receptor transcriptional regulator
- Entrez Gene ID
- 23532
- Genome
- hg19
- Position
- chr22:22,890,123-22,901,672
- Genome
- hg38
- Position
- chr22:22,547,701-22,559,265
- MIM
- 606021 OMIM
- HGNC
- HGNC:9336 HGNC
- Ensembl
- ENSG00000185686 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 68 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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82 |
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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
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 | CT130 |
| SYNONYM | MAPE |
| SYNONYM | OIP-4 |
| SYNONYM | OIP4 |
| MIM | 606021 OMIM |
| HGNC | HGNC:9336 HGNC |
| Ensembl | ENSG00000185686 Ensembl |
| AllianceGenome | HGNC:9336 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000406503.1 | hg38 | chr22 | 22,550,754 | 22,559,267 | 8,514 |
| ENST00000405655.8 | hg38 | chr22 | 22,547,701 | 22,559,265 | 11,565 |
| ENST00000402697.5 | hg38 | chr22 | 22,547,767 | 22,559,288 | 11,522 |
| ENST00000398741.5 | hg38 | chr22 | 22,547,702 | 22,559,143 | 11,442 |
| ENST00000398743.6 | hg38 | chr22 | 22,547,701 | 22,559,340 | 11,640 |
| ENST00000543184.5 | hg38 | chr22 | 22,547,702 | 22,559,289 | 11,588 |
| ENST00000405655.8 | hg19 | chr22 | 22,890,123 | 22,901,672 | 11,550 |
| ENST00000398743.6 | hg19 | chr22 | 22,890,123 | 22,901,747 | 11,625 |
| ENST00000398741.5 | hg19 | chr22 | 22,890,124 | 22,901,550 | 11,427 |
| ENST00000543184.5 | hg19 | chr22 | 22,890,124 | 22,901,696 | 11,573 |
| ENST00000402697.5 | hg19 | chr22 | 22,890,189 | 22,901,695 | 11,507 |
| ENST00000406503.1 | hg19 | chr22 | 22,893,176 | 22,901,674 | 8,499 |
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