Transport

Transport

• ABCA1: ATP-binding cassette, sub-family A (ABC1), member 1
• ABCA12: ATP-binding cassette, sub-family A (ABC1), member 12
• ABCB7: ATP-binding cassette, sub-family B (MDR/TAP), member 7
• ABCC2: ATP-binding cassette, sub-family C (CFTR/MRP), member 2
• ABCC6: ATP-binding cassette, sub-family C (CFTR/MRP), member 6
• ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
• AGXT: alanine-glyoxylate aminotransferase
• ANG: angiogenin, ribonuclease, RNase A family, 5
• APOE: apolipoprotein E
• AR: androgen receptor
• ARFGEF2: ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
• ATP1A2: ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide
• ATP2A2: ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
• ATP7A: ATPase, Cu++ transporting, alpha polypeptide
• ATP7B: ATPase, Cu++ transporting, beta polypeptide
• BARD1: BRCA1 associated RING domain 1
• BEST1: bestrophin 1
• BMPR1A: bone morphogenetic protein receptor, type IA
• CACNA1C: calcium channel, voltage-dependent, L type, alpha 1C subunit
• CACNA1S: calcium channel, voltage-dependent, L type, alpha 1S subunit
• CACNB4: calcium channel, voltage-dependent, beta 4 subunit
• CDH1: cadherin 1, type 1, E-cadherin (epithelial)
• CHD7: chromodomain helicase DNA binding protein 7
• CHRNA2: cholinergic receptor, nicotinic, alpha 2 (neuronal)
• CHRNA4: cholinergic receptor, nicotinic, alpha 4
• CHRNB2: cholinergic receptor, nicotinic, beta 2 (neuronal)
• CLN3: ceroid-lipofuscinosis, neuronal 3
• CPT2: carnitine palmitoyltransferase 2
• CTNS: cystinosis, nephropathic
• CTSA: cathepsin A
• DNAJC19: DnaJ (Hsp40) homolog, subfamily C, member 19
• DNM2: dynamin 2
• DRD3: dopamine receptor D3
• EDN3: endothelin 3
• F2: coagulation factor II (thrombin)
• FLNA: filamin A, alpha
• FOXP3: forkhead box P3
• GJB1: gap junction protein, beta 1, 32kDa
• GJB2: gap junction protein, beta 2, 26kDa
• GLI3: GLI family zinc finger 3
• GNAS: GNAS complex locus
• GRHPR: glyoxylate reductase/hydroxypyruvate reductase
• HBA2: hemoglobin, alpha 2
• HBB: hemoglobin, beta
• HFE: hemochromatosis
• IL1A: interleukin 1, alpha
• JPH3: junctophilin 3
• KCNA1: potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)
• KCNE1: potassium voltage-gated channel, Isk-related family, member 1
• KCNE2: potassium voltage-gated channel, Isk-related family, member 2
• KCNH2: potassium voltage-gated channel, subfamily H (eag-related), member 2
• KCNJ2: potassium inwardly-rectifying channel, subfamily J, member 2
• KCNQ4: potassium voltage-gated channel, KQT-like subfamily, member 4
• KIF1B: kinesin family member 1B
• LDLR: low density lipoprotein receptor
• LDLRAP1: low density lipoprotein receptor adaptor protein 1
• LRP2: low density lipoprotein-related protein 2
• LYST: lysosomal trafficking regulator
• MCOLN1: mucolipin 1
• MFN2: mitofusin 2
• MKKS: McKusick-Kaufman syndrome
• MT-ATP6: mitochondrially encoded ATP synthase 6
• MYH7: myosin, heavy chain 7, cardiac muscle, beta
• MYO6: myosin VI
• MYO7A: myosin VIIA
• NEFL: neurofilament, light polypeptide
• NF1: neurofibromin 1
• NLRP12: NLR family, pyrin domain containing 12
• NLRP3: NLR family, pyrin domain containing 3
• NOD2: nucleotide-binding oligomerization domain containing 2
• NPC1: Niemann-Pick disease, type C1
• NPC2: Niemann-Pick disease, type C2
• OPA1: optic atrophy 1 (autosomal dominant)
• PKD2: polycystic kidney disease 2 (autosomal dominant)
• PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
• PSAP: prosaposin
• RAB7A: RAB7A, member RAS oncogene family
• RPL11: ribosomal protein L11
• RPS19: ribosomal protein S19
• RYR1: ryanodine receptor 1 (skeletal)
• SAA1: serum amyloid A1
• SAR1B: SAR1 homolog B (S. cerevisiae)
• SCN1A: sodium channel, voltage-gated, type I, alpha subunit
• SCN4A: sodium channel, voltage-gated, type IV, alpha subunit
• SCN5A: sodium channel, voltage-gated, type V, alpha subunit
• SCN9A: sodium channel, voltage-gated, type IX, alpha subunit
• SEC23B: Sec23 homolog B (S. cerevisiae)
• SLC16A2: solute carrier family 16, member 2 (monocarboxylic acid transporter 8)
• SLC17A5: solute carrier family 17 (anion/sugar transporter), member 5
• SLC19A2: solute carrier family 19 (thiamine transporter), member 2
• SLC1A3: solute carrier family 1 (glial high affinity glutamate transporter), member 3
• SLC22A5: solute carrier family 22 (organic cation/carnitine transporter), member 5
• SLC25A13: solute carrier family 25, member 13 (citrin)
• SLC25A15: solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
• SLC25A19: solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
• SLC25A20: solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
• SLC26A2: solute carrier family 26 (sulfate transporter), member 2
• SLC26A4: solute carrier family 26, member 4
• SLC2A1: solute carrier family 2 (facilitated glucose transporter), member 1
• SLC3A1: solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1
• SLC40A1: solute carrier family 40 (iron-regulated transporter), member 1
• SLC46A1: solute carrier family 46 (folate transporter), member 1
• SLC5A1: solute carrier family 5 (sodium/glucose cotransporter), member 1
• SLC7A7: solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
• SLC7A9: solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
• SNCAIP: synuclein, alpha interacting protein
• TFR2: transferrin receptor 2
• TGFB1: transforming growth factor, beta 1
• TP53: tumor protein p53
• TRAPPC2: trafficking protein particle complex 2
• TRPS1: trichorhinophalangeal syndrome I
• TSC1: tuberous sclerosis 1
• TSC2: tuberous sclerosis 2
• TTPA: tocopherol (alpha) transfer protein
• TTR: transthyretin
• VCP: valosin-containing protein
• VPS13A: vacuolar protein sorting 13 homolog A (S. cerevisiae)
• WFS1: Wolfram syndrome 1 (wolframin)
• XK: X-linked Kx blood group (McLeod syndrome)

Source: Gene Ontology Consortium (June 2009).