PGA4 pepsinogen A4

Information
Symbol
PGA4
Type
protein-coding
Description
pepsinogen A4
Entrez Gene ID
643847
Genome
hg19
Position
chr11:60,989,819-60,999,166
Genome
hg38
Position
chr11:61,222,347-61,231,694
MIM
169720 OMIM
HGNC
HGNC:8886 HGNC
Ensembl
ENSG00000229183 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
8
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
MIM 169720 OMIM
HGNC HGNC:8886 HGNC
Ensembl ENSG00000229183 Ensembl
AllianceGenome HGNC:8886
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537932.5 hg38 chr11 61,228,377 61,231,566 3,190
ENST00000378149.9 hg38 chr11 61,222,347 61,231,694 9,348
ENST00000544899.1 hg38 chr11 61,229,583 61,231,668 2,086
ENST00000378149.9 hg19 chr11 60,989,819 60,999,166 9,348
ENST00000537932.5 hg19 chr11 60,995,849 60,999,038 3,190
ENST00000544899.1 hg19 chr11 60,997,055 60,999,140 2,086
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