FBXW9 F-box and WD repeat domain containing 9
Information
- Symbol
- FBXW9
- Type
- protein-coding
- Description
- F-box and WD repeat domain containing 9
- Entrez Gene ID
- 84261
- Genome
- hg19
- Position
- chr19:12,799,730-12,807,445
- Genome
- hg38
- Position
- chr19:12,688,916-12,696,631
- MIM
- 609074 OMIM
- HGNC
- HGNC:28136 HGNC
- Ensembl
- ENSG00000132004 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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72 |
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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 | Fbw9 |
SYNONYM | MEC-15 |
MIM | 609074 OMIM |
HGNC | HGNC:28136 HGNC |
Ensembl | ENSG00000132004 Ensembl |
AllianceGenome | HGNC:28136 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000393261.8 | hg38 | chr19 | 12,688,916 | 12,696,631 | 7,716 |
ENST00000587955.1 | hg38 | chr19 | 12,689,216 | 12,696,581 | 7,366 |
ENST00000393261.8 | hg19 | chr19 | 12,799,730 | 12,807,445 | 7,716 |
ENST00000587955.1 | hg19 | chr19 | 12,800,030 | 12,807,395 | 7,366 |
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