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.
Search for: (from the current location)    
  • 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.
10q11.2, CHAT to 10q11.23, PARG <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
10q11.2 CHAT, CMS1A2 Choline acetyltransferase   118490 Myasthenic syndrome, congenital, associated with episodic apnea,254210 (3)   REa, A  
10q11.2 DKK1 Dickkopf, Xenopus, homolog of, 1   605189     A  
10q11.2 MAPK8, PRKM8, JNK1, SAPK1 Mitogen-activated protein kinase 8   601158     R, REc  
10q11.2 MSMB, HPC13 Microseminoprotein, beta   157145 {Prostate cancer, hereditary, 13}, 611928 (3)   REa, A  
10q11.2 NCOA4, ELE1, PTC3 Nuclear receptor coactivator 4   601984 Thyroid carcinoma, papillary, 188550 (3) fused with RET to form PTC3 REn  
10q11.2 PRKG1, PRKG1B, PRKGR1B Protein kinase, cGMP-dependent, regulatory, type I   176894     REa, A  
10q11.2 RBP3 Retinol-binding protein-3, interstitial   180290     REa, A, Fd 14(Rbp3)
10q11.2 RET, MEN2A RET transforming sequence; oncogene RET   164761 Multiple endocrine neoplasia IIA, 171400 (3); Medullary thyroidcarcinoma, 155240 (3); Multiple endocrine neoplasia IIB, 162300 (3); Hirschsprung disease, 142623 (3); Central hypoventilation syndrome, congenital,209880 (3); Pheochromocytoma, 171300 (3); Renal agenesis, 191830 (3)   A, REn, Fd, Ch, D  
10q11.2 SGMS1, SMS1, TMEM23, MOB Sphingomyelin synthase 1   611573     REc  
10q11.2 SLC18A3, VACHT Solute carrier family 18 (vesicular acetylcholine), member 3   600336     REn  
10q11.2 ZNF22, KOX15 Zinc finger protein-22 (KOX15)   194529     A, REa  
10q11.2 ZNF33A, NF11A, KOX2 Zinc finger protein-33a   194521     REa, A  
10q11.2 ZNF33B, ZNF11B, KOX2 Zinc finger protein-33b   194522     REa, A  
10q11.2-q21 MBL2, MBL, MBP1 Mannose-binding lectin 2, soluble (opsonic defect)   154545 Mannose-binding protein deficiency (3); {Diabetes mellitus,gestational, susceptibility to} (3); {Meningococcal disease, susceptibility to} (3); {Chronic infections, due to MBL deficiency} (3) near MEN2A REa, A, Fd 14(Mbl1)
10q11.2-q21 UBE2D1, UBCH5A, UBCH5 Ubiquitin-conjugating enzyme E2D 1   602961     Psh, R  
10q11.2-q21.1 GPR7 G protein-coupled receptor-7   600730     A  
10q11.2-q21.2 PPYR1, NPY4R, PP1 Pancreatic polypeptide receptor-1   601790     REa, REc 14(Ppyr1)
10q11.21-q11.22 HNRPF Heterogeneous nuclear ribonucleoprotein F   601037     A  
10q11.21-q11.23 TIMM23 Translocase of inner mitochondrial membrane 23, Yeast, homolog of   605034     A  
10q11.23 ASAH2C, ASAH2L N-acylsphingosine amidohydrolase 2C   610987     REc  
10q11.23 PARG Poly(ADP-ribose) glycohydrolase   603501     A 14(Parg)
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

Disclaimer | Write to the Help Desk | Privacy Policy
NCBI | NLM | NIH