ID   GM20392
AC   CVCL_U305
DR   CLO; CLO_0029579
DR   Coriell; GM20392
DR   Wikidata; Q54850999
CC   Sequence variation: Mutation; HGNC; HGNC:5157; HPRT1; Simple; p.Val8Gly (c.23T>G); ClinVar=VCV001410753; Zygosity=Hemizygous (Coriell=GM20392).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   23Y
CA   Finite cell line
DT   Created: 03-02-14; Last updated: 19-12-24; Version: 15
//