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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11pter-p15.5, ALG8 to 11p15.5, KCNQ1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
11pter-p15.5 ALG8 Alg8, S. cerevisiae, homolog of   608103 Congenital disorder of glycosylation, type Ih, 608104 (3)   REc  
11pter-p15.5 RRAS2, TC21 Related Ras viral oncogene homolog 2   600098 Ovarian carcinoma (3)   R  
11pter-p13 AMPD3 Adenosine monophosphate deaminase-3, isoform E   102772 [AMP deaminase deficiency, erythrocytic], 612874 (3)   REa 7(Ampd3)
11pter-p13 CD44, MDU2, MDU3, MIC4 CD44 antigen (homing function)   107269 [Blood group, Indian system] (3)   S 2(Ly24)
11pter-p11.2 TP250 T-cell activation antigen p250   186710     S  
11p15.5 AP2A2, KIAA0899 Adaptor-related protein complex 2, alpha-2 subunit   607242     R, REc  
11p15.5 ASCL2 Achaete-scute complex, Drosophila, homolog-like 2   601886     A  
11p15.5 BM88 BM88 antigen   608213     REc, A  
11p15.5 C11orf13, HRC1 HRAS1-related cluster-1   143023   29kb 5' to HRAS1; divergently transcribed REn  
11p15.5 C11orf21 Chromosome 11 open reading frame 21   611033     REc  
11p15.5 CARS Cysteinyl-tRNA synthetase   123859     REa, A  
11p15.5 CD151, PETA3, SFA1, MER2 CD151 antigen   602243 Nephropathy with pretibial epidermolysis bullosa and deafness,609057 (3); [Blood group, Raph], 179620 (3)   A, S, REa  
11p15.5 CDKN1C, KIP2, BWS Cyclin-dependent kinase inhibitor 1C (p57, Kip2)   600856 Beckwith-Wiedemann syndrome, 130650 (3) rare cause of BWS A, Ch, Fd 7(Kip2)
11p15.5 CHRNA10 Cholinergic receptor, neuronal nicotinic, alpha polypeptide 10   606372     A, R  
11p15.5 CTSD, CPSD, CLN10 Cathepsin D (lysosomal aspartyl protease)   116840 Ceroid lipofuscinosis, neuronal, 10, 610127 (3)   REa, A  
11p15.5 DRD4 Dopamine receptor D4   126452 Autonomic nervous system dysfunction (3); [Novelty seekingpersonality], 601696 (1); {Attention deficit-hyperactivity disorder}, 143465 (3); {Parkinson disease, protection against}, 168600 (3) proximal to HRAS Fd  
11p15.5 DUSP8, HVH8 Dual specificity phosphatase-8   602038   pseudogene on 10q11.2 A 7(Dusp8)
11p15.5 H19, D11S813E, ASM1, BWS, WT2 H19 gene   103280 Beckwith-Wiedemann syndrome, 130650 (3); Silver-Russell syndrome,180860 (3); Wilms tumor 2, 194071 (3) same 200kb fragment as IGF2 REa, A, RE 7(H19)
11p15.5 HCCA2 HCCA2 gene   611969     REc  
11p15.5 IDDM2 Insulin-dependent diabetes mellitus-2   125852 {Diabetes mellitus, insulin-dependent, 2} (2)   Fd  
11p15.5 KCNQ1, KCNA9, LQT1, KVLQT1, ATFB3, SQT2 Potassium voltage-gated channel, KQT-like subfamily, member 1   607542 Long QT syndrome-1, 192500 (3); Jervell and Lange-Nielsen syndrome,220400 (3); Atrial fibrillation, familial, 3, 607554 (3); Torsades de pointes, drug-associated (3); Short QT syndrome-2, 609621 (3)   Fd 7(Kcnq1)
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