1: SLC6A4 Official Symbol SLC6A4 and Name: solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Homo sapiens] Other Aliases: 5-HTT, 5HTT, HTT, OCD1, SERT, hSERT Other Designations: 5-hydroxytryptamine transporter; 5HT transporter; Na+/Cl- dependent serotonin transporter; serotonin transporter; sodium-dependent serotonin transporter; solute carrier family 6 member 4 Chromosome: 17; Location: 17q11.1-q12 Annotation: Chromosome 17NC_000017.9 (25549032..25586831, complement) MIM: 182138 GeneID: 6532 2: SLC22A16 Official Symbol SLC22A16 and Name: solute carrier family 22 (organic cation transporter), member 16 [Homo sapiens] Other Aliases: RP1-261K5.1, CT2, FLIPT2, OCT6, OKB1, dJ261K5.1 Other Designations: OTTHUMP00000040478; WUGSC:RG331P03.1; carnitine transporter 2; fly-like putative organic ion transporter 2; organic cation transporter 6; solute carrier family 22, member 16 Chromosome: 6; Location: 6q21-q22.1 Annotation: Chromosome 6NC_000006.10 (110852599..110904537, complement) MIM: 608276 GeneID: 85413 3: SLC22A3 Official Symbol SLC22A3 and Name: solute carrier family 22 (extraneuronal monoamine transporter), member 3 [Homo sapiens] Other Aliases: EMT, EMTH, OCT3 Other Designations: EMT organic cation transporter 3; extraneuronal monoamine transporter; organic cation transporter 3; solute carrier family 22 member 3 Chromosome: 6; Location: 6q26-q27 Annotation: Chromosome 6NC_000006.10 (160689415..160796004) MIM: 604842 GeneID: 6581 4: SLC6A7 Official Symbol SLC6A7 and Name: solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 [Homo sapiens] Other Aliases: PROT Other Designations: brain-specific L-proline transporter; sodium-dependent proline transporter; solute carrier family 6, member 7 Chromosome: 5; Location: 5q31-q32 Annotation: Chromosome 5NC_000005.8 (149549713..149570828) MIM: 606205 GeneID: 6534 5: SLC37A4 Official Symbol SLC37A4 and Name: solute carrier family 37 (glucose-6-phosphate transporter), member 4 [Homo sapiens] Other Aliases: G6PT1, G6PT2, G6PT3, GSD1b, GSD1c, GSD1d, MGC15729, PRO0685, TRG19 Other Designations: glucose-6-phosphatase, transport (glucose) protein 3; glucose-6-phosphatase, transport (glucose-6-phosphate) protein 1; glucose-6-phosphatase, transport (phosphate/pyrophosphate) protein 2; glucose-6-phosphate translocase; glucose-6-phosphate transporter 1; microsomal glucose-6-phosphate transporter; solute carrier family 37 (glycerol-6-phosphate transporter), member 4 Chromosome: 11; Location: 11q23.3 Annotation: Chromosome 11NC_000011.8 (118400274..118406629, complement) MIM: 602671 GeneID: 2542 6: ABCA1 Official Symbol ABCA1 and Name: ATP-binding cassette, sub-family A (ABC1), member 1 [Homo sapiens] Other Aliases: ABC-1, ABC1, CERP, FLJ14958, HDLDT1, TGD Other Designations: ATP binding cassette transporter 1; ATP-binding cassette 1; ATP-binding cassette transporter-1; ATP-binding cassette, sub-family A member 1; cholesterol efflux regulatory protein; high density lipoprotein deficiency, Tangier type, 1; membrane-bound Chromosome: 9; Location: 9q31.1 Annotation: Chromosome 9NC_000009.10 (106583104..106730257, complement) MIM: 600046 GeneID: 19 7: SLC26A1 Official Symbol SLC26A1 and Name: solute carrier family 26 (sulfate transporter), member 1 [Homo sapiens] Other Aliases: EDM4, SAT-1, SAT1 Other Designations: solute carrier family 26, member 1; sulfate anion tranporter AT1; sulfate transporter; sulfate/anion transporter SAT-1 protein Chromosome: 4; Location: 4p16.3 Annotation: Chromosome 4NC_000004.10 (962861..977224, complement) MIM: 610130 GeneID: 10861 8: SLC2A3 Official Symbol SLC2A3 and Name: solute carrier family 2 (facilitated glucose transporter), member 3 [Homo sapiens] Other Aliases: FLJ90380, GLUT3 Other Designations: GLUCOSE TRANSPORTER TYPE 3, BRAIN Chromosome: 12; Location: 12p13.3 Annotation: Chromosome 12NC_000012.10 (7963094..7980138, complement) MIM: 138170 GeneID: 6515 9: SLC22A17 Official Symbol SLC22A17 and Name: solute carrier family 22 (organic cation transporter), member 17 [Homo sapiens] Other Aliases: BOCT, BOIT, NGALR, hBOIT Other Designations: NGAL receptor; neutrophil gelatinase-associated lipocalin receptor; potent brain type organic ion transporter Chromosome: 14; Location: 14q11.2 Annotation: Chromosome 14NC_000014.7 (22885367..22891920, complement) GeneID: 51310 10: SLC29A4 Official Symbol SLC29A4 and Name: solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens] Other Aliases: ENT4, FLJ34923, PMAT Other Designations: equilibrative nucleoside transporter 4; plasma membrane monoamine transporter Chromosome: 7; Location: 7p22.1 Annotation: Chromosome 7NC_000007.12 (5289101..5310216) MIM: 609149 GeneID: 222962 11: ABCC1 Official Symbol ABCC1 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [Homo sapiens] Other Aliases: ABC29, ABCC, DKFZp686N04233, DKFZp781G125, GS-X, MRP, MRP1 Other Designations: ATP-binding cassette, sub-family C, member 1; LTC4 transporter; leukotriene C(4) transporter; multidrug resistance protein; multiple drug resistance protein 1; multiple drug resistance-associated protein Chromosome: 16; Location: 16p13.1 Annotation: Chromosome 16NC_000016.8 (15950935..16143774) MIM: 158343 GeneID: 4363 12: SLC6A3 Official Symbol SLC6A3 and Name: solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 [Homo sapiens] Other Aliases: DAT, DAT1 Other Designations: dopamine transporter; variable number tandem repeat (VNTR) Chromosome: 5; Location: 5p15.3 Annotation: Chromosome 5NC_000005.8 (1445909..1498545, complement) MIM: 126455 GeneID: 6531 13: ABCG2 Official Symbol ABCG2 and Name: ATP-binding cassette, sub-family G (WHITE), member 2 [Homo sapiens] Other Aliases: ABC15, ABCP, BCRP, BCRP1, BMDP, CDw338, EST157481, MGC102821, MRX, MXR, MXR1 Other Designations: ABC transporter; ATP-binding cassette sub-family G (WHITE) member 2; ATP-binding cassette transporter G2; ATP-binding cassette, sub-family G, member 2; breast cancer resistance protein; mitoxantrone resistance protein; placenta specific MDR protein Chromosome: 4; Location: 4q22 Annotation: Chromosome 4NC_000004.10 (89230440..89299035, complement) MIM: 603756 GeneID: 9429 14: SLC1A3 Official Symbol SLC1A3 and Name: solute carrier family 1 (glial high affinity glutamate transporter), member 3 [Homo sapiens] Other Aliases: EA6, EAAT1, FLJ25094, GLAST, GLAST1 Other Designations: glutamate transporter variant EAAT1ex9skip Chromosome: 5; Location: 5p13 Annotation: Chromosome 5NC_000005.8 (36642446..36724191) MIM: 600111 GeneID: 6507 15: SLC1A1 Official Symbol SLC1A1 and Name: solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 [Homo sapiens] Other Aliases: EAAC1, EAAT3 Other Designations: excitatory amino acid carrier 1; excitatory amino acid transporter-3; solute carrier family 1, member 1 Chromosome: 9; Location: 9p24 Annotation: Chromosome 9NC_000009.10 (4480444..4577469) MIM: 133550 GeneID: 6505 16: SLCO3A1 Official Symbol SLCO3A1 and Name: solute carrier organic anion transporter family, member 3A1 [Homo sapiens] Other Aliases: FLJ40478, OATP-D, OATP3A1, SLC21A11 Other Designations: solute carrier family 21 (organic anion transporter), member 11 Chromosome: 15; Location: 15q26 Annotation: Chromosome 15NC_000015.8 (90197950..90507783) GeneID: 28232 17: SLCO1C1 Official Symbol SLCO1C1 and Name: solute carrier organic anion transporter family, member 1C1 [Homo sapiens] Other Aliases: OATP-F, OATP1, OATP1C1, SLC21A14 Other Designations: solute carrier family 21 (organic anion transporter), member 14 Chromosome: 12; Location: 12p12.2 Annotation: Chromosome 12NC_000012.10 (20739666..20797587) GeneID: 53919 18: SLC17A7 Official Symbol SLC17A7 and Name: solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 [Homo sapiens] Other Aliases: BNPI, VGLUT1 Other Designations: brain-specific Na-dependent inorganic phosphate cotransporter; solute carrier family 17, member 7; vesicular glutamate transporter 1 Chromosome: 19; Location: 19q13 Annotation: Chromosome 19NC_000019.8 (54624470..54636596, complement) MIM: 605208 GeneID: 57030 19: SLC22A15 Official Symbol SLC22A15 and Name: solute carrier family 22 (organic cation transporter), member 15 [Homo sapiens] Other Aliases: DKFZp761G0313, FLIPT1, PRO34686 Other Designations: fly-like putative organic ion transporter 1; trans-like protein Chromosome: 1; Location: 1p13.1 Annotation: Chromosome 1NC_000001.9 (116320642..116413548) MIM: 608275 GeneID: 55356 20: PITPNM1 Official Symbol PITPNM1 and Name: phosphatidylinositol transfer protein, membrane-associated 1 [Homo sapiens] Other Aliases: DRES9, FLJ44997, NIR2, PITPNM, RDGB, RDGB1, RDGBA1, Rd9 Other Designations: PYK2 N-terminal domain-interacting receptor 2; phosphatidylinositol transfer protein, membrane-associated; retinal degeneration B alpha 1 Chromosome: 11; Location: 11q13 Annotation: Chromosome 11NC_000011.8 (67015815..67028416, complement) MIM: 608794 GeneID: 9600 21: SLC2A1 Official Symbol SLC2A1 and Name: solute carrier family 2 (facilitated glucose transporter), member 1 [Homo sapiens] Other Aliases: GLUT, GLUT1, MGC141895, MGC141896 Chromosome: 1; Location: 1p35-p31.3 Annotation: Chromosome 1NC_000001.9 (43164102..43197088, complement) MIM: 138140 GeneID: 6513 22: PTGDS Official Symbol PTGDS and Name: prostaglandin D2 synthase 21kDa (brain) [Homo sapiens] Other Aliases: PDS, PGD2, PGDS, PGDS2 Other Designations: PGD2 synthase; beta-trace protein; glutathione-independent PGD synthase; lipocalin-type prostaglandin D synthase; prostaglandin D synthase; prostaglandin D2 synthase (21kD, brain); prostaglandin H2 D-isomerase; prostaglandin-H2 D-isomerase Chromosome: 9; Location: 9q34.2-q34.3 Annotation: Chromosome 9NC_000009.10 (138991777..138996015) MIM: 176803 GeneID: 5730 23: SLC2A2 Official Symbol SLC2A2 and Name: solute carrier family 2 (facilitated glucose transporter), member 2 [Homo sapiens] Other Aliases: GLUT2 Chromosome: 3; Location: 3q26.1-q26.2 Annotation: Chromosome 3NC_000003.10 (172196831..172227462, complement) MIM: 138160 GeneID: 6514 24: AQP1 Official Symbol AQP1 and Name: aquaporin 1 (Colton blood group) [Homo sapiens] Other Aliases: AQP-CHIP, CHIP28, CO, MGC26324 Other Designations: Colton blood group; aquaporin 1; aquaporin 1 (channel-forming integral protein, 28kDa); aquaporin 1 (channel-forming integral protein, 28kDa, CO blood group); channel-like integral membrane protein, 28-kDa Chromosome: 7; Location: 7p14 Annotation: Chromosome 7NC_000007.12 (30917993..30931656) MIM: 107776 GeneID: 358 25: STX1A Official Symbol STX1A and Name: syntaxin 1A (brain) [Homo sapiens] Other Aliases: HPC-1, STX1, p35-1 Chromosome: 7; Location: 7q11.23 Annotation: Chromosome 7NC_000007.12 (72751476..72771898, complement) MIM: 186590 GeneID: 6804 26: BACE1 Official Symbol BACE1 and Name: beta-site APP-cleaving enzyme 1 [Homo sapiens] Other Aliases: ASP2, BACE, FLJ90568, HSPC104, KIAA1149 Other Designations: APP beta-secretase; aspartyl protease 2; beta-secretase; beta-site amyloid beta A4 precursor protein-cleaving enzyme; beta-site amyloid precursor protein cleaving enzyme; memapsin-2; membrane-associated aspartic protease 2; transmembrane aspartic proteinase Asp2 Chromosome: 11; Location: 11q23.2-q23.3 Annotation: Chromosome 11NC_000011.8 (116661624..116692182, complement) MIM: 604252 GeneID: 23621 27: SLC17A8 Official Symbol SLC17A8 and Name: solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 [Homo sapiens] Other Aliases: VGLUT3 Other Designations: vesicular glutamate transporter 3 Chromosome: 12; Location: 12q23.1 Annotation: Chromosome 12NC_000012.10 (99275125..99339968) MIM: 607557 GeneID: 246213 28: ACCN4 Official Symbol ACCN4 and Name: amiloride-sensitive cation channel 4, pituitary [Homo sapiens] Other Aliases: ASIC4, BNAC4, MGC17248, MGC24860 Other Designations: acid-sensing ion channel 4; amiloride-sensitive cation channel 4; brain sodium channel 4 Chromosome: 2; Location: 2q35 Annotation: Chromosome 2NC_000002.10 (220087296..220111738) MIM: 606715 GeneID: 55515 29: ABCG4 Official Symbol ABCG4 and Name: ATP-binding cassette, sub-family G (WHITE), member 4 [Homo sapiens] Other Aliases: WHITE2 Other Designations: ATP-binding cassette, subfamily G, member 4; putative ABC transporter Chromosome: 11; Location: 11q23.3 Annotation: Chromosome 11NC_000011.8 (118524960..118538585) MIM: 607784 GeneID: 64137 30: SLC10A4 Official Symbol SLC10A4 and Name: solute carrier family 10 (sodium/bile acid cotransporter family), member 4 [Homo sapiens] Other Aliases: MGC29802, P4 Other Designations: bile acid transporter SLC10A4 Chromosome: 4; Location: 4p12 Annotation: Chromosome 4NC_000004.10 (48180206..48185921) GeneID: 201780 31: AQP4 Official Symbol AQP4 and Name: aquaporin 4 [Homo sapiens] Other Aliases: HMIWC2, MGC22454, MIWC Other Designations: aquaporin type4; aquaporin-4; mercurial-insensitive water channel Chromosome: 18; Location: 18q11.2-q12.1 Annotation: Chromosome 18NC_000018.8 (22686005..22699714, complement) MIM: 600308 GeneID: 361 32: ABCB1 Official Symbol ABCB1 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 1 [Homo sapiens] Other Aliases: ABC20, CD243, CLCS, GP170, MDR1, MGC163296, P-gp, PGY1 Other Designations: ATP-binding cassette sub-family B member 1; P glycoprotein 1; P-glycoprotein 1; colchicin sensitivity; doxorubicin resistance; multidrug resistance 1 Chromosome: 7; Location: 7q21.1 Annotation: Chromosome 7NC_000007.12 (86970884..87180500, complement) MIM: 171050 GeneID: 5243 33: ATP7B Official Symbol ATP7B and Name: ATPase, Cu++ transporting, beta polypeptide [Homo sapiens] Other Aliases: RP11-327P2.3, PWD, WC1, WD, WND Other Designations: ATPase, Cu(2+)- transporting, beta polypeptide; OTTHUMP00000040880; Wilson disease; Wilson disease-associated protein; copper pump 2; copper-transporting ATPase 2 Chromosome: 13; Location: 13q14.3 Annotation: Chromosome 13NC_000013.9 (51404806..51483631, complement) MIM: 606882 GeneID: 540 34: ABCA2 Official Symbol ABCA2 and Name: ATP-binding cassette, sub-family A (ABC1), member 2 [Homo sapiens] Other Aliases: ABC2, MGC129761 Other Designations: ATP-binding cassette, sub-family A, member 2; OTTHUMP00000064733 Chromosome: 9; Location: 9q34 Annotation: Chromosome 9NC_000009.10 (139021507..139043195, complement) MIM: 600047 GeneID: 20 35: UCP2 Official Symbol UCP2 and Name: uncoupling protein 2 (mitochondrial, proton carrier) [Homo sapiens] Other Aliases: SLC25A8, UCPH Other Designations: uncoupling protein 2; uncoupling protein-2 Chromosome: 11; Location: 11q13 Annotation: Chromosome 11NC_000011.8 (73363364..73371537, complement) MIM: 601693 GeneID: 7351 36: SLC25A27 Official Symbol SLC25A27 and Name: solute carrier family 25, member 27 [Homo sapiens] Other Aliases: RP11-446F17.2, FLJ33552, UCP4 Other Designations: uncoupling protein 4 Chromosome: 6; Location: 6p11.2-q12 Annotation: Chromosome 6NC_000006.10 (46728639..46752935) GeneID: 9481 37: SLC18A1 Official Symbol SLC18A1 and Name: solute carrier family 18 (vesicular monoamine), member 1 [Homo sapiens] Other Aliases: CGAT, VAT1, VMAT1 Chromosome: 8; Location: 8p21.3 Annotation: Chromosome 8NC_000008.9 (20046652..20084997, complement) MIM: 193002 GeneID: 6570 38: SLC11A2 Official Symbol SLC11A2 and Name: solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 [Homo sapiens] Other Aliases: DCT1, DMT1, FLJ37416, NRAMP2 Other Designations: natural resistance-associated macrophage protein 2 Chromosome: 12; Location: 12q13 Annotation: Chromosome 12NC_000012.10 (49666044..49706409, complement) MIM: 600523 GeneID: 4891 39: SNCA Official Symbol SNCA and Name: synuclein, alpha (non A4 component of amyloid precursor) [Homo sapiens] Other Aliases: MGC110988, NACP, PARK1, PARK4, PD1 Other Designations: alpha synuclein; alpha-synuclein; alpha-synuclein, isoform NACP140; non A-beta component of AD amyloid; non A4 component of amyloid Chromosome: 4; Location: 4q21 Annotation: Chromosome 4NC_000004.10 (90865728..90977156, complement) MIM: 163890 GeneID: 6622 40: DRD2 Official Symbol DRD2 and Name: dopamine receptor D2 [Homo sapiens] Other Aliases: D2DR, D2R Other Designations: seven transmembrane helix receptor Chromosome: 11; Location: 11q23 Annotation: Chromosome 11NC_000011.8 (112785527..112851091, complement) MIM: 126450 GeneID: 1813 41: SLC12A2 Official Symbol SLC12A2 and Name: solute carrier family 12 (sodium/potassium/chloride transporters), member 2 [Homo sapiens] Other Aliases: BSC, BSC2, MGC104233, NKCC1 Other Designations: basolateral Na-K-Cl symporter; bumetanide-sensitive sodium-(potassium)-chloride cotransporter 1 Chromosome: 5; Location: 5q23.3 Annotation: Chromosome 5NC_000005.8 (127447382..127553279) MIM: 600840 GeneID: 6558 42: SYP Official Symbol SYP and Name: synaptophysin [Homo sapiens] Other Designations: major synaptic vesicle protein P38 Chromosome: X; Location: Xp11.23-p11.22 Annotation: Chromosome XNC_000023.9 (48931209..48943605, complement) MIM: 313475 GeneID: 6855 43: LRP1 Official Symbol LRP1 and Name: low density lipoprotein-related protein 1 (alpha-2-macroglobulin receptor) [Homo sapiens] Other Aliases: A2MR, APOER, APR, CD91, FLJ16451, LRP, MGC88725, TGFBR5 Other Designations: alpha-2-macroglobulin receptor; low density lipoprotein-related protein 1; type V tgf-beta receptor Chromosome: 12; Location: 12q13-q14 Annotation: Chromosome 12NC_000012.10 (55808549..55893401) MIM: 107770 GeneID: 4035 44: TNF Official Symbol TNF and Name: tumor necrosis factor (TNF superfamily, member 2) [Homo sapiens] Other Aliases: DASS-280D8.2, DIF, TNF-alpha, TNFA, TNFSF2 Other Designations: APC1 protein; OTTHUMP00000037669; TNF superfamily, member 2; TNF, macrophage-derived; TNF, monocyte-derived; cachectin; tumor necrosis factor alpha Chromosome: 6; Location: 6p21.3 Annotation: Chromosome 6NC_000006.10 (31651329..31654091) MIM: 191160 GeneID: 7124 45: APOE Official Symbol APOE and Name: apolipoprotein E [Homo sapiens] Other Aliases: AD2, MGC1571, apoprotein Other Designations: Alzheimer disease 2 (APOE*E4-associated, late onset); apolipoprotein E3 Chromosome: 19; Location: 19q13.2 Annotation: Chromosome 19NC_000019.8 (50100879..50104490) MIM: 107741 GeneID: 348 46: SLC25A23 Official Symbol SLC25A23 and Name: solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 [Homo sapiens] Other Aliases: APC2, MCSC2, MGC2615, SCaMC-3 Other Designations: mitochondrial ATP-Mg/Pi carrier protein; mitochondrial Ca2+-dependent solute carrier protein 2; short calcium-binding mitochondrial carrier 3; solute carrier family 25, member 23 Chromosome: 19; Location: 19p13.3 Annotation: Chromosome 19NC_000019.8 (6391075..6410781, complement) MIM: 608746 GeneID: 79085 47: PTCH1 Official Symbol PTCH1 and Name: patched homolog 1 (Drosophila) [Homo sapiens] Other Aliases: RP11-435O5.3, BCNS, FLJ26746, FLJ42602, HPE7, NBCCS, PTC, PTC1, PTCH, PTCH11 Other Designations: PTCH protein +12b; PTCH protein +4'; PTCH protein -10; patched; patched homolog 1 splice variant 1C Chromosome: 9; Location: 9q22.3 Annotation: Chromosome 9NC_000009.10 (97246208..97310652, complement) MIM: 601309 GeneID: 5727 48: GJA1 Official Symbol GJA1 and Name: gap junction protein, alpha 1, 43kDa [Homo sapiens] Other Aliases: CX43, DFNB38, GJAL, ODDD Other Designations: connexin 43; gap junction 43 kDa heart protein; gap junction protein, alpha-like Chromosome: 6; Location: 6q21-q23.2 Annotation: Chromosome 6NC_000006.10 (121798487..121812571) MIM: 121014 GeneID: 2697 49: SORL1 Official Symbol SORL1 and Name: sortilin-related receptor, L(DLR class) A repeats-containing [Homo sapiens] Other Aliases: LR11, LRP9, SORLA, SorLA-1, gp250 Other Designations: mosaic protein LR11; sortilin-related receptor containing LDLR class A repeats Chromosome: 11; Location: 11q23.2-q24.2 Annotation: Chromosome 11NC_000011.8 (120828130..121005621) MIM: 602005 GeneID: 6653 50: SYT12 Official Symbol SYT12 and Name: synaptotagmin XII [Homo sapiens] Other Aliases: SRG1, SYT11 Chromosome: 11; Location: 11q13.1 Annotation: Chromosome 11NC_000011.8 (66547467..66574906) MIM: 606436 GeneID: 91683 51: CYP46A1 Official Symbol CYP46A1 and Name: cytochrome P450, family 46, subfamily A, polypeptide 1 [Homo sapiens] Other Aliases: CP46, CYP46 Other Designations: cholesterol 24-hydroxylase; cytochrome P450, family 46; cytochrome P450, subfamily 46 (cholesterol 24-hydroxylase) Chromosome: 14; Location: 14q32.1 Annotation: Chromosome 14NC_000014.7 (99220508..99263391) MIM: 604087 GeneID: 10858 52: SREBF2 Official Symbol SREBF2 and Name: sterol regulatory element binding transcription factor 2 [Homo sapiens] Other Aliases: SREBP2 Other Designations: OTTHUMP00000028740; sterol regulatory element-binding protein 2; sterol regulatory element-binding transcription factor 2 Chromosome: 22; Location: 22q13 Annotation: Chromosome 22NC_000022.9 (40559052..40632321) MIM: 600481 GeneID: 6721 53: GABRA6 Official Symbol GABRA6 and Name: gamma-aminobutyric acid (GABA) A receptor, alpha 6 [Homo sapiens] Other Aliases: MGC116903, MGC116904 Other Designations: GABA subunit A receptor alpha 6; gamma-aminobutyric acid A receptor, alpha 6 Chromosome: 5; Location: 5q34 Annotation: Chromosome 5NC_000005.8 (161045548..161061699) MIM: 137143 GeneID: 2559 54: LPL Official Symbol LPL and Name: lipoprotein lipase [Homo sapiens] Other Aliases: LIPD Chromosome: 8; Location: 8p22 Annotation: Chromosome 8NC_000008.9 (19841058..19869049) MIM: 609708 GeneID: 4023 55: CHRNA3 Official Symbol CHRNA3 and Name: cholinergic receptor, nicotinic, alpha 3 [Homo sapiens] Other Aliases: MGC104879 Other Designations: Cholinergic receptor, neuronal nicotinic, alpha polypeptide-3; cholinergic receptor, nicotinic, alpha polypeptide 3; neuronal nicotinic acetylcholine receptor, alpha3 subunit Chromosome: 15; Location: 15q24 Annotation: Chromosome 15NC_000015.8 (76674706..76700377, complement) MIM: 118503 GeneID: 1136 56: GLTP Official Symbol GLTP and Name: glycolipid transfer protein [Homo sapiens] Chromosome: 12; Location: 12q24.11 Annotation: Chromosome 12NC_000012.10 (108773131..108802676, complement) MIM: 608949 GeneID: 51228 57: GABRA5 Official Symbol GABRA5 and Name: gamma-aminobutyric acid (GABA) A receptor, alpha 5 [Homo sapiens] Other Aliases: MGC138184 Chromosome: 15; Location: 15q11.2-q12 Annotation: Chromosome 15NC_000015.8 (24742696..24776749) MIM: 137142 GeneID: 2558 58: DOC2A Official Symbol DOC2A and Name: double C2-like domains, alpha [Homo sapiens] Chromosome: 16; Location: 16p11.2 Annotation: Chromosome 16NC_000016.8 (29924336..29929902, complement) MIM: 604567 GeneID: 8448 59: MMP2 Official Symbol MMP2 and Name: matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) [Homo sapiens] Other Aliases: CLG4, CLG4A, MMP-II, MONA, TBE-1 Other Designations: 72kD type IV collagenase; collagenase type IV-A; matrix metalloproteinase 2; matrix metalloproteinase 2 (gelatinase A, 72kD gelatinase, 72kD type IV collagenase); matrix metalloproteinase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase); matrix metalloproteinase-II; neutrophil gelatinase Chromosome: 16; Location: 16q13-q21 Annotation: Chromosome 16NC_000016.8 (54070589..54098104) MIM: 120360 GeneID: 4313 60: NEWENTRY Record to support submission of GeneRIFs for a gene not in Entrez Gene (human; man). [Homo sapiens] GeneID: 192343 61: RALBP1 Official Symbol RALBP1 and Name: ralA binding protein 1 [Homo sapiens] Other Aliases: RIP, RIP1, RLIP76 Other Designations: ralA-binding protein Chromosome: 18; Location: 18p11.3 Annotation: Chromosome 18NC_000018.8 (9465530..9528106) MIM: 605801 GeneID: 10928 62: GABRR2 Official Symbol GABRR2 and Name: gamma-aminobutyric acid (GABA) receptor, rho 2 [Homo sapiens] Other Aliases: RP1-131H7.1 Other Designations: GABA-C receptor, rho-2 subunit; OTTHUMP00000040625 Chromosome: 6; Location: 6q13-q16.3 Annotation: Chromosome 6NC_000006.10 (90023958..90081668, complement) MIM: 137162 GeneID: 2570 63: GABRR1 Official Symbol GABRR1 and Name: gamma-aminobutyric acid (GABA) receptor, rho 1 [Homo sapiens] Other Aliases: MGC163216 Other Designations: bA135P14.1 (gamma-aminobutyric acid (GABA) receptor, rho 1); gamma-aminobutyric acid (GABA) A receptor, rho-1 Chromosome: 6; Location: 6q13-q16.3 Annotation: Chromosome 6NC_000006.10 (89944691..89983779, complement) MIM: 137161 GeneID: 2569 64: SOD1 Official Symbol SOD1 and Name: superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult)) [Homo sapiens] Other Aliases: ALS, ALS1, IPOA, SOD, homodimer Other Designations: Cu /Zn superoxide dismutase; Cu/Zn superoxide dismutase; SOD, soluble; indophenoloxidase A; superoxide dismutase (aa 120-154); superoxide dismutase 1, soluble; superoxide dismutase, cystolic Chromosome: 21; Location: 21q22.11 Annotation: Chromosome 21NC_000021.7 (31953806..31963115) MIM: 147450 GeneID: 6647 65: TOR1A Official Symbol TOR1A and Name: torsin family 1, member A (torsin A) [Homo sapiens] Other Aliases: DQ2, DYT1, torsin A Other Designations: dystonia 1, torsion (autosomal dominant; torsin A); torsin A Chromosome: 9; Location: 9q34 Annotation: Chromosome 9NC_000009.10 (131615042..131626262, complement) MIM: 605204 GeneID: 1861 66: RAB11A Official Symbol RAB11A and Name: RAB11A, member RAS oncogene family [Homo sapiens] Other Aliases: MGC1490, YL8 Other Designations: RAB 11A, member oncogene family; Ras-related protein Rab-11A Chromosome: 15; Location: 15q21.3-q22.31 Annotation: Chromosome 15NC_000015.8 (63948850..63968846) MIM: 605570 GeneID: 8766 67: STAR Official Symbol STAR and Name: steroidogenic acute regulatory protein [Homo sapiens] Other Aliases: STARD1 Other Designations: START domain containing 1; cholesterol trafficker; mitochondrial steroid acute regulatory protein; steroid acute regulatory protein; steroidogenic acute regulator Chromosome: 8; Location: 8p11.2 Annotation: Chromosome 8NC_000008.9 (38119375..38127757, complement) MIM: 600617 GeneID: 6770 68: TGFB1 Official Symbol TGFB1 and Name: transforming growth factor, beta 1 [Homo sapiens] Other Aliases: CED, DPD1, TGFB Other Designations: Camurati-Engelmann disease; TGF-beta 1 protein; diaphyseal dysplasia 1, progressive; transforming growth factor beta 1; transforming growth factor, beta 1 (Camurati-Engelmann disease); transforming growth factor-beta 1 Chromosome: 19; Location: 19q13.1 Annotation: Chromosome 19NC_000019.8 (46528491..46551656, complement) MIM: 190180 GeneID: 7040 69: TTR Official Symbol TTR and Name: transthyretin (prealbumin, amyloidosis type I) [Homo sapiens] Other Aliases: HsT2651, PALB, TBPA Other Designations: prealbumin; transthyretin Chromosome: 18; Location: 18q12.1 Annotation: Chromosome 18NC_000018.8 (27425838..27432781) MIM: 176300 GeneID: 7276 70: MAPK14 Official Symbol MAPK14 and Name: mitogen-activated protein kinase 14 [Homo sapiens] Other Aliases: CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA Other Designations: Csaids binding protein; MAP kinase Mxi2; MAX-interacting protein 2; cytokine suppressive anti-inflammatory drug binding protein; p38 MAP kinase; p38 mitogen activated protein kinase; p38alpha Exip; stress-activated protein kinase 2A Chromosome: 6; Location: 6p21.3-p21.2 Annotation: Chromosome 6NC_000006.10 (36103551..36186513) MIM: 600289 GeneID: 1432 71: HMOX1 Official Symbol HMOX1 and Name: heme oxygenase (decycling) 1 [Homo sapiens] Other Aliases: HO-1, bK286B10 Other Designations: OTTHUMP00000028925; heme oxygenase (decyclizing) 1 Chromosome: 22; Location: 22q13.1 Annotation: Chromosome 22NC_000022.9 (34107087..34120194) MIM: 141250 GeneID: 3162 72: APOD Official Symbol APOD and Name: apolipoprotein D [Homo sapiens] Chromosome: 3; Location: 3q26.2-qter Annotation: Chromosome 3NC_000003.10 (196776865..196792278, complement) MIM: 107740 GeneID: 347 73: IGF2 Official Symbol IGF2 and Name: insulin-like growth factor 2 (somatomedin A) [Homo sapiens] Other Aliases: C11orf43, FLJ22066, FLJ44734, INSIGF, pp9974 Other Designations: insulin-like growth factor 2; insulin-like growth factor II; insulin-like growth factor type 2; putative insulin-like growth factor II associated protein; somatomedin A Chromosome: 11; Location: 11p15.5 Annotation: Chromosome 11NC_000011.8 (2106926..2116578, complement) MIM: 147470 GeneID: 3481 74: PPARG Official Symbol PPARG and Name: peroxisome proliferator-activated receptor gamma [Homo sapiens] Other Aliases: NR1C3, PPARG1, PPARG2 Other Designations: PPAR gamma; peroxisome proliferative activated receptor gamma; peroxisome proliferative activated receptor, gamma; peroxisome proliferator-activated receptor gamma 1 Chromosome: 3; Location: 3p25 Annotation: Chromosome 3NC_000003.10 (12304359..12450843) MIM: 601487 GeneID: 5468 75: IGF1 Official Symbol IGF1 and Name: insulin-like growth factor 1 (somatomedin C) [Homo sapiens] Other Aliases: IGFI Other Designations: somatomedin C Chromosome: 12; Location: 12q22-q23 Annotation: Chromosome 12NC_000012.10 (101313806..101398454, complement) MIM: 147440 GeneID: 3479 76: GNB2L1 Official Symbol GNB2L1 and Name: guanine nucleotide binding protein (G protein), beta polypeptide 2-like 1 [Homo sapiens] Other Aliases: Gnb2-rs1, H12.3, HLC-7, PIG21, RACK1 Other Designations: lung cancer oncogene 7; proliferation-inducing gene 21; protein homologous to chicken B complex protein, guanine nucleotide binding Chromosome: 5; Location: 5q35.3 Annotation: Chromosome 5NC_000005.8 (180596534..180603512, complement) MIM: 176981 GeneID: 10399