Gene: [02p1/REL] avian reticuloendotheliosis viral homolog; — Gene: [03p142/FRA3B] fragile site 3p14.2, aphidicolin type, common;
Gene: [02p1/REL] avian
reticuloendotheliosis viral homolog;
Gene: [02p1/RPS27A] ribosomal
protein S27a;
Gene: [02p1/SFTPB] surfactant,
pulmonary-associated protein B (SP-B; 18kD); congenital alveolar
proteinosis (MIM:265120); [SFTP3 PSPB ]
Gene: [02p1/SLC1A4] solute carrier
family 1 (glutamate transporters), member 4; neutral amino acid transporter
ASCT1; [ASCT1 SATT ]
Gene: [02p1/SPR] sepiapterin reductase
(7,8-dihydrobiopterin:NADP+oxidoreductase);
Gene: [02p1/VRK2] vaccinia related
kinase 2;
Gene: [02p11/DRD5P1] dopamine
receptor D5 pseudogene 1;
Gene: [02p11/FAB1] fatty acid binding
protein 1, liver; [FABP1 FABPL ]
Gene: [02p11/TCF9] transcription
factor 9 (binds GC-rich sequences);
Gene: [02p112/LIS2] lissencephaly
sequence 2; lissencephaly 2?;
Gene: [02p112/SAMS2]
S-adenosylmethionine synthetase 2, gamma (non-hepatic or
kidney-specific);
Gene: [02p12/CD8A] antigen CD8, alpha
polypeptide (p32-33; monoclonal antibodies Leu2, T8); [CD8 LEU2 ]
Gene: [02p12/CD8B1] antigen CD8,
beta polypeptide 1 (p37; monoclonal antibodies T8/2T8-5H7); [CD8B P37 LY3H
]
Gene: [02p12/CD8B2] antigen CD8,
beta polypeptide 2 (p37);
Gene: [02p12/GGCX] gamma-glutamyl
carboxylase (vitamin K-dependent);
Gene: [02p12/IGKC] immunoglobulin,
kappa subunit, constant region;
Gene: [02p12/IGKJ1] immunoglobulin,
kappa subunit, J1 region;
Gene: [02p12/IGKJ2] immunoglobulin,
kappa subunit, J2 region;
Gene: [02p12/IGKJ3] immunoglobulin,
kappa subunit, J3 region;
Gene: [02p12/IGKJ4] immunoglobulin,
kappa subunit, J4 region;
Gene: [02p12/IGKJ5] immunoglobulin,
kappa subunit, J5 region;
Gene: [02p12/IGKV4F1]
immunoglobulin, kappa VAR-region, group IV, polypeptide 1;
Gene: [02p12/IGKVA10]
immunoglobulin, kappa VAR-region, group N/A, polypeptide 10;
Gene: [02p12/IGKVA11]
immunoglobulin, kappa VAR-region, group III/A, polypeptide 11;
Gene: [02p12/IGKVA13]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 13;
Gene: [02p12/IGKVA14]
immunoglobulin, kappa VAR-region, group N/A, polypeptide 14;
Gene: [02p12/IGKVA17]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 17;
Gene: [02p12/IGKVA18]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 18;
Gene: [02p12/IGKVA19]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 19;
Gene: [02p12/IGKVA1]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 1; [IGKV
]
Gene: [02p12/IGKVA23]
immunoglobulin, kappa VAR-region, group II/A, peptide 23;
Gene: [02p12/IGKVA24]
immunoglobulin, kappa VAR-region, group II/A, peptide 24;
Gene: [02p12/IGKVA25]
immunoglobulin, kappa VAR-region, group I/A, peptide 25;
Gene: [02p12/IGKVA26]
immunoglobulin, kappa VAR-region, group N/A, peptide 26;
Gene: [02p12/IGKVA27]
immunoglobulin, kappa VAR-region, group III/A, peptide 27;
Gene: [02p12/IGKVA29]
immunoglobulin, kappa VAR-region, group II/A, peptide 29;
Gene: [02p12/IGKVA2]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 2;
Gene: [02p12/IGKVA30]
immunoglobulin, kappa VAR-region, group I/A, peptide 30;
Gene: [02p12/IGKVA3]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 3;
Gene: [02p12/IGKVA7]
immunoglobulin, kappa VAR-region, group II/A, polypeptide 7;
Gene: [02p12/IGKVA8]
immunoglobulin, kappa VAR-region, group II/A, peptide 8;
Gene: [02p12/IGKVA9]
immunoglobulin, kappa VAR-region, group I/A, polypeptide 9;
Gene: [02p12/IGKVAP1]
immunoglobulin, kappa VAR-region, group I/A, psi-1;
Gene: [02p12/IGKVAP2]
immunoglobulin, kappa VAR-region, group II/A, psi-2;
Gene: [02p12/IGKVAP3]
immunoglobulin, kappa VAR-region, group III/A, psi-3;
Gene: [02p12/IGKVAP4]
immunoglobulin, kappa VAR-region, group II/A, psi-4;
Gene: [02p12/IGKVAP5]
immunoglobulin, kappa VAR-region, group I/A, psi-5;
Gene: [02p12/IGKVAP6]
immunoglobulin, kappa VAR-region, group II/A, psi-6;
Gene: [02p12/IGKVAP7]
immunoglobulin, kappa VAR-region, group III/A, psi-7;
Gene: [02p12/IGKVAP8]
immunoglobulin, kappa VAR-region, group II/A, psi-8;
Gene: [02p12/IGKVL10]
immunoglobulin, kappa VAR-region, group II/L, peptide 10;
Gene: [02p12/IGKVL12]
immunoglobulin, kappa VAR-region, group I/L, peptide 12;
Gene: [02p12/IGKVL13]
immunoglobulin, kappa VAR-region, group III/L, peptide 13;
Gene: [02p12/IGKVL15]
immunoglobulin, kappa VAR-region, group I/L, peptide 15;
Gene: [02p12/IGKVL16]
immunoglobulin, kappa VAR-region, group I/L, peptide 16;
Gene: [02p12/IGKVL17]
immunoglobulin, kappa VAR-region, group III/L, peptide 17;
Gene: [02p12/IGKVL18]
immunoglobulin, kappa VAR-region, group I/L, peptide 18;
Gene: [02p12/IGKVL1]
immunoglobulin, kappa VAR-region, group II/L, peptide 1;
Gene: [02p12/IGKVL3]
immunoglobulin, kappa VAR-region, group I/L, peptide 3;
Gene: [02p12/IGKVL4]
immunoglobulin, kappa VAR-region, group III/L, peptide 4;
Gene: [02p12/IGKVL6]
immunoglobulin, kappa VAR-region, group I/L, peptide 6;
Gene: [02p12/IGKVL7]
immunoglobulin, kappa VAR-region, group I/L, peptide 7;
Gene: [02p12/IGKVL8]
immunoglobulin, kappa VAR-region, group III/L, peptide 8;
Gene: [02p12/IGKVL9]
immunoglobulin, kappa VAR-region, group I/L, peptide 9;
Gene: [02p12/IGKVLP1]
immunoglobulin, kappa VAR-region, group I/L, psi-1;
Gene: [02p12/IGKVLP2]
immunoglobulin, kappa VAR-region, group II/L, psi-2;
Gene: [02p12/IGKVLP3]
immunoglobulin, kappa VAR-region, group I/L, psi-3;
Gene: [02p12/IGKVLP4]
immunoglobulin, kappa VAR-region, group II/L, psi-4;
Gene: [02p12/IGKVO10]
immunoglobulin, kappa VAR-region, group x/O, polypeptide 10;
Gene: [02p12/IGKVO9]
immunoglobulin, kappa VAR-region, group I/O, polypeptide 9;
Gene: [02p12/IGKVW1]
immunoglobulin, kappa VAR-region, group x/W, polypeptide 1;
Gene: [02p12/PAP]
pancreatitis-associated protein;
Gene: [02p12/REG1A] regenerating
islet-derived 1 alpha (pancreatic stone protein, pancreatic thread
protein); [REG PSP PTP ]
Gene: [02p12/REG1B] regenerating
islet-derived 1 beta (pancreatic stone protein, pancreatic thread
protein);
Gene: [02p12/REGP] regenerating
islet-derived pseudogene; [REGL
]
Gene: [02p13/ANX4] annexin IV
(lipocortin IV; endonexin I; chromobindin 4); placental anticoagulant
protein II (calcimedin 35-beta); [PAP2 ]
Gene: [02p13/AUP1] ancient ubiquitous
protein 1;
Gene: [02p13/DCTN1] dynactin 1 (p150
and p135, Glued (Drosophila) homolog);
Gene: [02p13/DGUOK] deoxyguanosine
kinase;
Gene: [02p13/EGR4] early growth
response 4 (transcription factor); zinc finger protein pAT133; [pAT133
]
Gene: [02p13/FRA2E] fragile site
2p13, aphidicolin type, common;
Gene: [02p13/GFPT]
glutamine-fructose-6-phosphate transaminase;
Gene: [02p13/LGMD2B] limb girdle
muscular dystrophy 2B (autosomal recessive);
Gene: [02p13/MAD] MAD protein
(MAX-binding protein; MAX dimerizer);
Gene: [02p13/OTX1] orthodenticle
(Drosophila) homolog 1; homeobox protein OTX1;
Gene: [02p13/PARK3] Parkinson
disease, dominant Lewy-body, 3;
Gene: [02p13/RTKN] rhotekin; [B5
]
Gene: [02p13/TGFA] transforming
growth factor, alpha; [TGF1 ETGF ]
Gene: [02p131/ACTA3] actin, alpha
3, smooth muscle, enteric (formerly: gamma-2 actin); [ACTG2 ]
Gene: [02p131/HK2] hexokinase 2;
noninsulin-dependent diabetes mellitus, association with (NIDDM;
MIM:125853);
Gene: [02p16/DHRD] Doyne honeycomb
retinal degeneration (autosomal dominant radial drusen);
Gene: [02p16/FBNL] fibrillin-like
peptide;
Gene: [02p16/GTBP] G/T
mismatch-binding protein (p160); mutS (E. coli) homolog 6; colorectal
cancer, hereditary, non-polyposis, type 5; [GTMBP MSH6 ]
Gene: [02p16/MSH2] mutS (E. coli)
homolog 2; colon cancer, nonpolyposis type 1; [COCA1]
Gene: [02p16/XPO1] exportin 1
(required for chromosome region maintenance; CRM1, yeast, homolog); [CRM1
]
Gene: [02p162/FRA2D] fragile site
2p16.2, aphidicolin type, common;
Gene: [02p163/SLC3A1] solute
carrier family 3, member 1; cystine, dibasic and neutral amino acid
transport, activator ATR1; cystinuria, type I (MIM:220100); [ATR1 D2H
]
Gene: [02p2/ADCY3] adenylate cyclase
3;
Gene: [02p2/APOB] apolipoprotein B
(including Agx antigen); normotriglyceridemic abetalipoproteinemia,
Steinberg type; familial hypobetalipoproteinemia; acanthocytosis
(deficiency of apolipoprotein B; MIM:200100); [APOB100 ]
Gene: [02p2/CAD] CAD trifunctional
protein; carbamoyl phosphate synthetase 2, soluble (EC:6.3.4.16); aspartate
transcarbamylase (EC:2.1.3.2); dihydroorotase (EC:3.5.2.3);
Gene: [02p2/DFNB9] deafness,
autosomal recessive 9; [NSRD9
]
Gene: [02p2/DTNB] dystrobrevin,
beta;
Gene: [02p2/ETM2] tremor, familiar
essential, 2; [ETM FET1
]
Gene: [02p2/FOSL2] FOS-like antigen
2;
Gene: [02p2/MPV17] MpV17 transgene,
murine homolog, glomerulosclerosis;
Gene: [02p2/PRKR] protein kinase,
interferon-inducible double stranded RNA dependent (p68);
Gene: [02p2/RRM2] ribonucleotide
reductase M2 polypeptide;
Gene: [02p2/SFRS7] splicing factor,
arginine/serine-rich 7 (35kD); [9G8
]
Gene: [02p2/SLC8A1] solute carrier
family 8 (sodium-calcium exchanger), member 1; [NCX1 ]
Gene: [02p2/SOS1] son of sevenless
(Drosophila) homolog 1; guanine nucleotide exchange factor SOS1;
Gene: [02p2/SPG4] spastic paraplegia 4
(autosomal dominant);
Gene: [02p2/TPO] thyroid peroxidase;
hypothyroidism due to thyroid peroxidase deficiency;
Gene: [02p2/XDH] xanthine dehydrogenase
(EC:1.1.1.204); xanthine oxidase (EC:1.1.3.22); xanthinuria, type 1 (due to
xanthine dehydrogenase deficiency);
Gene: [02p21/CALM2] calmodulin 2
(phosphorylase kinase, delta);
Gene: [02p21/CYP1B1] cytochrome
P450, subfamily IB (dioxin-inducible), polypeptide 1; glaucoma 3, primary
infantile, A (buphtalmos; MIM:231300);
Gene: [02p21/FSHR] follicle
stimulating hormone receptor; ovarian dysgenesis 1 (hypergonadotropic;
gonadal dysgenesis, type XX; MIM:233300); ovarian sex cord tumors; [ODG1
XXGD ]
Gene: [02p21/HPE2] holoprosencephaly
2, alobar or semilobar;
Gene: [02p21/LHCGR] luteinizing
hormone/choriogonadotropin receptor; male pseudohermaphroditism with Leydig
cell hypoplasia/agenesis; gonadotropin unresponsiveness (precocious
puberty, familial male; MIM:176410); micropenis; [LCGR ]
Gene: [02p21/LSL] leptin, serum levels
of; obesity, predisposition to?;
Gene: [02p21/SPTBN1] spectrin,
beta, non-erythrocytic 1;
Gene: [02p223/GCKR] glucokinase
(hexokinase 4) regulatory protein;
Gene: [02p23/ALK] anaplastic lymphoma
kinase (Ki-1); non-Hodgkin's lymphoma with t(2;5)(p23;q35);
Gene: [02p23/HADHA] trifunctional
protein, mitochondrial, alpha subunit; 3-hydroxyacyl-CoA dehydrogenase,
long chain (EC:1.1.1.35); enoyl-CoA hydratase, long chain (EC:4.2.1.7);
gastrin binding protein; long chain 3-hydroxyacyl-CoA dehydrog
Gene: [02p23/HADHB] trifunctional
protein, mitochondrial, beta subunit; 3-ketoacyl-CoA thiolase
(EC:2.3.1.16); trifunctional protein deficiency, type 2 (due to deficiency
of beta subunit);
Gene: [02p23/KHK] ketohexokinase
(fructokinase); fructosuria (hepatic fructokinase deficiency);
Gene: [02p23/KIF3C] kinesin family
member 3C;
Gene: [02p23/MDH1] malate
dehydrogenase, NAD (soluble);
Gene: [02p23/PPIL1] peptidylprolyl
cis-trans-isomerase (cyclophilin)-like 1; cyclophilin-related protein 1;
[CYPL1
]
Gene: [02p23/PPP1CB] protein
phosphatase 1, catalytic subunit, beta isoform;
Gene: [02p23/SRD5A2]
steroid-5-alpha-reductase, alpha polypeptide 2; pseudohermaphroditism, male
(steroid-5-alpha-reductase alpha 2 deficiency); pseudovaginal
perineoscrotal hypospadias;
Gene: [02p233/POMC]
proopiomelanocortin (adrenocorticotropin/beta-lipotropin); lipotropins
(alpha-, beta-, gamma-LPH); melanotropins (alpha-, beta-, gamma-MSH);
endorphins (alpha, beta, gamma); obesity, adrenal insufficiency, and red
hair;
Gene: [02p24/DDX1] DEAD/H
(Asp-Glu-Ala-Asp/His) box polypeptide 1;
Gene: [02p24/KCNS3] potassium
voltage-gated channel, delayed-rectifier, subfamily S, member 3; [Kv9.3
]
Gene: [02p241/MYCN] avian
myelocytomatosis viral related oncogene; [NMYC]
Gene: [02p242/FRA2C] fragile site
2p24.2, aphidicolin type, common;
Gene: [02p25/ACP1] acid phosphatase
1, soluble;
Gene: [02p25/ID2] inhibitor of DNA
binding 2, dominant negative helix-loop-helix protein;
Gene: [02p25/ODC1] ornithine
decarboxylase 1;
Gene: [02p25/RPS7] ribosomal protein
S7;
Gene: [02p25/SOX11] SRY (sex
determining region Y)-box 11;
Gene: [02p25/YWHAZ] tyrosine
3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta
polypeptide; tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation
protein, delta polypeptide (phosphorylated); brain protein 14-3-3,
Gene: [02q/BARD1] BRCA1-associated
RING domain gene 1; ovarian cancer;
Gene: [02q/EN1] homeobox engrailed
homolog 1;
Gene: [02q/EVX2] even-skipped homeo box
2 (homolog of Drosophila eve);
Gene: [02q/EXTL2P] exostoses
(multiple)-like 2 pseudogene;
Gene: [02q/FRZB] frizzled-related
protein; frizzled (Drosophila) homolog-related; [SFRP3
]
Gene: [02q/GAPDL3]
glyceraldehyde-3-phosphate dehydrogenase-like 3;
Gene: [02q/GNAQP] guanine nucleotide
binding protein (G protein), alpha q pseudogene;
Gene: [02q/GYPC] glycophorin C (Gerbich
blood group); [GE GPC GLPC ]
Gene: [02q/IL1R2] interleukin 1
receptor, type II (beta); [IL1RB ]
Gene: [02q/LCO] protooncogene LCO (liver
cancer oncogene); hepatocellular carcinoma (HCC; protooncogene LCO); [LCA
HCC
]
Gene: [02q/NCL] nucleolin;
Gene: [02q/NIDDM1]
non-insulin-dependent diabetes mellitus (common, type 2) 1
(MIM:125853);
Gene: [02q/NPPC] natriuretic peptide
precursor C;
Gene: [02q/RAB6] oncogene RAS-family,
member rab6;
Gene: [02q/RNU20] RNA, U20 small
nuclear;
Gene: [02q/SCN3A] sodium channel,
voltage-gated, type III, alpha polypeptide;
Gene: [02q/SRMS] src-related kinase
lacking C-terminal regulatory tyrosine and N-terminal myristylation
sites;
Gene: [02q/TUBA1] tubulin, alpha 1
(testis specific); [TUBAT ]
Gene: [02q/VIS1] viral integration site
1 (oncogene HIS-1); [HIS-1 HS1
]
Gene: [02q1/ATP6B1] ATPase, H+
transporting, lysosomal (vacuolar proton pump), beta polypeptide, 56/58kD,
isoform 1 (kidney); vacuolar proton pump 3 (58kD subunit), isoform 1
(kidney);
Gene: [02q1/BUB1] budding uninhibited
by benzimidazoles 1 (yeast homolog); mitotic checkpoint protein kinase
BUB1; colorectal cancer with chromosomal instability;
Gene: [02q1/COX5B] cytochrome c
oxidase subunit Vb;
Gene: [02q1/ED3] ectodermal dysplasia
3, anhidrotic; [ADHED
]
Gene: [02q1/GABRI] diazepam binding
inhibitor; acyl-CoA binding protein; anxiety, pathologic (liability?); [DBI
ACBP ]
Gene: [02q1/GLC1B] glaucoma 1, open
angle, B (adult-onset); [POAG
]
Gene: [02q1/HTR5B]
5-hydroxytryptamine (serotonin) receptor 5B;
Gene: [02q1/IGKDEL] immunoglobulin
kappa deleting element or like; [IGKDE
]
Gene: [02q1/IGO1] immunoglobulin
orphon (transposed element) 1;
Gene: [02q1/INHBB] inhibin, beta B;
activin, beta B;
Gene: [02q1/LAF4] lymphoid nuclear
protein 4;
Gene: [02q1/MAL] mal, T-cell
differentiation protein;
Gene: [02q1/PAX8] paired box homeotic
gene 8;
Gene: [02q1/RALB] simian leukemia
viral oncogene homolog B (ras related);
Gene: [02q1/RANBP2L1] RAN binding
protein 2 like 1 (RANBP2-alpha);
Gene: [02q1/RANBP2] RAN binding
protein 2; nucleoporin, 358kD; [NUP358 ]
Gene: [02q1/SLC20A1] solute carrier
family 20 (phosphate transporter), member 1; gibbon ape leukemia virus
receptor 1; [GLVR1
]
Gene: [02q11/DUSP2] dual specificity
phosphatase 2 (EC:3.1.3.48 and EC:3.1.3.16);
Gene: [02q11/SULT1C1]
sulfotransferase family 1C1;
Gene: [02q112/FRA2A] fragile site
2q11.2, folic acid type, rare;
Gene: [02q112/RPL31] ribosomal
protein L31;
Gene: [02q112/ST2H] growth
stimulation-expressed gene (mouse) homolog; ST2 protein;
Gene: [02q12/IL1R1] interleukin 1
receptor, type I (alpha; antigen CDW121A); [IL1R IL1RA ]
Gene: [02q12/ZAP70] zeta-chain (TCR)
associated protein kinase (70 kD); syk-related tyrosine kinase; protein
tyrosine kinase ZAP-70 (zeta-associated protein, 70kD); selective T-cell
defect;
Gene: [02q13/FRA2B] fragile site
2q13, folic acid type, rare;
Gene: [02q13/IL1A] interleukin 1,
alpha (hematopoietin-1); rheumatoid arthritis, juvenile, association with;
[IL1 ]
Gene: [02q13/IL1B] interleukin 1,
beta;
Gene: [02q13/LIS2P1] lissencephaly
sequence pseudogene; [LISP1
]
Gene: [02q13/MALL] mal, T-cell
differentiation protein-like;
Gene: [02q13/NPHP1] src homology 3
domain containing protein NPHP1; nephronophthisis 1 (juvenile); medullary
cystic kidney disease (autosomal recessive);
Gene: [02q13/PROC] protein C (serine
protease destroying coagulation factors Va and VIIIa); thrombophilia,
hereditary (recurrent venous thrombosis, protein C deficiency);
Gene: [02q14/AMPHL]
amphiphysin-like; box dependent MYC interacting protein 1 (BIN1);
amphiphysin II; [BIN1 SH3P9
]
Gene: [02q14/GLI2]
chromatin-associated GLI-phosphoprotein 2; zinc finger oncoprotein GLI2;
GLI-Kruppel family member GLI2;
Gene: [02q141/SCTR] secretin
receptor;
Gene: [02q142/IL1RN] interleukin 1
receptor antagonist;
Gene: [02q2/ACVR1] activin A
receptor, type I (65kD); activin A receptor, type II-like kinase
2;
Gene: [02q2/CACNB4] calcium channel,
voltage-dependent, beta 4 subunit;
Gene: [02q2/GPR39] G protein-coupled
receptor 39;
Gene: [02q2/GRB14] growth factor
receptor-bound protein 14;
Gene: [02q2/NEM2] nemaline myopathy 2,
autosomal recessive;
Gene: [02q2/NURR1] nuclear receptor
related 1 (transcriptionally inducible); nuclear receptor of T cells (NOT);
transcriptionally inducible nuclear receptor (TINUR); [NOT TINUR]
Gene: [02q2/SCN6A] sodium channel,
voltage-gated, type VI, alpha polypeptide;
Gene: [02q21/CHRNG] cholinergic
receptor, nicotinic, gamma polypeptide (muscle); [ACHRG ]
Gene: [02q21/ERCC3] excision repair
cross-complementing rodent repair deficiency, complementation group 3;
basic transcription factor 2 (transcription factor TFIIH p89 polypeptide);
xeroderma pigmentosum, complementation group B; trichothio
Gene: [02q21/LCT] lactase, intestinal
(EC:3.2.1.108); phlorizin hydrolase (EC:3.2.1.62); disaccharide intolerance
II (lactase deficiency); disaccharide intolerance III (adult lactase
deficiency; MIM:223100);
Gene: [02q21/MCM6] minichromosome
maintenance deficient (S. pombe) 6; DNA replication licensing factor
MCM6;
Gene: [02q21/MGAT5] mannosyl
(alpha-1,6-)-glycoprotein
beta-1,6-N-acetylglucosaminyltransferase;
Gene: [02q21/NPY3R] neuropeptide Y
receptor Y3-like receptor; G protein-coupled receptor LCR1 homolog; fusin
(HIV-1 entry cofactor); leukocyte-derived seven-transmembrane domain
receptor (LESTR); CXC chemokine receptor 4 (CXCR4); [NPYY3 LCR
Gene: [02q21/PHBP4] prohibitin
pseudogene 4;
Gene: [02q21/POLR2D] RNA polymerase
II (DNA directed) polypeptide D (16kD);
Gene: [02q213/FRA2F] fragile site
2q21.3, aphidicolin type, common;
Gene: [02q223/FRA2K] fragile site
2q22.3, folic acid type, rare;
Gene: [02q23/FAP] fibroblast
activation protein, alpha;
Gene: [02q23/GCG] glucagon;
hyperproglucagonemia (glucagon);
Gene: [02q23/SCN2A] sodium channel,
voltage-gated, type II, alpha polypeptide (brain) (see also MIM:601219);
[NAC2 HBSCII ]
Gene: [02q24/NEB] nebulin;
Gene: [02q24/PFIC2] progressive
familial intrahepatic cholestasis 2;
Gene: [02q24/SCN1A] sodium channel,
voltage-gated, type I, alpha polypeptide (brain); [SCN1 NAC1 ]
Gene: [02q241/GPD2]
glycerol-3-phosphate dehydrogenase 2 (beta, mitochondrial); diabetes
mellitus, type II;
Gene: [02q241/KCNJ3] potassium
inwardly-rectifying channel, subfamily J, member 3;
Gene: [02q243/DPP4]
dipeptidylpeptidase IV (antigen CD26); antigen CD26 (p250; monoclonal
antibodies B1.19.2); adenosine deaminase complexing protein 2;
Gene: [02q3/ACADL] acyl-CoA
dehydrogenase L (fatty acid long straight-chain C8 to C16); hypoglycemia,
intermittent non-ketotic (LCAD deficiency); dicarboxylicaciduria (LCAD
deficiency);
Gene: [02q3/ALS2] amyotrophic lateral
sclerosis 2 (juvenile);
Gene: [02q3/CASP10] caspase 10,
apoptosis-related cysteine protease;
Gene: [02q3/CHE2] cholinesterase 2
(serum; C5 band; pseudocholinesterase 2);
Gene: [02q3/CHGC] chromogranin C
(secretogranin 2); [SCG2 ]
Gene: [02q3/CHN1] chimerin (chimaerin)
1 (alpha-chimerin, n-chimerin); [RhoGAP2 ]
Gene: [02q3/CHRND] cholinergic
receptor, nicotinic, delta polypeptide (muscle); [ACHRD ]
Gene: [02q3/COL3A1] collagen, type
III, alpha 1; Ehlers-Danlos syndrome, type IV (ecchymotic, Sack-Barabas
type; autosomal dominant, MIM:130050); Ehlers-Danlos syndrome, type IV
(ecchymotic, Sack-Barabas type; autosomal recessive, MIM:22535
Gene: [02q3/COL4A3] collagen, type
IV, alpha 3 (Goodpasture antigen); Alport syndrome, autosomal recessive,
type I (MIM:203780); Goodpasture syndrome (MIM:233450);
Gene: [02q3/COL4A4] collagen, type
IV, alpha 4; Alport syndrome, autosomal recessive, type II (MIM:203780);
hematuria, benign familial (141200);
Gene: [02q3/COL5A2] collagen, type
V, alpha 2;
Gene: [02q3/CREB1] cAMP responsive
element binding protein 1;
Gene: [02q3/CRYBA2] crystallin, beta
A2 polypeptide;
Gene: [02q3/CRYGA] crystallin, gamma
A polypeptide; [CRYG1 CRYG1P ]
Gene: [02q3/CRYGB] crystallin, gamma
B polypeptide; [CRYG2 CRYG2P ]
Gene: [02q3/CRYGC] crystallin, gamma
C polypeptide; [CRYG3 ]
Gene: [02q3/CRYGD] crystallin, gamma
D polypeptide; cataract, Coppock-like; [CCL CRYG4 ]
Gene: [02q3/CRYGEP1] crystallin,
gamma E pseudogene 1; [CRYG5
]
Gene: [02q3/CRYGFP1] crystallin,
gamma F pseudogene 1; [CRYG6
]
Gene: [02q3/CRYGGP1] crystallin,
gamma G pseudogene 1;
Gene: [02q3/CRYGP1] crystallin,
gamma polypeptide pseudogene 1;
Gene: [02q3/CRYGP2] crystallin,
gamma polypeptide pseudogene 2;
Gene: [02q3/CYP27A1] cytochrome
P450, subfamily XXVIIA (steroid 27-hydroxylase), polypeptide 1;
cerebrotendinous xanthomatosis (cerebral cholesterinosis; van
Bogaert-Scherer-Epstein disease);
Gene: [02q3/E2F3P2] E2F
transcription factor 3 pseudogene 2;
Gene: [02q3/FACL3] fatty-acid-CoA
ligase, long-chain 3;
Gene: [02q3/FTHL3] ferritin, heavy
polypeptide-like 3;
Gene: [02q3/FUCA1P]
alpha-L-fucosidase 1 pseudogene;
Gene: [02q3/FZD5] frizzled
(Drosophila) homolog 5;
Gene: [02q3/GBX2] gastrulation brain
homeo box 2;
Gene: [02q3/GLS] glutaminase
(phosphate-activated);
Gene: [02q3/GPC1] glypican 1;
Gene: [02q3/HTR2B]
5-hydroxytryptamine (serotonin) receptor 2B;
Gene: [02q3/ICR2B] ichthyosis
congenita IIB (lamellar ichthyosis, type 2); [LI2
]
Gene: [02q3/IGFB2] insulin-like
growth factor binding protein 2 (36kD); [IBP2 IGFBP2 ]
Gene: [02q3/IHH] Indian hedgehog
(Drosophila) homolog;
Gene: [02q3/INHA] inhibin, alpha;
activin, alpha;
Gene: [02q3/INPP5D] inositol
polyphosphate-5-phosphatase, type IV, 145kD;
Gene: [02q3/ITGA4] integrin, alpha 4
(antigen CD49D; alpha 4 subunit of VLA-4 receptor); very late activation
protein-4 receptor (MIM:192972); [CD49D VLA4 ]
Gene: [02q3/ITGAV] integrin, alpha V
(antigen CD51); vitronectin receptor, alpha polypeptide; [CD51 VNRA
]
Gene: [02q3/LRP2] low density
lipoprotein receptor-related protein 2 (glycoprotein 330;
megalin);
Gene: [02q3/MYL1] myosin, light
polypeptide 1, alkali; skeletal, fast; [MLC1F HSLC1 ]
Gene: [02q3/NDUFS1] NADH
dehydrogenase (ubiquinone) Fe-S protein 1 (75kD; NADH-CoQ reductase;
EC:1.6.5.3, EC:1.6.99.3);
Gene: [02q3/PI7] protease inhibitor 7
(protease nexin I); [PNI ]
Gene: [02q3/PMS1] postmeiotic
segregation increased (S. cerevisiae) 1 (mismatch repair gene); hereditary
nonpolyposis colon cancer (HNPCC); [PMSL1 ]
Gene: [02q3/PNKD] paroxysmal
nonkinesiogenic dyskinesia; choreoathetosis, familial paroxysmal
(Mount-Reback syndrome); dystonia 8; [FPD1 PDC
]
Gene: [02q3/PPH1] primary pulmonary
hypertension 1; [PPH
]
Gene: [02q3/PTPRN] protein tyrosine
phosphatase, receptor type, N; islet cell antigen 512 (IA-2); islet cell
autoantigen 3 (ICA512);
Gene: [02q3/RPE]
ribulose-5-phosphate-3-epimerase;
Gene: [02q3/RPL37A] ribosomal
protein L37a;
Gene: [02q3/SCYA20] small inducible
cytokine subfamily A (Cys-Cys), member 20; beta-chemokine Exodus;
macrophage inflammatory protein 3 alpha (MIP-3-alpha); liver and
activation-regulated chemokine (LARC); [MIP3A LARC ]
Gene: [02q3/TNS] tensin;
Gene: [02q3/UBL1] ubiquitin-like 1,
12kD; sentrin; ubiquitin-like protein SMT3C; [SMTH3 SMT3C ]
Gene: [02q3/VGL] vigilin;
Gene: [02q3/ZNF142] zinc finger
protein 142 (clone pHZ-49); [KIAA0236 ]
Gene: [02q31/FRA2G] fragile site
2q31, aphidicolin type, common;
Gene: [02q31/GAD1] glutamate
decarboxilase 1 (brain, 67kD); pyridoxine dependency with seizures (GAD
deficiency);
Gene: [02q31/HOXD10] homeo box
D10(4D), homologous to mouse Hox-4.4; [HOX4D
]
Gene: [02q31/HOXD11] homeo box
D11(4F), homologous to mouse Hox-4.6; [HOX4F
]
Gene: [02q31/HOXD12] homeo box
D12(4H), homologous to mouse Hox-4.8; [HOX5 HOX4H
]
Gene: [02q31/HOXD13] homeo box
D13(4I), homologous to mouse Hox-4.9; synpolydactyly (syndactyly type II;
MIM:186000); [HOX5 HOX4I
]
Gene: [02q31/HOXD1] homeo box
D1(4G), homologous to mouse Hox-4.7; [HOX4G
]
Gene: [02q31/HOXD3] homeo box
D3(4A), homologous to mouse Hox-4.1; [HOX4 HOX4A
]
Gene: [02q31/HOXD4] homeo box
D4(4B), homologous to mouse Hox-4.2; [HOX4B HOX5
]
Gene: [02q31/HOXD8] homeo box
D8(4E), homologous to mouse Hox-4.5; [HOX4E
]
Gene: [02q31/HOXD9] homeo box
D9(4C), homologous to mouse Hox-4.3; [HOX4C
]
Gene: [02q31/IDDM7]
insulin-dependent diabetes mellitus 7;
Gene: [02q31/IL17] interleukin 17;
cytotoxic T-lymphocyte-associated serine esterase 8;
Gene: [02q31/NFE2L2] nuclear
factor, erythroid-derived 2-like 2; [NRF2
]
Gene: [02q31/SP3] Sp3 transcription
factor;
Gene: [02q31/TMD] tibial muscular
dystrophy, tardive;
Gene: [02q31/TTN] titin;
Gene: [02q32/ARVD4] arrhythmogenic
right ventricular dysplasia 4;
Gene: [02q32/ATF4] activating
transcription factor 4; tax-responsive enhancer element B67; [TXREB
]
Gene: [02q32/CHRNA1] cholinergic
receptor, nicotinic, alpha polypeptide 1 (muscle); [CHRNA ACHRA
]
Gene: [02q32/CREB2] cAMP responsive
element binding protein 2; activating transcription factor 2; [ATF2 TREB7
]
Gene: [02q32/DLX1] distal-less homeo
box 1;
Gene: [02q32/DLX2] distal-less homeo
box 2;
Gene: [02q32/INPP1] inositol
polyphosphate-1-phosphatase;
Gene: [02q32/NEUROD1] neurogenic
differentiation 1;
Gene: [02q32/TFPI] tissue factor
pathway inhibitor; lipoprotein-associated coagulation inhibitor; [LACI
]
Gene: [02q321/FRA2H] fragile site
2q32.1, aphidicolin type, common;
Gene: [02q321/GDF8] growth
differentiation factor 8 (myostatin); [MSTN
]
Gene: [02q33/AOX1] aldehyde oxidase
1; molybdenum cofactor deficiency, type A;
Gene: [02q33/CD28] antigen CD28
(Tp44; T-cell-specific);
Gene: [02q33/CLK1] CDC-like kinase
1;
Gene: [02q33/CTLA4] cytotoxic
T-lymphocyte-associated serine esterase 4; T cell/natural killer cells
serine esterase 4;
Gene: [02q33/FRA2I] fragile site
2q33, aphidicolin type, common;
Gene: [02q33/FZD7] frizzled
(Drosophila) homolog 7; [FzE3
]
Gene: [02q33/IDDM12]
insulin-dependent diabetes mellitus 12;
Gene: [02q33/ORC2L] origin
recognition complex, subunit 2 (yeast homolog)-like; origin of replication
2 (Saccharomyes) homolog-like;
Gene: [02q33/PLCE] phospholipase C,
epsilon (lung carcinoma-related); lung carcinoma?;
Gene: [02q33/PTHR2] parathyroid
hormone receptor 2; [PTHR2R
]
Gene: [02q333/IDH1] isocitrate
dehydrogenase 1 (NADP+), soluble;
Gene: [02q34/EGFR4] avian
erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4; oncogene
homolog ERBB4; protein tyrosine kinase, receptor ERBB4;
Gene: [02q34/FN1] fibronectin 1
(dysfibronectinemic Ehlers-Danlos syndrome X); Ehlers-Danlos syndrome, type
X (dysfibronectinemic; MIM:225310);
Gene: [02q34/IDDM13]
insulin-dependent diabetes mellitus 13;
Gene: [02q34/MAP2]
microtubule-associated protein 2 (280kD; dendrite-specific); [MTB
]
Gene: [02q34/TNP1] transition protein
1 (during histone to protamine replacement);
Gene: [02q35/CPS1] carbamoyl
phosphate synthetase 1, mitochondrial; hyperammonemia II (due to carbamoyl
phosphate synthetase 1 deficiency);
Gene: [02q35/DES] desmin (skeletin;
intermediate filament, muscle type); distal myopathy with
cardiomyopathy;
Gene: [02q35/IL8RA] interleukin 8
receptor, alpha (high affinity; antigen CDW128); chemokine (C-X-C) receptor
1; [CMKAR1 CXCR1
]
Gene: [02q35/IL8RBP] interleukin 8
receptor, beta (high affinity) pseudogene;
Gene: [02q35/IL8RB] interleukin 8
receptor, beta (high affinity);
Gene: [02q35/NRAMP1] natural
resistance-associated macrophage protein 1 (might include Leishmaniasis);
[LSH NRAMP ]
Gene: [02q35/PSMB3] proteasome
(prosome, macropain) subunit, beta type, 3 (homolog of yeast PUP3);
[HC10-II ]
Gene: [02q35/VIL1] villin 1;
Gene: [02q35/XRCC5] X-ray repair
complementing defective repair in Chinese hamster cells 5; thyroid
autoantigen, 80kD (antigen Ku; p80; lupus antigen); ATP-dependent DNA
helicase II, 86kD;
Gene: [02q36/IRS1] insulin receptor
substrate 1; noninsulin-dependent diabetes mellitus (NIDDM, MIM:125853);
[HIRS-1 ]
Gene: [02q36/PAX3] paired box
homeotic gene 3; Waardenburg syndrome, type 1; Waardenburg syndrome, type 3
(with upper limb anomalies; Klein-Waardenburg syndrome; MIM:148820);
rhabdomyosarcoma, type 2 (alveolar; MIM:268220); craniofacial-dea
Gene: [02q36/PDE6D]
phosphodiesterase 6D, cGMP-specific, rod, delta (17kD);
Gene: [02q36/SLC4A3] solute carrier
family 4, anion exchanger, member 3 (neuronal and cardiac); [AE3 SLC2C
]
Gene: [02q37/ALPIF] alkaline
phosphatase, intestinal, fetal (Kasahara isozyme);
Gene: [02q37/ALPT] alkaline
phosphatase, testicular/T-cell (placental-like 2); alkaline phosphatase,
placental-like (Nagao isozyme); alkaline phosphatase, placental-like
2;
Gene: [02q37/BDMR]
brachydactyly-mental retardation syndrome; Albright hereditary
osteodystrophy, type 3; brachydactyly, type E (MIM:113300);
Gene: [02q37/HDLBP] high density
lipoprotein binding protein;
Gene: [02q37/NEDD5] neural precursor
cell expressed, developmentally down-regulated 5; differentiation 6;
deoxyguanosine triphosphate triphosphohydrolase (deoxy-GTPase);
Gene: [02q37/PSMD1] proteasome
(prosome, macropain) 26S subunit, non-ATPase, 1 (homolog of yeast SEN3);
[S1 P112
]
Gene: [02q37/SPP2] secreted
phosphoprotein 2, 24kD; [spp24 ]
Gene: [02q37/UGT1]
UDP-glucuronosyltransferase 1; Crigler-Najjar syndrome type I (MIM:218800);
Crigler-Najjar syndrome type II (Gilbert syndrome; MIM:143500);
Gene: [02q371/ALPIA] alkaline
phosphatase, intestinal, adult;
Gene: [02q371/ALPPR] alkaline
phosphatase, placental (Regan isozyme);
Gene: [02q371/SAG] S-antigen (retinal
and pineal protein 45 kD; arrestin S); arrestin S (S-antigen); Oguchi
disease (stationary nightblindness; MIM:258100);
Gene: [02q373/AGXT]
alanine-glyoxylate aminotransferase (EC:2.6.1.44; hyperoxaluria I);
serine-pyruvate aminotransferase (EC:2.6.1.51); oxalosis I (hyperoxaluria
I; glycolicaciduria);
Gene: [02q373/COL6A3] collagen,
type VI, alpha 3; Bethlem myopathy;
Gene: [02q373/FRA2J] fragile site
2q37.3, aphidicolin type, common;
Gene: [02q373/GPR35] G
protein-coupled receptor 35;
Gene: [02q373/PDCD1] programmed
cell death 1;
Gene: [02q373/PPP1R7] protein
phosphatase 1, regulatory (inhibitor) subunit 7;
Gene: [02^/ACHM2] achromatopsia (rod
monochromacy) 2; rod monochromacy (RMCH; total colorblindness); [RMCH
]
Gene: [02^/ACTL3] actin-like sequence
3;
Gene: [02^/ADRA2B] adrenergic,
alpha-2B-, receptor; [ADRA2RL1 ]
Gene: [02^/ATP5BL1] ATP synthase, H+
transporting, mitochondrial F1 complex, beta polypeptide-like 1; [ATPMBL1
]
Gene: [02^/ATP5G3] ATP synthase, H+
transporting, mitochondrial F0 complex, subunit c (subunit 9), isoform
3;
Gene: [02^/CYP1ARA] aryl hydrocarbon
hydroxylase inducibility; bronchogenic cancer (liability?); [AHHR AHHI
]
Gene: [02^/DTYMK] deoxythymidylate
kinase;
Gene: [02^/EEF1B2] eukaryotic
translation elongation factor 1 beta 2;
Gene: [02^/HNMT] histamine
N-methyltransferase;
Gene: [02^/HPCAL1] hippocalcin-like
peptide 1;
Gene: [02^/HVBS4] hepatitis B virus
integration site 4;
Gene: [02^/IFNB5] interferon, beta 5,
fibroblast;
Gene: [02^/INSL1] insulin-like
1;
Gene: [02^/ITGA6] integrin, alpha 6;
epidermolysis bullosa, junctional;
Gene: [02^/ITGB6] integrin, beta
6;
Gene: [02^/LDHAL3] lactate
dehydrogenase A-like 3;
Gene: [02^/LTBP1] latent transforming
growth factor beta binding protein 1;
Gene: [02^/MIC18] antigen MIC18
(monoclonal antibody AUA1);
Gene: [02^/MSK8] antigen MSK8
(monoclonal antibody L230);
Gene: [02^/NEFLL1] neurofilament,
light polypeptide-like 1;
Gene: [02^/NPAS2] neuronal PAS domain
protein 2; [MOP4
]
Gene: [02^/PCH1] protein spot in 2-D
gels (MM 250 kD; pI 7.0);
Gene: [02^/PLGL]
plasminogen-like;
Gene: [02^/PTMA] prothymosin, alpha
(gene sequence 28); [TMSA ]
Gene: [02^/RACH] acetylcholinesterase
derepressor; [ACEE
]
Gene: [02^/RAD52P] RAD52
pseudogene;
Gene: [02^/SLC9A2] solute carrier
family 9 (sodium/hydrogen exchanger), isoform 2; [NHE2
]
Gene: [02^/SLC9A4] solute carrier
family 9 (sodium/hydrogen exchanger), isoform 4; [NHE4
]
Gene: [02^/TACR1] tachykinin receptor
1 (substance P receptor, neurokinin 1 receptor); [NK1R ]
Gene: [02^/TMSL2] thymosin-like
2;
Gene: [02^/TNFAI6] tumor necrosis
factor, alpha-induced protein 6; [TNFAIP6 ]
Gene: [02^/TSE2] tissue specific
extinguisher 2;
Gene: [02^/UCN] urocortin; [UROC
]
Gene: [02^/UGP2] UDP-glucose
pyrophosphorylase 2;
Gene: [02^/ZNF2] zinc finger protein 2
(A1-5);
Gene: [03p/BBS3] Bardet-Biedl syndrome
3;
Gene: [03p/DFNB6] deafness, autosomal
recessive 6; [NSRD6
]
Gene: [03p/DNASE1L3]
deoxyribonuclease I-like 3;
Gene: [03p/ITIH4] inter-alpha
(globulin) inhibitor, H polypeptide-like 1; inter-alpha (globulin)
inhibitor H4; inter-alpha-trypsin inhibitor, heavy chain-related protein;
plasma kallikrein-sensitive glycoprotein; [IHRP PK120 ]
Gene: [03p/LRS1] Larsen syndrome 1
(autosomal dominant);
Gene: [03p/MSK10] antigen MSK10
(monoclonal antibody AJ425);
Gene: [03p/MSK32] antigen MSK32
(monoclonal antibody K66);
Gene: [03p/MSK33] antigen MSK33
(monoclonal antibody SR3);
Gene: [03p/MSK9] antigen MSK9
(monoclonal antibody K15);
Gene: [03p/PEO2] progressive external
ophthalmoplegia, type 2;
Gene: [03p/SCA7] spinocerebellar ataxia
7 (olivopontocerebellar atrophy with retinal degeneration);
Gene: [03p/SEX2] transmembrane protein
SEP;
Gene: [03p/TMF1] TATA element
modulatory factor 1 (123kD);
Gene: [03p/TNNC1] troponin C1, cardiac
and skeletal, slow; [TNCC TNC ]
Gene: [03p/WNT5A] wingless-type MMTV
integration site 5A, human homolog;
Gene: [03p1/HTR1F]
5-hydroxytryptamine (serotonin) receptor 1F;
Gene: [03p1/MITF]
microphthalmia-associated transcription factor; Waardenburg syndrome, type
2A (WS2A; MIM:193510); [WS2A
]
Gene: [03p1/RPL24] ribosomal protein
L24;
Gene: [03p11/POU1F1] POU domain,
class 1, transcription factor 1; pituitary-specific transcription factor 1;
growth hormone factor 1; combined pituitary hormone deficiency; [PIT1
GHF1]
Gene: [03p112/EPHA3] ephrin
receptor EphA3; eph-like tyrosine kinase 1; human embryo kinase 1;
Gene: [03p12/ALDRP] aldehyde
reductase (aldose reductase) pseudogene;
Gene: [03p142/FHIT] fragile
histidine triad gene;
Gene: [03p142/FRA3B] fragile site
3p14.2, aphidicolin type, common;