RDH13 retinol dehydrogenase 13
Information
- Symbol
- RDH13
- Type
- protein-coding
- Description
- retinol dehydrogenase 13
- Entrez Gene ID
- 112724
- Genome
- hg19
- Position
- chr19:55,555,684-55,574,516
- Genome
- hg38
- Position
- chr19:55,044,316-55,063,148
- HGNC
- HGNC:19978 HGNC
- Ensembl
- ENSG00000160439 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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
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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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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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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 | SDR7C3 |
HGNC | HGNC:19978 HGNC |
Ensembl | ENSG00000160439 Ensembl |
AllianceGenome | HGNC:19978 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000610356.4 | hg38 | chr19 | 55,044,324 | 55,063,217 | 18,894 |
ENST00000415061.8 | hg38 | chr19 | 55,044,316 | 55,063,148 | 18,833 |
ENST00000396247.7 | hg38 | chr19 | 55,044,343 | 55,069,529 | 25,187 |
ENST00000415061.8 | hg19 | chr19 | 55,555,684 | 55,574,516 | 18,833 |
ENST00000396247.7 | hg19 | chr19 | 55,555,711 | 55,580,897 | 25,187 |
ENST00000610356.4 | hg19 | chr19 | 55,555,692 | 55,574,585 | 18,894 |
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