ID   GM07861
AC   CVCL_AY25
DR   CLO; CLO_0010301
DR   Coriell; GM07861
DR   Wikidata; Q54842974
CC   Sequence variation: Mutation; HGNC; HGNC:3775; FMR1; Repeat_expansion; CGG[351-400]; ClinVar=VCV000009972; Zygosity=Hemizygous (Coriell=GM07861).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Donor information: Established from monozygotic twin of GM07862 (Cellosaurus=CVCL_AY26).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84717; Fragile X syndrome
DI   ORDO; Orphanet_908; Fragile X syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   25Y
CA   Transformed cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 14
//