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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17q23, ACE to 17q23-qter, PEPE <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q23 ACE, DCP1, ACE1, MVCD3 Angiotensin I converting enzyme (dipeptidyl carboxypeptidase-1)   106180 {Myocardial infarction, susceptibility to} (3); {Alzheimer disease,susceptibility to}, 104300 (3); {Microvascular complications of diabetes 3, 612624 (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  
17q23-q24 SMARCD2, BAF60B SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily d, member 2 601736     Psh, R  
17q23-q25 DDX5, HLR1, G17P1 DEAD/H box-5 (RNA helicase, 68kD)   180630   near BRCA1 REa, REn  
17q23-q25 ICAM2 Intercellular adhesion molecule-2   146630     REa, C  
17q23-q25 MRPL38 Mitodhondrial ribosomal protein L38   611844     R, REc  
17q23-q25 MRPS7 Mitochondrial ribosomal protein S7   611974     R, REc  
17q23-q25 NT5C, UMPH2, DNT1 5', 3' nucleotidase, cytosolic   191720     REa 11(Umph2)
17q23-qter APOH Apolipoprotein H (beta-2-glycoprotein I)   138700 [Apolipoprotein H deficiency] (3)   Fd, REa 11(Apoh)
17q23-qter PEPE Peptidase E   170200     S  
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