EMB embigin

Information
Symbol
EMB
Type
protein-coding
Description
embigin
Entrez Gene ID
133418
Genome
hg19
Position
chr5:49,692,026-49,737,122
Genome
hg38
Position
chr5:50,396,192-50,441,288
MIM
615669 OMIM
HGNC
HGNC:30465 HGNC
Ensembl
ENSG00000170571 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
30
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 GP70
MIM 615669 OMIM
HGNC HGNC:30465 HGNC
Ensembl ENSG00000170571 Ensembl
AllianceGenome HGNC:30465
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303221.10 hg38 chr5 50,396,192 50,441,288 45,097
ENST00000508934.5 hg38 chr5 50,398,677 50,441,350 42,674
ENST00000514111.1 hg38 chr5 50,398,939 50,428,727 29,789
ENST00000303221.10 hg19 chr5 49,692,026 49,737,122 45,097
ENST00000508934.5 hg19 chr5 49,694,511 49,737,184 42,674
ENST00000514111.1 hg19 chr5 49,694,773 49,724,561 29,789
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