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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11p15.2-p15.1, CALCB to 11p15.1, SAA2 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
11p15.2-p15.1 CALCB, CALC2 Calcitonin-related polypeptide, beta   114160     A, REa, REb, D  
11p15.2-p15.1 NELL1 Nel-like 1   602319     A  
11p15.2-p15.1 PTPN5, STEP Protein tyrosine phosphatase, nonreceptor-type, 5 (striatum-enriched)   176879     Psh, A 7(Ptpn5)
11p15.2-p15.1 SLC6A5, GLYT2 Solute carrier family 6 (neurotransmitter transporter, glycine), member 5 604159 Hyperekplexia, 149400 (3)   R  
11p15.2-p15.1 TSG101 Tumor susceptibility gene 101   601387 Breast cancer (3)   R, A  
11p15.2-p15.1 UEVLD, UEV3, ATTP Ubiquitin E2 variant and lactate/malate dehydrogenase domains-containing protein 610985     REc  
11p15.2-p14.3 GAS2 Growth arrest-specific 2   602835     R, A, H 7(Gas2)
11p15.1 ABCC8, SUR, PHHI, SUR1, HHF1, TNDM2 ATP-binding cassette, subfamily C, member 8 (sulfonylurea receptor)   600509 Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3);Hypoglycemia of infancy, leucine-sensitive, 240800 (3); Diabetes mellitus, transient neonatal 2, 610374 (3); Diabetes mellitus, noninsulin-dependent,125853 (3); Diabetes mellitus, permanent neonatal, 606176 (3)   A, REn, Fd, LD  
11p15.1 CSRP3, CRP3, CLP, CMD1M, CMH12 Cysteine- and glycine-rich protein 3   600824 Cardiomyopathy, dilated, 1M, 607482 (3); Cardiomyopathy,familial hypertrophic, 12, 612124 (3)   A  
11p15.1 E2F8 E2F transcription factor 8   612047     REc 7(E2f8)
11p15.1 HTATIP2, TIP30, CC3 HIV-1 TAT-interacting protein 2, 30kD   605628     R, REc  
11p15.1 KCNJ11, BIR, PHHI, HHF2, TNDM3 Potassium inwardly-rectifying channel, subfamily J, member 11   600937 Hyperinsulinemic hypoglycemia, familial, 2, 601820 (3);Diabetes, permanent neonatal, 606176 (3); Diabetes mellitus, permanent neonatal, with neurologic features, 606176 (3); {Diabetes mellitus, type 2,susceptibility to}, 125853 (3); Diabetes mellitus, transient neonatal, 3, 610582 (3) 4.5kb 3' of SUR A, REn, Fd, LD  
11p15.1 MRGPRX1, MRGX1 Mas-related G protein-coupled receptor family, member X1   607227     REc  
11p15.1 MRGPRX2, MRGX2 Mas-related G protein-coupled receptor family, member X2   607228     REc  
11p15.1 MRGPRX3, MRGX3 Mas-related G protein-coupled receptor family, member X3   607229     REc  
11p15.1 MRGPRX4, MRGX4 Mas-related G protein-coupled receptor family, member X4   607230     REc  
11p15.1 NAV2, RAINB1, KIAA1419 Neuron navigator 2   607026     R, REc  
11p15.1 PLEKHA7 Pleckstrin homology domain-containing protein, family A, member 7   612686     REc  
11p15.1 PSMA1, PROS30 Proteasome subunit, alpha-type, 1   602854     A  
11p15.1 SAA1 Serum amyloid A1   104750     REa, H, A, Psh 7(Saa1)
11p15.1 SAA2 Serum amyloid A2   104751   pseudogene = SAA3 REn, A, Fd, Psh  
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