PA2G4 proliferation-associated 2G4

Information
Symbol
PA2G4
Type
protein-coding
Description
proliferation-associated 2G4
Entrez Gene ID
5036
Genome
hg19
Position
chr12:56,498,343-56,507,694
Genome
hg38
Position
chr12:56,104,559-56,113,910
MIM
602145 OMIM
HGNC
HGNC:8550 HGNC
Ensembl
ENSG00000170515 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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 :
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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 :
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 EBP1
SYNONYM HG4-1
SYNONYM ITAF45
SYNONYM p38-2G4
MIM 602145 OMIM
HGNC HGNC:8550 HGNC
Ensembl ENSG00000170515 Ensembl
AllianceGenome HGNC:8550
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303305.11 hg38 chr12 56,104,559 56,113,910 9,352
ENST00000552766.5 hg38 chr12 56,104,537 56,113,907 9,371
ENST00000552766.5 hg19 chr12 56,498,321 56,507,691 9,371
ENST00000303305.11 hg19 chr12 56,498,343 56,507,694 9,352
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