CYP3A51P cytochrome P450 family 3 subfamily A member 51, pseudogene
Information
- Symbol
- CYP3A51P
- Type
- pseudo
- Description
- cytochrome P450 family 3 subfamily A member 51, pseudogene
- Entrez Gene ID
- 1578
- Genome
- hg19
- Position
- chr7:99,282,768-99,297,657
- Genome
- hg38
- Position
- chr7:99,685,145-99,700,034
- HGNC
- HGNC:42418 HGNC
- Ensembl
- ENSG00000282277 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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0 |
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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
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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 | ||||||||||||||
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CYP3A5-de13c |
| SYNONYM | CYP3A5-de1b2b |
| SYNONYM | CYP3A5P1 |
| SYNONYM | CYP3AP1 |
| HGNC | HGNC:42418 HGNC |
| Ensembl | ENSG00000282277 Ensembl |
| AllianceGenome | HGNC:42418 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000633513.1 | hg38 | chr7 | 99,685,145 | 99,700,034 | 14,890 |
| ENST00000633513.1 | hg19 | chr7 | 99,282,768 | 99,297,657 | 14,890 |
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