ID   WC012i-CMT2A-1.3
AC   CVCL_UB81
DR   WiCell; wc012i-cmt2a-1.3
DR   Wikidata; Q98134785
CC   Sequence variation: Mutation; HGNC; 16877; MFN2; Unexplicit; Not described; Zygosity=Unspecified (WiCell=wc012i-cmt2a-1.3).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C150646; Charcot-Marie-Tooth disease type 2A2A
DI   ORDO; Orphanet_99947; Autosomal dominant Charcot-Marie-Tooth disease type 2A2
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_UB79 ! WC010i-CMT2A-1.1
OI   CVCL_UB80 ! WC011i-CMT2A-1.2
SX   Male
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 05-10-23; Version: 9
//