CYP26B1 cytochrome P450 family 26 subfamily B member 1
Information
- Symbol
- CYP26B1
- Type
- protein-coding
- Description
- cytochrome P450 family 26 subfamily B member 1
- Entrez Gene ID
- 56603
- Genome
- hg19
- Position
- chr2:72,356,367-72,374,991
- Genome
- hg38
- Position
- chr2:72,129,238-72,147,862
- MIM
- 605207 OMIM
- HGNC
- HGNC:20581 HGNC
- Ensembl
- ENSG00000003137 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely pathogenic | 0 | 6 |
Benign | 0 | 50 |
Likely benign | 0 | 94 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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42 |
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188 |
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4 |
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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Search word | : | |
Filtering | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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
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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 | CYP26A2 |
SYNONYM | P450RAI-2 |
SYNONYM | P450RAI2 |
SYNONYM | RHFCA |
MIM | 605207 OMIM |
HGNC | HGNC:20581 HGNC |
Ensembl | ENSG00000003137 Ensembl |
AllianceGenome | HGNC:20581 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000001146.7 | hg38 | chr2 | 72,129,238 | 72,147,862 | 18,625 |
ENST00000546307.5 | hg38 | chr2 | 72,129,238 | 72,147,862 | 18,625 |
ENST00000412253.1 | hg38 | chr2 | 72,129,393 | 72,143,084 | 13,692 |
ENST00000001146.7 | hg19 | chr2 | 72,356,367 | 72,374,991 | 18,625 |
ENST00000546307.5 | hg19 | chr2 | 72,356,367 | 72,374,991 | 18,625 |
ENST00000412253.1 | hg19 | chr2 | 72,356,522 | 72,370,213 | 13,692 |
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