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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5q11.2-q13.1, TAF9 to 5q12.1, IPO11 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
5q11.2-q13.1 TAF9, TAF2G, TAFII32 TAF9 RNA polymerase II, TATA box-binding protein-associated factor, 32kD 600822     REa, Psh, A  
5q11.2-q13.2 DHFR Dihydrofolate reductase   126060 ?Anemia, megaloblastic, due to DHFR deficiency (1) 5q23 = conflicting localization; to other chrs. with amplification;absence/presence of polymorphism pseudogene DHFRP1 on chr. 18 S, REa, H, D 13(Dhfr)
5q11.2-q13.3 CRHBP Corticotropin releasing hormone-binding protein   122559     Psh 13(Crhbp)
5q12 ADAMTS6 A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 6 605008     REa, REc  
5q12 CCNB1 Cyclin B1   123836     A, REa 13(Cycb4)
5q12 ERBB2IP, ERBIN ERBB2 interacting protein   606944     R, REc  
5q12 ERCC8, CKN1, CSA Excision repair cross-complementing rodent repair deficiency, complementation group 8 609412 Cockayne syndrome, type A, 216400 (3)   Psh  
5q12 LY64, RP105 Lymphocyte antigen-64, radioprotective, 105kD   602226     A 13(Ly64)
5q12 PART1 Prostate androgen-regulated transcript 1   604991     R, A  
5q12 PDE4D, DPDE3, STRK1 Phosphodiesterase-4D, cAMP-specific (dunce, Drosophila, homolog of, phosphodiesterase-E3) 600129 {Stroke, susceptibility to, 1}, 606799 (3)   REa, A, Fd 13(Pde4D)
5q12-q13 ANKRA2, ANKRA Ankyrin repeat-containing protein, family A, member 2   605787     R, Psh  
5q12-q13 CMYA5, MYOSPRYN, TRIM76 Cardiomyopathy-associated protein 5   612193     REc 13(Cmya5)
5q12-q13 FOXD1, FKHL8 Forkhead box D1   601091     A  
5q12-q13 KIF2 Kinesin, heavy chain, 2   602591     R  
5q12-q13 MCCC2, MCCB 3-Methylcrotonyl-CoA carboxylase 2   609014 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210 (3)   R  
5q12-q13 PLK2, SNK Polo-like kinase 2   607023     R  
5q12-q13 PMCHL2 Pro-melanin-concentrating hormone-like 2   176794     REa, A  
5q12-q14 CSPG2, WGN, WGN1, ERVR Chondroitin sulfate proteoglycan-2 (versican)   118661 Wagner syndrome 1, 143200 (3)   REa, A, H, Fd 13(Cspg2)
5q12-q14 EEF1B3 Eukaryotic translation elongation factor-1, beta-3   600656   ?pseudogene Psh, A  
5q12-q14 EJM4 Myoclonic epilepsy, juvenile, 4   611364 Myoclonic epilepsy, juvenile, 4 (2) max lod at D5S459 Fd  
5q12.1 IPO11, RANBP11, SLRN Importin 11   610889     REc  
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