REXO2 RNA exonuclease 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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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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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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 | CGI-114 |
SYNONYM | REX2 |
SYNONYM | RFN |
SYNONYM | SFN |
MIM | 607149 OMIM |
HGNC | HGNC:17851 HGNC |
Ensembl | ENSG00000076043 Ensembl |
AllianceGenome | HGNC:17851 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000544196.5 | hg38 | chr11 | 114,439,466 | 114,441,902 | 2,437 |
ENST00000544827.5 | hg38 | chr11 | 114,440,121 | 114,450,262 | 10,142 |
ENST00000539754.5 | hg38 | chr11 | 114,439,471 | 114,450,039 | 10,569 |
ENST00000265881.10 | hg38 | chr11 | 114,439,467 | 114,450,279 | 10,813 |
ENST00000539275.5 | hg38 | chr11 | 114,439,484 | 114,450,279 | 10,796 |
ENST00000544196.5 | hg19 | chr11 | 114,310,188 | 114,312,624 | 2,437 |
ENST00000265881.10 | hg19 | chr11 | 114,310,189 | 114,321,001 | 10,813 |
ENST00000539275.5 | hg19 | chr11 | 114,310,206 | 114,321,001 | 10,796 |
ENST00000539754.5 | hg19 | chr11 | 114,310,193 | 114,320,761 | 10,569 |
ENST00000544827.5 | hg19 | chr11 | 114,310,843 | 114,320,984 | 10,142 |
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