FOS Fos proto-oncogene, AP-1 transcription factor subunit
Information
- Symbol
- FOS
- Type
- protein-coding
- Description
- Fos proto-oncogene, AP-1 transcription factor subunit
- Entrez Gene ID
- 2353
- Genome
- hg19
- Position
- chr14:75,745,531-75,748,933
- Genome
- hg38
- Position
- chr14:75,278,828-75,282,230
- MIM
- 164810 OMIM
- HGNC
- HGNC:3796 HGNC
- Ensembl
- ENSG00000170345 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 18 |
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
6 |
 |
44 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 | AP-1 |
| SYNONYM | C-FOS |
| SYNONYM | p55 |
| MIM | 164810 OMIM |
| HGNC | HGNC:3796 HGNC |
| Ensembl | ENSG00000170345 Ensembl |
| AllianceGenome | HGNC:3796 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000555686.1 | hg38 | chr14 | 75,279,643 | 75,281,684 | 2,042 |
| ENST00000554617.1 | hg38 | chr14 | 75,278,826 | 75,280,374 | 1,549 |
| ENST00000555347.1 | hg38 | chr14 | 75,280,193 | 75,281,587 | 1,395 |
| ENST00000535987.5 | hg38 | chr14 | 75,278,828 | 75,281,636 | 2,809 |
| ENST00000555242.1 | hg38 | chr14 | 75,278,977 | 75,280,789 | 1,813 |
| ENST00000303562.9 | hg38 | chr14 | 75,278,828 | 75,282,230 | 3,403 |
| ENST00000554617.1 | hg19 | chr14 | 75,745,529 | 75,747,077 | 1,549 |
| ENST00000535987.5 | hg19 | chr14 | 75,745,531 | 75,748,339 | 2,809 |
| ENST00000303562.9 | hg19 | chr14 | 75,745,531 | 75,748,933 | 3,403 |
| ENST00000555242.1 | hg19 | chr14 | 75,745,680 | 75,747,492 | 1,813 |
| ENST00000555686.1 | hg19 | chr14 | 75,746,346 | 75,748,387 | 2,042 |
| ENST00000555347.1 | hg19 | chr14 | 75,746,896 | 75,748,290 | 1,395 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | OG |
| start | 75,745,480 |
| Gene Symbol | FOS |
| Entrez GeneId | 2,353 |
| Chr Band | 14q24.3 |
| end | 75,748,936 |
| chr | chr14 |
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