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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13p12, RNR1 to 13q12, KL <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
13p12 RNR1 Ribosomal RNA-1   180450     A  
13p11 IL17D Interleukin 17D   607587   ?associated with Hodgkin lymphoma REc  
13q CLQTL1, CLF Cholesterol level quantitative trait locus 1   604595 [Cholesterol level QTL 1] (2)   Fd  
13q RPL21 Ribosomal protein L21   603636     REa, R  
13q11 GJA3, CX46, CZP3, CAE3 Gap junction protein, alpha-3, 46kD (connexin 46)   121015 Cataract, zonular pulverulent-3, 601885 (3)   REa, A, Fd 14(Gja3)
13q11 PARP4, ADPRTL1, VPARP, KIAA0177 Poly(ADP-ribose) polymerase 4   607519     REc  
13q11 TUBA2 Tubulin, alpha 2   602528     REc  
13q11-q12 FGF9, SYNS3 Fibroblast growth factor-9 (glia-activating factor)   600921 Multiple synostoses syndrome 3, 612961 (3)   A  
13q11-q12 GJB2, CX26, DFNB1A, PPK, DFNA3A, KID, HID Gap junction protein, beta-2, 26kD (connexin 26)   121011 Deafness, autosomal recessive 1A, 220290 (3); Deafness, autosomaldominant 3A, 601544 (3); Vohwinkel syndrome, 124500 (3); Keratoderma, palmoplantar, with deafness, 148350 (3); Keratitis-ichthyosis-deafnesssyndrome, 148210 (3); Hystrix-like ichthyosis with deafness, 602540 (3); Bart-Pumphrey syndrome, 149200 (3)   REa, A, Fd 14(Gjb2)
13q11-q12 LATS2 Large tumor suppressor, Drosophila, homolog of, 2   604861     A 14(Lats2)
13q11-q12 PABPC3, PABP3, PABPL3 Polyadenylate-binding protein, cytoplasmic, 3   604680     Psh  
13q11-q12 ZNF198, SCLL, RAMP, FIM Zinc finger protein-198   602221 Stem-cell leukemia/lymphoma syndrome (3)   REc, R, Ch  
13q12 ALOX5AP, FLAP Arachidonate 5-lipoxygenase-activating protein   603700 {Stroke, susceptibility to}, 601367 (3)   R, A, REc  
13q12 ATP8A2, ATPIB ATPase, class I, type 8A, member 2   605870     A  
13q12 CDK8 Cyclin-dependent kinase 8   603184     REc  
13q12 FLT1 fms-related tyrosine kinase-1 (vascular endothelial growth factor/vascular permeability factor receptor) 165070   150kb from FLT3 REa, A  
13q12 FLT3 fms-related tyrosine kinase-3   136351 Leukemia, acute myeloid, reduced survival in (3); Leukemia,acute myeloid, 601626 (3); Leukemia, acute lymphoblastic (3)   A, Psh, REn 5(Flt3)
13q12 GJB6, CX30, DFNA3B, HED, ED2, DFNB1B Gap junction protein, beta-6 (connexin-30)   604418 Deafness, autosomal dominant 3B, 612643 (3); Ectodermal dysplasia,hidrotic, 129500 (3); Deafness, autosomal recessive 1B, 612645 (3); Deafness, digenic GJB2/GJB6, 220290 (3)   Fd, H  
13q12 GPR12 G protein-coupled receptor-12   600752     A  
13q12 HMGB1, HMG1 High-mobility group box 1 (high-mobility group (nonhistone chromosomal) protein 1) 163905     A 5(Hmg1)
13q12 KL, KLOTHO Klotho   604824 {Coronary artery disease, susceptibility to} (3); Tumoral calcinosis,hyperphosphatemic, 211900 (3)   A, REc  
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