MEP1B meprin A subunit beta

Information
Symbol
MEP1B
Type
protein-coding
Description
meprin A subunit beta
Entrez Gene ID
4225
Genome
hg19
Position
chr18:29,770,002-29,800,367
Genome
hg38
Position
chr18:32,190,039-32,220,404
MIM
600389 OMIM
HGNC
HGNC:7020 HGNC
Ensembl
ENSG00000141434 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
70
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 600389 OMIM
HGNC HGNC:7020 HGNC
Ensembl ENSG00000141434 Ensembl
AllianceGenome HGNC:7020
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000269202.11 hg38 chr18 32,190,039 32,220,404 30,366
ENST00000581447.1 hg38 chr18 32,190,025 32,220,404 30,380
ENST00000581447.1 hg19 chr18 29,769,988 29,800,367 30,380
ENST00000269202.11 hg19 chr18 29,770,002 29,800,367 30,366
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