PCGF2 polycomb group ring finger 2

Information
Symbol
PCGF2
Type
protein-coding
Description
polycomb group ring finger 2
Entrez Gene ID
7703
Genome
hg19
Position
chr17:36,890,151-36,906,070
Genome
hg38
Position
chr17:38,733,898-38,749,817
MIM
600346 OMIM
HGNC
HGNC:12929 HGNC
Ensembl
ENSG00000277258 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 6
Benign 0 60
Likely benign 0 174
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 168
Ranking
ClinVar
0
0
48
352
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
Category :
Search word :
Filtering :
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 :
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
Category :
Search word :
Filtering :
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 MEL-18
SYNONYM RNF110
SYNONYM TPFS
SYNONYM ZNF144
MIM 600346 OMIM
HGNC HGNC:12929 HGNC
Ensembl ENSG00000277258 Ensembl
AllianceGenome HGNC:12929
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000620225.5 hg38 chr17 38,733,898 38,748,336 14,439
ENST00000616199.4 hg38 chr17 38,733,898 38,749,817 15,920
ENST00000618941.4 hg38 chr17 38,735,109 38,748,184 13,076
ENST00000616129.4 hg38 chr17 38,735,044 38,748,378 13,335
ENST00000618506.1 hg38 chr17 38,735,112 38,748,353 13,242
ENST00000611883.4 hg38 chr17 38,734,280 38,746,628 12,349
ENST00000620225.5 hg19 chr17 36,890,151 36,904,589 14,439
ENST00000616199.4 hg19 chr17 36,890,151 36,906,070 15,920
ENST00000611883.4 hg19 chr17 36,890,533 36,902,881 12,349
ENST00000616129.4 hg19 chr17 36,891,297 36,904,631 13,335
ENST00000618941.4 hg19 chr17 36,891,362 36,904,437 13,076
ENST00000618506.1 hg19 chr17 36,891,365 36,904,606 13,242
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