Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B77900ef26135fef51927837f5a90871f> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B77900ef26135fef51927837f5a90871f NCIT_P378 "NCI" @default.
- B77900ef26135fef51927837f5a90871f type Axiom @default.
- B77900ef26135fef51927837f5a90871f annotatedProperty IAO_0000115 @default.
- B77900ef26135fef51927837f5a90871f annotatedSource NCIT_C52318 @default.
- B77900ef26135fef51927837f5a90871f annotatedTarget "Human CYP11A1 wild-type allele is located within 15q23-q24 and is approximately 30 kb in length. This allele, which encodes cytochrome P450 11A1, mitochondrial protein, is involved in steroid synthesis. Certain allelic variants of the CYP11A1 gene result in 17-alpha-hydroxylase/17,20-lyase deficiency. Defects in this gene cause congenital adrenal insufficiency and congenital lipoid adrenal hyperplasia." @default.