TOX2 TOX high mobility group box family member 2
Information
- Symbol
- TOX2
- Type
- protein-coding
- Description
- TOX high mobility group box family member 2
- Entrez Gene ID
- 84969
- Genome
- hg19
- Position
- chr20:42,543,492-42,698,256
- Genome
- hg38
- Position
- chr20:43,914,852-44,069,616
- MIM
- 611163 OMIM
- HGNC
- HGNC:16095 HGNC
- Ensembl
- ENSG00000124191 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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62 |
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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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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
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| 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
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| Category | : |
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| 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 | C20orf100 |
| SYNONYM | GCX-1 |
| SYNONYM | GCX1 |
| SYNONYM | dJ1108D11.2 |
| SYNONYM | dJ495O3.1 |
| MIM | 611163 OMIM |
| HGNC | HGNC:16095 HGNC |
| Ensembl | ENSG00000124191 Ensembl |
| AllianceGenome | HGNC:16095 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000372999.5 | hg38 | chr20 | 43,916,167 | 44,069,616 | 153,450 |
| ENST00000358131.5 | hg38 | chr20 | 43,945,705 | 44,069,616 | 123,912 |
| ENST00000423191.6 | hg38 | chr20 | 43,916,150 | 44,068,914 | 152,765 |
| ENST00000341197.9 | hg38 | chr20 | 43,914,852 | 44,069,616 | 154,765 |
| ENST00000341197.9 | hg19 | chr20 | 42,543,492 | 42,698,256 | 154,765 |
| ENST00000423191.6 | hg19 | chr20 | 42,544,790 | 42,697,554 | 152,765 |
| ENST00000372999.5 | hg19 | chr20 | 42,544,807 | 42,698,256 | 153,450 |
| ENST00000358131.5 | hg19 | chr20 | 42,574,345 | 42,698,256 | 123,912 |
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