KEGG   VARIANT: 4047v1
Entry
4047v1                      Variant                                
Name
LSS deficiency
Type
Loss of function
Gene
LSS  lanosterol synthase [KO:K01852]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 600909
Network
nt06034  Cholesterol biosynthesis
Disease
H02303  Alopecia-mental retardation syndrome
Reference
  Authors
Besnard T, Sloboda N, Goldenberg A, Kury S, Cogne B, Breheret F, Trochu E, Conrad S, Vincent M, Deb W, Balguerie X, Barbarot S, Baujat G, Ben-Omran T, Bursztejn AC, Carmignac V, Datta AN, Delignieres A, Faivre L, Gardie B, Gueant JL, Kuentz P, Lenglet M, Nassogne MC, Ramaekers V, Schnur RE, Si Y, Torti E, Thevenon J, Vabres P, Van Maldergem L, Wand D, Wiedemann A, Cariou B, Redon R, Lamaziere A, Bezieau S, Feillet F, Isidor B
  Title
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome.
  Journal
Genet Med 21:2025-2035 (2019)
DOI:10.1038/s41436-019-0445-x
LinkDB

DBGET integrated database retrieval system