Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®

Intrinsic component of organelle membrane

Intrinsic component of organelle membrane

  • ABCD1: ATP binding cassette subfamily D member 1
  • BSCL2: Berardinelli-Seip congenital lipodystrophy 2 (seipin)
  • CALR: calreticulin
  • CLN3: ceroid-lipofuscinosis, neuronal 3
  • CPT1A: carnitine palmitoyltransferase 1A (liver)
  • DHCR7: 7-dehydrocholesterol reductase
  • DMPK: dystrophia myotonica protein kinase
  • ELOVL4: ELOVL fatty acid elongase 4
  • ETFDH: electron transfer flavoprotein dehydrogenase
  • EXT1: exostosin glycosyltransferase 1
  • FAM134B: family with sequence similarity 134 member B
  • G6PC: glucose-6-phosphatase, catalytic subunit
  • GDAP1: ganglioside induced differentiation associated protein 1
  • HLA-B: major histocompatibility complex, class I, B
  • HLA-DPB1: major histocompatibility complex, class II, DP beta 1
  • HLA-DQA1: major histocompatibility complex, class II, DQ alpha 1
  • HLA-DQB1: major histocompatibility complex, class II, DQ beta 1
  • HLA-DRB1: major histocompatibility complex, class II, DR beta 1
  • ITM2B: integral membrane protein 2B
  • L2HGDH: L-2-hydroxyglutarate dehydrogenase
  • LARGE: like-glycosyltransferase
  • LBR: lamin B receptor
  • LEMD3: LEM domain containing 3
  • MFN2: mitofusin 2
  • PINK1: PTEN induced putative kinase 1
  • PKD2: polycystin 2, transient receptor potential cation channel
  • PPOX: protoporphyrinogen oxidase
  • SLC37A4: solute carrier family 37 (glucose-6-phosphate transporter), member 4
  • STIM1: stromal interaction molecule 1
  • WFS1: Wolfram syndrome 1 (wolframin)

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference..

 
Published: February 8, 2016