FMO5 flavin containing dimethylaniline monoxygenase 5
Information
- Symbol
- FMO5
- Type
- protein-coding
- Description
- flavin containing dimethylaniline monoxygenase 5
- Entrez Gene ID
- 2330
- Genome
- hg19
- Position
- chr1:146,657,840-146,696,931
- Genome
- hg38
- Position
- chr1:147,186,261-147,225,339
- MIM
- 603957 OMIM
- HGNC
- HGNC:3773 HGNC
- Ensembl
- ENSG00000131781 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 4 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 94 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
100 |
 |
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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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| 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 | hBVMO1 |
| MIM | 603957 OMIM |
| HGNC | HGNC:3773 HGNC |
| Ensembl | ENSG00000131781 Ensembl |
| AllianceGenome | HGNC:3773 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000578284.5 | hg38 | chr1 | 147,184,492 | 147,225,638 | 41,147 |
| ENST00000369272.7 | hg38 | chr1 | 147,186,261 | 147,225,309 | 39,049 |
| ENST00000254090.9 | hg38 | chr1 | 147,186,261 | 147,225,339 | 39,079 |
| ENST00000441068.6 | hg38 | chr1 | 147,184,305 | 147,225,353 | 41,049 |
| ENST00000441068.6 | hg19 | chr1 | 146,655,884 | 146,696,945 | 41,062 |
| ENST00000578284.5 | hg19 | chr1 | 146,656,071 | 146,697,230 | 41,160 |
| ENST00000369272.7 | hg19 | chr1 | 146,657,840 | 146,696,901 | 39,062 |
| ENST00000254090.9 | hg19 | chr1 | 146,657,840 | 146,696,931 | 39,092 |
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