Gene: [11p15/PNIA4] protein spot in 2-D gels (70kD; pI 5.6); — Gene: [12p13/PTPN6] protein tyrosine phosphatase, non-receptor type 6;

  • Gene: [11p15/PNIA4] protein spot in 2-D gels (70kD; pI 5.6);
  • Gene: [11p15/POLR2L] RNA polymerase II (DNA directed) polypeptide L (7.6kD);
  • Gene: [11p15/PTH] parathyroid hormone (parathyrin); hypocalcemia, autosomal dominant (MIM:601198); hyperparathyroidism, familial isolated (FIH; MIM:146200);
  • Gene: [11p15/PTPN5] protein tyrosine phosphatase, non-receptor type 5 (striatum-enriched);
  • Gene: [11p15/RPL27A] ribosomal protein L27a;
  • Gene: [11p15/RRM1] ribonucleotide reductase M1 polypeptide;
  • Gene: [11p15/SSA1] ribonucleoprotein autoantigen SS-A/Ro, 52kD; Sjogren syndrome antigen A1;
  • Gene: [11p15/TALDO1] transaldolase 1;
  • Gene: [11p15/TSG101] tumor susceptibility gene 101; breast cancer;
  • Gene: [11p15/ZNF143] zinc finger protein 143 (clone pHZ-1);
  • Gene: [11p151/FRA11C] fragile site 11p15.1, aphidicolin type, common;
  • Gene: [11p151/FRA11I] fragile site 11p15.1, distamycin A type, rare;
  • Gene: [11p151/KCNC1] potassium voltage-gated channel, Shaw-related subfamily, member 1;
  • Gene: [11p151/KCNJ11] potassium inwardly-rectifying channel, subfamily J, member 11; hyperinsulinism; hypoglycaemia, persistent hyperinsulinaemic (PHHI; MIM:256450); [BIR Kir6.2 ]
  • Gene: [11p151/LDHA] lactate dehydrogenase A (M chain; muscle); exertional myoglobinuria (lactate dehydrogenase A deficiency);
  • Gene: [11p151/LDHC] lactate dehydrogenase C (X chain; testicular);
  • Gene: [11p151/LMO4] LIM domain only 4 (cardiac LIM protein; CLP); [CLP ]
  • Gene: [11p151/SAA1] serum amyloid A1; reactive, secondary amyloidosis;
  • Gene: [11p151/SAA2] serum amyloid A2; reactive, secondary amyloidosis;
  • Gene: [11p151/SAA3] serum amyloid A3 (probably a pseudogene);
  • Gene: [11p151/SAA4] serum amyloid A4, constitutive; reactive, secondary amyloidosis;
  • Gene: [11p151/SUR] sulfonylurea receptor (hyperinsulinemia); persistent hyperinsulinemic hypoglycemia of infancy (MIM:256450); [HRINS PHHI ]
  • Gene: [11p151/USH1C] Usher syndrome 1C (autosomal recessive, severe; retinitis/deafness);
  • Gene: [11p152/TEAD1] TEA domain family member 1; transcriptional enhancer factor 1; transcription factor 13 (SV40 transcriptional enhancer factor); [TEF-1 NTEF-1 ]
  • Gene: [11p153/LMO1] LIM domain only 1 (rhombotin 1); rhombotin 1 (rhombosine; T cell lymphoma associated breakpoint); T cell acute lymphoblastic leukemia 1 (rhombotin); T cell lymphoma 6 associated breakpoint; [RBTN1 TCL6 ]
  • Gene: [11p153/ST5] suppression of tumorigenicity 5;
  • Gene: [11p153/TAF2H] TATA box binding protein (TBP)-associated factor, RNA polymerase II, H, 30kD; [TAFII30 ]
  • Gene: [11p153/WEE1] cell division cycle control WEE1 (human homolog of S. pombe wee1+); protein kinase, WEE1 like;
  • Gene: [11p154/CALCA] calcitonin/calcitonin gene related peptide, alpha polypeptide; [CALC1 CT CGRP ]
  • Gene: [11p154/CCKBR] cholecystokinin B receptor (gastrin receptor);
  • Gene: [11p154/MYOD1] myogenic differentiation antigen 1 (myogenic factor 3); rhabdomyosarcoma? (MIM:268210; liability); [MYF3 RMS ]
  • Gene: [11p154/SMPD1] sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase); Niemann-Pick disease A/B (sphingomyelin lipidosis);
  • Gene: [11p155/ADCR] adrenocortical carcinoma; breast cancer chromosome region? (liability); [ADCC ACC BCCR ]
  • Gene: [11p155/AMCD2B] arthrogryposis multiplex congenita, distal, type 2B; Freeman-Sheldon syndrome variant; [DA2B ]
  • Gene: [11p155/ASCL2] achaete-scute complex (Drosophila) homolog-like transcription factor 2; [ASH2 HASH2 ]
  • Gene: [11p155/BWSCR1A] Beckwith-Wiedemann syndrome chromosome region 1, candidate a; imprinted polyspecific membrane transporter 1; organic cation transporter-like 2; solute carrier family 22, member 1-like; [BWR1A IMPT1 ]
  • Gene: [11p155/BWSCR1B] Beckwith-Wiedemann syndrome chromosome region 1, candidate b; [BWR1B ]
  • Gene: [11p155/CARS] cysteinyl-tRNA synthetase;
  • Gene: [11p155/CD151] CD151 antigen (platelet-endothelial cell tetra-span antigen 3); [SFA-1 PETA3 ]
  • Gene: [11p155/CD81] antigen CD81 (26kD cell surface protein TAPA-1); target of antiproliferative antibody 1 (CD81); [TAPA1 ]
  • Gene: [11p155/CDKN1C] cyclin-dependent kinase inhibitor 1C (p57, Kip2); Beckwith-Wiedemann syndrome (exomphalos-macroglossia-gigantism; MIM:130650); [Kip2 ]
  • Gene: [11p155/CTSD] cathepsin D (lysosomal aspartyl protease);
  • Gene: [11p155/DRD4] dopamine receptor D4;
  • Gene: [11p155/DUSP8] dual specificity phosphatase 8 (EC:3.1.3.48 and EC:3.1.3.16);
  • Gene: [11p155/HBBP] hemoglobin, beta pseudogene; [HBBP1 ]
  • Gene: [11p155/HBB] hemoglobin, beta;
  • Gene: [11p155/HBD] hemoglobin, delta;
  • Gene: [11p155/HBE] hemoglobin, epsilon; [HBE1 ]
  • Gene: [11p155/HBG1] hemoglobin, gamma A (position 136 = Ala); hereditary persistence of fetal hemoglobin, pancellular type (MIM:141749); F-cell production, pancellular type;
  • Gene: [11p155/HBG2] hemoglobin, gamma G (position 136 = Gly); hereditary persistence of fetal hemoglobin, pancellular type (MIM:141749); F-cell production, pancellular type;
  • Gene: [11p155/HBGR] Hb gamma regulator;
  • Gene: [11p155/HBHPAI] HpaI recognition polymorphism, beta-globin-related; [HPA1 ]
  • Gene: [11p155/HPFH1] hereditary persistence of fetal hemoglobin, heterocellular 1; F-cell production, heterocellular 1; [FCP ]
  • Gene: [11p155/HRAS] Harvey rat sarcoma viral oncogene homolog; [RASH1 HAMSV H ]
  • Gene: [11p155/IDDM2] insulin-dependent diabetes mellitus 2; [IDDM1 IDDM ]
  • Gene: [11p155/IGF2AP] insulin-like growth factor 2 associated protein;
  • Gene: [11p155/IGF2] insulin-like growth factor 2 (somatomedin A); [SMA ]
  • Gene: [11p155/INSHVR] insulin-related DNA polymorphism; [IRDN ]
  • Gene: [11p155/INS] insulin; proinsulinemia;
  • Gene: [11p155/KCNQ1] potassium voltage-gated channel, KQT-like subfamily, member 1; potassium voltage-gated channel, shaker-related subfamily, member 9; potassium voltage-gated channel, shaker-related subfamily, member 8; long (electrocardi
  • Gene: [11p155/LSP1] lymphocyte-specific protein 1;
  • Gene: [11p155/MER2] antigen MER2 (monoclonal antibodies 1D12, 2F7);
  • Gene: [11p155/MTACR1] multiple tumor-associated chromosome region 1; Wilms tumor suppressor 2 (MTACR1); Wilms tumor 2 (nephroblastoma); [WT2 ]
  • Gene: [11p155/MUC2] mucin 2, intestinal/tracheal;
  • Gene: [11p155/MUC5AC] mucin 5, subtypes A and C, tracheobronchial; [MUC5 ]
  • Gene: [11p155/MUC5B] mucin 5, subtype B, tracheobronchial; mucin 9, salivary (high molecular weight); [MG1 MUC5 MUC9 ]
  • Gene: [11p155/MUC6] mucin 6, gastric;
  • Gene: [11p155/NAP1L4] nucleosome assembly protein 1-like 4 (NAP2-related protein); [NAP2 ]
  • Gene: [11p155/NDUFA5P1] NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene; NADH:ubiquinone oxidoreductase subunit B13 pseudogene;
  • Gene: [11p155/ORCTL2S] organic cation transporter-like 2 antisense;
  • Gene: [11p155/ORCTL2] organic cation transporter-like 2;
  • Gene: [11p155/RNH] ribonuclease/angiogenin inhibitor; [RAI ]
  • Gene: [11p155/RPL23L] ribosomal protein L23-like; ribosomal protein related to L23 (mitochondrial); [L23MRP RPL23 ]
  • Gene: [11p155/RPLP2] ribosomal protein, large, P2;
  • Gene: [11p155/STIM1] stromal interaction molecule 1;
  • Gene: [11p155/TH] tyrosine hydroxylase;
  • Gene: [11p155/TNNI2] troponin I2, skeletal, fast;
  • Gene: [11p155/TNNT3] troponin T3, skeletal, fast;
  • Gene: [11p155/ZNF195] zinc finger protein 195;
  • Gene: [11q/ASSP13] argininosuccinate synthetase pseudogene 13;
  • Gene: [11q/CD57] antigen CD57 (leukocyte antigen 7; HNK-1); [LEU7 ]
  • Gene: [11q/COX5BL4] cytochrome c oxidase subunit Vb-like 4;
  • Gene: [11q/ESA4] esterase A4;
  • Gene: [11q/GANAB] glucosidase, alpha; neutral AB;
  • Gene: [11q/HPRTP3] hypoxanthine phosphoribosyltransferase pseudogene 3;
  • Gene: [11q/HPRTP4] hypoxanthine phosphoribosyltransferase pseudogene 4;
  • Gene: [11q/MSK13] antigen MSK13 (monoclonal antibody Q14);
  • Gene: [11q/MSK25] antigen MSK25 (monoclonal antibody MC139);
  • Gene: [11q/MSK26] antigen MSK26 (monoclonal antibody K117);
  • Gene: [11q/MSK39] antigen MSK39 (monoclonal antibody 5.1H11);
  • Gene: [11q/P200] cell surface protein;
  • Gene: [11q/PSMA1] proteasome (prosome, macropain) subunit, alpha type, 1 (homolog of yeast PRE5); multicatalytic endopeptidase complex subunit C2 (30kD prosomal protein);
  • Gene: [11q/SCZD2] schizophrenia disorder 2;
  • Gene: [11q/ST3] suppression of tumorigenicity 3 (HeLa-transformation suppressor); tumor suppressor 3 (HeLa-transformation suppressor); [TSHL ]
  • Gene: [11q/TCF6L3] transcription factor 6-like 3 (mitochondrial transcription factor 1-like);
  • Gene: [11q1/BKMA] BKM (banded krait minor) satellite DNA;
  • Gene: [11q1/C1NH] complement component 1 inhibitor; hereditary angioneurotic edema, type II (HANE, C1 inhibitor deficiency); partial deficiency of complement component 4 (due to dysfunctional C1 inhibitor; MIM:120790); [HANE CINH ]
  • Gene: [11q1/CD20L] antigen CD20-like (hematopoietic cell-specific);
  • Gene: [11q1/CD20] antigen CD20 (lymphocyte differentiation antigen B1/1F5); [1F5/B1 B1/1F5 ]
  • Gene: [11q1/CHRM1] cholinergic receptor, muscarinic 1;
  • Gene: [11q1/CLNS1A] chloride channel, nucleotide-sensitive, 1A; chloride channel current inducer; [CLCI ICln ]
  • Gene: [11q1/COX8] cytochrome c oxidase subunit VIII (cytochrome a3/aa3); mitochondrial myopathy? (MIM:220110);
  • Gene: [11q1/DDB1] damage-specific DNA binding protein 1 (127kD); xeroderma pigmentosum, complementation group E (MIM:278740);
  • Gene: [11q1/EMK1] ELKL motif kinase;
  • Gene: [11q1/FNL2] fibronectin-like 2;
  • Gene: [11q1/FNTAL1] farnesyltransferase, CAAX box, alpha-like 1;
  • Gene: [11q1/GARP] glycoprotein A repetitions predominant; [D11S833E ]
  • Gene: [11q1/GIF] gastric intrinsic factor (vitamin B synthesis); pernicious anemia, congenital, due to defect of intrinsic factor; [IF ]
  • Gene: [11q1/IGHER1B] immunoglobulin E Fc-receptor I, beta subunit (high affinity); [FCER1B ]
  • Gene: [11q1/MDU1] antigen MDU1, heavy subunit (p40, monoclonal antibodies 4F2, 44D7); sodium-calcium exchanger (NACAE); [M4F2 MGP4F2 ]
  • Gene: [11q1/MSK22] antigen MSK22 (monoclonal antibody A124);
  • Gene: [11q1/MSK23] antigen MSK23 (monoclonal antibody T43);
  • Gene: [11q1/OPPG] osteoporosis pseudoglioma syndrome; osteogenesis imperfecta, ocular form; [OPS ]
  • Gene: [11q1/P2RY2] purinergic receptor P2Y, G-protein coupled, 2; [HP2U P2U ]
  • Gene: [11q1/TCN1] transcobalamin I (vitamin B12 binding protein, R binder family); [TC1 ]
  • Gene: [11q1/UGB] uteroglobin (blastokinin); Clara cells 10kD secretory protein; [CC10 ]
  • Gene: [11q11/CTNND1] catenin (cadherin-associated protein), delta 1; [CTNND ]
  • Gene: [11q11/OSBP] oxysterol binding protein;
  • Gene: [11q12/AGTRL1] angiotensin receptor-like 1 (G protein-coupled receptor APJ); [APJ ]
  • Gene: [11q12/AHNAK] AHNAK nucleoprotein (desmoyokin);
  • Gene: [11q12/CNTF] ciliary neurotrophic factor;
  • Gene: [11q12/ESRRA] estrogen-related receptor alpha; estrogen receptor-like 1; [ESRL1 ERR1 ]
  • Gene: [11q12/FEN1] flap structure-specific endonuclease 1 (maturation factor 1);
  • Gene: [11q12/LTBP3] latent transforming growth factor beta binding protein 3;
  • Gene: [11q12/P2RX3] purinergic receptor P2X, ligand-gated ion channel, 3 (purinoceptor P2X3); [P2X3 ]
  • Gene: [11q12/SSRP1] structure specific recognition protein 1;
  • Gene: [11q13/ACMG] acromegaly;
  • Gene: [11q13/ACTN3] actinin, alpha 3;
  • Gene: [11q13/ADRBK1] adrenergic, beta, receptor kinase 1;
  • Gene: [11q13/ALDH7] aldehyde dehydrogenase 7, kidney;
  • Gene: [11q13/ALDH8] aldehyde dehydrogenase 8, salivary gland;
  • Gene: [11q13/ARIX] aristaless (Drosophila) homeobox;
  • Gene: [11q13/ARRB1] arrestin, beta 1; [ARR1 ]
  • Gene: [11q13/ART2P] ADP-ribosyltransferase 2 pseudogene; RT6 antigen (rat) homolog; [ART1P RT6 ]
  • Gene: [11q13/BBS1] Bardet-Biedl syndrome 1;
  • Gene: [11q13/CAPN1] calpain, large polypeptide L1 (catalytic); calcium-activated neutral proteinase Mu;
  • Gene: [11q13/CCND2P] cyclin D2 pseudogene;
  • Gene: [11q13/CD6] antigen CD6 (monoclonal antibodies Tp120); T cell differentiation antigen (Tp120; CD6); [Tp120 ]
  • Gene: [11q13/CFL1] cofilin 1 (non-muscle); [CFL ]
  • Gene: [11q13/CPT1A] carnitine palmitoyltransferase I, liver; hypoglycemia, hypoketotic (deficiency of carnitine palmitoyltransferase I; MIM:255120);
  • Gene: [11q13/CST6] cystatin M;
  • Gene: [11q13/DHCR7] 7-dehydrocholesterol reductase; delta-7-dehydrocholesterol reductase; Smith-Lemli-Opitz syndrome, type 1? (MIM:270400);
  • Gene: [11q13/EMS1] ems1 oncogene (mammory tumor and squamous cell carcinoma-associated (p80/p85 src substrate)); SRC substrate cortactin (amplaxin);
  • Gene: [11q13/EVR1] exudative vitreoretinopathy 1 (autosomal dominant; Criswick-Schepens syndrome); [FEVR ]
  • Gene: [11q13/FKBP2] FK506-binding protein 2 (13kD);
  • Gene: [11q13/FOLR1P] folate receptor 1 (adult) pseudogene;
  • Gene: [11q13/FOLR1] folate receptor 1 (adult); folate binding protein (adult); [FOLR FBP ]
  • Gene: [11q13/FOLR2L] folate receptor 2 (fetal)-like;
  • Gene: [11q13/FOLR2] folate receptor 2 (fetal); folate binding protein (fetal);
  • Gene: [11q13/FOLR3] folate receptor 3 (gamma);
  • Gene: [11q13/FOSL1] FOS-like antigen 1; [FOSL ]
  • Gene: [11q13/FRA11H] fragile site 11q13, aphidicolin type, common;
  • Gene: [11q13/FTH1] ferritin, heavy polypeptide 1; [FTHL6 FTH ]
  • Gene: [11q13/FTHL16] ferritin, heavy polypeptide-like 16 (pseudogene?); [FTH2 ]
  • Gene: [11q13/GALN] galanin;
  • Gene: [11q13/GSTP1] glutathione S-transferase pi (placental; EC:2.5.1.18); fatty acid ethyl ester synthase III, myocardial (EC:3.1.1.67);
  • Gene: [11q13/HNP36] hydrophobic nucleolar protein, 36kD; delayed-early response gene 12; equilibrative nucleoside transporter 2 (ei; nitrobenzylthioinosine-insensitive); [DER12 ENT2 ]
  • Gene: [11q13/HPAST] PAST-1 (Drosophila) homolog;
  • Gene: [11q13/IDDM4] insulin-dependent diabetes mellitus 4;
  • Gene: [11q13/IGER] IgE responsiveness (atopic); atopic hypersensitivity (allergic asthma and rhinitis, liability 2); [APY ]
  • Gene: [11q13/IGHMBP2] immunoglobulin mu binding protein 2; cardiac transcription factor 1 (CATF1); [SMUBP2 CATF1 ]
  • Gene: [11q13/KRN1] keratin, cuticle, ultrahigh sulphur 1; [UHRSK1 ]
  • Gene: [11q13/MEN1] menin; multiple endocrine neoplasia, type I (Wermer syndrome); [MEAI ]
  • Gene: [11q13/MLK3] mixed lineage kinase 3;
  • Gene: [11q13/NDUFV1] NADH dehydrogenase (ubiquinone) flavoprotein 1 (51kD; EC:1.6.5.3, EC:1.6.99.3);
  • Gene: [11q13/NFKB3] nuclear factor of kappa light chain gene enhancer in B-cells 3 (p65); transcription factor kappa-B, subunit 3 (p65); v-rel avian reticuloendotheliosis viral oncogene homolog A; [RELA ]
  • Gene: [11q13/NUMA1] nuclear mitotic apparatus protein 1;
  • Gene: [11q13/PC] pyruvate carboxylase; Leigh necrotizing encephalopathy (pyruvate carboxylase deficiency);
  • Gene: [11q13/PGA3] pepsinogen 3, group I;
  • Gene: [11q13/PGA4] pepsinogen 4, group I;
  • Gene: [11q13/PGA5] pepsinogen 5, group I;
  • Gene: [11q13/PLCB3] phospholipase C, beta 3 (phosphatidylinositol-specific);
  • Gene: [11q13/PNG] phospholipase c, beta 3 neighboring gene; [SOM172 ]
  • Gene: [11q13/PPP1CA] protein phosphatase 1, catalytic subunit, alpha isoform;
  • Gene: [11q13/PPP2R5B] protein phosphatase 2, regulatory subunit B (B56), beta isoform;
  • Gene: [11q13/RAB8IP] Rab8 interacting protein (GC kinase); germinal center kinase;
  • Gene: [11q13/RBM4] RNA binding motif protein 4; [LARK ]
  • Gene: [11q13/REQ] requiem, apoptosis response zinc finger gene; ubi-d4/requiem (mouse) homolog; [UBI-D4 ]
  • Gene: [11q13/RNU15A] RNA, U15a small nucleolar;
  • Gene: [11q13/ROM1] rod outer segment membrane protein 1; retinal degeneration, slow? (rds-like protein); [ROSP1 ]
  • Gene: [11q13/RPS30] ribosomal protein S30; Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV) ubiquitously expressed (fox derived); [FAU ]
  • Gene: [11q13/RPS3] ribosomal protein S3;
  • Gene: [11q13/SEA] S13 avian erythroblastosis oncogene homolog;
  • Gene: [11q13/TBX10] T-box 10;
  • Gene: [11q13/TM7SF2] transmembrane 7 superfamily member 2; [ANG1 ]
  • Gene: [11q13/UCP2] uncoupling protein 2 (mitochondrial, proton carrier);
  • Gene: [11q13/UCP3] uncoupling protein 3 (mitochondrial, proton carrier);
  • Gene: [11q13/UVRAG] UV radiation resistance associated gene;
  • Gene: [11q13/VEGFB] vascular endothelial growth factor B; [VRF ]
  • Gene: [11q13/VMD2] bestrophin; vitelliform macular dystrophy (Best disease);
  • Gene: [11q13/VRNI] vitreoretinopathy, neovascular inflammatory;
  • Gene: [11q13/ZNF126] zinc finger protein 126 (HZF-2; clone c11q-1c3);
  • Gene: [11q13/ZNF130] zinc finger protein 130 (HZF-6; clone c11q-5e11);
  • Gene: [11q13/ZNF162] zinc finger protein 162; [ZFM1 D11S363 ]
  • Gene: [11q131/CD5] antigen CD5 (p56-62; T1; monoclonal antibodies LEU1); T cell antigen T1 (CD5; Leu-1); [T1 LEU1 ]
  • Gene: [11q131/FEOM2] fibrosis of the extraocular muscles, congenital 2; [CFEOM2 ]
  • Gene: [11q131/PGL2] paraganglioma or familial glomus tumors 2;
  • Gene: [11q131/POLR2G] RNA polymerase II (DNA directed) polypeptide G (19kD);
  • Gene: [11q131/PYGM] phosphorylase; muscle (McArdle disease); McArdle disease (muscle glycogen phosphorylase deficiency); glycogen storage disease V (McArdle);
  • Gene: [11q133/BCL1] B-cell chronic lymphatic leukemia 1 (B-CLL: lymphoma 1);
  • Gene: [11q133/CCND1] cyclin D1; parathyroid adenomatosis 1 (cyclin D1 deficiency); [PRAD1 ]
  • Gene: [11q133/FGF3] fibroblast growth factor 3; murine mammary tumor virus integration site homolog; [INT2 ]
  • Gene: [11q133/FGF4] fibroblast growth factor 4; heparin secretory transforming protein 1 (Kaposi sarcoma oncogene); [HST1 KS3 ]
  • Gene: [11q133/FRA11A] fragile site 11q13.3, folic acid type, rare;
  • Gene: [11q133/PTPRCAP] protein tyrosine phosphatase, receptor type, c polypeptide-associated protein; lymphocyte phosphatase-associated phosphoprotein; [LPAP ]
  • Gene: [11q133/SIPA1] signal-induced proliferation-associated gene 1; [SPA1 ]
  • Gene: [11q135/CBP2] collagen-binding protein 2 (colligin 2); colligin 2 (collagen binding protein 2);
  • Gene: [11q135/MYO7A] myosin VIIA (Usher syndrome 1B, autosomal recessive, severe); Usher syndrome 1B (autosomal recessive, severe; retinitis/deafness); deafness, autosomal dominant 11 (DFNA11; MIM:601317); deafness, autosomal recessive 2 (D
  • Gene: [11q135/OMP] olfactory marker protein, neuronal specific;
  • Gene: [11q135/P2RY6] purinergic receptor P2Y, G-protein coupled, 6;
  • Gene: [11q135/THRSP] thyroid hormone responsive SPOT14 (rat) homolog; [SPOT14 ]
  • Gene: [11q14/CTSC] cathepsin C;
  • Gene: [11q14/ELA3] elastase 3, neutrophil (medullasin, bone marrow serine protease);
  • Gene: [11q14/FOLH1] folate hydrolase 1; prostate-specific membrane antigen;
  • Gene: [11q14/KCNA4L] potassium voltage-gated channel, shaker-related subfamily, member 4-like;
  • Gene: [11q14/PALS] Papillon-Lefevre syndrome; [PLS ]
  • Gene: [11q14/PRCP] prolylcarboxypeptidase (peptidyl prolylamino acid hydrolase); lysosomal pro-X carboxypeptidase (angiotensinase C);
  • Gene: [11q142/FRA11F] fragile site 11q14.2, aphidicolin type, common;
  • Gene: [11q2/ACAT1] acetyl-CoA acetyltransferase 1 (acetoacetyl Coenzyme A thiolase); alpha-methylacetoaceticaciduria (beta-ketothiolase deficiency);
  • Gene: [11q2/ANC] anal canal carcinoma;
  • Gene: [11q2/APLP2] amyloid beta (A4) precursor-like protein 2; [APPL2 ]
  • Gene: [11q2/ATDC] ataxia telangiectasia (complementation group D); [ATD ]
  • Gene: [11q2/ATM] ataxia telangiectasia mutated locus; ataxia telangiectasia, Louis-Bar syndrome; [AT1 ATA ATB ]
  • Gene: [11q2/CRYAB] crystallin, alpha B polypeptide; myopathy, desmin-related, cardioskeletal; [CRYA2]
  • Gene: [11q2/DDX10] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 10 (RNA helicase); [HRH-J8 ]
  • Gene: [11q2/FDX1] ferredoxin 1 (adrenodoxin; adrenal ferredoxin); [FDX ADX ]
  • Gene: [11q2/GUCY1A2] guanylate cyclase 1, soluble, alpha 2;
  • Gene: [11q2/HSPA8] heat shock 70kD protein 8 (HSP73);
  • Gene: [11q2/HSPB2] heat shock 27kD protein 2;
  • Gene: [11q2/MTNR1B] melatonin receptor 1B;
  • Gene: [11q2/NCAM1] neural cell adhesion molecule 1 (CD56); [NCAM CD56 ]
  • Gene: [11q2/NFRKB] nuclear factor related to kappa B binding protein; transcription factor kappa-B-related factor;
  • Gene: [11q2/NPAT] nuclear protein, ataxia-telangiectasia locus; [E14 ]
  • Gene: [11q2/PGL1] paraganglioma or familial glomus tumors 1; carotid body tumor-1; [PGL CBT1 ]
  • Gene: [11q2/PTS] 6-pyruvoyltetrahydropterin synthase; hyperphenylalaninemia (due to PTS deficiency);
  • Gene: [11q2/PVRL1] poliovirus receptor-like 1; poliovirus receptor related 1; [PVRR1 PRR1 ]
  • Gene: [11q2/SCN2B] sodium channel, voltage-gated, type II, beta polypeptide;
  • Gene: [11q2/SLN] sarcolipin;
  • Gene: [11q2/SORL1] sortilin-related receptor, L(DLR class) A repeats-containing; [sorLA-1 ]
  • Gene: [11q2/TECTA] tectorin alpha; deafness, autosomal dominant 8 (MIM:601543); deafness, autosomal dominant 12 (MIM:601842); [DFNA8 DFNA12 ]
  • Gene: [11q2/THY1] Thy-1 cell surface antigen;
  • Gene: [11q2/TMC] transmembrane conserved protein;
  • Gene: [11q2/VACM1] vasopressin-activated calcium-mobilizing receptor 1 (cullin homolog 5); [CUL5]
  • Gene: [11q21/CLA1] cerebellar ataxia 1 (autosomal recessive); [CPD3 ]
  • Gene: [11q21/FUT4] fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific); antigen CD15 (monoclonal antibodies RIB-19, S4.7.13);
  • Gene: [11q21/MRE11A] meiotic recombination (S. cerevisiae) 11 homolog A;
  • Gene: [11q21/TYR] tyrosinase (tyrosinase-negative albinism, I; ATN#); oculocutaneous albinism, tyrosinase-negative;
  • Gene: [11q22/API1] apoptosis inhibitor 1; inhibitor of apoptosis 2; [cIAP1 HIAP2 ]
  • Gene: [11q22/API2] apoptosis inhibitor 2; [CIAP2 HIAP1 ]
  • Gene: [11q22/CASP1] caspase 1, apoptosis-related cysteine protease; interleukin 1, beta, convertase;
  • Gene: [11q22/CASP4] caspase 4, apoptosis-related cysteine protease (TX protease); interleukin 1, beta convertase (Ice/Ced-3) homolog 2;
  • Gene: [11q22/CASP5] caspase 5, apoptosis-related cysteine protease; interleukin 1, beta convertase (Ice/Ced-3) homolog 3;
  • Gene: [11q22/DRD2] dopamine receptor D2; alcoholism, liability?; schizophrenia, susceptibility to;
  • Gene: [11q22/GRIA4] glutamate receptor, ionotropic, AMPA 4; [GLUR4 ]
  • Gene: [11q22/MMP20] matrix metalloproteinase 20 (enamelysin);
  • Gene: [11q22/PGR] progesterone receptor;
  • Gene: [11q22/TSC4] tuberous sclerosis 4;
  • Gene: [11q223/MMP10] matrix metalloproteinase 10; stromelysin 2 (transin 2);
  • Gene: [11q223/MMP12] matrix metalloproteinase 12 (macrophage elastase);
  • Gene: [11q223/MMP13] matrix metalloproteinase 13 (zinc); collagenase 3;
  • Gene: [11q223/MMP1] matrix metalloproteinase 1; collagenase, interstitial (fibroblast); epidermolysis bullosa, dystrophic (Hallopeau-Siemens, recessive; MIM:226600);
  • Gene: [11q223/MMP3] matrix metalloproteinase 3; stromelysin 1 (proteoglycanase; transin 1);
  • Gene: [11q223/MMP7] matrix metalloproteinase 7 (matrilysin, uterine); stromelysin-like metalloproteinase (Pump-1);
  • Gene: [11q223/MMP8] matrix metalloproteinase 8; collagenase I, neutrophil;
  • Gene: [11q23/CMT4B] Charcot-Marie-Tooth neuropathy 4B;
  • Gene: [11q23/G6PT1] glucose-6-phosphatase, transport (glucose-6-phosphate) protein 1; glucose-6-phosphate translocase; glycogen storage disease type Ib (MIM:232220); [GSD1b ]
  • Gene: [11q23/GRIK4] glutamate receptor, ionotropic, kainate 4; [GRIK ]
  • Gene: [11q23/H2AX] histone H2AX (basal);
  • Gene: [11q23/HTR3] 5-hydroxytryptamine (serotonin) receptor 3;
  • Gene: [11q23/INPPL1] inositol polyphosphate phosphatase-like 1;
  • Gene: [11q23/LH11CR2A] loss of heterozygosity, chromosome 11, chromosomal region 2, gene A;
  • Gene: [11q23/MIC9] antigen MIC9 (p100, monoclonal antibody 4D12, 2E2);
  • Gene: [11q23/MLL] trithorax (Drosophila) homolog; zink finger protein HRX (ALL-1); myeloid/lymphoid or mixed-lineage leukemia; [TRX1 HRX ALL- ]
  • Gene: [11q23/RDX] radixin;
  • Gene: [11q23/SDHD] succinate dehydrogenase complex, subunit D, integral membrane protein;
  • Gene: [11q23/ZNF123] zinc finger protein 123 (HZF-1);
  • Gene: [11q23/ZNF128] zinc finger protein 128 (clone c11q-8e8);
  • Gene: [11q23/ZNF129] zinc finger protein 129 (HZF-5; clone c11q-2g4);
  • Gene: [11q23/ZNF145] zinc finger protein 145 (Kruppel-like, expressed in promyelocytic leukemia); promyelocytic leukemia;
  • Gene: [11q231/DLAT] dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex); primary biliary cirrhosis;
  • Gene: [11q231/EBVM1] Epstein-Barr virus modification site 1;
  • Gene: [11q231/NNMT] nicotinamide N-methyltransferase;
  • Gene: [11q231/PORC] porphyria, acute; Chester type;
  • Gene: [11q231/POU2AF1] POU domain, class 2, associating factor 1; Oct binding factor 1 (OBF1); [OBF1 ]
  • Gene: [11q231/ZNF125] zinc finger protein 125 (HZF-3; clone c11q-3c1);
  • Gene: [11q232/TAGLN] transgelin (calponin-related, smooth muscle cell specific; SM22-alpha); [SM22 WS3-10 ]
  • Gene: [11q233/APOA1] apolipoprotein A-I; amyloidosis IV, Iowa type (van Allen type); amyloidosis VIII (systemic nonneuropathic, Ostertag type, German type; MIM:105200); hypoalphalipoproteinemia, primary;
  • Gene: [11q233/APOA4] apolipoprotein A-IV;
  • Gene: [11q233/APOC3] apolipoprotein C-III;
  • Gene: [11q233/ARCN1] archain 1; delta coat protein (coatomer protein complex, subunit delta); [COPD ]
  • Gene: [11q233/CBL2] Cas-Br-M (murine) ecotropic retroviral transforming sequence (oncogene CBL2); Jacobsen syndrome? (11q- syndrome, partial 11q monosomy syndrome; MIM:147791); [CBL ]
  • Gene: [11q233/DDX6] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 6 (RNA helicase, 54kD); RNA-dependent ATPase 2 (nuclear; p54; RNA-helicase 2);
  • Gene: [11q233/DPAGT1] dolichyl-phosphate alpha-N-acetylglucosaminyltransferase 1;
  • Gene: [11q233/ETS1] avian erythroblastosis virus E26 homolog 1;
  • Gene: [11q233/FRA11B] fragile site 11q23.3, folic acid type, rare;
  • Gene: [11q233/FRA11G] fragile site 11q23.3, aphidicolin type, common;
  • Gene: [11q233/HMBS] hydroxymethylbilane synthase; porphobilinogen deaminase (uroporphyrinogen-I synthase); porphyria, acute intermittent (AIP, Swedish type; UPS-deficiency);
  • Gene: [11q233/IL10RA] interleukin 10 receptor, alpha; [IL10R HIL-10R ]
  • Gene: [11q233/ITM1] integral transmembrane protein 1; [B5 TMC ]
  • Gene: [11q233/JBS] Jacobsen syndrome (partial 11q monosomy syndrome);
  • Gene: [11q233/RPS25] ribosomal protein S25;
  • Gene: [11q233/SC5DL] sterol-C5-desaturase-like protein (fungal ERG3, delta-5-desaturase homolog); [ERG3 ]
  • Gene: [11q233/TCR2D] T cell receptor, signal T3-delta polypeptide (TiT3 complex); antigen CD3D/T3, delta polypeptide (T cell receptor); [CD3D T3D ]
  • Gene: [11q233/TCR2E] T cell receptor, signal T3-epsilon polypeptide (TiT3 complex); antigen CD3E/T3, epsilon polypeptide (T cell receptor); [CD3E T3E ]
  • Gene: [11q233/TCR2G] T cell receptor, signal T3-gamma polypeptide (TiT3 complex); antigen CD3G/T3, gamma polypeptide (T cell receptor); [CD3G T3G ]
  • Gene: [11q24/CHEK1] checkpoint kinase (S.pombe) homolog;
  • Gene: [11q24/FLI1] oncogene FLI-1 (transcription factor ERGB?); Friend leukemia virus integration 1; Ewing sarcoma breakpoint region 2; [EWSR2 ]
  • Gene: [11q24/GLULL3] glutamate-ammonia ligase (glutamine synthase)-like 3;
  • Gene: [11q24/KCNJ1] potassium inwardly-rectifying channel, subfamily J, member 1; Bartter syndrome, type 2 (antenatal hypercalciuric; MIM:601678); hyperprostaglandin E syndrome (MIM:601678);
  • Gene: [11q24/KCNJ5] potassium inwardly-rectifying channel, subfamily J, member 5;
  • Gene: [11q24/NRGN] neurogranin (protein kinase C substrate, RC3); [RC3 ]
  • Gene: [11q241/SRPR] signal recognition particle receptor alpha (docking protein alpha);
  • Gene: [11q25/HJCD] histiocytosis with joint contractures and sensorineural deafness (Faisalabad);
  • Gene: [11^/ACRV1] acrosomal vesicle protein 1;
  • Gene: [11^/ADM] adrenomedullin;
  • Gene: [11^/BAK3] BCL-2 homolog (apoptosis regulator) BAK3; BCL2-like 7 pseudogene 2; [BCL2L7P2 ]
  • Gene: [11^/D11Z1] alphoid satellite DNA from chr 11 (probe pHS53);
  • Gene: [11^/ERVF1] endogenous retroviral sequence, full length 1 (band F6, 14.5 kb); [FRV1 ]
  • Gene: [11^/ERVT2] endogenous retroviral sequence, truncated 2 (band T2, 21.0 kb);
  • Gene: [11^/F2] coagulation factor II (prothrombin; fibrinogenase); disprothrombinemia; hypoprothrombinemia (prothrombin);
  • Gene: [11^/GABRIL3] diazepam binding inhibitor, like 3; [DBIL3 ]
  • Gene: [11^/GAPDL15] glyceraldehyde-3-phosphate dehydrogenase-like 15;
  • Gene: [11^/INSL2] insulin-like 2;
  • Gene: [11^/KRT18L4] keratin 18-like 4;
  • Gene: [11^/MUW53] cell surface antigen MUW 53 (monoclonal antibody 53.6);
  • Gene: [11^/MYODL] myogenic differentiation antigen 1-like 1; myogenic factor 3, like; [MYF3L1 ]
  • Gene: [11^/OPCML] opioid-binding protein/cell adhesion molecule-like;
  • Gene: [11^/PHKGL] phosphorylase kinase, gamma-like;
  • Gene: [11^/PTP4A2] protein tyrosine phosphatase 4A2;
  • Gene: [11^/PYHG2] protein spot in 2-D gels (MM 178 kD);
  • Gene: [11^/SCA5] spinocerebellar ataxia 5;
  • Gene: [11^/SIAT4C] sialyltransferase 4C (beta-galactosidase alpha-2,3-sialytransferase);
  • Gene: [11^/TMSL5] thymosin-like 5;
  • Gene: [11^/TUBAL] tubulin, alpha-like (gene or pseudogene);
  • Gene: [11^/ZNF75C] zinc finger protein 75C;
  • Gene: [12p1/A2MP] alpha-2-macroglobulin, pseudogene;
  • Gene: [12p1/A2M] alpha-2-macroglobulin;
  • Gene: [12p1/ACLS] acrocallosal syndrome;
  • Gene: [12p1/ATD] asphyxiating thoracic dystrophy (of newborn); chondroectodermal dysplasia-like syndrome; Jeune syndrome; thoracic-pelvic-phalangeal dystrophy;
  • Gene: [12p1/BCAT1] branched chain aminotransferase 1, cytosolic; transaminase 1 of branched chain amino acids (BCAA); hyperleucinemia-isoleucinemia (BCAA transaminase 1 deficiency);
  • Gene: [12p1/CD4] antigen CD4 (p55; monoclonal antibodies T4, Leu3a, 9106); T cell OKT4/CD4 deficiency (immunodeficiency?); [OKT4 T4 LEU3 ]
  • Gene: [12p1/CD69] antigen CD69 (p60; early T-cell activation antigen); [LEU23 ]
  • Gene: [12p1/ELA1] elastase 1 (pancreatic);
  • Gene: [12p1/GNAI2L] guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2(h)-like; [GNAIH GNAI2A ]
  • Gene: [12p1/GPR19] G protein-coupled receptor 19;
  • Gene: [12p1/HBP1] high blood pressure type 1 (autosomal dominant hypertension and brachydactyly); [HTNB ]
  • Gene: [12p1/KLRA1] killer cell lectin-like receptor subfamily A, member 1 (homologous to mouse Ly49); [Ly49 ]
  • Gene: [12p1/KLRB1] killer cell lectin-like receptor subfamily B, member 1; natural killer receptor; antigen CD161; [NKR-P1A CD161 ]
  • Gene: [12p1/KLRC1] killer cell lectin-like receptor subfamily C, member 1; natural killer cell group 2, sequences A and B; [NKG2-A NKG2-B ]
  • Gene: [12p1/KLRD1] killer cell lectin-like receptor subfamily D, member 1; antigen CD94 (type II membrane glycoprotein; NK/T-cell C-type lectin receptor); [CD94 ]
  • Gene: [12p1/MFAP5] microfibrillar-associated protein 5; [MAGP-2 ]
  • Gene: [12p1/MGP] matrix Gla protein; [MGLAP MGLA ]
  • Gene: [12p1/MIC17] antigen MIC17 (monoclonal antibody BB1);
  • Gene: [12p1/MSK3] antigen MSK3 (monoclonal antibody M68);
  • Gene: [12p1/NDUFS2L] NADH dehydrogenase (ubiquinone) Fe-S protein 2-like (49kD; NADH-CoQ reductase);
  • Gene: [12p1/PTHLH] parathyroid hormone-like hormone; humoral hypercalcemia of malignancy, protein-causing; [HHM PTHRP ]
  • Gene: [12p1/PZP] pregnancy zone protein;
  • Gene: [12p1/RAD52] RAD52 (S. cerevisiae) homolog;
  • Gene: [12p1/SIAT8] sialyltransferase 8 (alpha-N-acetylneuraminate: alpha-2,8-sialytransferase, GD3 synthase);
  • Gene: [12p1/SYB1] synaptobrevin 1; [VAMP-1 ]
  • Gene: [12p11/DDX11] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 (S.cerevisiae CHL1-like helicase); keratinocyte growth factor regulated gene 2 (KRG2); [CHLR1 KRG2 ]
  • Gene: [12p11/ITPR2] inositol 1,4,5-triphosphate receptor, type 2;
  • Gene: [12p1123/KCNJ8] potassium inwardly-rectifying channel, subfamily J, member 8; [Kir6.1 ]
  • Gene: [12p12/GRIN2B] glutamate receptor, ionotropic, N-methyl-D-aspartate 2B; [NMDAR2B ]
  • Gene: [12p12/GUCY2C] guanylate cyclase 2C, intestinal (heat stable enterotoxin receptor);
  • Gene: [12p12/LDHB] lactate dehydrogenase B (H chain; heart muscle);
  • Gene: [12p12/RECQL] RecQ protein-like (ATP-dependent DNA helicase Q1-like);
  • Gene: [12p12/SKP1B] S-phase kinase-associated protein 1B (p19B); CDK2/cyclin A-associated protein p19B;
  • Gene: [12p12/SLC21A3] solute carrier family 21 (organic anion transporter), member 3; [OATP ]
  • Gene: [12p121/IAPP] islet amyloid polypeptide (amylin); diabetes mellitus, associated peptide (amylin); [IAP DAP AMYN ]
  • Gene: [12p121/KRAS2] Kirsten rat sarcoma 2 viral homolog;
  • Gene: [12p121/SOX5] SRY (sex determining region Y)-box 5;
  • Gene: [12p122/GYS2] glycogen synthase 2 (liver);
  • Gene: [12p123/ARHGDIB] GDP association inhibitor, Aplasia-ras related 2; Rho GDP dissociation inhibitor (GDI) beta; [GDID4 GDI ]
  • Gene: [12p13/C1R] complement component 1, r subcomponent;
  • Gene: [12p13/C1S] complement component 1, s subcomponent (C1 esterase); complement C1S deficiency;
  • Gene: [12p13/CACNA1C] calcium channel, voltage-dependent, L type, alpha 1C subunit; calcium channel, L type, alpha 1 polypeptide, isoform 1 (cardiac muscle); [CACNL1A1 ]
  • Gene: [12p13/CCND2] cyclin D2 (G1/S-specific);
  • Gene: [12p13/CD27] antigen CD27;
  • Gene: [12p13/CD9] antigen CD9 (MIC3; p24; monoclonal antibodies 602-29); [MIC3 P24 BA2 ]
  • Gene: [12p13/CDKN1B] cyclin-dependent kinase inhibitor 1B (p27, Kip1); [Kip1 ]
  • Gene: [12p13/CHD4] chromodomain helicase DNA binding protein 4 (218kD); [Mi-2b ]
  • Gene: [12p13/CLAPS3] clathrin-associated/assembly/adaptor protein, small 3 (22kD);
  • Gene: [12p13/DDX12] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 12 (S.cerevisiae CHL1-like helicase); [CHLR2 ]
  • Gene: [12p13/ENO2] enolase 2 (gamma-enolase; neuron-specific);
  • Gene: [12p13/ETV6] ets translocation variant gene 6 (TEL oncogene); [TEL ]
  • Gene: [12p13/F8VWF] coagulation factor VIII VWF (von Willebrand factor); von Willebrand pseudohemophilia (coagulation factor VIII VWF deficiency; also MIM:277480); [VWF ]
  • Gene: [12p13/FGF6] fibroblast growth factor 6 (fgf.6 oncogene);
  • Gene: [12p13/GAPD] glyceraldehyde-3-phosphate dehydrogenase;
  • Gene: [12p13/GNB3] guanine nucleotide binding protein (G protein), beta polypeptide 3; adenylate cyclase modulator G(I,S,T), beta-3;
  • Gene: [12p13/GOT2L3] glutamic-oxaloacetic transaminase 2-like 3;
  • Gene: [12p13/KCNA1] potassium voltage-gated channel, shaker-related subfamily, member 1; ataxia, episodic with myokymia (AEM; MIM:160120); paroxysmal ataxia with neuromyotonia, hereditary (MIM:160120); [AEMK EA1 EAM ]
  • Gene: [12p13/KCNA5] potassium voltage-gated channel, shaker-related subfamily, member 5;
  • Gene: [12p13/KCNA6] potassium voltage-gated channel, shaker-related subfamily, member 6;
  • Gene: [12p13/KLRC2] killer cell lectin-like receptor subfamily C, member 2; natural killer cell group 2, sequence C; [NKG2C ]
  • Gene: [12p13/KLRC3] killer cell lectin-like receptor subfamily C, member 3; natural killer cell group 2, sequence E; [NKG2E ]
  • Gene: [12p13/KLRC4] killer cell lectin-like receptor subfamily C, member 4; natural killer cell group 2, sequence D; [NKG2D NKG2F ]
  • Gene: [12p13/LMO3] LIM domain only 3 (rhombotin-like 2); [RBTNL2 RHOM3 ]
  • Gene: [12p13/LTBR] lymphotoxin B receptor; tumor necrosis factor C receptor; [TNFCR ]
  • Gene: [12p13/M6PRD] mannose 6-phosphate receptor, cation-dependent; [M6PR MAN6PRD]
  • Gene: [12p13/MLF2] myeloid leukemia factor 2;
  • Gene: [12p13/MPE] eosinophil malignant proliferation;
  • Gene: [12p13/NOL1] nucleolar protein 1 (120kD); [NOP120 ]
  • Gene: [12p13/NTF3] neurotrophin 3;
  • Gene: [12p13/PDE6H] phosphodiesterase 6H, cGMP-specific, cone, gamma;
  • Gene: [12p13/POU5F1L] POU domain, class 5, transcription factor 1-like; octamer-binding transcription factor 3-like; [OTF3L ]
  • Gene: [12p13/PTPN6] protein tyrosine phosphatase, non-receptor type 6;

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