EPOP elongin BC and polycomb repressive complex 2 associated protein
Information
- Symbol
- EPOP
- Type
- protein-coding
- Description
- elongin BC and polycomb repressive complex 2 associated protein
- Entrez Gene ID
- 100170841
- Genome
- hg19
- Position
- chr17:36,827,956-36,831,210
- Genome
- hg38
- Position
- chr17:38,671,703-38,674,957
- MIM
- 617795 OMIM
- HGNC
- HGNC:34493 HGNC
- Ensembl
- ENSG00000273604 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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8 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C17orf96 |
SYNONYM | PRR28 |
MIM | 617795 OMIM |
HGNC | HGNC:34493 HGNC |
Ensembl | ENSG00000273604 Ensembl |
AllianceGenome | HGNC:34493 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000621654.2 | hg38 | chr17 | 38,671,703 | 38,674,957 | 3,255 |
ENST00000621654.2 | hg19 | chr17 | 36,827,956 | 36,831,210 | 3,255 |
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