ART5 ADP-ribosyltransferase 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
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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44 |
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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 |
Prediction | |||||
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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 | ARTC5 |
MIM | 610625 OMIM |
HGNC | HGNC:24049 HGNC |
Ensembl | ENSG00000167311 Ensembl |
AllianceGenome | HGNC:24049 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000397068.8 | hg38 | chr11 | 3,638,512 | 3,641,992 | 3,481 |
ENST00000397067.7 | hg38 | chr11 | 3,638,512 | 3,641,992 | 3,481 |
ENST00000359918.8 | hg38 | chr11 | 3,638,514 | 3,642,316 | 3,803 |
ENST00000397067.7 | hg19 | chr11 | 3,659,742 | 3,663,222 | 3,481 |
ENST00000397068.8 | hg19 | chr11 | 3,659,742 | 3,663,222 | 3,481 |
ENST00000359918.8 | hg19 | chr11 | 3,659,744 | 3,663,546 | 3,803 |
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