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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2p24-p23, MATN3 to 2p23.1, YPEL5 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
2p24-p23 MATN3, EDM5, HOA Matrilin 3   602109 Epiphyseal dysplasia, multiple, 5, 607078 (3); {Osteoarthritis,hand, susceptibility to}, 607850 (3); Spondyloepimetaphyseal dysplasia, 608728 (3)   A, Fd 12(Matn3)
2p24-p23 TCF23 Transcription factor 23   609635     REc 5(Tcf23)
2p24-p22 ADCY3 Adenylate cyclase-3   600291     REa, A  
2p24-p21 CENPA Centromere protein A, 17kD   117139     R, Psh 5(Cenpa)
2p23.3 ABHD1, LABH1 Abhydrolase domain-containing 1   612195     REc 5(Abhd1)
2p23.3 CENPO Centromeric protein O   611504     R, REc  
2p23.3 DPYSL5, CRMP5, CRAM Dihydropyrimidinase-like 5   608383     R, REc 5(Dpysl5)
2p23.3 EIF2B4 Eukaryotic translation initiation factor 2B, subunit 4   606687 Leukoencephaly with vanishing white matter, 603896 (3);Ovarioleukodystrophy, 603896 (3)   R  
2p23 EMILIN1, EMILIN Elastin microfibril interfacer 1   130660     REc  
2p23.3 FNDC4, FRCP1 Fibrinectin type III domain-containing protein 4   611905     R, REc, H 5(Fndc4)
2p23.3 POMC Proopiomelanocortin (adrenocorticotropin/beta-lipotropin)   176830 Obesity, adrenal insufficiency, and red hair due to POMC deficiency,609734 (3); {Obesity, early-onset, susceptibility to}, 601665 (3)   REa, A 12(Pomc1)
2p23.3 SLC30A3, ZNT3 Solute carrier family 30 (zinc transporter), member 3   602878     REc 5(Slc30a3)
2p23.3-p23.2 GCKR, GKRP Glucokinase (hexokinase 4) regulatory protein   600842     A, Fd, REc  
2p23.3-p23.2 KHK Ketohexokinase (fructokinase)   229800 [Fructosuria] (3)   A, Fd, REc, Psh  
2p23.3-p23.1 MAPRE3, EB3, RP3, EBF3 Microtubule-associated protein, RP/EB family, member 3   605788     A, R  
2p23.3-p22.3 GINGF3, HGF3, GGF3 Fibromatosis, gingival, 3   609955 Fibromatosis, gingival, 3 (2) between D2S2221 and D2S1788 Fd  
2p23.2 GALNT14 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 608225     REc  
2p23.2 PLB1, PLB, FLJ30866 Phospholipase B1   610179     R, REc  
2p23.2 RBKS Ribokinase   611132     REc  
2p23.1 LBH Limb bud and heart development, mouse, homolog of   611763     R, REc  
2p23.1 YPEL5 Yippee-like 5   609726     REc 17(Ypel5)
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