TOM1L2 target of myb1 like 2 membrane trafficking protein
Information
- Symbol
- TOM1L2
- Type
- protein-coding
- Description
- target of myb1 like 2 membrane trafficking protein
- Entrez Gene ID
- 146691
- Genome
- hg19
- Position
- chr17:17,746,825-17,875,714
- Genome
- hg38
- Position
- chr17:17,843,511-17,972,400
- MIM
- 615519 OMIM
- HGNC
- HGNC:11984 HGNC
- Ensembl
- ENSG00000175662 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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56 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
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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
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Category | : |
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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 |
Type | ID |
---|---|
MIM | 615519 OMIM |
HGNC | HGNC:11984 HGNC |
Ensembl | ENSG00000175662 Ensembl |
AllianceGenome | HGNC:11984 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000318094.14 | hg38 | chr17 | 17,846,849 | 17,972,397 | 125,549 |
ENST00000395739.8 | hg38 | chr17 | 17,847,349 | 17,972,404 | 125,056 |
ENST00000478943.5 | hg38 | chr17 | 17,846,825 | 17,872,064 | 25,240 |
ENST00000379504.8 | hg38 | chr17 | 17,843,511 | 17,972,400 | 128,890 |
ENST00000542206.5 | hg38 | chr17 | 17,847,569 | 17,972,400 | 124,832 |
ENST00000535933.5 | hg38 | chr17 | 17,847,446 | 17,972,420 | 124,975 |
ENST00000540946.5 | hg38 | chr17 | 17,847,469 | 17,972,397 | 124,929 |
ENST00000581396.5 | hg38 | chr17 | 17,843,511 | 17,972,410 | 128,900 |
ENST00000379504.8 | hg19 | chr17 | 17,746,825 | 17,875,714 | 128,890 |
ENST00000581396.5 | hg19 | chr17 | 17,746,825 | 17,875,724 | 128,900 |
ENST00000478943.5 | hg19 | chr17 | 17,750,139 | 17,775,378 | 25,240 |
ENST00000318094.14 | hg19 | chr17 | 17,750,163 | 17,875,711 | 125,549 |
ENST00000395739.8 | hg19 | chr17 | 17,750,663 | 17,875,718 | 125,056 |
ENST00000535933.5 | hg19 | chr17 | 17,750,760 | 17,875,734 | 124,975 |
ENST00000540946.5 | hg19 | chr17 | 17,750,783 | 17,875,711 | 124,929 |
ENST00000542206.5 | hg19 | chr17 | 17,750,883 | 17,875,714 | 124,832 |
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