OLFM2 olfactomedin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 22 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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68 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | NOE2 |
SYNONYM | NOELIN2 |
SYNONYM | NOELIN2_V1 |
SYNONYM | OlfC |
MIM | 617492 OMIM |
HGNC | HGNC:17189 HGNC |
Ensembl | ENSG00000105088 Ensembl |
AllianceGenome | HGNC:17189 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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