ERP29 endoplasmic reticulum protein 29
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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 | |||||
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | C12orf8 |
SYNONYM | ERp28 |
SYNONYM | ERp31 |
SYNONYM | HEL-S-107 |
SYNONYM | PDI-DB |
SYNONYM | PDIA9 |
MIM | 602287 OMIM |
HGNC | HGNC:13799 HGNC |
Ensembl | ENSG00000089248 Ensembl |
AllianceGenome | HGNC:13799 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000261735.4 | hg38 | chr12 | 112,013,426 | 112,023,449 | 10,024 |
ENST00000455836.1 | hg38 | chr12 | 112,013,348 | 112,023,220 | 9,873 |
ENST00000546477.1 | hg38 | chr12 | 112,018,804 | 112,023,168 | 4,365 |
ENST00000455836.1 | hg19 | chr12 | 112,451,152 | 112,461,024 | 9,873 |
ENST00000261735.4 | hg19 | chr12 | 112,451,230 | 112,461,253 | 10,024 |
ENST00000546477.1 | hg19 | chr12 | 112,456,608 | 112,460,972 | 4,365 |
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