ID   GM24585
AC   CVCL_AZ37
DR   Coriell; GM24585
DR   Wikidata; Q54853786
CC   Sequence variation: Gene deletion; HGNC; HGNC:20444; MBD5; Zygosity=Heterozygous (Coriell=GM24585).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C141424; Mental retardation, autosomal dominant 1
DI   ORDO; Orphanet_178469; Autosomal dominant non-syndromic intellectual disability
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_5T12 ! GM23711
SX   Female
AG   3Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 11
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