ETS2 ETS proto-oncogene 2, transcription factor
Information
- Symbol
- ETS2
- Type
- protein-coding
- Description
- ETS proto-oncogene 2, transcription factor
- Entrez Gene ID
- 2114
- Genome
- hg19
- Position
- chr21:40,177,107-40,196,879
- Genome
- hg38
- Position
- chr21:38,805,183-38,824,955
- MIM
- 164740 OMIM
- HGNC
- HGNC:3489 HGNC
- Ensembl
- ENSG00000157557 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 52 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
4 |
 |
56 |
 |
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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| 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 | ETS2IT1 |
| MIM | 164740 OMIM |
| HGNC | HGNC:3489 HGNC |
| Ensembl | ENSG00000157557 Ensembl |
| AllianceGenome | HGNC:3489 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000662305.1 | hg38 | chr21 | 38,809,403 | 38,823,783 | 14,381 |
| ENST00000360938.8 | hg38 | chr21 | 38,805,929 | 38,824,955 | 19,027 |
| ENST00000667466.1 | hg38 | chr21 | 38,805,895 | 38,824,936 | 19,042 |
| ENST00000360214.8 | hg38 | chr21 | 38,805,183 | 38,824,955 | 19,773 |
| ENST00000653642.1 | hg38 | chr21 | 38,808,094 | 38,824,928 | 16,835 |
| ENST00000666778.1 | hg38 | chr21 | 38,805,983 | 38,824,936 | 18,954 |
| ENST00000360214.8 | hg19 | chr21 | 40,177,107 | 40,196,879 | 19,773 |
| ENST00000667466.1 | hg19 | chr21 | 40,177,819 | 40,196,860 | 19,042 |
| ENST00000360938.8 | hg19 | chr21 | 40,177,853 | 40,196,879 | 19,027 |
| ENST00000666778.1 | hg19 | chr21 | 40,177,907 | 40,196,860 | 18,954 |
| ENST00000653642.1 | hg19 | chr21 | 40,180,018 | 40,196,852 | 16,835 |
| ENST00000662305.1 | hg19 | chr21 | 40,181,327 | 40,195,707 | 14,381 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | OG |
| start | 40,177,230 |
| Gene Symbol | ETS2 |
| Entrez GeneId | 2,114 |
| Chr Band | 21q22.2 |
| end | 40,196,877 |
| chr | chr21 |
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