Substrate-specific transporter activity
- ABCA1: ATP-binding cassette, sub-family A (ABC1), member 1
- ABCB11: ATP-binding cassette, sub-family B (MDR/TAP), member 11
- ABCC2: ATP-binding cassette, sub-family C (CFTR/MRP), member 2
- ABCC8: ATP-binding cassette, sub-family C (CFTR/MRP), member 8
- ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
- ABCG5: ATP-binding cassette, sub-family G (WHITE), member 5
- ABCG8: ATP-binding cassette, sub-family G (WHITE), member 8
- ANKH: ankylosis, progressive homolog (mouse)
- APOA1: apolipoprotein A-I
- APOB: apolipoprotein B (including Ag(x) antigen)
- APOE: apolipoprotein E
- AQP2: aquaporin 2 (collecting duct)
- ATP1A2: ATPase, Na+/K+ transporting, alpha 2 polypeptide
- ATP1A3: ATPase, Na+/K+ transporting, alpha 3 polypeptide
- ATP2A1: ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
- ATP2A2: ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
- ATP2B2: ATPase, Ca++ transporting, plasma membrane 2
- 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: Bartter syndrome, infantile, with sensorineural deafness (Barttin)
- CACNA1A: calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
- CACNA1C: calcium channel, voltage-dependent, L type, alpha 1C subunit
- CACNA1F: calcium channel, voltage-dependent, L type, alpha 1F subunit
- CACNA1S: calcium channel, voltage-dependent, L type, alpha 1S subunit
- CACNB4: calcium channel, voltage-dependent, beta 4 subunit
- CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
- CHRNA2: cholinergic receptor, nicotinic, alpha 2 (neuronal)
- CHRNA4: cholinergic receptor, nicotinic, alpha 4 (neuronal)
- CHRNB2: cholinergic receptor, nicotinic, beta 2 (neuronal)
- CHRNE: cholinergic receptor, nicotinic, epsilon (muscle)
- CLCN1: chloride channel, voltage-sensitive 1
- CLCN5: chloride channel, voltage-sensitive 5
- CLCN7: chloride channel, voltage-sensitive 7
- CNGA3: cyclic nucleotide gated channel alpha 3
- CTNS: cystinosin, lysosomal cystine transporter
- GJA1: gap junction protein, alpha 1, 43kDa
- GLRA1: glycine receptor, alpha 1
- HBB: hemoglobin, beta
- KCNA1: potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)
- KCNE1: potassium voltage-gated channel, Isk-related family, member 1
- KCNH2: potassium voltage-gated channel, subfamily H (eag-related), member 2
- KCNJ11: potassium inwardly-rectifying channel, subfamily J, member 11
- KCNJ2: potassium inwardly-rectifying channel, subfamily J, member 2
- KCNQ1: potassium voltage-gated channel, KQT-like subfamily, member 1
- KCNQ2: potassium voltage-gated channel, KQT-like subfamily, member 2
- KCNQ3: potassium voltage-gated channel, KQT-like subfamily, member 3
- KCNQ4: potassium voltage-gated channel, KQT-like subfamily, member 4
- MCOLN1: mucolipin 1
- MLC1: megalencephalic leukoencephalopathy with subcortical cysts 1
- MTTP: microsomal triglyceride transfer protein
- NPC1: Niemann-Pick disease, type C1
- OCA2: oculocutaneous albinism II
- PKD1: polycystic kidney disease 1 (autosomal dominant)
- PKD2: polycystic kidney disease 2 (autosomal dominant)
- PSEN1: presenilin 1
- RYR1: ryanodine receptor 1 (skeletal)
- RYR2: ryanodine receptor 2 (cardiac)
- SCN10A: sodium channel, voltage-gated, type X, alpha subunit
- SCN1A: sodium channel, voltage-gated, type I, alpha subunit
- SCN5A: sodium channel, voltage-gated, type V, alpha subunit
- SCNN1G: sodium channel, non-voltage-gated 1, gamma subunit
- SLC12A1: solute carrier family 12 (sodium/potassium/chloride transporters), member 1
- SLC12A3: solute carrier family 12 (sodium/chloride transporters), member 3
- SLC12A6: solute carrier family 12 (potassium/chloride transporters), member 6
- SLC16A2: solute carrier family 16, member 2 (thyroid hormone transporter)
- 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
- SLC20A2: solute carrier family 20 (phosphate transporter), member 2
- SLC22A5: solute carrier family 22 (organic cation/carnitine transporter), member 5
- SLC25A13: solute carrier family 25 (aspartate/glutamate carrier), member 13
- SLC25A15: solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
- SLC25A19: solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
- SLC25A4: solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
- 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
- SLC2A10: solute carrier family 2 (facilitated glucose transporter), member 10
- 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
- SLC5A1: solute carrier family 5 (sodium/glucose cotransporter), member 1
- SLC5A5: solute carrier family 5 (sodium iodide symporter), member 5
- SLC6A8: solute carrier family 6 (neurotransmitter transporter, creatine), member 8
- SLC7A9: solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9
- SLCO1B1: solute carrier organic anion transporter family, member 1B1
- SLCO1B3: solute carrier organic anion transporter family, member 1B3
- TRPV4: transient receptor potential cation channel, subfamily V, member 4
- VLDLR: very low density lipoprotein receptor
Source: Gene Ontology Consortium
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