Genomic Map
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Target Gene Details
Entrez Gene ID: | 56603 |
Gene Name: | cytochrome P450 family 26 subfamily B member 1 |
Gene Aliases: |
CYP26A2, P450RAI-2, P450RAI2, RHFCA |
Location: |
Chr.2:72129238-72147862 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP26B1 | NM_001277742.1 | NP_001264671.1 | ||
| NM_019885.3 | NP_063938.1 | |||
| XM_005264433.4 | XP_005264490.1 | |||
| XM_011532988.1 | XP_011531290.1 | |||
| AF252297.1 | AAF76003.1 | |||
| AK294814.1 | ||||
| AK294933.1 | ||||
| AK295683.1 | ||||
| AK313433.1 | ||||
| BC069443.1 | AAH69443.1 | |||
| BC109205.2 | AAI09206.1 | |||
| CR749631.1 | CAH18425.1 | |||
| DC308258.1 | ||||
| FJ467289.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv582207 | Chr.2:72102473 - 72162205 on Build GRCh38 | Loss |
 CYP26B1
|
| nsv953147 | Chr.2:72126972 - 72160571 on Build GRCh38 | Deletion |
CYP26B1
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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