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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7q35-q36, SMARCD3 to 7q36, RHEB2 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
7q35-q36 SMARCD3, BAF60C SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 3 601737     Psh, R  
7q35-q36 TAS2R38, T2R61, PTC Taste receptor, type 2, member 38   607751 [Phenylthiocarbamide tasting], 171200 (3)   Fd, REc  
7q36 ABCF2, HUSSY18 ATP-binding cassette, subfamily F, member 2   612510     Psh, R, REc  
7q36 ACRPS Acropectoral syndrome   605967 Acropectoral syndrome (2)   Fd  
7q36 AD10 Alzheimer disease-10   609636 Alzheimer disease-10, 104300 (2) max lod with D7S798 Fd  
7q36 ATP6V0E2 ATPase, H+ transporting, lysosomal, 9kD, V- subunit E2   611019     REc  
7q36 FLACE B-cell acute lymphoblastic leukemia-expressed gene   608450     R  
7q36 CDK5 Cyclin-dependent kinase 5   123831     A 5(cdk5)
7q36 EN2, AUTS10 Engrailed-2   131310 {Autism, susceptibility to, 10}, 611016 (3)   REa, A, Fd 5(En2)
7q36 GBX1 Gastrulatin brain homeo box 1   603354     A 5(Gbx1)
7q36 HLXB9, HOXHB9, SCRA1 Homeo box-HB9   142994 Currarino syndrome, 176450 (3)   Fd, REc  
7q36 HPFH2 Hereditary persistence of fetal hemoglobin, heterocellular, Indian type 142335 ?Hereditary persistence of fetal hemoglobin, heterocellular,Indian type (2)   Fd  
7q36 INSIG1 Insulin-induced gene 1   602055     A  
7q36 LMBR1, ACHP, C7orf2, PPD2 Limb region 1, mouse, homolog of   605522 Acheiropody, 200500 (3); Polydactyly, preaxial type II, 174500 (3);Triphalangeal thumb, type I, 174500 (3); Triphalangeal thumb-polysyndactyly syndrome, 174500 (3); Syndactyly, type IV, 186200 (3)   Fd, HZ, Fd 5(Lmbr1)
7q36 MLL3, KIAA1506 Myeloid/lymphoid or mixed-lineage leukemia 3   606833     A  
7q36 MYP4 Myopia 4   608367 Myopia 4 (2)   Fd  
7q36 NOS3 Nitric oxide synthase 3, endothelial cell   163729 {Coronary spasms, susceptibility to} (3); {Alzheimer disease,late-onset, susceptibility to}, 104300 (3); {Hypertension, susceptibility to}, 145500 (3); {Hypertension, pregnancy-induced}, 189800 (3); {Placentalabruption} (3); {Ischemic stroke, susceptibility to}, 601367 (3)   REa, A, Psh 5(Nos3)
7q36 PACIP1, PAXIP1L, PTIP PAX transcription activation domain-interacting protein 1   608254 {Alzheimer disease, susceptibility to}, 104300 (3)   R, A  
7q36 PRKAG2, WPWS, CMH6 Protein kinase, AMP-activated, noncatalytic, gamma-2   602743 Wolff-Parkinson-White syndrome, 194200 (3); Cardiomyopathy,hypertrophic 6, with WPW, 600858 (3); Glycogen storage disease of heart, lethal congenital, 261740 (3)   REc, R, Fd  
7q36 PTPRN2, IAR, ICAAR Protein-tyrosine phosphatase, receptor-type, N, polypeptide 2   601698     A, R  
7q36 RHEB2 Ras homolog enriched in brain 2   601293     A  
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