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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  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer".
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10q24, HPV6AI1 to 10q24-q25, LDB1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
10q24 HPV6AI1 Human papillomavirus type 6A integration site 1   604461     A  
10q24 IOSCA, SCA8 Infantile-onset spinocerebellar ataxia   271245 Spinocerebellar ataxia, infantile-onset, with sensory neuropathy (2)   Fd  
10q24 LGI1, EPT, ETL1 Leucine-rich gene, glioma-inactivated, 1   604619 Epilepsy, partial, with auditory features, 600512 (3); Glioblastoma,somatic, 137800 (3)   Ch, Fd  
10q24 LBX1, LBX1H Lady bird late, Drosophila, homolog of, 1   604255     A 19(Lbx1)
10q24 LOXL4 Lysyl oxidate-like 4   607318     REc  
10q24 MRPL43 Mitochondrial ribosomal protein L43   611848     R, REc  
10q24 NFKB2, LYT10 Nuclear factor of kappa light chain gene enhancer in B-cells 2 (p49/p100); oncogene Lyt-10 164012     REa, A, Ch  
10q24 NOC3L, FAD24 Nucleolar complex-associated 3, S. cerevisiae, homolog of   610769     REc  
10q24 PDCD4 Programmed cell death 4   608610     A  
10q24 PDE6C, PDEA2 Phosphodiesterase-6C, cGMP-specific, cone, alpha prime   600827     A  
10q24 PI4K2A Phosphatidylinositol 4-kinase type 2 alpha   609763     R, REc  
10q24 PLAU, URK Plasminogen activator, urokinase   191840 {Alzheimer disease, late-onset, susceptibility to}, 104300 (3) proximal to HOX11 REa, A, Psh 14(Plau)
10q24 PSD Pleckstrin and Sec7 domain protein   602327     REn  
10q24 RBP4 Retinol-binding protein-4, interstitial   180250 Retinol binding protein, deficiency of (3) just centromeric of CYP2C cluster REa, A 19(Rbp4)
10q24 SHFM3, SHSF3 Split-hand/foot malformation 3   600095 Split-hand/foot malformation 3 (2) ?contiguous gene syndrome involving BTRC and SUFU Fd  
10q24 SLC25A28, MRS4L, NPD016 Solute carrier family 25 (mitochondrial carrier), member 28   609767     Psh, REn  
10q24 TLX1, HOX11, TCL3 T-cell leukemia, homeobox 1   186770 Leukemia, T-cell acute lymphocytic (2) t(7;10) or t(10;4) Ch, RE, H  
10q24 WNT8B Wingless-type MMTV integration site family, member 8B   601396     Psh, A  
10q24-q25 BTRC, BTRCP Beta-transducin repeat-containing protein   603482     R, A  
10q24-q25 GSTO2 Glutathione S-transferase, omega-2   612314     REc  
10q24-q25 LDB1, CLIM2, NLI LIM domain-binding factor-1   603451     R, H 19(Ldb1)
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