FBXO44 F-box protein 44
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
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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48 |
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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
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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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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 |
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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 |
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SYNONYM | FBG3 |
SYNONYM | FBX30 |
SYNONYM | FBX6A |
SYNONYM | Fbx44 |
SYNONYM | Fbxo6a |
MIM | 609111 OMIM |
HGNC | HGNC:24847 HGNC |
Ensembl | ENSG00000132879 Ensembl |
AllianceGenome | HGNC:24847 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000251547.10 | hg38 | chr1 | 11,654,877 | 11,663,327 | 8,451 |
ENST00000376762.8 | hg38 | chr1 | 11,654,910 | 11,662,291 | 7,382 |
ENST00000376760.5 | hg38 | chr1 | 11,654,910 | 11,661,349 | 6,440 |
ENST00000376768.5 | hg38 | chr1 | 11,654,881 | 11,661,391 | 6,511 |
ENST00000251546.8 | hg38 | chr1 | 11,654,375 | 11,662,289 | 7,915 |
ENST00000376770.5 | hg38 | chr1 | 11,654,857 | 11,663,327 | 8,471 |
ENST00000251546.8 | hg19 | chr1 | 11,714,432 | 11,722,346 | 7,915 |
ENST00000376770.5 | hg19 | chr1 | 11,714,914 | 11,723,384 | 8,471 |
ENST00000251547.10 | hg19 | chr1 | 11,714,934 | 11,723,384 | 8,451 |
ENST00000376768.5 | hg19 | chr1 | 11,714,938 | 11,721,448 | 6,511 |
ENST00000376760.5 | hg19 | chr1 | 11,714,967 | 11,721,406 | 6,440 |
ENST00000376762.8 | hg19 | chr1 | 11,714,967 | 11,722,348 | 7,382 |
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