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Plasma membrane region

Plasma membrane region

  • ABCA4: ATP-binding cassette, sub-family A (ABC1), member 4
  • ABCC2: ATP-binding cassette, sub-family C (CFTR/MRP), member 2
  • ABCG5: ATP-binding cassette, sub-family G (WHITE), member 5
  • ABCG8: ATP-binding cassette, sub-family G (WHITE), member 8
  • AMN: amnion associated transmembrane protein
  • ANK1: ankyrin 1, erythrocytic
  • ANK2: ankyrin 2, neuronal
  • AQP2: aquaporin 2 (collecting duct)
  • ATP6V0A4: ATPase, H+ transporting, lysosomal V0 subunit a4
  • ATP6V1B1: ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
  • ATP7A: ATPase, Cu++ transporting, alpha polypeptide
  • ATP7B: ATPase, Cu++ transporting, beta polypeptide
  • ATP8B1: ATPase, aminophospholipid transporter, class I, type 8B, member 1
  • BEST1: bestrophin 1
  • BSND: barttin CLCNK-type chloride channel accessory beta subunit
  • CASK: calcium/calmodulin-dependent serine protein kinase (MAGUK family)
  • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
  • CUBN: cubilin (intrinsic factor-cobalamin receptor)
  • EPCAM: epithelial cell adhesion molecule
  • ERBB2: v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2
  • GNAT1: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
  • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
  • GPR143: G protein-coupled receptor 143
  • GUCY2D: guanylate cyclase 2D, membrane (retina-specific)
  • KCNQ1: potassium voltage-gated channel, KQT-like subfamily, member 1
  • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • LRP2: low density lipoprotein receptor-related protein 2
  • MLC1: megalencephalic leukoencephalopathy with subcortical cysts 1
  • MUC1: mucin 1, cell surface associated
  • MYO1A: myosin IA
  • OPN1LW: opsin 1 (cone pigments), long-wave-sensitive
  • OPN1MW: opsin 1 (cone pigments), medium-wave-sensitive
  • OPN1SW: opsin 1 (cone pigments), short-wave-sensitive
  • PDE6B: phosphodiesterase 6B, cGMP-specific, rod, beta
  • PDGFB: platelet-derived growth factor beta polypeptide
  • PDGFRB: platelet-derived growth factor receptor, beta polypeptide
  • PFKM: phosphofructokinase, muscle
  • PKD1: polycystic kidney disease 1 (autosomal dominant)
  • PKD2: polycystic kidney disease 2 (autosomal dominant)
  • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
  • PSEN1: presenilin 1
  • PSEN2: presenilin 2
  • RHO: rhodopsin
  • SCNN1A: sodium channel, non-voltage-gated 1 alpha subunit
  • SHANK3: SH3 and multiple ankyrin repeat domains 3
  • SLC12A3: solute carrier family 12 (sodium/chloride transporter), member 3
  • SLC12A6: solute carrier family 12 (potassium/chloride transporter), member 6
  • SLC22A5: solute carrier family 22 (organic cation/carnitine transporter), member 5
  • SLC26A4: solute carrier family 26 (anion exchanger), member 4
  • SLC40A1: solute carrier family 40 (iron-regulated transporter), member 1
  • SLC46A1: solute carrier family 46 (folate transporter), member 1
  • TCIRG1: T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
  • TEK: TEK tyrosine kinase, endothelial
  • UMOD: uromodulin
  • USH2A: Usher syndrome 2A (autosomal recessive, mild)

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

 
Published: August 18, 2014