CYP4F11 cytochrome P450 family 4 subfamily F member 11
Information
- Symbol
- CYP4F11
- Type
- protein-coding
- Description
- cytochrome P450 family 4 subfamily F member 11
- Entrez Gene ID
- 57834
- Genome
- hg19
- Position
- chr19:16,023,187-16,045,339
- Genome
- hg38
- Position
- chr19:15,912,377-15,934,529
- MIM
- 611517 OMIM
- HGNC
- HGNC:13265 HGNC
- Ensembl
- ENSG00000171903 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 82 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
88 |
 |
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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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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 | CYPIVF11 |
| MIM | 611517 OMIM |
| HGNC | HGNC:13265 HGNC |
| Ensembl | ENSG00000171903 Ensembl |
| AllianceGenome | HGNC:13265 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000620614.4 | hg38 | chr19 | 15,912,370 | 15,934,866 | 22,497 |
| ENST00000591841.1 | hg38 | chr19 | 15,912,939 | 15,928,111 | 15,173 |
| ENST00000402119.9 | hg38 | chr19 | 15,912,377 | 15,934,529 | 22,153 |
| ENST00000326742.12 | hg38 | chr19 | 15,912,367 | 15,934,410 | 22,044 |
| ENST00000248041.12 | hg38 | chr19 | 15,912,367 | 15,934,867 | 22,501 |
| ENST00000326742.12 | hg19 | chr19 | 16,023,177 | 16,045,220 | 22,044 |
| ENST00000248041.12 | hg19 | chr19 | 16,023,177 | 16,045,677 | 22,501 |
| ENST00000620614.4 | hg19 | chr19 | 16,023,180 | 16,045,676 | 22,497 |
| ENST00000402119.9 | hg19 | chr19 | 16,023,187 | 16,045,339 | 22,153 |
| ENST00000591841.1 | hg19 | chr19 | 16,023,749 | 16,038,921 | 15,173 |
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