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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11p13-p12, DFNB51 to 11p12-p11, ACP2 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
11p13-p12 DFNB51 Deafness, autosomal recessive 51   609941 Deafness, autosomal recessive 51 (2) max lod at D11S4102 Fd  
11p13-p12 EVR3 Exudative vitreoretinopathy 3   605750 Exudative vitreoretinopathy-3 (2)   Fd  
11p13-p12 LGMD2L Muscular dystrophy, limb-girdle, type 2L   611307 Muscular dystrophy, limb-girdle, type 2L (2) max lod at D11S1360 Fd  
11p13-p12 LHX1, LIM1 LIM/homeodomain protein LHX1   601999   by homology, should be 17q A 11(Lhx1)
11p13-p12 PROTOR2, FLJ14213 Protein observed with rictor 2   611728     R, REc  
11p13-p12 PSMC3, TBP1 Proteasome (prosome, macropain) 26S subunit, ATPase, 3   186852     Psh, A  
11p13-p12 SLC1A2, EAAT2 Solute carrier family 1 (glial high affinity glutamate transporter), member 2 600300     A, REa 2(Eaat2)
11p13-p11.1 FOLH1B, PSMAL, GCP3 Folate hydrolase 1B   609020     A, REc  
11p13-q11 SCA20 Spinocerebellar ataxia 20   608687 Spinocerebellar ataxia 20 (2) highest lod with D11S4191 Fd  
11p13-q12 CANDN1, FCNC Candidiasis, familial chronic nail, with ICAM1 deficiency   607644 Candidiasis, familial chronic nail, with ICAM1 deficiency (2) between D11S1312 and D11S4191 Fd  
11p13-p12 WAGRO, DEL11p14p12 Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome 612469 WAGRO syndrome (4) contiguous gene deletion syndrome Ch  
11p12 API5, AAC11 Apoptosis inhibitor 5   609774     REc  
11p12 BMND8 Bone mineral density QTL 8   611739 {Osteoporosis}, 166710 (2) between D11S1392 and D11S4102 Fd  
11p12 EHF, ESE3 ETS homologous factor   605439     REa, A  
11p12 LRRC4C, NGL1, KIAA1580 Leucine rich repeat containing 4C (netrin-G1 ligand)   608817     R, REc  
11p12 TRAF6 TNF receptor-associated factor 6   602355     REc, R  
11p12-p11.2 CHRM4 Cholinergic receptor, muscarinic, 4   118495     A, REa, Fd  
11p12-p11.2 LRP4, MEGF7 Low density lipoprotein receptor-related protein 4   604270     R  
11p12-p11.2 MAPK8IP1, IB1 Mitogen-activated protein kinase 8-interacting protein 1   604641 {Diabetes mellitus, noninsulin-dependent}, 125853 (3)   R, A  
11p12-p11.2 PEX16 Peroxisome biogenesis factor 16   603360 Zellweger syndrome, complementation group 9 (3)   R, H 2(Pex16)
11p12-p11 ACP2 Acid phosphatase 2, lysosomal   171650 ?Lysosomal acid phosphatase deficiency, 200950 (1)   S, REa 2(Acp2)
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