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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16pter, SYNGR3 to 16p13.3, CCNF <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
16pter SYNGR3 Synaptogyrin 3   603927     A  
16pter-p13.3 HBA1 Hemoglobin alpha-1   141800 Thalassemias, alpha-, 604131 (3); Methemoglobinemias, alpha- (3);Erythremias, alpha- (3); Heinz body anemias, alpha-, 140700 (3) 1, 2, or 3 loci;5'-zeta-pseudozeta-pseudoalpha-alpha-2-alpha-1-3' HS 11(Hba)
16pter-p13.3 HBA2 Hemoglobin alpha-2   141850 Thalassemia, alpha-, 604131 (3); Hemoglobin H disease (3); Heinz bodyanemia, 140700 (3); Erythrocytosis (3); Hypochromic microcytic anemia (3)   HS 11(Hba)
16pter-p13.3 HBQ1 Hemoglobin theta-1   142240     RE  
16pter-p13.3 HBZ Hemoglobin, zeta   142310     RE  
16pter-p13.3 HBHR, ATR1 Alpha-thalassemia/mental retardation syndrome, type 1   141750 Alpha-thalassemia/mental retardation syndrome, type 1 (1) contiguous gene syndrome involving deletion of HBA1 and HBA2 Fd, RE, D  
16pter-p13.3 MPG, MDG N-methylpurine DNA glycosylase   156565   75kb upstream of HBZ REa, REn 11(Mpg)
16pter-p13 CHDS1 Coronary heart disease, susceptibility to, 1   607339 {Coronary heart disease, susceptibility to} (2)   Fd  
16pter-p11 ZNF75A Zinc finger protein-75A   601473     REa  
16p13.3 ABAT, GABAT 4-aminobutyrate aminotransferase   137150 GABA-transaminase deficiency (3)   R  
16p13.3 ABCA3, ABC3, SMDP3 ATP-binding cassette-3   601615 Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3)   REc  
16p13.3 ADCY9 Adenylate cyclase-9   603302     A 16(Adcy9)
16p13.3 ALG1, HMAT1, HMT1 Alg1, yeast, homolog of (beta-1,4 mannosyltransferase)   605907 Congenital disorder of glycosylation, type Ik, 608540 (3)   REc  
16p13.3 AXIN1, AXIN Axis inhibitor 1   603816 Hepatocellular carcinoma, somatic, 114550 (3); Caudal duplicationanomaly, 607864 (3)   REc  
16p13.3 ATP6V0C, ATP6L, ATP6C ATPase, H+ transporting, lysosomal, 16kD, V0 subunit c   108745     REc  
16p13.3 BAIAP3, BAP3 BAI1-associated protein 3   604009     A, R  
16p13.3 C16orf5 Chromosome 16 open reading frame 5   610503     A, Psh  
16p13.3 C16orf30, CLP24 Claudin-like protein 24   611002     REc  
16p13.3 CACNA1H, EIG6, ECA6 Calcium channel, voltage-dependent, T type, alpha-1H subunit   607904 {Epilepsy, idiopathic generalized, susceptibility to, 6}, 611942 (3);{Epilepsy, childhood absence, susceptibility to, 6}, 611942 (3)   R, A 17(Cacna1h)
16p13.3 CASKIN1, KIAA1306 CASK-interacting protein 1   612184     R, REc  
16p13.3 CCNF, FBX1 Cyclin F   600227     REn 17(Ccnf)
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