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PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM
The OMIM Gene map presents the cytogenetic map location of disease genes and other expressed genes described in OMIM. See the OMIM Morbid Map for a list of disease genes organized by disease. For more refined maps of genes and DNA segments click on the Location to invoke NCBI Entrez Map Viewer.
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Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer". You must capitalize X and Y to search for those chromosomes.
17q22-q24, CMRF35 to 17q23-q24, RGS9 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q22-q24 CMRF35, CMRF35A CMRF35 antigen   606786     Psh, A  
17q22-q24 CSH1, CSA, PL Chorionic somatomammotropin hormone-1   150200 [Placental lactogen deficiency] (1)   REa, A 13(Pl1)
17q22-q24 CSH2, CSB Chorionic somatomammotropin B   118820     REa, A 13(Pl2)
17q22-q24 CSHL1, CSL Chorionic somatomammotropin hormone-like 1   603515     A  
17q22-q24 GH1, GHN Growth hormone-1   139250 Growth hormone deficiency (3); Growth hormone deficiency, isolated,type IA, 262400 (3); Growth hormone deficiency, isolated, type IB, 262400 (3); Growth hormone deficiency, isolated, type II, 173100 (3); Kowarski syndrome,262650 (3); Short stature, familial, 604271 (3) 5'-GH1-CSHP1-CSH1-GH2-CSH2-3' REa, A, Fd 11(Gh)
17q22-q24 GH2, GHV Growth hormone-2   139240     REa, A  
17q22-q25 FOXJ1, FKHL13, HFH4 Forkhead box J1   602291     REc  
17q22-qter CDK3 Cyclin-dependent kinase 3   123828   distal to BRCA1 Psh  
17q23 ACE, DCP1, ACE1 Angiotensin I converting enzyme (dipeptidyl carboxypeptidase-1)   106180 {Myocardial infarction, susceptibility to} (3); {Alzheimerdisease, susceptibility to}, 104300 (3); {Diabetic nephropathy, susceptibility to}, 603933 (3); [Angiotensin I-converting enzyme, benign serum increase] (3);{SARS, progression of} (3); Renal tubular dysgenesis, 267430 (3)   A, H, Fd  
17q23 BSZQTL Bone size quantitative trait locus 1   609656 {Bone size QTL} (2)   Fd  
17q23 CA4, RP17 Carbonic anhydrase IV   114760 Retinitis pigmentosa-17, 600852 (3)   REa, A, Fd  
17q23 CD79B, IGB, B29 Immunoglobulin-associated protein (B29)   147245     A  
17q23 CLTC Clathrin, heavy polypeptide (Hc)   118955   fusion gene with TFE3 in renal adenocarcinoma REc, Ch  
17q23 MKS1, MKS, BBS13 MKS1 gene   609883 Meckel syndrome, type 1, 249000 (3); Bardet-Biedl syndrome 13,209900 (3) frequent in Finland Fd, REc  
17q23 PECAM1 Platelet/endothelial cell adhesion molecule (CD31 antigen)   173445     Psh, A 6(Pecam1)
17q23 SEPT4, PNUTL2 Septin 4   603696     A, REc 11(Sept4)
17q23 TBX2 T-box 2   600747     A, H 11(Tbx2)
17q23-q24 KPNA2, RCH1, QIP2 Karyopherin alpha-2   600685     REc  
17q23-q24 POLG2, POLGB, PEOA4 Polymerase, DNA, gamma-2   604983 Progressive external ophthalmoplegia with mitochondrial DNAdeletions, autosomal dominant 4, 610131 (3)   REc  
17q23-q24 PRKAR1A, TSE1, CNC1, CAR, PPNAD1 Protein kinase, cAMP-dependent, regulatory, type I, alpha   188830 Carney complex, type 1, 160980 (3); Myxoma, intracardiac, 255960 (3);Thyroid carcinoma, papillary, 188550 (3); Pigmented adrenocortical disease, primary, 1, 610489 (3); Adrenocortical tumor, somatic (3) fused with RET to form PTC2 S, M, REa, RE, Fd 11(Tse1)
17q23-q24 RGS9, PERRS Regulator of G protein signaling 9   604067 Bradyopsia, 608415 (3)   R, A  
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