FCGR2A (Fc gamma receptor IIa) - Rat Genome Database

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Gene: FCGR2A (Fc gamma receptor IIa) Homo sapiens
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Symbol: FCGR2A
Name: Fc gamma receptor IIa
RGD ID: 1316933
HGNC Page HGNC:3616
Description: Predicted to enable IgG binding activity and IgG receptor activity. Predicted to be involved in several processes, including antibody-dependent cellular cytotoxicity; positive regulation of phagocytosis; and positive regulation of tumor necrosis factor production. Predicted to be located in plasma membrane and secretory granule membrane. Predicted to be active in external side of plasma membrane. Implicated in several diseases, including autoimmune disease (multiple); dengue disease (multiple); hematologic cancer (multiple); leukopenia (multiple); and malaria (multiple). Biomarker of asthma; atopic dermatitis; autoimmune disease (multiple); and chronic myeloid leukemia.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CD32; CD32A; CDw32; Fc fragment of IgG receptor IIa; Fc fragment of IgG, low affinity IIa, receptor (CD32); fc fragment of igg, low affinity iia, receptor for (cd32); Fc gamma receptor RIIa3; fc-gamma RII-a; fc-gamma-RIIa; FCG2; FcgammaRIIa; FcGR; FCGR2; FCGR2A1; fcRII-a; IGFR2; igG Fc receptor II-a; Immunoglobulin G Fc receptor II; low affinity immunoglobulin gamma Fc region receptor II-a; MGC23887; MGC30032
RGD Orthologs
Rat
Bonobo
Squirrel
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381161,505,457 - 161,524,048 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1161,505,430 - 161,524,013 (+)EnsemblGRCh38hg38GRCh38
GRCh371161,475,247 - 161,489,619 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361159,741,844 - 159,755,984 (+)NCBINCBI36Build 36hg18NCBI36
Build 341158,288,274 - 158,302,415NCBI
Celera1134,591,741 - 134,592,404 (-)NCBICelera
Celera1134,682,428 - 134,687,972 (+)NCBICelera
Cytogenetic Map1q23.3NCBI
HuRef1132,800,353 - 132,814,372 (+)NCBIHuRef
CHM1_11162,897,042 - 162,911,192 (+)NCBICHM1_1
T2T-CHM13v2.01160,768,080 - 160,786,676 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
Acute Lung Injury  (ISO)
Anaphylaxis  (IAGP,IMP)
arthus reaction  (IDA)
asthma  (IEP)
atherosclerosis  (IAGP)
atopic dermatitis  (IEP,ISO)
autoimmune hemolytic anemia  (ISO)
autoimmune interstitial lung, joint, and kidney disease  (IAGP)
autoimmune thrombocytopenic purpura  (IAGP,IEP,ISO)
Bacteremia  (IAGP)
bacterial pneumonia  (ISO)
Charcot-Marie-Tooth disease type 1  (IAGP)
chronic myeloid leukemia  (IEP)
common variable immunodeficiency  (IEP)
coronary artery disease  (IAGP)
crescentic glomerulonephritis  (ISO)
Crohn's disease  (IAGP)
cystic fibrosis  (EXP,IAGP)
dengue disease  (IAGP)
dengue hemorrhagic fever  (IAGP)
diffuse large B-cell lymphoma  (IAGP)
diffuse scleroderma  (IDA)
Experimental Arthritis  (ISO)
Experimental Autoimmune Encephalomyelitis  (ISO)
factor VIII deficiency  (IAGP)
gastrointestinal stromal tumor  (IAGP)
glomerulonephritis  (ISO)
haemophilus meningitis  (IAGP)
hemolytic anemia  (IMP)
hemolytic disease of the fetus  (IAGP)
Heparin-induced Thrombocytopenia  (IAGP)
Kawasaki disease  (EXP)
lupus nephritis  (IAGP)
lymphoid leukemia  (IAGP)
lymphopenia  (IAGP)
malaria  (EXP,IAGP)
Meningococcal Infections  (IAGP)
multiple myeloma  (IAGP)
multiple sclerosis  (IAGP)
neutropenia  (IAGP)
non-Hodgkin lymphoma  (IAGP)
osteoarthritis  (IDA)
parathyroid carcinoma  (IAGP)
Plasmodium falciparum malaria  (IAGP)
Pseudomonas Infections  (IAGP)
psoriasis  (IEP)
respiratory system disease  (IAGP)
rheumatoid arthritis  (EXP,IAGP,IDA)
Sjogren's syndrome  (EXP)
Stroke  (IAGP)
systemic lupus erythematosus  (EXP,IAGP,IDA,IEP)
temporal arteritis  (IAGP)
thrombocytopenia  (EXP,IMP)
thrombosis  (EXP,IAGP,IMP)
Transplant Rejection  (IDA)
type 1 diabetes mellitus  (ISO)
ulcerative colitis  (EXP,IAGP)
visual epilepsy  (IAGP)
Wallerian Degeneration  (ISO)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane  (ISO)
1,3,5-trinitro-1,3,5-triazinane  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
17beta-estradiol 3-benzoate  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-nitrofluorene  (ISO)
3',5'-cyclic AMP  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3-chloropropane-1,2-diol  (ISO)
6-propyl-2-thiouracil  (ISO)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
antirheumatic drug  (EXP)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
buspirone  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calcitriol  (EXP)
cefaloridine  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
cisplatin  (EXP)
cyclosporin A  (ISO)
cytarabine  (EXP)
Dibutyl phosphate  (EXP)
dibutyl phthalate  (ISO)
diuron  (ISO)
endosulfan  (ISO)
ethanol  (ISO)
fipronil  (ISO)
flavonoids  (ISO)
flutamide  (ISO)
fulvestrant  (EXP)
gentamycin  (ISO)
heparin  (EXP)
hexachlorobenzene  (ISO)
lead diacetate  (EXP)
lipopolysaccharide  (EXP)
mercury dichloride  (EXP)
methotrexate  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
nefazodone  (ISO)
nickel atom  (EXP)
nimesulide  (ISO)
nitrofen  (ISO)
Nor-9-carboxy-delta9-THC  (EXP)
oxycodone  (ISO)
ozone  (ISO)
paclitaxel  (ISO)
paracetamol  (EXP,ISO)
perfluorooctanoic acid  (EXP,ISO)
pirinixic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
S-nitroso-N-acetyl-D-penicillamine  (ISO)
silicon dioxide  (EXP)
Soman  (ISO)
streptozocin  (ISO)
tamoxifen  (ISO)
testosterone  (ISO)
testosterone enanthate  (EXP)
thioacetamide  (ISO)
toluene  (ISO)
trichloroethene  (ISO)
triphenyl phosphate  (EXP)
undecane  (ISO)
vanadyl sulfate  (ISO)
vinclozolin  (ISO)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Antinuclear antibody positivity  (IAGP)
Antiphospholipid antibody positivity  (IAGP)
Arthritis  (IAGP)
Asthma  (IAGP)
Autosomal dominant inheritance  (IAGP)
Autosomal recessive inheritance  (IAGP)
Biliary cirrhosis  (IAGP)
Bronchiectasis  (IAGP)
Childhood onset  (IAGP)
Chronic lung disease  (IAGP)
Chronic sinusitis  (IAGP)
Cirrhosis  (IAGP)
Clubbing of fingers  (IAGP)
Cor pulmonale  (IAGP)
Cutaneous photosensitivity  (IAGP)
Decreased forced expiratory flow 25-75%  (IAGP)
Dehydration  (IAGP)
Diarrhea  (IAGP)
Elevated sweat chloride  (IAGP)
Exocrine pancreatic insufficiency  (IAGP)
Failure to thrive  (IAGP)
Fever  (IAGP)
Gastrointestinal stroma tumor  (IAGP)
Glomerulonephritis  (IAGP)
Hemolytic anemia  (IAGP)
Hemoptysis  (IAGP)
Hepatomegaly  (IAGP)
Hepatosplenomegaly  (IAGP)
Hypercalciuria  (IAGP)
Hyperpolarized transepithelial nasal potential difference  (IAGP)
Ileus  (IAGP)
Infantile onset  (IAGP)
Invasive parasitic infection  (IAGP)
Ischemic stroke  (IAGP)
Leukopenia  (IAGP)
Lupus nephritis  (IAGP)
Malar rash  (IAGP)
Male infertility  (IAGP)
Meconium ileus  (IAGP)
Nasal polyposis  (IAGP)
Nephritis  (IAGP)
Neutropenia in presence of anti-neutropil antibodies  (IAGP)
Opportunistic bacterial infection  (IAGP)
Pancreatitis  (IAGP)
Parathyroid carcinoma  (IAGP)
Pericarditis  (IAGP)
Pleuritis  (IAGP)
Psychosis  (IAGP)
Rectal prolapse  (IAGP)
Recurrent bronchopulmonary infections  (IAGP)
Recurrent pneumonia  (IAGP)
Reduced forced expiratory volume in one second  (IAGP)
Reduced forced vital capacity  (IAGP)
Salty tasting skin  (IAGP)
Seizure  (IAGP)
Steatorrhea  (IAGP)
Systemic lupus erythematosus  (IAGP)
Thrombocytopenia  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Fc(epsilon)RI and FcgammaRIII/CD16 differentially regulate atopic dermatitis in mice. Abboud G, etal., J Immunol. 2009 May 15;182(10):6517-26.
2. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Aitman TJ, etal., Nature. 2006 Feb 16;439(7078):851-5.
3. Expression of Fc gamma and complement receptors in monocytes of X-linked agammaglobulinaemia and common variable immunodeficiency patients. Amoras AL, etal., Clin Exp Immunol. 2007 Dec;150(3):422-8. Epub 2007 Sep 27.
4. FcgammaRIII-expressing macrophages are essential for development of collagen-induced arthritis. Andren M, etal., Scand J Immunol. 2006 Apr;63(4):282-9.
5. Fc gamma RIIA H/R 131 polymorphism, subclass-specific IgG anti-heparin/platelet factor 4 antibodies and clinical course in patients with heparin-induced thrombocytopenia and thrombosis. Arepally G, etal., Blood. 1997 Jan 15;89(2):370-5.
6. A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. Asano K, etal., Nat Genet. 2009 Dec;41(12):1325-9. Epub 2009 Nov 15.
7. Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele. Balada E, etal., Tissue Antigens. 2006 Nov;68(5):432-8.
8. Differential contribution of three activating IgG Fc receptors (FcgammaRI, FcgammaRIII, and FcgammaRIV) to IgG2a- and IgG2b-induced autoimmune hemolytic anemia in mice. Baudino L, etal., J Immunol. 2008 Feb 1;180(3):1948-53.
9. Fc gamma RIIa polymorphism: a susceptibility factor for immune complex-mediated lupus nephritis in Brazilian patients. Bazilio AP, etal., Nephrol Dial Transplant. 2004 Jun;19(6):1427-31. Epub 2004 Mar 5.
10. Specificity and class distribution of Fc gamma R-specific autoantibodies in patients with autoimmune disease. Boros P, etal., J Immunol. 1994 Jan 1;152(1):302-6.
11. Destructive arthritis in the absence of both FcgammaRI and FcgammaRIII. Boross P, etal., J Immunol. 2008 Apr 1;180(7):5083-91.
12. On the role of platelet Fc gamma RIIa phenotype in heparin-induced thrombocytopenia. Brandt JT, etal., Thromb Haemost. 1995 Dec;74(6):1564-72.
13. No association of Fc gamma RIIa, Fc gamma RIIIa and Fc gamma RIIIb polymorphisms with MS. Breij EC, etal., J Neuroimmunol. 2003 Jul;140(1-2):210-5.
14. Common variants in genes that mediate immunity and risk of multiple myeloma. Brown EE, etal., Int J Cancer. 2007 Jun 15;120(12):2715-22.
15. Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis. De Rose V, etal., Eur J Hum Genet. 2005 Jan;13(1):96-101.
16. Associations between Fc gamma receptor IIA polymorphisms and the risk and prognosis of meningococcal disease. Domingo P, etal., Am J Med. 2002 Jan;112(1):19-25.
17. Effect of FCGR2A and FCGR3A variants on CLL outcome. Dornan D, etal., Blood. 2010 Nov 18;116(20):4212-22. doi: 10.1182/blood-2010-03-272765. Epub 2010 Aug 12.
18. The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia A. Eckhardt CL, etal., J Thromb Haemost. 2014 Aug;12(8):1294-301. doi: 10.1111/jth.12631. Epub 2014 Jul 16.
19. FcgammaRIIa and FcgammaRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt. Eyada TK, etal., Blood Coagul Fibrinolysis. 2012 Jan;23(1):64-8. doi: 10.1097/MBC.0b013e32834ddf2f.
20. The role of Fcgamma receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individuals. Fijen CA, etal., Clin Exp Immunol. 2000 May;120(2):338-45.
21. [Low-affinity Fcgamma receptor IIa gene polymorphism and dengue bleeding disorder]. Garcia G, etal., Enferm Infecc Microbiol Clin. 2012 Dec;30(10):621-3. doi: 10.1016/j.eimc.2012.05.011. Epub 2012 Jul 18.
22. FCGR3A/2A polymorphisms and diffuse large B-cell lymphoma outcome treated with immunochemotherapy: a meta-analysis on 1134 patients from two prospective cohorts. Ghesquieres H, etal., Hematol Oncol. 2016 Jun 10. doi: 10.1002/hon.2305.
23. Fc gamma RIII and Fc gamma RIV are indispensable for acute glomerular inflammation induced by switch variant monoclonal antibodies. Giorgini A, etal., J Immunol. 2008 Dec 15;181(12):8745-52.
24. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
25. Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Harley JB, etal., Nat Genet. 2008 Feb;40(2):204-10. Epub 2008 Jan 20.
26. Expression of Fcgamma and complement receptors on peripheral blood monocytes in systemic lupus erythematosus and rheumatoid arthritis. Hepburn AL, etal., Rheumatology (Oxford). 2004 May;43(5):547-54. Epub 2004 Jan 27.
27. Dendritic cells modulate platelet activity in IVIg-mediated amelioration of ITP in mice. Huang HS, etal., Blood. 2010 Dec 2;116(23):5002-9. doi: 10.1182/blood-2010-03-275123. Epub 2010 Aug 10.
28. Activating Fc gamma receptors participate in the development of autoimmune diabetes in NOD mice. Inoue Y, etal., J Immunol. 2007 Jul 15;179(2):764-74.
29. Association between SLE nephritis and polymorphic variants of the CRP and FcgammaRIIIa genes. Jonsen A, etal., Rheumatology (Oxford). 2007 Sep;46(9):1417-21. Epub 2007 Jun 27.
30. Decreased expression of both Fc gamma RII and Fc gamma RIII mRNA in leukemic granulocytes. Kant A, etal., Leuk Res. 1995 Dec;19(12):997-1000.
31. Susceptibility for ischemic stroke in Korean population is associated with polymorphisms of the Fc gamma receptor IIA. Kim YS, etal., Blood Coagul Fibrinolysis. 2009 Jul;20(5):353-7.
32. The association between a common FCGR2A polymorphism and C-reactive protein and coronary artery disease revisited. Kroupis C, etal., Genet Test Mol Biomarkers. 2010 Dec;14(6):839-46. Epub 2010 Oct 25.
33. Inhibition of hyperacute transplant rejection by soluble proteins with the functional domains of CD46 and FcgammaRII. Lanteri MB, etal., Transplantation. 2000 Mar 27;69(6):1128-36.
34. Susceptibility for ischemic stroke in four constitution medicine is associated with polymorphisms of FCGR2A and IL1RN genes. Lee BC, etal., Neurol Res. 2010 Feb;32 Suppl 1:43-7.
35. FCGR3A and FCGR2A polymorphisms may not correlate with response to alemtuzumab in chronic lymphocytic leukemia. Lin TS, etal., Blood. 2005 Jan 1;105(1):289-91. Epub 2004 Jun 24.
36. High-dose dexamethasone shifts the balance of stimulatory and inhibitory Fcgamma receptors on monocytes in patients with primary immune thrombocytopenia. Liu XG, etal., Blood. 2011 Feb 10;117(6):2061-9. doi: 10.1182/blood-2010-07-295477. Epub 2010 Dec 3.
37. The role of the human Fc receptor Fc gamma RIIA in the immune clearance of platelets: a transgenic mouse model. McKenzie SE, etal., J Immunol. 1999 Apr 1;162(7):4311-8.
38. FcgammaRIII (CD16)-deficient mice show IgG isotype-dependent protection to experimental autoimmune hemolytic anemia. Meyer D, etal., Blood. 1998 Dec 1;92(11):3997-4002.
39. CD32a antibodies induce thrombocytopenia and type II hypersensitivity reactions in FCGR2A mice. Meyer T, etal., Blood. 2015 Nov 5;126(19):2230-8. doi: 10.1182/blood-2015-04-638684. Epub 2015 Sep 22.
40. Bevacizumab immune complexes activate platelets and induce thrombosis in FCGR2A transgenic mice. Meyer T, etal., J Thromb Haemost. 2009 Jan;7(1):171-81. doi: 10.1111/j.1538-7836.2008.03212.x. Epub 2008 Oct 30.
41. Association of Fc¿RIIa Polymorphism with Clinical Outcome of Dengue Infection: First Insight from Pakistan. Mohsin SN, etal., Am J Trop Med Hyg. 2015 Oct;93(4):691-6. doi: 10.4269/ajtmh.15-0199. Epub 2015 Aug 3.
42. Association of FCGR2A and FCGR2A-FCGR3A haplotypes with susceptibility to giant cell arteritis. Morgan AW, etal., Arthritis Res Ther. 2006;8(4):R109.
43. Relationships between eosinophil-associated parameters and disease severity in atopic dermatitis. Nakama T Kurume Med J. 1995;42(2):95-106.
44. [The diagnostic of defects of inborn immunity under B-cell tumors of lymphatic system]. Nazarova EL, etal., Klin Lab Diagn. 2014 Nov;59(11):39-42.
45. Relationship between Fc receptor IIA polymorphism and infection in children with sickle cell disease. Norris CF, etal., J Pediatr. 1996 Jun;128(6):813-9.
46. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
47. Fc gamma RIIa, IIIa and IIIb polymorphisms in Turkish children susceptible to recurrent infectious diseases. Ozturk C, etal., Clin Exp Med. 2006 Mar;6(1):27-32.
48. Role of novel rat-specific Fc receptor in macrophage activation associated with crescentic glomerulonephritis. Page TH, etal., J Biol Chem. 2012 Feb 17;287(8):5710-9. doi: 10.1074/jbc.M111.260695. Epub 2011 Dec 19.
49. FcgammaRIIa and FcgammaRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome. Papagianni A, etal., Blood Coagul Fibrinolysis. 2013 Jan;24(1):35-9. doi: 10.1097/MBC.0b013e328359bc3b.
50. FC gamma RIIa polymorphism in patients with rheumatoid arthritis. Pawlik A, etal., Clin Exp Rheumatol. 2002 Nov-Dec;20(6):841-4.
51. Multiple elements of the allergic arm of the immune response modulate autoimmune demyelination. Pedotti R, etal., Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):1867-72. Epub 2003 Feb 7.
52. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
53. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
54. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
55. FcgammaRIII is protective against Pseudomonas aeruginosa pneumonia. Rhein LM, etal., Am J Respir Cell Mol Biol. 2008 Apr;38(4):401-6. Epub 2007 Nov 1.
56. Anti-CD40L immune complexes potently activate platelets in vitro and cause thrombosis in FCGR2A transgenic mice. Robles-Carrillo L, etal., J Immunol. 2010 Aug 1;185(3):1577-83. Epub 2010 Jun 28.
57. Early atherosclerosis and IgG2 to bacteria are associated with FcgammaRIIa genotype in non-smokers. Sampi M, etal., Eur J Clin Invest. 2009 Jun;39(6):517-26.
58. Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus. Sanchez E, etal., Ann Rheum Dis. 2011 Jun 30.
59. FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children. Schuldt K, etal., J Med Genet. 2010 Jul;47(7):471-5. Epub 2009 Dec 3.
60. Polymorphisms of TNF-enhancer and gene for FcgammaRIIa correlate with the severity of falciparum malaria in the ethnically diverse Indian population. Sinha S, etal., Malar J. 2008 Jan 14;7:13.
61. The Fcgamma receptor IIA-H/H131 genotype is associated with bacteremia in pneumococcal community-acquired pneumonia. Sole-Violan J, etal., Crit Care Med. 2011 Jun;39(6):1388-93.
62. A single-nucleotide polymorphism of the Fcgamma receptor type IIIA gene in the recipient predicts transplant outcomes after HLA fully matched unrelated BMT for myeloid malignancies. Takami A, etal., Bone Marrow Transplant. 2011 Feb;46(2):238-43. doi: 10.1038/bmt.2010.88. Epub 2010 Apr 19.
63. FcgammaRIII b and FcgammaRIIa polymorphism may affect the production of specific NA1 autoantibody and clinical course of autoimmune neutropenia of infancy. Taniuchi S, etal., Hum Immunol. 2001 Apr;62(4):408-13.
64. A novel splice variant of FcgammaRIIa: a risk factor for anaphylaxis in patients with hypogammaglobulinemia. van der Heijden J, etal., J Allergy Clin Immunol. 2013 May;131(5):1408-16.e5. doi: 10.1016/j.jaci.2013.02.009. Epub 2013 Mar 29.
65. A novel human CD32 mAb blocks experimental immune haemolytic anaemia in FcgammaRIIA transgenic mice. van Royen-Kerkhof A, etal., Br J Haematol. 2005 Jul;130(1):130-7.
66. Expression of genes encoding receptors for IgG (FcRIII) and for C3b/C4b (Crry) in rat sciatic nerve during development and Wallerian degeneration. Vedeler CA, etal., J Neurosci Res. 1992 Apr;31(4):654-61.
67. Phenotypic analysis of alveolar macrophages and monocytes in allergic airway inflammation. I. Evidence for activation of alveolar macrophages, but not peripheral blood monocytes, in subjects with allergic rhinitis and asthma. Viksman MY, etal., Am J Respir Crit Care Med. 1997 Mar;155(3):858-63.
68. Mannose binding lectin and FcgammaRIIa (CD32) polymorphism in Spanish systemic lupus erythematosus patients. Villarreal J, etal., Rheumatology (Oxford). 2001 Sep;40(9):1009-12.
69. Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations. Weersma RK, etal., Inflamm Bowel Dis. 2010 Dec;16(12):2080-9. doi: 10.1002/ibd.21342.
70. Treatment of lupus-prone NZB/NZW F1 mice with recombinant soluble Fc gamma receptor II (CD32). Werwitzke S, etal., Ann Rheum Dis. 2008 Feb;67(2):154-61. Epub 2007 Jun 8.
71. Delay of LPS-induced acute lung injury resolution by soluble immune complexes is neutrophil dependent. Wu CL, etal., Shock. 2009 Sep;32(3):276-85.
72. Correlation of Fc(gamma)RIIa (CD32) Polymorphism and IgG Antibody Subclasses in Hemolytic Disease of Newborn. Wu Q, etal., Neonatology. 2009;96(1):1-5. doi: 10.1159/000189239. Epub 2009 Jan 8.
73. Identification of TNF-related apoptosis-inducing ligand and other molecules that distinguish inflammatory from resident dendritic cells in patients with psoriasis. Zaba LC, etal., J Allergy Clin Immunol. 2010 Jun;125(6):1261-1268.e9. Epub 2010 May 14.
Additional References at PubMed
PMID:1379234   PMID:2139735   PMID:2526077   PMID:2527651   PMID:2529342   PMID:2531919   PMID:2824655   PMID:2965389   PMID:2967437   PMID:2971615   PMID:3402431   PMID:8125298  
PMID:8631888   PMID:8636449   PMID:8756631   PMID:8940017   PMID:8994865   PMID:9268059   PMID:9280292   PMID:9295288   PMID:9490697   PMID:10331870   PMID:10382761   PMID:10397151  
PMID:10675363   PMID:10704522   PMID:10781611   PMID:11099670   PMID:11110978   PMID:11141335   PMID:11145038   PMID:11229467   PMID:11237133   PMID:11263776   PMID:11398118   PMID:11453982  
PMID:11480843   PMID:11528518   PMID:11699473   PMID:11740730   PMID:11835346   PMID:11913983   PMID:11937562   PMID:11953994   PMID:11976734   PMID:12027254   PMID:12064825   PMID:12095061  
PMID:12115187   PMID:12121275   PMID:12176802   PMID:12215902   PMID:12363051   PMID:12390315   PMID:12393699   PMID:12421634   PMID:12447772   PMID:12477932   PMID:12486608   PMID:12492589  
PMID:12493400   PMID:12501257   PMID:12571856   PMID:12626795   PMID:12643213   PMID:12690104   PMID:12710759   PMID:12729187   PMID:12752683   PMID:12830330   PMID:12832410   PMID:12834496  
PMID:12847687   PMID:12857726   PMID:12858454   PMID:12867584   PMID:12871511   PMID:12893767   PMID:12960360   PMID:14514134   PMID:14597109   PMID:14641546   PMID:14651519   PMID:14734773  
PMID:14740869   PMID:14761117   PMID:14976391   PMID:15140146   PMID:15152814   PMID:15153543   PMID:15166534   PMID:15171001   PMID:15190804   PMID:15191947   PMID:15194589   PMID:15194692  
PMID:15251320   PMID:15319871   PMID:15351857   PMID:15369725   PMID:15371685   PMID:15457442   PMID:15483014   PMID:15535834   PMID:15583733   PMID:15675264   PMID:15735807   PMID:15742161  
PMID:15744239   PMID:15833371   PMID:15878871   PMID:15910853   PMID:15946259   PMID:16005880   PMID:16107886   PMID:16110781   PMID:16133986   PMID:16150646   PMID:16160618   PMID:16169188  
PMID:16177087   PMID:16185324   PMID:16198451   PMID:16200626   PMID:16221721   PMID:16277670   PMID:16356189   PMID:16421008   PMID:16511922   PMID:16542359   PMID:16551965   PMID:16569263  
PMID:16606986   PMID:16682723   PMID:16709925   PMID:16751395   PMID:16785568   PMID:16805673   PMID:16846215   PMID:16880255   PMID:16889631   PMID:16893392   PMID:17005690   PMID:17018637  
PMID:17020818   PMID:17046568   PMID:17092253   PMID:17118455   PMID:17134755   PMID:17142741   PMID:17291475   PMID:17324336   PMID:17335370   PMID:17523948   PMID:17582430   PMID:17587350  
PMID:17588661   PMID:17594928   PMID:17606457   PMID:17642530   PMID:17650444   PMID:17652100   PMID:17665457   PMID:17673295   PMID:17704420   PMID:17710620   PMID:17785206   PMID:17845308  
PMID:17848620   PMID:17877745   PMID:17921137   PMID:18022136   PMID:18025239   PMID:18029348   PMID:18052703   PMID:18071035   PMID:18165525   PMID:18180796   PMID:18311806   PMID:18337560  
PMID:18347005   PMID:18349392   PMID:18372357   PMID:18418394   PMID:18474295   PMID:18535921   PMID:18539895   PMID:18633131   PMID:18636124   PMID:18641368   PMID:18793404   PMID:18832675  
PMID:18843786   PMID:18930989   PMID:18936436   PMID:18957413   PMID:19012493   PMID:19026120   PMID:19040302   PMID:19055599   PMID:19088437   PMID:19100392   PMID:19127818   PMID:19140833  
PMID:19164213   PMID:19184295   PMID:19197137   PMID:19201892   PMID:19232413   PMID:19235048   PMID:19262684   PMID:19284648   PMID:19309690   PMID:19331818   PMID:19372459   PMID:19420354  
PMID:19423540   PMID:19480687   PMID:19494086   PMID:19494328   PMID:19497711   PMID:19573080   PMID:19640933   PMID:19664613   PMID:19672774   PMID:19692168   PMID:19720214   PMID:19773279  
PMID:19776239   PMID:19892918   PMID:19898481   PMID:19913121   PMID:19926792   PMID:19933905   PMID:20007585   PMID:20047592   PMID:20054293   PMID:20148910   PMID:20149216   PMID:20154205  
PMID:20207250   PMID:20215002   PMID:20228799   PMID:20237496   PMID:20301428   PMID:20356573   PMID:20367096   PMID:20406964   PMID:20438785   PMID:20439102   PMID:20439936   PMID:20453000  
PMID:20508037   PMID:20519616   PMID:20542180   PMID:20550522   PMID:20551103   PMID:20568250   PMID:20588308   PMID:20628086   PMID:20634666   PMID:20644561   PMID:20697800   PMID:20707220  
PMID:20716621   PMID:20720565   PMID:20736173   PMID:20802378   PMID:20848568   PMID:20881011   PMID:20929558   PMID:20935224   PMID:21042730   PMID:21044892   PMID:21048031   PMID:21054877  
PMID:21123174   PMID:21168221   PMID:21297633   PMID:21324097   PMID:21357544   PMID:21372129   PMID:21607711   PMID:21657954   PMID:21768177   PMID:21780194   PMID:21818580   PMID:21831733  
PMID:21832933   PMID:21856937   PMID:21873635   PMID:21945020   PMID:21956105   PMID:22081228   PMID:22138510   PMID:22167032   PMID:22268665   PMID:22286219   PMID:22289203   PMID:22305465  
PMID:22446962   PMID:22489915   PMID:22540264   PMID:22542851   PMID:22559288   PMID:22565545   PMID:22623428   PMID:22628489   PMID:22649103   PMID:22677127   PMID:22885164   PMID:22903236  
PMID:22906996   PMID:22908332   PMID:22945762   PMID:22955924   PMID:23023090   PMID:23030766   PMID:23128233   PMID:23239500   PMID:23270585   PMID:23286345   PMID:23345329   PMID:23372157  
PMID:23376485   PMID:23444610   PMID:23458236   PMID:23483488   PMID:23498761   PMID:23504312   PMID:23509345   PMID:23517907   PMID:23551080   PMID:23616574   PMID:23649770   PMID:23652523  
PMID:23780683   PMID:23782136   PMID:23965133   PMID:23994584   PMID:24039173   PMID:24117665   PMID:24191245   PMID:24258815   PMID:24356554   PMID:24366619   PMID:24390342   PMID:24554771  
PMID:24583628   PMID:24586589   PMID:24594077   PMID:24665136   PMID:24667440   PMID:24775607   PMID:24802006   PMID:24871463   PMID:24884501   PMID:24896836   PMID:24911936   PMID:24945596  
PMID:24987061   PMID:24997134   PMID:25011934   PMID:25061875   PMID:25093412   PMID:25100508   PMID:25108563   PMID:25242138   PMID:25312792   PMID:25345863   PMID:25416956   PMID:25447268  
PMID:25457587   PMID:25470559   PMID:25484053   PMID:25553878   PMID:25568316   PMID:25680756   PMID:25787843   PMID:25802446   PMID:25811666   PMID:25823785   PMID:25879560   PMID:25900780  
PMID:26089602   PMID:26125827   PMID:26133275   PMID:26186194   PMID:26314337   PMID:26363448   PMID:26427148   PMID:26429304   PMID:26429310   PMID:26429312   PMID:26450443   PMID:26490967  
PMID:26496101   PMID:26510856   PMID:26748351   PMID:26774660   PMID:26801149   PMID:26996483   PMID:27025455   PMID:27064330   PMID:27074847   PMID:27267995   PMID:27270653   PMID:27315784  
PMID:27376362   PMID:27490376   PMID:27609290   PMID:27742794   PMID:27765766   PMID:27769046   PMID:27893416   PMID:27984611   PMID:28005267   PMID:28039707   PMID:28239647   PMID:28297712  
PMID:28427365   PMID:28514442   PMID:28605553   PMID:28606989   PMID:28719596   PMID:28815933   PMID:28856973   PMID:28886140   PMID:28891817   PMID:28942727   PMID:28952147   PMID:28988621  
PMID:29041009   PMID:29155175   PMID:29164277   PMID:29233917   PMID:29350833   PMID:29351998   PMID:29443373   PMID:29482947   PMID:29597194   PMID:29692344   PMID:29780387   PMID:29858387  
PMID:29879453   PMID:29908029   PMID:29928276   PMID:29976297   PMID:29976671   PMID:29977032   PMID:30013105   PMID:30232664   PMID:30260678   PMID:30278383   PMID:30299252   PMID:30318772  
PMID:30341387   PMID:30412591   PMID:30475382   PMID:30498196   PMID:30555482   PMID:30610165   PMID:30638300   PMID:30888406   PMID:30968301   PMID:31211444   PMID:31239514   PMID:31249568  
PMID:31509231   PMID:31589165   PMID:31741433   PMID:31884867   PMID:31992246   PMID:32072832   PMID:32076121   PMID:32235430   PMID:32252656   PMID:32296183   PMID:32755599   PMID:32759994  
PMID:33208458   PMID:33392111   PMID:33424858   PMID:33961781   PMID:34082682   PMID:34285919   PMID:34497614   PMID:34551786   PMID:34743150   PMID:34871197   PMID:34970970   PMID:35149195  
PMID:35626650   PMID:37114884   PMID:37149714   PMID:37174624   PMID:38029355   PMID:38335505   PMID:38408113   PMID:38455048   PMID:38544414  


Genomics

Comparative Map Data
FCGR2A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381161,505,457 - 161,524,048 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1161,505,430 - 161,524,013 (+)EnsemblGRCh38hg38GRCh38
GRCh371161,475,247 - 161,489,619 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361159,741,844 - 159,755,984 (+)NCBINCBI36Build 36hg18NCBI36
Build 341158,288,274 - 158,302,415NCBI
Celera1134,591,741 - 134,592,404 (-)NCBICelera
Celera1134,682,428 - 134,687,972 (+)NCBICelera
Cytogenetic Map1q23.3NCBI
HuRef1132,800,353 - 132,814,372 (+)NCBIHuRef
CHM1_11162,897,042 - 162,911,192 (+)NCBICHM1_1
T2T-CHM13v2.01160,768,080 - 160,786,676 (+)NCBIT2T-CHM13v2.0
Fcgr2a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81385,813,516 - 85,830,269 (-)NCBIGRCr8
mRatBN7.21383,280,782 - 83,297,535 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1383,280,784 - 83,295,967 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1385,900,776 - 85,913,853 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01387,194,261 - 87,207,344 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01384,432,186 - 84,445,276 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01391,146,878 - 91,163,691 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1391,168,973 - 91,198,036 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl1391,146,876 - 91,229,066 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01395,665,044 - 95,682,068 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41386,898,651 - 86,911,743NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1382,933,510 - 83,125,911 (-)NCBICelera
Cytogenetic Map13q24NCBI
LOC100991644
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2188,268,426 - 88,282,501 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1187,936,861 - 87,950,937 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01136,892,311 - 136,906,450 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
Fcgr2a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244050587,496,110 - 7,502,712 (+)NCBIHiC_Itri_2
SpeTri2.0NW_00493713115,542 - 22,099 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FCGR2A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1202,480,710 - 2,512,429 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660381,557,192 - 1,570,636 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Fcgr2a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462482623,930 - 34,735 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in FCGR2A
41 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001136219.3(FCGR2A):c.500A>G (p.His167Arg) single nucleotide variant Lupus nephritis, susceptibility to [RCV000015946]|Malaria, severe, susceptibility to [RCV000054529]|Pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis [RCV000015947]|not specified [RCV000454909] Chr1:161509955 [GRCh38]
Chr1:161479745 [GRCh37]
Chr1:1q23.3
risk factor|benign|drug response
GRCh38/hg38 1q23.3(chr1:161513195-161671153)x3 copy number gain See cases [RCV000051556] Chr1:161513195..161671153 [GRCh38]
Chr1:161482985..161640943 [GRCh37]
Chr1:159749609..159907567 [NCBI36]
Chr1:1q23.3
uncertain significance
GRCh38/hg38 1q23.2-24.1(chr1:159479887-166895086)x1 copy number loss See cases [RCV000051172] Chr1:159479887..166895086 [GRCh38]
Chr1:159449677..166864323 [GRCh37]
Chr1:157716301..165130947 [NCBI36]
Chr1:1q23.2-24.1
pathogenic
GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3 copy number gain See cases [RCV000051854] Chr1:157747246..176021247 [GRCh38]
Chr1:157717036..175990383 [GRCh37]
Chr1:155983660..174257006 [NCBI36]
Chr1:1q23.1-25.1
pathogenic
GRCh38/hg38 1q23.3-24.2(chr1:160789732-168617494)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|See cases [RCV000053913] Chr1:160789732..168617494 [GRCh38]
Chr1:160759522..168586732 [GRCh37]
Chr1:159026146..166853356 [NCBI36]
Chr1:1q23.3-24.2
pathogenic
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
NM_002155.4(HSPA6):c.-1862_*5145del deletion Small for gestational age [RCV000161186] Chr1:161522797..161531735 [GRCh38]
Chr1:161492587..161501525 [GRCh37]
Chr1:1q23.3
not provided
GRCh37/hg19 1q23.2-25.1(chr1:160369890-175796325) copy number loss not provided [RCV000767779] Chr1:160369890..175796325 [GRCh37]
Chr1:1q23.2-25.1
pathogenic
NM_001136219.3(FCGR2A):c.187C>T (p.Gln63Ter) single nucleotide variant FCGR2A-related disorder [RCV003972704]|not specified [RCV000455363] Chr1:161506414 [GRCh38]
Chr1:161476204 [GRCh37]
Chr1:1q23.3
benign
NM_001136219.3(FCGR2A):c.645A>G (p.Pro215=) single nucleotide variant not specified [RCV000455589] Chr1:161510859 [GRCh38]
Chr1:161480649 [GRCh37]
Chr1:1q23.3
benign
NM_001136219.3(FCGR2A):c.879C>T (p.Pro293=) single nucleotide variant not specified [RCV000455964] Chr1:161518073 [GRCh38]
Chr1:161487863 [GRCh37]
Chr1:1q23.3
benign
NM_001136219.3(FCGR2A):c.188A>G (p.Gln63Arg) single nucleotide variant FCGR2A-related disorder [RCV003970260]|not specified [RCV000456029] Chr1:161506415 [GRCh38]
Chr1:161476205 [GRCh37]
Chr1:1q23.3
benign
NM_001136219.3(FCGR2A):c.365-11G>A single nucleotide variant not specified [RCV000456031] Chr1:161509809 [GRCh38]
Chr1:161479599 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.3(chr1:161469309-162517412)x3 copy number gain not provided [RCV000684667] Chr1:161469309..162517412 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.2-25.2(chr1:159815642-177026983)x1 copy number loss not provided [RCV000736717] Chr1:159815642..177026983 [GRCh37]
Chr1:1q23.2-25.2
pathogenic
GRCh37/hg19 1q23.3(chr1:161477028-161643125)x3 copy number gain not provided [RCV000749209] Chr1:161477028..161643125 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161482520-161519610)x3 copy number gain not provided [RCV000749210] Chr1:161482520..161519610 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161483723-161611004)x1 copy number loss not provided [RCV000749211] Chr1:161483723..161611004 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161483843-161643125)x3 copy number gain not provided [RCV000749212] Chr1:161483843..161643125 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161486615-161643984)x0 copy number loss not provided [RCV000749213] Chr1:161486615..161643984 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161486615-161645259)x1 copy number loss not provided [RCV000749214] Chr1:161486615..161645259 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:160744174-162583871)x3 copy number gain not provided [RCV000849025] Chr1:160744174..162583871 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1 copy number loss not provided [RCV000848773] Chr1:157321299..167391423 [GRCh37]
Chr1:1q23.1-24.2
pathogenic
NM_001136219.3(FCGR2A):c.210C>T (p.Ser70=) single nucleotide variant not provided [RCV000887332] Chr1:161506437 [GRCh38]
Chr1:161476227 [GRCh37]
Chr1:1q23.3
benign|likely benign
NM_001136219.3(FCGR2A):c.733C>T (p.Arg245Trp) single nucleotide variant not provided [RCV000890879] Chr1:161510947 [GRCh38]
Chr1:161480737 [GRCh37]
Chr1:1q23.3
benign
GRCh37/hg19 1q23.3(chr1:161134675-161652307)x3 copy number gain not provided [RCV001005146] Chr1:161134675..161652307 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.418A>G (p.Met140Val) single nucleotide variant not provided [RCV001702155] Chr1:161509873 [GRCh38]
Chr1:161479663 [GRCh37]
Chr1:1q23.3
likely benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance
NM_001136219.3(FCGR2A):c.363C>T (p.Ser121=) single nucleotide variant not provided [RCV001702143] Chr1:161506590 [GRCh38]
Chr1:161476380 [GRCh37]
Chr1:1q23.3
likely benign
GRCh37/hg19 1q23.2-24.1(chr1:160417296-166197042) copy number loss not specified [RCV002053658] Chr1:160417296..166197042 [GRCh37]
Chr1:1q23.2-24.1
pathogenic
NC_000001.10:g.(?_158581054)_(162750036_?)dup duplication Autoimmune interstitial lung disease-arthritis syndrome [RCV001918952]|not provided [RCV001918953] Chr1:158581054..162750036 [GRCh37]
Chr1:1q23.1-23.3
uncertain significance|no classifications from unflagged records
NM_001136219.3(FCGR2A):c.497C>T (p.Ser166Phe) single nucleotide variant Cystic fibrosis [RCV002208746] Chr1:161509952 [GRCh38]
Chr1:161479742 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.780+1G>A single nucleotide variant Cystic fibrosis [RCV002204527] Chr1:161513933 [GRCh38]
Chr1:161483723 [GRCh37]
Chr1:1q23.3
uncertain significance
NC_000001.10:g.(?_161279609)_(161751809_?)dup duplication Charcot-Marie-Tooth disease, type I [RCV003111375] Chr1:161279609..161751809 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.614T>C (p.Val205Ala) single nucleotide variant not specified [RCV004246601] Chr1:161510069 [GRCh38]
Chr1:161479859 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.776T>C (p.Phe259Ser) single nucleotide variant not specified [RCV004076148] Chr1:161513928 [GRCh38]
Chr1:161483718 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.221A>C (p.Gln74Pro) single nucleotide variant not specified [RCV004143913] Chr1:161506448 [GRCh38]
Chr1:161476238 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.895G>A (p.Asp299Asn) single nucleotide variant not specified [RCV004230384] Chr1:161518089 [GRCh38]
Chr1:161487879 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.514T>C (p.Phe172Leu) single nucleotide variant not specified [RCV004170961] Chr1:161509969 [GRCh38]
Chr1:161479759 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.671T>C (p.Ile224Thr) single nucleotide variant not specified [RCV004086625] Chr1:161510885 [GRCh38]
Chr1:161480675 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.677C>T (p.Thr226Ile) single nucleotide variant not specified [RCV004086627] Chr1:161510891 [GRCh38]
Chr1:161480681 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.281C>T (p.Ala94Val) single nucleotide variant not specified [RCV004096671] Chr1:161506508 [GRCh38]
Chr1:161476298 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.674C>G (p.Ala225Gly) single nucleotide variant not specified [RCV004086626] Chr1:161510888 [GRCh38]
Chr1:161480678 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.449C>G (p.Pro150Arg) single nucleotide variant not specified [RCV004270051] Chr1:161509904 [GRCh38]
Chr1:161479694 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.734G>A (p.Arg245Gln) single nucleotide variant not specified [RCV004253767] Chr1:161510948 [GRCh38]
Chr1:161480738 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.635G>A (p.Ser212Asn) single nucleotide variant not specified [RCV004348480] Chr1:161510849 [GRCh38]
Chr1:161480639 [GRCh37]
Chr1:1q23.3
uncertain significance
GRCh37/hg19 1q23.1-23.3(chr1:158001058-162858285)x1 copy number loss not provided [RCV003483944] Chr1:158001058..162858285 [GRCh37]
Chr1:1q23.1-23.3
likely pathogenic
NM_001136219.3(FCGR2A):c.943A>G (p.Ser315Gly) single nucleotide variant not provided [RCV003456673] Chr1:161518137 [GRCh38]
Chr1:161487927 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.153C>T (p.Asn51=) single nucleotide variant FCGR2A-related disorder [RCV003974633] Chr1:161506380 [GRCh38]
Chr1:161476170 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.144G>A (p.Pro48=) single nucleotide variant FCGR2A-related disorder [RCV003914393] Chr1:161506371 [GRCh38]
Chr1:161476161 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.308C>T (p.Thr103Met) single nucleotide variant not specified [RCV004389341] Chr1:161506535 [GRCh38]
Chr1:161476325 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.257C>T (p.Thr86Met) single nucleotide variant not specified [RCV004389340] Chr1:161506484 [GRCh38]
Chr1:161476274 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.341C>T (p.Pro114Leu) single nucleotide variant not specified [RCV004389342] Chr1:161506568 [GRCh38]
Chr1:161476358 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.799A>C (p.Ile267Leu) single nucleotide variant not specified [RCV004391415] Chr1:161517993 [GRCh38]
Chr1:161487783 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.943A>T (p.Ser315Cys) single nucleotide variant not specified [RCV004391416] Chr1:161518137 [GRCh38]
Chr1:161487927 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.944G>A (p.Ser315Asn) single nucleotide variant not specified [RCV004391417] Chr1:161518138 [GRCh38]
Chr1:161487928 [GRCh37]
Chr1:1q23.3
uncertain significance
NM_001136219.3(FCGR2A):c.648G>A (p.Met216Ile) single nucleotide variant not provided [RCV003409205] Chr1:161510862 [GRCh38]
Chr1:161480652 [GRCh37]
Chr1:1q23.3
likely benign
NM_001136219.3(FCGR2A):c.626G>C (p.Ser209Thr) single nucleotide variant not specified [RCV004324439] Chr1:161510840 [GRCh38]
Chr1:161480630 [GRCh37]
Chr1:1q23.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3303
Count of miRNA genes:1112
Interacting mature miRNAs:1375
Transcripts:ENST00000271450, ENST00000367972, ENST00000459885, ENST00000461298, ENST00000467525, ENST00000467654, ENST00000471026, ENST00000473080, ENST00000482233, ENST00000483665, ENST00000486608, ENST00000491841, ENST00000497474, ENST00000536731
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
AL009695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,485,115 - 161,485,255UniSTSGRCh37
Build 361159,751,739 - 159,751,879RGDNCBI36
Cytogenetic Map1q23UniSTS
HuRef1132,810,126 - 132,810,266UniSTS
RH17750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,479,506 - 161,479,751UniSTSGRCh37
Build 361159,746,130 - 159,746,375RGDNCBI36
Celera1134,686,728 - 134,686,973RGD
Cytogenetic Map1q23UniSTS
HuRef1132,804,518 - 132,804,763UniSTS
GeneMap99-GB4 RH Map1591.58UniSTS
NCBI RH Map11443.7UniSTS
D1S3418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,569,712 - 161,569,985UniSTSGRCh37
GRCh371161,488,056 - 161,488,329UniSTSGRCh37
Build 361159,754,680 - 159,754,953RGDNCBI36
Cytogenetic Map1q23UniSTS
Cytogenetic Map1q23.3UniSTS
HuRef1132,813,067 - 132,813,340UniSTS
GeneMap99-GB4 RH Map1596.62UniSTS
GeneMap99-GB4 RH Map1576.12UniSTS
Whitehead-RH Map1732.4UniSTS
Whitehead-YAC Contig Map1 UniSTS
RH68292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371161,570,755 - 161,570,950UniSTSGRCh37
GRCh371161,489,104 - 161,489,299UniSTSGRCh37
Build 361159,755,728 - 159,755,923RGDNCBI36
Celera1134,591,802 - 134,591,997RGD
Cytogenetic Map1q23UniSTS
HuRef1132,814,116 - 132,814,311UniSTS
GeneMap99-GB4 RH Map1589.09UniSTS
GDB:190031  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q23UniSTS
Cytogenetic Map1q23.3UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 42 42
Medium 613 1751 449 114 1137 68 1546 245 976 149 238 834 47 962 979 3
Low 1729 1161 1244 488 519 371 2508 1723 2419 241 1126 602 120 1 242 1649 1 2
Below cutoff 46 33 21 16 193 18 289 218 314 14 43 71 1 160

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001136219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_021642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454041 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737042 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide A21604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AA634082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC243509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF416711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF481857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH003095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI250177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225601 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK226059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC019931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC020823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX379627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF064737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  J03619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M28697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M31932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MH558549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X62572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X68090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y00644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000271450   ⟹   ENSP00000271450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,457 - 161,519,829 (+)Ensembl
RefSeq Acc Id: ENST00000367972   ⟹   ENSP00000356949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,430 - 161,518,558 (+)Ensembl
RefSeq Acc Id: ENST00000459885   ⟹   ENSP00000476411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,513,898 - 161,519,967 (+)Ensembl
RefSeq Acc Id: ENST00000461298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,513,377 - 161,518,590 (+)Ensembl
RefSeq Acc Id: ENST00000467525   ⟹   ENSP00000476495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,506,333 - 161,524,013 (+)Ensembl
RefSeq Acc Id: ENST00000467654
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,446 - 161,510,350 (+)Ensembl
RefSeq Acc Id: ENST00000471026
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,506,651 - 161,518,355 (+)Ensembl
RefSeq Acc Id: ENST00000473080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,453 - 161,506,368 (+)Ensembl
RefSeq Acc Id: ENST00000482233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,868 - 161,506,640 (+)Ensembl
RefSeq Acc Id: ENST00000483665   ⟹   ENSP00000440148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,457 - 161,518,565 (+)Ensembl
RefSeq Acc Id: ENST00000486608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,514,620 - 161,518,603 (+)Ensembl
RefSeq Acc Id: ENST00000491841
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,517,975 - 161,523,099 (+)Ensembl
RefSeq Acc Id: ENST00000497474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,459 - 161,506,449 (+)Ensembl
RefSeq Acc Id: ENST00000536731   ⟹   ENSP00000441156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,457 - 161,509,899 (+)Ensembl
RefSeq Acc Id: ENST00000699277   ⟹   ENSP00000514258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,456 - 161,519,553 (+)Ensembl
RefSeq Acc Id: ENST00000699278   ⟹   ENSP00000514259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,457 - 161,519,554 (+)Ensembl
RefSeq Acc Id: ENST00000699279   ⟹   ENSP00000514260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1161,505,869 - 161,519,554 (+)Ensembl
RefSeq Acc Id: NM_001136219   ⟹   NP_001129691
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
GRCh371161,475,205 - 161,489,360 (+)ENTREZGENE
HuRef1132,800,353 - 132,814,372 (+)ENTREZGENE
CHM1_11162,897,042 - 162,911,192 (+)NCBI
T2T-CHM13v2.01160,768,080 - 160,782,453 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375296   ⟹   NP_001362225
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
T2T-CHM13v2.01160,768,080 - 160,782,453 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375297   ⟹   NP_001362226
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
T2T-CHM13v2.01160,768,080 - 160,782,453 (+)NCBI
Sequence:
RefSeq Acc Id: NM_021642   ⟹   NP_067674
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
GRCh371161,475,205 - 161,489,360 (+)ENTREZGENE
Build 361159,741,844 - 159,755,984 (+)NCBI Archive
HuRef1132,800,353 - 132,814,372 (+)ENTREZGENE
CHM1_11162,897,042 - 162,911,192 (+)NCBI
T2T-CHM13v2.01160,768,080 - 160,782,453 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509290   ⟹   XP_011507592
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509291   ⟹   XP_011507593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,519,829 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000663   ⟹   XP_016856152
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,520,183 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000664   ⟹   XP_016856153
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,524,048 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000665   ⟹   XP_016856154
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,524,048 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000666   ⟹   XP_016856155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,520,187 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024454040   ⟹   XP_024309808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,506,633 - 161,520,190 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047449441   ⟹   XP_047305397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,520,183 (+)NCBI
RefSeq Acc Id: XM_054335132   ⟹   XP_054191107
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,782,806 (+)NCBI
RefSeq Acc Id: XM_054335133   ⟹   XP_054191108
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,782,806 (+)NCBI
RefSeq Acc Id: XM_054335134   ⟹   XP_054191109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,786,676 (+)NCBI
RefSeq Acc Id: XM_054335135   ⟹   XP_054191110
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,786,676 (+)NCBI
RefSeq Acc Id: XM_054335136   ⟹   XP_054191111
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,782,811 (+)NCBI
RefSeq Acc Id: XM_054335137   ⟹   XP_054191112
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,768,080 - 160,782,390 (+)NCBI
RefSeq Acc Id: XM_054335138   ⟹   XP_054191113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01160,769,257 - 160,782,813 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001129691 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362225 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362226 (Get FASTA)   NCBI Sequence Viewer  
  NP_067674 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507592 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507593 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856152 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856153 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856154 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856155 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309808 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305397 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191107 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191108 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191109 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191110 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191111 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191112 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191113 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA35827 (Get FASTA)   NCBI Sequence Viewer  
  AAA35932 (Get FASTA)   NCBI Sequence Viewer  
  AAA36050 (Get FASTA)   NCBI Sequence Viewer  
  AAH19931 (Get FASTA)   NCBI Sequence Viewer  
  AAH20823 (Get FASTA)   NCBI Sequence Viewer  
  AAL78867 (Get FASTA)   NCBI Sequence Viewer  
  AAL99539 (Get FASTA)   NCBI Sequence Viewer  
  ABK41920 (Get FASTA)   NCBI Sequence Viewer  
  AXP32131 (Get FASTA)   NCBI Sequence Viewer  
  BAG37654 (Get FASTA)   NCBI Sequence Viewer  
  BAH12840 (Get FASTA)   NCBI Sequence Viewer  
  BAH12860 (Get FASTA)   NCBI Sequence Viewer  
  CAA01563 (Get FASTA)   NCBI Sequence Viewer  
  CAA48217 (Get FASTA)   NCBI Sequence Viewer  
  CAA68672 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000271450
  ENSP00000271450.6
  ENSP00000356949
  ENSP00000356949.4
  ENSP00000440148.1
  ENSP00000441156.1
  ENSP00000476411.1
  ENSP00000476495.1
  ENSP00000514258
  ENSP00000514258.1
  ENSP00000514259.1
  ENSP00000514260.1
GenBank Protein P12318 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001129691   ⟸   NM_001136219
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8WUN1 (UniProtKB/Swiss-Prot),   Q8WW64 (UniProtKB/Swiss-Prot),   P12318 (UniProtKB/Swiss-Prot),   A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_067674   ⟸   NM_021642
- Peptide Label: isoform 2 precursor
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507592   ⟸   XM_011509290
- Peptide Label: isoform X5
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507593   ⟸   XM_011509291
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016856153   ⟸   XM_017000664
- Peptide Label: isoform X3
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856154   ⟸   XM_017000665
- Peptide Label: isoform X3
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856155   ⟸   XM_017000666
- Peptide Label: isoform X4
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856152   ⟸   XM_017000663
- Peptide Label: isoform X2
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024309808   ⟸   XM_024454040
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: NP_001362225   ⟸   NM_001375296
- Peptide Label: isoform 3 precursor
- UniProtKB: A0A8V8TPS4 (UniProtKB/TrEMBL),   A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362226   ⟸   NM_001375297
- Peptide Label: isoform 4 precursor
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000476495   ⟸   ENST00000467525
RefSeq Acc Id: ENSP00000271450   ⟸   ENST00000271450
RefSeq Acc Id: ENSP00000441156   ⟸   ENST00000536731
RefSeq Acc Id: ENSP00000440148   ⟸   ENST00000483665
RefSeq Acc Id: ENSP00000476411   ⟸   ENST00000459885
RefSeq Acc Id: ENSP00000356949   ⟸   ENST00000367972
RefSeq Acc Id: XP_047305397   ⟸   XM_047449441
- Peptide Label: isoform X1
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000514258   ⟸   ENST00000699277
RefSeq Acc Id: ENSP00000514260   ⟸   ENST00000699279
RefSeq Acc Id: ENSP00000514259   ⟸   ENST00000699278
RefSeq Acc Id: XP_054191109   ⟸   XM_054335134
- Peptide Label: isoform X3
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191110   ⟸   XM_054335135
- Peptide Label: isoform X3
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191111   ⟸   XM_054335136
- Peptide Label: isoform X4
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191107   ⟸   XM_054335132
- Peptide Label: isoform X1
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191108   ⟸   XM_054335133
- Peptide Label: isoform X2
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191112   ⟸   XM_054335137
- Peptide Label: isoform X5
- UniProtKB: A0A346JF56 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191113   ⟸   XM_054335138
- Peptide Label: isoform X7
Protein Domains
Ig-like   Ig-like C2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P12318-F1-model_v2 AlphaFold P12318 1-317 view protein structure

Promoters
RGD ID:6785570
Promoter ID:HG_KWN:5859
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000271450,   ENST00000367972,   OTTHUMT00000083324,   OTTHUMT00000083326,   OTTHUMT00000083327,   OTTHUMT00000083328,   OTTHUMT00000315965,   OTTHUMT00000315966
Position:
Human AssemblyChrPosition (strand)Source
Build 361159,741,901 - 159,743,007 (+)MPROMDB
RGD ID:6858020
Promoter ID:EPDNEW_H2111
Type:initiation region
Name:FCGR2A_1
Description:Fc fragment of IgG receptor IIa
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381161,505,457 - 161,505,517EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3616 AgrOrtholog
COSMIC FCGR2A COSMIC
Ensembl Genes ENSG00000143226 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000271450 ENTREZGENE
  ENST00000271450.12 UniProtKB/Swiss-Prot
  ENST00000367972 ENTREZGENE
  ENST00000367972.8 UniProtKB/Swiss-Prot
  ENST00000459885.1 UniProtKB/TrEMBL
  ENST00000467525.5 UniProtKB/TrEMBL
  ENST00000483665.6 UniProtKB/TrEMBL
  ENST00000536731.5 UniProtKB/TrEMBL
  ENST00000699277 ENTREZGENE
  ENST00000699277.1 UniProtKB/TrEMBL
  ENST00000699278.1 UniProtKB/TrEMBL
  ENST00000699279.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000143226 GTEx
HGNC ID HGNC:3616 ENTREZGENE
Human Proteome Map FCGR2A Human Proteome Map
InterPro Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:2212 UniProtKB/Swiss-Prot
NCBI Gene 2212 ENTREZGENE
OMIM 146790 OMIM
PANTHER IMMUNOGLOBULIN FC RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LOW AFFINITY IMMUNOGLOBULIN GAMMA FC REGION RECEPTOR II-A-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ig_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB FCGR2A RGD, PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A346JF56 ENTREZGENE, UniProtKB/TrEMBL
  A0A8V8TN00_HUMAN UniProtKB/TrEMBL
  A0A8V8TN30_HUMAN UniProtKB/TrEMBL
  A0A8V8TPS4 ENTREZGENE, UniProtKB/TrEMBL
  F5GX41_HUMAN UniProtKB/TrEMBL
  F5GXY9_HUMAN UniProtKB/TrEMBL
  FCG2A_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q8WUN1 ENTREZGENE
  Q8WW64 ENTREZGENE
  V9GY55_HUMAN UniProtKB/TrEMBL
  V9GY83_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q8WUN1 UniProtKB/Swiss-Prot
  Q8WW64 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-11-08 FCGR2A  Fc gamma receptor IIa  FCGR2A  Fc fragment of IgG receptor IIa  Symbol and/or name change 19259463 PROVISIONAL
2016-01-19 FCGR2A  Fc fragment of IgG receptor IIa  FCGR2A  Fc fragment of IgG, low affinity IIa, receptor (CD32)  Symbol and/or name change 5135510 APPROVED