FOSL1 FOS like 1, AP-1 transcription factor subunit
Information
- Symbol
- FOSL1
- Type
- protein-coding
- Description
- FOS like 1, AP-1 transcription factor subunit
- Entrez Gene ID
- 8061
- Genome
- hg19
- Position
- chr11:65,659,520-65,667,859
- Genome
- hg38
- Position
- chr11:65,892,049-65,900,388
- MIM
- 136515 OMIM
- HGNC
- HGNC:13718 HGNC
- Ensembl
- ENSG00000175592 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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
[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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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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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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FRA |
SYNONYM | FRA1 |
SYNONYM | fra-1 |
MIM | 136515 OMIM |
HGNC | HGNC:13718 HGNC |
Ensembl | ENSG00000175592 Ensembl |
AllianceGenome | HGNC:13718 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000448083.6 | hg38 | chr11 | 65,892,049 | 65,900,419 | 8,371 |
ENST00000312562.7 | hg38 | chr11 | 65,892,049 | 65,900,388 | 8,340 |
ENST00000531493.5 | hg38 | chr11 | 65,892,474 | 65,900,419 | 7,946 |
ENST00000532401.1 | hg38 | chr11 | 65,892,645 | 65,900,419 | 7,775 |
ENST00000312562.7 | hg19 | chr11 | 65,659,520 | 65,667,859 | 8,340 |
ENST00000448083.6 | hg19 | chr11 | 65,659,520 | 65,667,890 | 8,371 |
ENST00000531493.5 | hg19 | chr11 | 65,659,945 | 65,667,890 | 7,946 |
ENST00000532401.1 | hg19 | chr11 | 65,660,116 | 65,667,890 | 7,775 |
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