VMO1 vitelline membrane outer layer 1 homolog
Information
- Symbol
- VMO1
- Type
- protein-coding
- Description
- vitelline membrane outer layer 1 homolog
- Entrez Gene ID
- 284013
- Genome
- hg19
- Position
- chr17:4,688,580-4,689,659
- Genome
- hg38
- Position
- chr17:4,785,285-4,786,364
- HGNC
- HGNC:30387 HGNC
- Ensembl
- ENSG00000182853 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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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
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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 |
---|---|
SYNONYM | ERGA6350 |
SYNONYM | PRO21055 |
HGNC | HGNC:30387 HGNC |
Ensembl | ENSG00000182853 Ensembl |
AllianceGenome | HGNC:30387 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000354194.4 | hg38 | chr17 | 4,785,285 | 4,786,433 | 1,149 |
ENST00000441199.2 | hg38 | chr17 | 4,785,285 | 4,786,371 | 1,087 |
ENST00000416307.6 | hg38 | chr17 | 4,785,285 | 4,786,398 | 1,114 |
ENST00000328739.6 | hg38 | chr17 | 4,785,285 | 4,786,364 | 1,080 |
ENST00000328739.6 | hg19 | chr17 | 4,688,580 | 4,689,659 | 1,080 |
ENST00000441199.2 | hg19 | chr17 | 4,688,580 | 4,689,666 | 1,087 |
ENST00000416307.6 | hg19 | chr17 | 4,688,580 | 4,689,693 | 1,114 |
ENST00000354194.4 | hg19 | chr17 | 4,688,580 | 4,689,728 | 1,149 |
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