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CYP26C1;jsessionid=C1845BF8A366A4594F3FD1D8732D6E23
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
No tissues found
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Disease Atlas
Most Correlated Diseases
Vesicular stomatitis Indiana virus disease
Waardenburg's syndrome
Enteric campylobacteriosis
Alpha-1-antitrypsin deficiency
Anomaly of chromosome pair 6
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Pharmaco Atlas
Most Correlated Compounds
Tretinoin
Sunscreening Agents
Benzodiazepines
IL17F protein, human
Pneumovax
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Knockdown Atlas
Most Correlated Gene Perturbations
TSPYL2
CHMP2B
BCAR1
NR2F1
CUL3
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.
Association of CYP26C1 Promoter Hypomethylation with Small Vessel Occlusion in Korean Subjects.
Retinoic acid production, regulation and containment through Zic1, Pitx2c and Cyp26c1 control crania…
Mandibulofacial Dysostosis Attributed to a Recessive Mutation of CYP26C1 in Hereford Cattle.
Cell fate specification in the lingual epithelium is controlled by antagonistic activities of Sonic …
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for CYP26C1;jsessionid=C1845BF8A366A4594F3FD1D8732D6E23
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