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Disease Info Card
Por Deficiency
Information about Por Deficiency: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Por Deficiency
Most recent studies have shown that Por Deficiency shares some biological mechanisms with 46-xy-disorders-of-sex-development, adrenal-gland-hypofunction, adrenal-hyperplasia, ambiguous-genitalia, antley-bixler-syndrome-autosomal-dominant, congenital-abnormal-synostosis, congenital-adrenal-hyperplasia, congenital-anomaly-of-skeletal-bone, craniosynostosis, disorders-of-sex-development, dysplasia, hyperplasia, hypoplasia, infertility, mutation-out-of-frame, virilism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Por Deficiency, and have been seen in publications frequently: Excretion, Localization, Methylation, Pathogenesis
Quite a number of genes have been found to play important roles in Por Deficiency, such as AR, BRCA2, CYCS, CYP17A1, CYP19A1, CYP1A2, CYP21A2, CYP26A1, CYP2C19, DDX41, FANCD2, FGFR2, FMN1, HMOX1, POMC, POR, PORCN, VDAC2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Por Deficiency
This information is being compiled and will come in a future update
| Excretion | Localization | Methylation |
| Pathogenesis |