CYB5R2 cytochrome b5 reductase 2
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
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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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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 | B5R.2 |
MIM | 608342 OMIM |
HGNC | HGNC:24376 HGNC |
Ensembl | ENSG00000166394 Ensembl |
AllianceGenome | HGNC:24376 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000299498.11 | hg38 | chr11 | 7,665,104 | 7,673,500 | 8,397 |
ENST00000533558.5 | hg38 | chr11 | 7,665,104 | 7,674,208 | 9,105 |
ENST00000524790.5 | hg38 | chr11 | 7,665,100 | 7,673,472 | 8,373 |
ENST00000524790.5 | hg19 | chr11 | 7,686,331 | 7,694,703 | 8,373 |
ENST00000299498.11 | hg19 | chr11 | 7,686,335 | 7,694,731 | 8,397 |
ENST00000533558.5 | hg19 | chr11 | 7,686,335 | 7,695,439 | 9,105 |
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