URGCP upregulator of cell proliferation
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 16 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 58 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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80 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | URG4 |
| MIM | 610337 OMIM |
| HGNC | HGNC:30890 HGNC |
| Ensembl | ENSG00000106608 Ensembl |
| AllianceGenome | HGNC:30890 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000443736.5 | hg38 | chr7 | 43,875,913 | 43,906,626 | 30,714 |
| ENST00000446958.1 | hg38 | chr7 | 43,881,138 | 43,906,627 | 25,490 |
| ENST00000402306.7 | hg38 | chr7 | 43,875,913 | 43,906,615 | 30,703 |
| ENST00000336086.10 | hg38 | chr7 | 43,875,913 | 43,889,634 | 13,722 |
| ENST00000453200.6 | hg38 | chr7 | 43,875,913 | 43,906,596 | 30,684 |
| ENST00000336086.10 | hg19 | chr7 | 43,915,512 | 43,929,233 | 13,722 |
| ENST00000453200.6 | hg19 | chr7 | 43,915,512 | 43,946,195 | 30,684 |
| ENST00000402306.7 | hg19 | chr7 | 43,915,512 | 43,946,214 | 30,703 |
| ENST00000443736.5 | hg19 | chr7 | 43,915,512 | 43,946,225 | 30,714 |
| ENST00000446958.1 | hg19 | chr7 | 43,920,737 | 43,946,226 | 25,490 |
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