UPF1 UPF1 RNA helicase and ATPase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 44 |
Likely benign | 0 | 28 |
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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140 |
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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 |
Search Word
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 |
---|---|
SYNONYM | HUPF1 |
SYNONYM | NORF1 |
SYNONYM | RENT1 |
SYNONYM | UTF |
SYNONYM | pNORF1 |
SYNONYM | smg-2 |
MIM | 601430 OMIM |
HGNC | HGNC:9962 HGNC |
Ensembl | ENSG00000005007 Ensembl |
AllianceGenome | HGNC:9962 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000599848.5 | hg38 | chr19 | 18,832,001 | 18,868,229 | 36,229 |
ENST00000704676.1 | hg38 | chr19 | 18,831,959 | 18,868,230 | 36,272 |
ENST00000262803.10 | hg38 | chr19 | 18,831,959 | 18,868,230 | 36,272 |
ENST00000262803.10 | hg19 | chr19 | 18,942,768 | 18,979,039 | 36,272 |
ENST00000599848.5 | hg19 | chr19 | 18,942,810 | 18,979,038 | 36,229 |
ENST00000704676.1 | hg19 | chr19 | 18,942,768 | 18,979,039 | 36,272 |
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