disorder is caused by homozygous and compound heterozygous mutations in the DNAJC12 gene, which encodes a molecular chaperone belonging to the DnaJ/HSP40 family...
Click to read more »family (Hsp40) member C12 is a protein that in humans is encoded by the DNAJC12 gene. This gene encodes a member of a subclass of the HSP40/DnaJ protein...
Click to read more »Disco interacting protein 2 homolog c DKK1: Dickkopf-related protein 1 DNAJC12: DnaJ (Hsp40) homolog, subfamily c, member 12 DNAJC9: DnaJ (Hsp40) homolog...
Click to read more »Q8WXX5 4408 DNAJC10 HGNC:24637; Q8IXB1 4409 DNAJC11 HGNC:25570; Q9NVH1 4410 DNAJC12 HGNC:28908; Q9UKB3 4411 DNAJC13 HGNC:30343; O75165 4412 DNAJC14 HGNC:24581;...
Click to read more »non-BH4-deficient hyperphenylalaninemia - disorder arising due to mutations of the DNAJC12 gene. Ponzone A, Spada M, Ferraris S, Dianzani I, de Sanctis L (2004)....
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