URGCP upregulator of cell proliferation

Information
Symbol
URGCP
Type
protein-coding
Description
upregulator of cell proliferation
Entrez Gene ID
55665
Genome
hg19
Position
chr7:43,915,512-43,946,195
Genome
hg38
Position
chr7:43,875,913-43,906,596
MIM
610337 OMIM
HGNC
HGNC:30890 HGNC
Ensembl
ENSG00000106608 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 6
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
80
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
Category :
Search word :
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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
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
Entry Origin Type Annotation
TypeID
SYNONYM URG4
MIM 610337 OMIM
HGNC HGNC:30890 HGNC
Ensembl ENSG00000106608 Ensembl
AllianceGenome HGNC:30890
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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