Regulation of localization

Regulation of localization

• ABCA1: ATP-binding cassette, sub-family A (ABC1), member 1
• ACVRL1: activin A receptor type II-like 1
• ANG: angiogenin, ribonuclease, RNase A family, 5
• APC: adenomatous polyposis coli
• APOB: apolipoprotein B (including Ag(x) antigen)
• APOE: apolipoprotein E
• BARD1: BRCA1 associated RING domain 1
• BMPR1A: bone morphogenetic protein receptor, type IA
• CACNB4: calcium channel, voltage-dependent, beta 4 subunit
• CDH1: cadherin 1, type 1, E-cadherin (epithelial)
• CHD7: chromodomain helicase DNA binding protein 7
• CHRNA4: cholinergic receptor, nicotinic, alpha 4
• CHRNB2: cholinergic receptor, nicotinic, beta 2 (neuronal)
• DRD3: dopamine receptor D3
• EDN3: endothelin 3
• F2: coagulation factor II (thrombin)
• FLNA: filamin A, alpha
• FOXP3: forkhead box P3
• IL1A: interleukin 1, alpha
• JAG1: jagged 1 (Alagille syndrome)
• JPH3: junctophilin 3
• LDLRAP1: low density lipoprotein receptor adaptor protein 1
• LPL: lipoprotein lipase
• MYO6: myosin VI
• NF1: neurofibromin 1
• NF2: neurofibromin 2 (merlin)
• NLRP12: NLR family, pyrin domain containing 12
• NLRP3: NLR family, pyrin domain containing 3
• NOD2: nucleotide-binding oligomerization domain containing 2
• PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
• PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
• PTEN: phosphatase and tensin homolog
• RPS19: ribosomal protein S19
• RYR1: ryanodine receptor 1 (skeletal)
• SAA1: serum amyloid A1
• SLC26A4: solute carrier family 26, member 4
• SNCAIP: synuclein, alpha interacting protein
• TBX5: T-box 5
• TGFB1: transforming growth factor, beta 1
• TSC2: tuberous sclerosis 2
• WFS1: Wolfram syndrome 1 (wolframin)

Source: Gene Ontology Consortium (June 2009).