RETREG2 reticulophagy regulator family member 2

Information
Symbol
RETREG2
Type
protein-coding
Description
reticulophagy regulator family member 2
Entrez Gene ID
79137
Genome
hg19
Position
chr2:220,042,997-220,050,197
Genome
hg38
Position
chr2:219,178,275-219,185,475
HGNC
HGNC:28450 HGNC
Ensembl
ENSG00000144567 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
62
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 :
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 C2orf17
SYNONYM FAM134A
SYNONYM MAG-2
HGNC HGNC:28450 HGNC
Ensembl ENSG00000144567 Ensembl
AllianceGenome HGNC:28450
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000430297.7 hg38 chr2 219,178,275 219,185,475 7,201
ENST00000430297.7 hg19 chr2 220,042,997 220,050,197 7,201
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