FBXL3 F-box and leucine rich repeat protein 3
Information
- Symbol
- FBXL3
- Type
- protein-coding
- Description
- F-box and leucine rich repeat protein 3
- Entrez Gene ID
- 26224
- Genome
- hg19
- Position
- chr13:77,579,395-77,601,294
- Genome
- hg38
- Position
- chr13:77,005,260-77,027,159
- MIM
- 605653 OMIM
- HGNC
- HGNC:13599 HGNC
- Ensembl
- ENSG00000005812 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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6 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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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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 | FBL3 |
SYNONYM | FBL3A |
SYNONYM | FBXL3A |
SYNONYM | IDDSFAS |
MIM | 605653 OMIM |
HGNC | HGNC:13599 HGNC |
Ensembl | ENSG00000005812 Ensembl |
AllianceGenome | HGNC:13599 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000355619.10 | hg38 | chr13 | 77,005,260 | 77,027,159 | 21,900 |
ENST00000355619.10 | hg19 | chr13 | 77,579,395 | 77,601,294 | 21,900 |
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