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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15p12, RNR3 to 15q11-q13, MKRN3 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
15p12 RNR3 Ribosomal RNA-3   180452     A  
15q AP3B2, NAPTB Adaptor-related protein complex 3, beta 2 subunit   602166     H 7(Naptb)
15q APBA2 Amyloid beta A4 precursor protein-binding, family A, member 2   602712     R 7(Apba2)
15q HYT2 Hypertension, essential, susceptibility to, 2   604329 {Hypertension, essential, susceptibility to, 2}, 145500 (2)   Fd  
15q LCS1, CHLS Cholestasis-lymphedema syndrome   214900 Cholestasis-lymphedema syndrome (2)   Fd, HZ  
15q NEDD4 Neural precursor cell expressed, developmentally downregulated-4   602278     H, A  
15q RPL4 Ribosomal protein L4   180479     REa, R  
15q RPS17, RPS17L1, RPS17L2, DBA4 Ribosomal protein S17   180472 Diamond-Blackfan anemia 4, 612527 (3) previously on chr.11; pseudogenes on 5q33-qter and 17q Psh, R  
15q11 AUTS4 Autism, susceptibility to, 4   608636 {Autism, susceptibility to, 4} (2)   Ch  
15q11 CYFIP1, KIAA0068 Cytoplasmic FMRP interacting protein 1   606322     R, REc  
15q11-q12 IGHDY2 Immunoglobulin heavy chain diversity region-2   146990   ?functional A  
15q11-q12 MIC7 Attached cell antigen 28.3.7   108990     S  
15q11-q13 ATP10A, ATP10C, ATPVC ATPase, class V, type 10A   605855     R, REc, D  
15q11-q13 BCL8 B-cell CLL/lymphoma-8   601889 Lymphoma, diffuse large cell (3)   REc, A  
15q11-q13 C15orf2 Chromosome 15 open reading frame 2   610922     REc  
15q11-q13 CELIAC5, GSES Celiac disease, susceptibility to, 5   607202 {Celiac disease, susceptibility to, 5} (2) in homogeneous Finnish population Fd  
15q11-q13 GLC1I Glaucoma 1, open angle, I   609745 Glaucoma 1, open angle, I (2) max lod at GABRB3 Fd  
15q11-q13 IPW Imprinted in Prader-Willi syndrome   601491     REc  
15q11-q13 MAGEL2, NDNL1 MAGE-like 2   605283     REc 7(Magel2)
15q11-q13 MAN2C1, MANA Mannosidase, alpha, class 2C, member 1   154580     S, D  
15q11-q13 MKRN3, ZFP127, ZNF127 Makorin 3   603856   expressed only from paternal allele REc 7(Znf127)
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