FOSB FosB proto-oncogene, AP-1 transcription factor subunit
Information
- Symbol
- FOSB
- Type
- protein-coding
- Description
- FosB proto-oncogene, AP-1 transcription factor subunit
- Entrez Gene ID
- 2354
- Genome
- hg19
- Position
- chr19:45,971,254-45,978,437
- Genome
- hg38
- Position
- chr19:45,467,996-45,475,179
- MIM
- 164772 OMIM
- HGNC
- HGNC:3797 HGNC
- Ensembl
- ENSG00000125740 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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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Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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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 | |||
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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 | AP-1 |
SYNONYM | G0S3 |
SYNONYM | GOS3 |
SYNONYM | GOSB |
MIM | 164772 OMIM |
HGNC | HGNC:3797 HGNC |
Ensembl | ENSG00000125740 Ensembl |
AllianceGenome | HGNC:3797 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000417353.6 | hg38 | chr19 | 45,467,995 | 45,475,178 | 7,184 |
ENST00000592436.5 | hg38 | chr19 | 45,468,435 | 45,473,040 | 4,606 |
ENST00000590335.1 | hg38 | chr19 | 45,467,996 | 45,472,081 | 4,086 |
ENST00000592811.5 | hg38 | chr19 | 45,469,876 | 45,474,597 | 4,722 |
ENST00000353609.8 | hg38 | chr19 | 45,467,996 | 45,475,179 | 7,184 |
ENST00000586615.5 | hg38 | chr19 | 45,469,913 | 45,475,179 | 5,267 |
ENST00000591858.5 | hg38 | chr19 | 45,467,995 | 45,475,178 | 7,184 |
ENST00000443841.6 | hg38 | chr19 | 45,467,995 | 45,475,178 | 7,184 |
ENST00000585836.5 | hg38 | chr19 | 45,467,995 | 45,475,178 | 7,184 |
ENST00000417353.6 | hg19 | chr19 | 45,971,253 | 45,978,436 | 7,184 |
ENST00000443841.6 | hg19 | chr19 | 45,971,253 | 45,978,436 | 7,184 |
ENST00000585836.5 | hg19 | chr19 | 45,971,253 | 45,978,436 | 7,184 |
ENST00000591858.5 | hg19 | chr19 | 45,971,253 | 45,978,436 | 7,184 |
ENST00000590335.1 | hg19 | chr19 | 45,971,254 | 45,975,339 | 4,086 |
ENST00000353609.8 | hg19 | chr19 | 45,971,254 | 45,978,437 | 7,184 |
ENST00000592436.5 | hg19 | chr19 | 45,971,693 | 45,976,298 | 4,606 |
ENST00000592811.5 | hg19 | chr19 | 45,973,134 | 45,977,855 | 4,722 |
ENST00000586615.5 | hg19 | chr19 | 45,973,171 | 45,978,437 | 5,267 |
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