Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6f85bb1dcb7d6850017db5d828e62f9e> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B6f85bb1dcb7d6850017db5d828e62f9e NCIT_P378 "NCI" @default.
- B6f85bb1dcb7d6850017db5d828e62f9e type Axiom @default.
- B6f85bb1dcb7d6850017db5d828e62f9e annotatedProperty IAO_0000115 @default.
- B6f85bb1dcb7d6850017db5d828e62f9e annotatedSource NCIT_C52351 @default.
- B6f85bb1dcb7d6850017db5d828e62f9e annotatedTarget "Human CYP21A2 wild-type allele is located in the vicinity of 6p21.3 and is approximately 3 kb in length. This allele, which encodes cytochrome P450 21 protein, plays a role in the 21-hydroxylation of steroids. Gene conversion events involving the CYP21A2 gene and a nearby pseudogene putatively account for many cases of steroid 21-hydroxylase deficiency. CYP21A2 gene dysfunction causes congenital adrenal hyperplasia." @default.