OLFM2 olfactomedin 2

Information
Symbol
OLFM2
Type
protein-coding
Description
olfactomedin 2
Entrez Gene ID
93145
Genome
hg19
Position
chr19:9,964,394-10,024,512
Genome
hg38
Position
chr19:9,853,718-9,913,836
MIM
617492 OMIM
HGNC
HGNC:17189 HGNC
Ensembl
ENSG00000105088 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 22
Likely benign 0 4
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
68
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 :
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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 :
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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 NOE2
SYNONYM NOELIN2
SYNONYM NOELIN2_V1
SYNONYM OlfC
MIM 617492 OMIM
HGNC HGNC:17189 HGNC
Ensembl ENSG00000105088 Ensembl
AllianceGenome HGNC:17189
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000593091.2 hg38 chr19 9,853,718 9,913,836 60,119
ENST00000590841.5 hg38 chr19 9,853,745 9,858,168 4,424
ENST00000264833.9 hg38 chr19 9,853,718 9,936,515 82,798
ENST00000593091.2 hg19 chr19 9,964,394 10,024,512 60,119
ENST00000264833.9 hg19 chr19 9,964,394 10,047,191 82,798
ENST00000590841.5 hg19 chr19 9,964,421 9,968,844 4,424
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