PGA5 pepsinogen A5

Information
Symbol
PGA5
Type
protein-coding
Description
pepsinogen A5
Entrez Gene ID
5222
Genome
hg19
Position
chr11:61,008,647-61,018,916
Genome
hg38
Position
chr11:61,241,175-61,251,444
MIM
169730 OMIM
HGNC
HGNC:8887 HGNC
Ensembl
ENSG00000256713 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
26
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 :
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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 Pg5
MIM 169730 OMIM
HGNC HGNC:8887 HGNC
Ensembl ENSG00000256713 Ensembl
AllianceGenome HGNC:8887
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000451616.6 hg38 chr11 61,248,122 61,251,444 3,323
ENST00000312403.10 hg38 chr11 61,241,175 61,251,444 10,270
ENST00000541528.1 hg38 chr11 61,249,333 61,251,418 2,086
ENST00000312403.10 hg19 chr11 61,008,647 61,018,916 10,270
ENST00000451616.6 hg19 chr11 61,015,594 61,018,916 3,323
ENST00000541528.1 hg19 chr11 61,016,805 61,018,890 2,086
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