The Chromosome 7 Annotation Project
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Disease Genes on Chromosome 7

Gene#  Symbol  Full name  OMIM#  Disorder  Location 
AASS  Aminoadipate-semialdehyde synthase  605113  "Saccharopinuria, 268700; Hyperlysinemia, 238700 "  7q31.3 
ABCB1  "ATP-binding cassette, sub-family B (MDR/TAP), member 1"  171050  Colchicine resistance (3)   7q21.1 
ABCB4  "ATP-binding cassette, sub-family B (MDR/TAP), member 4"  171060  "Cholestasis, progressive familial intrahepatic 3, 602347 "  7q21.1 
ABCB8  "ATP-binding cassette, sub-family B (MDR/TAP), member 8"  605464    7q36 
ABP1  Amiloride binding protein 1 (amine oxidase (copper-containing))  104610    7q34-q36 
ACHE  Acetylcholinesterase (YT blood group)  100740  Acute sensitivity to anti-acetylcholinesterases [OMIM:100740]   7q22 
ACRPS  Acropectoral syndrome  605967  Acropectoral syndrome (2)   7q36 
ACTB  "Actin, beta"  102630    7p15-p12 
ADAM22  A disintegrin and metalloproteinase domain 22  603709    7q21 
10  ADCY1  Adenylate cyclase 1 (brain)  103072    7p13-p12 
11  ADCYAP1R1  Adenylate cyclase activating polypeptide 1 (pituitary) receptor type I  102981    7p14 
12  AGR2  Anterior gradient 2 homolog (Xenepus laevis)  606358    7p21.3 
13  AHR  Aryl hydrocarbon receptor  600253    7p15 
14  AIB  "Aneurysm, intracranial berry"  105800  "Aneurysm, intracranial berry (2) "  7q11.2 
15  AIP1  Atrophin-1 interacting protein 1; activin receptor interacting protein 1  606382    7q21 
16  AKR1B1  "Aldo-keto reductase family 1, member B1 (aldose reductase)"  103880    7q35 
17  AMPH  Amphiphysin (Stiff-Man syndrome with breast cancer 128kD autoantigen)  600418  Paraneoplastic Stiff-man syndrome [OMIM:600418]  7p14-p13 
18  AOAH  Acyloxyacyl hydrolase (neutrophil)  102593    7p14-p12 
19  AP1S1  "Adaptor-related protein complex 1, sigma 1 subunit"  603531    7q11.22 
20  APS  Adaptor protein with pleckstrin homology and src homology 2 domains  605300    7q22 
21  AQP1  "Aquaporin 1 (channel-forming integral protein, 28kD)"  107776  "Blood group--colton, 110450; [Aquaporin-1 deficiency] (3) "  7p14 
22  ARF5  ADP-ribosylation factor 5  103188    7q31.3 
23  ARHGEF5  Rho guanine nucleotide exchange factor (GEF) 5  600888    7q33-q35 
24  ARL4  ADP-ribosylation factor-like 4  604786    7p21-p15.3 
25  ASB4  Ankyrin repeat and SOCS box-containing 4  605761    7q21-q22 
26  ASK  Activator of S phase kinase  604281    7q21.3 
27  ASL  Argininosuccinate lyase  207900  Argininosuccinicaciduria (3)   7cen-q11.2 
28  ASNS  Asparagine synthetase  108370    7q21.3 
29  ATP6V0A4  "ATPase, H+ transporting, lysosomal V0 subunit a isoform 4"  605239  "Renal tubular acidosis, distal, autosomal recessive, 602722 "  7q33-q34 
30  AUTS1  Autism susceptibility 1  209850  "{Autism, susceptibility to} (2) "  7q 
31  AZGP1  "Alpha-2-glycoprotein 1, zinc"  194460    7q22.1 
32  BAZ1B  "Bromodomain adjacent to zinc finger domain, 1B"  605681    7q11.23 
33  BCL7B  B-cell CLL/lymphoma 7B  605846    7q11.23 
34  BLVRA  Biliverdin reductase A  109750    7p14-cen 
35  BMIQ1  Body mass index QTL on chromosome 7  606642  "Body mass index, 606641 "  7q32.3 
36  BPGM  "2,3-bisphosphoglycerate mutase"  222800  Hemolytic anemia due to bisphosphoglycerate mutase deficiency (1)   7q31-q34 
37  BRAF  V-raf murine sarcoma viral oncogene homolog B1  164757    7q34 
38  C7orf2  Chromosome 7 open reading frame 2  605522  "Acheiropody, 200500 "  7q36 
39  CACNA2D1  "Calcium channel, voltage-dependent, alpha 2/delta subunit 1"  114204    7q21-q22 
40  CALCR  Calcitonin receptor  114131  "Osteoporosis, involutional, 166710 "  7q21.3 
41  CALD1  Caldesmon 1  114213    7q33 
42  CALML1  Calmodulin-like 1  114181    7pter-p13 
43  CALU  Calumenin  603420    7q32 
44  CAPZA2  "Capping protein (actin filament) muscle Z-line, alpha 2"  601571    7q31.2-q31.3 
45  CARD4  "Caspase recruitment domain family, member 4"  605980    7p15-p14 
46  CASP2  "Caspase 2, apoptosis-related cysteine protease "  600639    7q34-q35 
47  CATR1  CATR tumorigenicity conversion 1  600676    7q32 
48  CAV1  "Caveolin 1, caveolae protein, 22kD"  601047    7q31.1 
49  CAV2  Caveolin 2  601048    7q31.1 
50  CCM1  Cerebral cavernous malformations 1  604214  "Cerebral cavernous malformations 1, 116860 "  7q21-q22 
51  CCM2  Cerebral cavernous malformation 2  603284  Cerebral cavernous malformations-2 (2)   7p15-p13 
52  CD36  "CD36 antigen (collagen type I receptor, thrombospondin receptor)"  173510  Platelet glycoprotein IV deficiency(3); [Macrothrombocytopenia] (1)   7q11.2 
53  CDK5  Cyclin-dependent kinase 5  123831    7q36 
54  CDK6  Cyclin-dependent kinase 6  603368  Splenic lymphoma [OMIM:603368]  7q21-q22 
55  CFTR  "Cystic fibrosis transmembrane conductance regulator, ATP-binding cassette"  602421  "Vas deferens, congenital bilateral aplasia of; Cystic fibrosis; Sweat chloride elevation without CF; {Hypertrypsinemia, neonatal} ; {Pancreatitis, idiopathic} "  7q31.2 
56  CGRP-RCP  Calcitonin gene-related peptide-receptor component protein  606121    7p13 
57  CHDM  Chordoma  215400  Chordoma (2)   7q33 
58  CHN2  Chimerin (chimaerin) 2  602857    7p15.3 
59  CHRM2  "Cholinergic receptor, muscarinic 2"  118493    7q31-q35 
60  CLCN1  "Chloride channel 1, skeletal muscle (Thomsen disease, autosomal dominant)"  118425  "Myotonia, generalized, Myotonia congenita, autosomal dominant, Myotonia levior, recessive"  7q35 
61  CLDN3  Claudin 3  602910    7q11.23 
62  CLECSF5  "C-type (calcium dependent, carbohydrate-recognition domain) lectin, superfamily member 5"  604987    7q33 
63  CMH6  "Cardiomyopathy, hypertrophic 6"  600858  "Cardiomyopathy, familial hypertrophic withWolff-Parkinson-White syndrome"  7q31-qter 
64  CMT2D  Charcot-Marie-Tooth neuropathy 2D  601472  "Charcot-Marie-Tooth neuropathy, type 2D (2) "  7p14 
65  CMT2F  "Charcot-Marie-Tooth disease, axonal, F"  606595  "Charcot-Marie-Tooth disease, type 2F (2) "  7q11-q21 
66  CNTNAP2  Contactin associated protein-like 2  604569    7q35-q36 
67  COG5  Component of oligomeric golgi complex 5  606821    7q31 
68  COL1A2  "Collagen, type I, alpha 2"  120160  "Osteoporosis, involutional, Ehlers-danlos syndrome, type vii, autosomal dominant, Marfan syndrome, atypical "  7q22.1 
69  COPG2  "Coatomer protein complex, subunit gamma 2"  604355    7q32 
70  CPA1  Carboxypeptidase A1 (pancreatic)  114850    7q32 
71  CPA2  Carboxypeptidase A2 (pancreatic)  600688    7q32 
72  CPSF4  "Cleavage and polyadenylation specific factor 4, 30kD subunit"  603052    7q22.1 
73  CRHR2  Corticotropin releasing hormone receptor 2  602034    7p15.3 
74  CRIP1  Cysteine-rich protein 1 (intestinal)  123875    7q11.23 
75  CROT  Carnitine O-octanoyltransferase  606090    7q21.1 
76  CRS  Craniosynostosis  123100  "Craniosynostosis, type 1 (2) "  7p21 
77  CUTL1  "Cut-like 1, CCAAT displacement protein (Drosophila)"  116896    7q22 
78  CYLN2  Cytoplasmic linker 2  603432    7q11.23 
79  CYP3A4  "Cytochrome P450, subfamily IIIA (niphedipine oxidase), polypeptide 4"  124010    7q21.1 
80  CYP3A43  "Cytochrome P450, subfamily IIIA, polypeptide 43"  606534    7q21.1 
81  CYP3A5  "Cytochrome P450, subfamily IIIA (niphedipine oxidase), polypeptide 5"  605325    7q21.1 
82  CYP51  "Cytochrome P450, 51 (lanosterol 14-alpha-demethylase)"  601637    7q21.2-q21.3 
83  DDC  Dopa decarboxylase (aromatic L-amino acid decarboxylase)  107930    7p11 
84  DFNA5  "Deafness, autosomal dominant 5"  600994  "Deafness, autosomal dominant 5 (3) "  7p15 
85  DFNB13  "Deafness, autosomal recessive 13"  603098  "Deafness, autosomal recessive 13 (2) "  7q34-q36 
86  DFNB14  "Deafness, autosomal recessive 14"  603678  "Deafness, autosomal recessive 14 (2) "  7q31 
87  DFNB17  "Deafness, autosomal recessive 17"  603010  "Deafness, autosomal recessive 17 (2) "  7q31 
88  DGKB  "Diacylglycerol kinase, beta (90kD)"  604070    7p22.1 
89  DGKI  "Diacylglycerol kinase, iota"  604072    7q32.3-q33 
90  DIA2  Diaphorase-2  125870   
91  DLD  Dihydrolipoamide dehydrogenase   246900  Lipoamide dehydrogenase deficiency (3)   7q31-q32 
92  DLX5  Distal-less homeo box 5  600028    7q22 
93  DLX6  Distal-less homeo box 6  600030    7q22 
94  DNAH11  "Dynein, axonemal, heavy polypeptide 11"  603339    7p21 
95  DNCI1  "Dynein, cytoplasmic, intermediate polypeptide 1"  603772    7q21.3-q22.1 
96  DNHBL  "Dynein, heavy chain beta-like"  603299    7p15 
97  DPP6  Dipeptidylpeptidase VI  126141    7q36.1-q36.2 
98  DSS1  Deleted in split-hand/split-foot 1 region  601285    7q21.3-q22.1 
99  EEC1  "Ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1"  129900  EEC syndrome-1 (2)   7q11.2-q21.3 
100  EGFR  Epidermal growth factor receptor   131550    7p12 
101  ELMO1  "Engulfment and cell motility 1 (ced-12 homolog, C. elegans)"  606420    7p15.3-p15.2 
102  ELN  "Elastin (supravalvular aortic stenosis, Williams-Beuren syndrome)"  130160  "Williams-beuren syndrome, Supravalvular aortic stenosis, Cutis laxa, "  7q11.23 
103  EN2  Engrailed homolog 2  131310    7q36 
104  EPHA1  EphA1  179610    7q32-q36 
105  EPHB4  EphB4  600011    7q22 
106  EPHB6  EphB6  602757    7q33-q35 
107  EPIM  Epimorphin  132350   
108  EPO  Erythropoietin  133170  Erythremia (1)   7q22 
109  ERV3  Endogenous retroviral sequence 3 (includes zinc finger protein H-plk/HPF9)  131170    7p11.2 
110  ERVK6  "Endogenous retroviral sequence K, 6"  605626   
111  ERVWE1  "Endogenous retroviral family W, env(C7), member 1 (syncytin)"  604659    7q21-q22 
112  ETV1  Ets variant gene 1  600541    7p22 
113  EVX1  "Eve, even-skipped homeo box homolog 1 (Drosophila)"  142996    7p15-p14 
114  EZH2  Enhancer of zeste homolog 2 (Drosophila)  601573    7q35-q36 
115  FDPSL2  Farnesyl diphosphate synthase-like 2 (farnesyl pyrophosphate synthetase-like 2)  134632   
116  FGL2  Fibrinogen-like 2  605351    7q11.23 
117  FHA2  "Hyperaldosteronism, familial, type II"  605635  "Hyperaldosteronism, familial, type II (2) "  7p22 
118  FKBP6  FK506 binding protein 6 (36kD)  604839    7q11.23 
119  FLNC  "Filamin C, gamma (actin binding protein 280)"  102565    7q32-q35 
120  FOXP2  Forkhead box P2  605317  "Specific language impairment, 602081 "  7q31 
121  FTSJ2  FtsJ homolog 2 (E. coli)  606906    7p22 
122  FZD1  Frizzled homolog 1 (Drosophila)  603408    7q21 
123  FZD9  Frizzled homolog 9 (Drosophila)  601766    7q11.23 
124  G7P1  Kinase-like protein  148750    7q22-q32 
125  GABPB1  "GA binding protein transcription factor, beta subunit 1 (53kD)"  600610    7q11.2 
126  GARS  Glycyl-tRNA synthetase  600287    7p15 
127  GBAS  Glioblastoma amplified sequence  603004    7p12 
128  GBX1  Gastrulation brain homeo box 1  603354    7q36 
129  GCF1  Growth control factor 1  139220   
130  GCK  "Glucokinase (hexokinase 4, maturity onset diabetes of the young 2)"  138079  "Hyperinsulinism,, Maturity-onset diabetes of the young, type ii, "  7p15.3-p15.1 
131  GCTG  Gamma-glutamylcyclotransferase  137170    7pter-p14 
132  GHRHR  Growth hormone releasing hormone receptor  139191  Growth hormone deficient dwarfism (3)   7p14 
133  GLC1F  "Glaucoma 1, open angle, F (adult-onset)"  603383  Glaucoma 1F (2)   7q35-q36 
134  GLI3  GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)  165240  "Greig cephalopolysyndactyly syndrome, Polydactyly, preaxial iv, Polydactyly, postaxial, type a1, Pallister-hall syndrome, "  7p13 
135  GNAI1  "Guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1"  139310    7q21 
136  GNB2  "Guanine nucleotide binding protein (G protein), beta polypeptide 2"  139390    7q22 
137  GNGT1  "Guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1"  189970    7q21.3 
138  GPDS1  Glaucoma-related pigment dispersion syndrome 1  600510  Pigment dispersion syndrome (2)   7q35-q36 
139  GPR22  G protein-coupled receptor 22  601910    7q22-q31.1 
140  GPR30  G protein-coupled receptor 30  601805    7p22 
141  GPR37  G protein-coupled receptor 37 (endothelin receptor type B-like)  602583    7q31 
142  GPR85  G protein-coupled receptor 85  605188    7q31 
143  GRB10  Growth factor receptor-bound protein 10  601523    7p12-p11.2 
144  GRM3  "Glutamate receptor, metabotropic 3"  601115    7q21.1-q21.2 
145  GRM8  "Glutamate receptor, metabotropic 8"  601116    7q31.3-q32.1 
146  GSBS  G-substrate  604088    7p15 
147  GTF2I  "General transcription factor II, i"  601679    7q11.23 
148  GTF2IRD1  GTF2I repeat domain containing 1  604318    7q11.23 
149  GUSB  "Glucuronidase, beta"  253220  Mucopolysaccharidosis VII (3)   7q21.11 
150  HAKAI  Hypothetical protein FLJ23109  606872    7q21.11 
151  HDAC9  Histone deacetylase 9  606543    7p21-p15 
152  HGF  Hepatocyte growth factor (hepapoietin A; scatter factor)  142409    7q21.1 
153  HIP1  Huntingtin interacting protein 1  601767    7q11.23 
154  HIPK2  Homeodomain interacting protein kinase 2  606868    7q32-q34 
155  HLXB9  Homeo box HB9  176450  "Currarino syndrome, 176450; Sacral agenesis-1 (2) "  7q36 
156  HNRPA2B1  Heterogeneous nuclear ribonucleoprotein A2/B1  600124    7p15 
157  HOXA1  Homeo box A1  142955    7p15.3 
158  HOXA10  Homeo box A10  142957    7p15-p14 
159  HOXA11  Homeo box A11  142958  "Radioulnar synostosis with amegakaryocytic thrombocytopenia, 605432(3) "  7p15-p14 
160  HOXA13  Homeo box A13  142959  "Hand-foot-uterus syndrome, 140000; Guttmacher syndrome, 176305(3) "  7p15-p14 
161  HOXA3  Homeo box A3  142954    7p15-p14 
162  HOXA4  Homeo box A4  142953    7p15-p14 
163  HOXA5  Homeo box A5  142952    7p15-p14 
164  HOXA6  Homeo box A6  142951    7p15-p14 
165  HOXA7  Homeo box A7  142950    7p15-p14 
166  HOXA9  Homeo box A9  142956    7p15-p14 
167  HPFH2  "Hereditary persistence of fetal hemoglobin, heterocellular, Indian type"  142335  "Hereditary persistence of fetal hemoglobin, heterocellular,Indian type (2) "  7q36 
168  HPVC1  Human papillomavirus (type 18) E5 central sequence-like 1  600762    7p14-p13 
169  HRX  Hyperreflexia  145290    7q 
170  HSPB1  Heat shock 27kD protein 1  602195    7p12.3 
171  HTR5A  5-hydroxytryptamine (serotonin) receptor 5A  601305    7q36.1 
172  HUS1  HUS1 checkpoint homolog (S. pombe)  603760    7p13-p12 
173  HYAL4  Hyaluronoglucosaminidase 4  604510    7q31.3 
174  ICA1  Islet cell autoantigen 1 (69kD)  147625    7p22 
175  IFRD1  Interferon-related developmental regulator 1  603502    7q22-q31 
176  IGFBP1  Insulin-like growth factor binding protein 1  146730    7p13-p12 
177  IGFBP3  Insulin-like growth factor binding protein 3  146732    7p13-p12 
178  IL6  "Interleukin 6 (interferon, beta 2)"  147620  "Osteoporosis, involutional, 166710; Kaposi sarcoma, 148000 "  7p21 
179  IMMP2L  Inner mitochondrial membrane peptidase 2 like  605977  Gilles de la Tourette syndrome [candidate OMIM:605977]  7q31 
180  IMPDH1  IMP (inosine monophosphate) dehydrogenase 1  146690    7q31.3-q32 
181  INHBA  "Inhibin, beta A (activin A, activin AB alpha polypeptide)"  147290    7p15-p13 
182  INMT  Indolethylamine N-methyltransferase  604854    7p15.3-p15.2 
183  INSIG1  Insulin induced gene 1  602055    7q36 
184  JAZF1  Juxtaposed with another zinc finger gene 1  606246  Endometrial stromal tumors (2)   7p15 
185  JTV1  JTV1 gene  600859    7p22 
186  KCND2  "Potassium voltage-gated channel, Shal-related subfamily, member 2"  605410    7q31-q32 
187  KCNH2  "Potassium voltage-gated channel, subfamily H (eag-related), member 2"  152427  Long QT syndrome-2 (3)   7q35-q36 
188  KEL  Kell blood group  110900    7q33 
189  LAMB1  "Laminin, beta 1"  150240  "Cutis laxa, marfanoid neonatal type (1) "  7q22 
190  LEP  "Leptin (obesity homolog, mouse)"  164160  "Obesity, morbid, withhypogonadism (3); Obesity, severe, due to leptin deficiency "  7q31.3 
191  LFNG  Lunatic fringe homolog (Drosophila)  602576    7p22 
192  LGMD1D  Limb girdle muscular dystrophy 1D (autosomal dominant)  603511  "Muscular dystrophy, limb-girdle, type 1D (2) "  7q 
193  LIMK1  LIM domain kinase 1  601329    7q11.23 
194  MAD1L1  MAD1 mitotic arrest deficient-like 1 (yeast)  602686  "Prostate cancer, 176807; Lymphoma, somatic (3) "  7p22 
195  MAFK  V-maf musculoaponeurotic fibrosarcoma oncogene homolog K (avian)  600197    7p22 
196  MAP2K2  Mitogen-activated protein kinase kinase 2  601263    7q32 
197  MCM7  MCM7 minichromosome maintenance deficient 7 (S. cerevisiae)  600592    7q21.3-q22.1 
198  MDDC  "Macular dystrophy, dominant cystoid (2) "  153880  "Macular dystrophy, dominant cystoid (2) "  7p21-p15 
199  MDH2  "Malate dehydrogenase 2, NAD (mitochondrial)"  154100    7p12.3-q11.2 
200  MEOX2  Mesenchyme homeo box 2 (growth arrest-specific homeo box)  600535    7p22.1-p21.3 
201  MEST  Mesoderm specific transcript homolog (mouse)  601029    7q32 
202  MET  Met proto-oncogene (hepatocyte growth factor receptor)  164860  "Renal cell carcinoma, papillary, 605074 "  7q31 
203  MGAM  Maltase-glucoamylase (alpha-glucosidase)  154360    7q32.3 
204  MHS3  Malignant hyperthermia susceptibility 3  154276  {Malignant hyperthermia susceptibility 3} (2)   7q21-q22 
205  MKLN1  "Muskelin 1, intracellular mediator containing kelch motifs"  605623    7q32 
206  MTERF  "Transcription termination factor, mitochondrial"  602318    7q21-q22 
207  MTPN  Myotrophin  606484    7q33-q35 
208  MUC11  Mucin 11  604608    7q22 
209  MUC12  Mucin 12  604609    7q22 
210  MUC3A  "Mucin 3A, intestinal"  158371  "Ulcerative colitis, susceptibility to, 191390 "  7q22 
211  MUC3B  Mucin 3B  605633    7q22 
212  MYCLK1  V-myc myelocytomatosis viral oncogene homolog (avian)-like 1  164865    7p15 
213  NCF1  "Neutrophil cytosolic factor 1 (47kD, chronic granulomatous disease, autosomal 1)"  233700  Chronic granulomatous disease due to deficiency of NCF-1 (3)   7q11.23 
214  NDUFA5  "NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 (13kD, B13)"  601677    7q32 
215  NFE2L3  Nuclear factor (erythroid-derived 2)-like 3  604135    7p15-p14 
216  NHCP2  Non-histone chromosome protein 2  118880   
217  NM  Neutrophil migration  162820    7q22-qter 
218  NOS3  Nitric oxide synthase 3 (endothelial cell)  163729  "Hypertension, pregnancy-induced (PEE1) [OMIM:189800]"  7q36 
219  NPTX2  Neuronal pentraxin II  600750    7q21.3-q22.1 
220  NPY  Neuropeptide Y  162640    7p15.1 
221  NRCAM  Neuronal cell adhesion molecule  601581    7q31.1-q31.2 
222  NRF1  Nuclear respiratory factor 1  600879    7q32 
223  NT5C3  "5-nucleotidase, cytosolic III"  606224  "Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to"  7p15.3 
224  NUDT1  Nudix (nucleoside diphosphate linked moiety X)-type motif 1  600312    7p22 
225  OCM  Oncomodulin  164795    7p13-p11 
226  OGDH  Oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)  203740  Alpha-ketoglutarate dehydrogenase deficiency (1)   7p14-p13 
227  OPN1SW  "Opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)"  190900  "Colorblindness, tritan (3) "  7q31.3-q32 
228  ORC5L  "Origin recognition complex, subunit 5-like (yeast)"  602331    7q22.1 
229  OTSC2  Otosclerosis 2  605727  Otosclerosis-2 (2)   7q34-q36 
230  p100  EBNA-2 co-activator (100kD)  602181    7q31.3 
231  PAX4  Paired box gene 4  167413    7q32 
232  PCLO  Piccolo (presynaptic cytomatrix protein)  604918    7q11.23-q21.3 
233  PCOLCE  Procollagen C-endopeptidase enhancer  600270    7q22 
234  PDAP1  PDGFA associated protein 1  607075    7q11.21 
235  PDGFA  Platelet-derived growth factor alpha polypeptide  173430    7p22 
236  PDK4  "Pyruvate dehydrogenase kinase, isoenzyme 4"  602527    7q21.3-q22.1 
237  PEX1  Peroxisome biogenesis factor 1  602136  "Refsum disease, infantile form, Zellweger syndrome, Adrenoleukodystrophy, autosomal neonatal form,"  7q21-q22 
238  PGAM2  Phosphoglycerate mutase 2 (muscle)  261670  Myopathy due to phosphoglycerate mutase deficiency (3)   7p13-p12 
239  PHKG1  "Phosphorylase kinase, gamma 1 (muscle)"  172470    7p12-q21 
240  PIK3CG  "Phosphoinositide-3-kinase, catalytic, gamma polypeptide"  601232    7q21.11 
241  PILR  Paired immunoglobulin-like receptor alpha  605341    7q22 
242  PILR  Paired immunoglobulin-like receptor beta  605342    7q22 
243  PIP  Prolactin-induced protein  176720    7q34 
244  PLOD3  "Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3"  603066    7q22 
245  PLXNA4  Plexin A4  604280   
246  PMPCB  Peptidase (mitochondrial processing) beta  603131    7q22-q32 
247  PMS2  PMS2 postmeiotic segregation increased 2 (S. cerevisiae)  600259  "Turcot syndrome, 276300; Colorectal cancer, hereditary nonpolyposis, 114500 "  7p22 
248  PODXL  Podocalyxin-like  602632    7q32-q33 
249  POLD2  "Polymerase (DNA directed), delta 2, regulatory subunit (50kD)"  600815    7p15.1 
250  POLR2J  Polymerase (RNA) II (DNA directed) polypeptide J (13.3kD)  604150    7q11.2 
251  POMZP3  POM (POM121 rat homolog) and ZP3 fusion  600587    7q11.23 
252  PON1  Paraoxonase 1  168820  "Coronary artery disease, susceptibility to; Coronary arteryspasm, susceptibility to"  7q21.3 
253  PON2  Paraoxonase 2  602447  "{Coronary artery disease, susceptibility to} (3) "  7q21.3 
254  PON3  Paraoxonase 3  602720    7q21.3 
255  POR  P450 (cytochrome) oxidoreductase  124015    7q11.2 
256  PPD2  "Polydactyly, preaxial II"  174500  "Polydactyly, preaxial II (2) "  7q36 
257  PPIA  Peptidylprolyl isomerase A (cyclophilin A)  123840    7p13-p11.2 
258  PPP1R3A  "Protein phosphatase 1, regulatory (inhibitor) subunit 3A "  600917  "Diabetes mellitus, insulin-resistant, with acanthosis nigricans and hypertension, "  7q11.23 
259  PRES  Prestin (motor protein)  604943    7q22 
260  PRKAG2  "Protein kinase, AMP-activated, gamma 2 non-catalytic subunit"  602743  "Cardiomyopathy, familial hypertrophic, with Wolff-parkinson-white syndrome, "  7q35-q36 
261  PRKAR1B  "Protein kinase, cAMP-dependent, regulatory, type I, beta"  176911    7pter-p22 
262  PRKAR2B  "Protein kinase, cAMP-dependent, regulatory, type II, beta"  176912    7q22-q31.1 
263  PRSS1  "Protease, serine, 1 (trypsin 1)"  276000  "Pancreatitis, hereditary, 167800; Trypsinogen deficiency (1) "  7q34 
264  PRSS2  "Protease, serine, 2 (trypsin 2)"  601564    7q34 
265  PSCD3  "Pleckstrin homology, Sec7 and coiled/coil domains 3"  605081    7p22.3-p22.2 
266  PSMC2  "Proteasome (prosome, macropain) 26S subunit, ATPase, 2"  154365    7q22.1-q22.3 
267  PSPH  Phosphoserine phosphatase  172480    7p15.2-p15.1 
268  PSPHL  Phosphoserine phosphatase-like  604239    7q11.2 
269  PTN  "Pleiotrophin (heparin binding growth factor 8, neurite growth-promoting factor 1)"  162095    7q33-q34 
270  PTPN12  "Protein tyrosine phosphatase, non-receptor type 12"  600079  Colon cancer (3)   7q11.23 
271  PTPRN2  "Protein tyrosine phosphatase, receptor type, N polypeptide 2"  601698    7q36 
272  PTPRZ1  "Protein tyrosine phosphatase, receptor-type, Z polypeptide 1"  176891    7q31.3 
273  RALA  V-ral simian leukemia viral oncogene homolog A (ras related)  179550    7p22-p15 
274  RAMP3  Receptor (calcitonin) activity modifying protein 3  605155    7p13-p12 
275  RELN  Reelin  600514  "Lissencephaly syndrome, norman-roberts type, 257320 "  7q22 
276  RFC2  Replication factor C (activator 1) 2 (40kD)  600404    7q11.23 
277  RHEB2  Ras homolog enriched in brain 2  601293    7q36 
278  RNY1  "RNA, Y1 small cytoplasmic (associated with Ro protein)"  601821    7q36 
279  RNY3  "RNA, Y3 small cytoplasmic (associated with Ro protein)"  601822    7q36 
280  RNY4  "RNA, Y4 small cytoplasmic (associated with Ro protein)"  601823    7q36 
281  RNY5  "RNA, Y5 small cytoplasmic (associated with Ro protein)"  601824    7q36 
282  RP10  Retinitis pigmentosa 10 (autosomal dominant)  180105  Retinitis pigmentosa-10 (2)   7q31-q35 
283  RP9  Retinitis pigmentosa 9 (autosomal dominant)  180104  Retinitis pigmentosa-9 (2)   7p14.3 
284  RPA3  Replication protein A3 (14kD)  179837    7p22 
285  RPP20  "POP7 (processing of precursor, S. cerevisiae) homolog"  606113    7q22 
286  SCAP2  Src family associated phosphoprotein 2  605215    7p21-p15 
287  SCYA24  "Small inducible cytokine subfamily A (Cys-Cys), member 24"  602495    7q11.23 
288  SDS  Shwachman-Diamond syndrome  260400  Shwachman-Diamond syndrome (2)   7p11-q11 
289  SERPINE1  "Serine (or cysteine) proteinase inhibitor, clade E "  173360  Thrombophilia due to excessive plasminogen activator inhibitor ; Hemorrhagic diathesis due to PAI1 deficiency  7q21.3-q22.1 
290  SFRP4  Secreted frizzled-related protein 4  606570    7p14.1 
291  SGCE  "Sarcoglycan, epsilon"  604149  "Myoclonic dystonia, 159900 "  7q21-q22 
292  SHFM1  Split hand/foot malformation (ectrodactyly) type 1  183600  "Split hand/foot malformation, type 1 (2) "  7q21.3-q22.1 
293  SHFM1D  Split hand/foot malformation type 1 with deafness  605617  Split hand/foot malformation type 1 with deafness (2)   7q21.2-q21.3 
294  SHH  Sonic hedgehog homolog (Drosophila)  600725  "Solitary median maxillary central incisor, Holoprosencephaly 3, Basal cell carcinoma "  7q36 
295  SLC13A1  "Solute carrier family 13 (sodium/sulfate symporters), member 1"  606193    7q31-q32 
296  SLC13A4  "Solute carrier family 13 (sodium/sulfate symporters), member 4"  604309    7q33 
297  SLC25A13  "Solute carrier family 25, member 13 (citrin)"  603859  "Citrullinemia, type ii, adult-onset, 603471 "  7q21.3  
298  SLC26A3  "Solute carrier family 26, member 3"  126650  "Chloride diarrhea, familial, 214700; ?Colon cancer (1) "  7q31 
299  SLC26A4  "Solute carrier family 26, member 4"  605646  "Deafness, neurosensory, autosomal recessive 4, Pendred syndrome, Enlarged vestibular aqueduct"  7q31 
300  SLC30A3  "Solute carrier family 30 (zinc transporter), member 3"  602878   
301  SLC4A2  "Solute carrier family 4, anion exchanger, member 2 "  109280    7q35-q36 
302  SMAD1    600794  "Spinal muscular atrophy, distal, with upper limb predominance (2) "  7p 
303  SMARCD3  "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3"  601737    7q35-q36 
304  SMOH  Smoothened homolog (Drosophila)  601500  "Basal cell carcinoma, sporadic (3) "  7p22 
305  SMURF1  E3 ubiquitin ligase SMURF1  605568    7p21.3 
306  SNL  "Singed-like (fascin homolog, sea urchin) (Drosophila)"  602689    7p22 
307  SNX13  Sorting nexin 13  606589    7p21.1 
308  SP4  Sp4 transcription factor  600540    7p15 
309  SPAM1  "Sperm adhesion molecule 1 (PH-20 hyaluronidase, zona pellucida binding)"  600930    7q31.3-q32 
310  SRI  Sorcin  182520    7q21.1 
311  SSBP1  Single-stranded DNA binding protein  600439    7q34 
312  ST7  Suppression of tumorigenicity 7  600833  Colon cancer [OMIM:600833]  7q31.1-q31.3 
313  STEAP  Six transmembrane epithelial antigen of the prostate  604415    7q21 
314  STK31  Serine/threonine kinase 31  605790    7p21.3-p21.2 
315  STQTL7  Stature QTL on chromosome 7  606256  [Stature QTL] (2)   7q 
316  STX1A  Syntaxin 1A (brain)  186590    7q11.23 
317  TAC1  "Tachykinin, precursor 1 "  162320    7q21-q22 
318  TAF6  "TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 80 kD"  602955    7q22.1 
319  TAS2R16  "Taste receptor, type 2, member 16"  604867    7q31.1-q31.3 
320  TAS2R3  "Taste receptor, type 2, member 3"  604868    7q31.3-q32 
321  TAS2R4  "Taste receptor, type 2, member 4"  604869    7q31.3-q32 
322  TAS2R5  "Taste receptor, type 2, member 5"  605062    7q31.3-q32 
323  TAX1BP1  Tax1 (human T-cell leukemia virus type I) binding protein 1  605326    7p15 
324  TBL2  Transducin (beta)-like 2  605842    7q11.23 
325  TBX20  T-box 20  606061    7p15-p14 
326  TBXAS1  "Thromboxane A synthase 1 (platelet, cytochrome P450, subfamily V)"  274180  Thromboxane synthase deficiency (2)   7q34-q35 
327  TCF6L1  Transcription factor 6-like 1 (mitochondrial transcription factor 1-like)  157670    7pter-cen 
328  TEM6  Tumor endothelial marker 6  606825    7p15.1 
329  TES  Testis derived transcript (3 LIM domains)  606085    7q31.2 
330  TFPI2  Tissue factor pathway inhibitor 2  600033    7q22 
331  TFR2  Transferrin receptor 2  604720  "Hemochromatosis, type 3, 604250 "  7q22 
332  TIF1  Transcriptional intermediary factor 1  603406  "Thyroid carcinoma, papillary, 188550 "  7q32-q34 
333  TPK1  Thiamin pyrophosphokinase 1  606370    7q34-q35 
334  TPST1  Tyrosylprotein sulfotransferase 1  603125    7q11.21 
335  TPTPS  Triphalangeal thumb-polysyndactyly syndrome  190605  Triphalangeal thumb-polysyndactyly syndrome (2)   7q36 
336  TRB@  T cell receptor beta locus  186930    7q34 
337  TRG@  T cell receptor gamma locus  186970    7p15-p14 
338  TRIP6  Thyroid hormone receptor interactor 6  602933    7q22 
339  TRRAP  Transformation/transcription domain-associated protein  603015    7q21.2-q22.1 
340  TTIM1  T-cell tumor invasion and metastasis 1  147830    7p12-cen 
341  TWIST  Twist homolog (acrocephalosyndactyly 3; Saethre-Chotzen syndrome)   601622  "Saethre-chotzen syndrome, 101400 "  7p21.2 
342  UBE2H  "Ubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast)"  601082    7q32 
343  UP  Uridine phosphorylase  191730   
344  VGF  VGF nerve growth factor inducible  602186    7q22 
345  VIPR2  Vasoactive intestinal peptide receptor 2  601970    7q36.3 
346  VPS41  Vacuolar protein sorting 41 (yeast)  605485    7p14-p13 
347  WBSCR1  Williams-Beuren syndrome chromosome region 1  603431    7q11.23 
348  WBSCR14  Williams Beuren syndrome chromosome region 14  605678    7q11.23 
349  WBSCR5  Williams-Beuren syndrome chromosome region 5  605719    7q11.23 
350  WNT2  Wingless-type MMTV integration site family member 2  147870    7q31 
351  WTSL  Wilms tumor suppressor locus  601583  {Wilms tumor susceptibility-5} (2)   7p15-p11.2 
352  XRCC2  X-ray repair complementing defective repair in Chinese hamster cells 2  600375    7q36.1 
353  YWHAG  "Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide"  605356    7q11.23 
354  ZAN  Zonadhesin  602372    7q22 
355  ZNF107  Zinc finger protein 107 (Y8)  603989    7q11.2 
356  ZNF117  Zinc finger protein 117 (HPF9)  194624    7q11.2 
357  ZNF12  Zinc finger protein 12 (KOX 3)  194536    7p22-p21 
358  ZNF138  Zinc finger protein 138 (clone pHZ-32)  604080    7q11.21-q11.23 
359  ZNF212  Zinc finger protein 212  602386    7q36.1 
360  ZNF277  Zinc finger protein 277  605465    7q31.1 
361  ZNF36  Zinc finger protein 36 (KOX 18)  601260    7q21.3-q22.1 
362  ZNF38  Zinc finger protein 38 (KOX 25)  601261    7q21-q22 
363  ZNFN1A1  "Zinc finger protein, subfamily 1A, 1 (Ikaros)"  603023  "Leukemia, acute lymphoblastic (3) "  7p13-p11.1 
364  ZP3A  Zona pellucida glycoprotein 3A (sperm receptor)  182889    7q11.23 
365  ZP3B  Zona pellucida glycoprotein 3B (sperm receptor)  195002   
366  ZRF1  Zuotin related factor 1  605502    7q22-q32 
367  ZYX  Zyxin  602002    7q32 

Note: Data source originated from NCBI.