TOM1 target of myb1 membrane trafficking protein
Information
- Symbol
- TOM1
- Type
- protein-coding
- Description
- target of myb1 membrane trafficking protein
- Entrez Gene ID
- 10043
- Genome
- hg19
- Position
- chr22:35,695,797-35,743,985
- Genome
- hg38
- Position
- chr22:35,299,804-35,347,992
- MIM
- 604700 OMIM
- HGNC
- HGNC:11982 HGNC
- Ensembl
- ENSG00000100284 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 18 |
| Likely benign | 0 | 10 |
| Conflicting classifications of pathogenicity | 0 | 4 |
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
112 |
 |
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
[No Data.]
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 | : |
|
| 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 |
|---|---|
| SYNONYM | IMD85 |
| MIM | 604700 OMIM |
| HGNC | HGNC:11982 HGNC |
| Ensembl | ENSG00000100284 Ensembl |
| AllianceGenome | HGNC:11982 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000447733.5 | hg38 | chr22 | 35,299,275 | 35,347,992 | 48,718 |
| ENST00000449058.7 | hg38 | chr22 | 35,299,894 | 35,347,973 | 48,080 |
| ENST00000411850.5 | hg38 | chr22 | 35,299,804 | 35,347,992 | 48,189 |
| ENST00000425375.5 | hg38 | chr22 | 35,299,804 | 35,347,992 | 48,189 |
| ENST00000447733.5 | hg19 | chr22 | 35,695,268 | 35,743,985 | 48,718 |
| ENST00000425375.5 | hg19 | chr22 | 35,695,797 | 35,743,985 | 48,189 |
| ENST00000411850.5 | hg19 | chr22 | 35,695,797 | 35,743,985 | 48,189 |
| ENST00000449058.7 | hg19 | chr22 | 35,695,887 | 35,743,966 | 48,080 |
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