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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2p22-p21, CYP1B1 to 2p21, FBXO11 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
2p22-p21 CYP1B1, GLC3A Cytochrome P450, subfamily I, dioxin-inducible, polypeptide 1   601771 Glaucoma 3A, primary congenital, 231300 (3); Peters anomaly, 604229(3); Glaucoma, early-onset, digenic (3); Glaucoma, primary open angle, adult-onset, 137760 (3); Glaucoma, primary open angle, juvenile-onset, 137750(3)   REa, REn, A, Fd  
2p22-p21 EML4, ROPP120 Echinoderm microtubule associated protein like-4   607442     R, A  
2p22-p21 MEMO1, MEMO, C2orf4 Mediator of cell motility 1   611786     REc  
2p22-p21 MSH2, COCA1, FCC1, HNPCC1 mutS, E. coli, homolog of, 2   609309 Colorectal cancer, hereditary nonpolyposis, type 1, 120435 (3);Muir-Torre syndrome, 158320 (3); Mismatch repair cancer syndrome, 276300 (3)   Fd, REa, Ch  
2p22-p21 PUM2, KIAA0235 Pumilio, Drosophila, homolog of, 2   607205     REa, REc  
2p22-p21 SFRS7 Splicing factor, arginine/serine-rich 7, 35kD   600572     A  
2p22-p21 SLC30A6, ZNT6 Solute carrier family 30 (zinc transporter), member 6   611148     REc, H 17(Slc30a6)
2p22-p21 SOS1, GINGF, GF1, HGF, NS4 Son of sevenless, Drosophila, homolog of, 1   182530 Fibromatosis, gingival, 135300 (3); Noonan syndrome 4, 610733 (3);Noonan-like/multiple giant cell lesion syndrome, 163955 (3)   A, Fd, REc 17(Sos1)
2p22-p21 SPAST, SPG4 Spastin   604277 Spastic paraplegia-4, 182601 (3)   Fd  
2p22-p21 THUMPD2, C2orf8 THUMP domain-containing 2   611751     A  
2p22-p16 HTLF Human T-cell leukemia virus enhancer factor   143089     REa, A  
2p22-p11 GLAT Galactose enzyme activator   137030     S  
2p21 ABCG5 ATP-binding cassette, subfamily G, member 5   605459 Sitosterolemia, 210250 (3)   REc  
2p21 ABCG8, GBD4 ATP-binding cassette, subfamily G, member 8   605460 Sitosterolemia, 210250 (3); Gallbladder disease 4, 611465 (3)   REc  
2p21 ARHQ, TC10 Ras-homolog gene family, member Q   605857     R  
2p21 CAD CAD trifunctional protein of pyrimidine biosynthesis   114010   proximal to 21.01 REa, A, S, D  
2p21 CALM2 Calmodulin-2   114182     Psh, A  
2p21 CDC42EP3, CEP3, BORG2 CDC42 effector protein 3   606133     R, REc  
2p21 COX7A2L, COX7RP, EB1 Cytochrome c oxidase subunit VIIA, polypeptide 2-like   605771     R, REc  
2p21 EHD3 EH domain-containing 3   605891     R  
2p21 FBXO11, FBX11, VIT1, PRMT9 F-box only protein 11   607871   ?2p16 REc 17(Fbxo11)
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