ID   GM18436
AC   CVCL_W152
DR   CLO; CLO_0031148
DR   Coriell; GM18436
DR   Wikidata; Q54849542
RX   PubMed=12955717;
CC   Population: Caucasian; Canadian/Italian.
CC   Sequence variation: Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Pro543Argfs*20 (c.1628delC) (p.Phe542fs); ClinVar=VCV000556403; Zygosity=Heterozygous (Coriell=GM18436).
CC   Sequence variation: Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Glu612Asp (c.1836A>C); ClinVar=VCV000555407; Zygosity=Heterozygous (Coriell=GM18436).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C126864; Niemann-Pick disease, type C1
DI   ORDO; Orphanet_646; Niemann-Pick disease type C
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 19-12-24; Version: 15
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RX   PubMed=12955717; DOI=10.1002/humu.10255;
RA   Park W.D., O'Brien J.F., Lundquist P.A., Kraft D.L., Vockley C.W.,
RA   Karnes P.S., Patterson M.C., Snow K.;
RT   "Identification of 58 novel mutations in Niemann-Pick disease type C:
RT   correlation with biochemical phenotype and importance of PTC1-like
RT   domains in NPC1.";
RL   Hum. Mutat. 22:313-325(2003).
//