ID   GM25541
AC   CVCL_5T44
SY   GM25541*B
DR   Coriell; GM25541
DR   SKIP; SKIP001195
DR   Wikidata; Q54854004
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 5157; HPRT1; Unexplicit; Ex2-3dup; Zygosity=Hemizygous (Coriell=GM25541).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
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)
HI   CVCL_F602 ! GM01662
SX   Male
AG   9Y
CA   Induced pluripotent stem cell
DT   Created: 23-02-16; Last updated: 30-01-24; Version: 11
//