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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1p36.2, KIF1B to 1p36.2-p34, RHCE <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
1p36.2 KIF1B, CMT2A, CMT2A1, NBLST1 Kinesin family member 1B   605995 Charcot-Marie-Tooth disease, type 2A1, 118210 (3); Pheochromocytoma,171300 (3); {Neuroblastoma, susceptibility to, 1}, 256700 (3)   Fd, REc, D 4(Kif1b)
1p36.2 MFN2, KIAA0214, CMT2A2 Mitofusin 2   608507 Charcot-Marie-Tooth disease, type 2A2, 609260 (3); Hereditary motorand sensory neuropathy VI, 601152 (3)   R, REa, REc  
1p36.2 NBPF1, KIAA1693 Neuroblastoma breakpoint family, member 1   610501     REc  
1p36.2 NPPA, PND, ANP, ATFB6 Natriuretic peptide precursor A   108780 Atrial fibrillation, familial, 6, 612201 (3)   REa, A, H 4(Pnd)
1p36.2 NPPB, BNP Natriuretic peptide precursor B   600295     H, REa, A, REn 4(Nppb)
1p36.2 PEX14 Peroxisome biogenesis factor 14   601791 Zellweger syndrome, 214100 (3)   R, REc  
1p36.2 PIK3CD Phosphatidylinositol 3-kinase, catalytic, 110kD, delta   602839     A, R  
1p36.2 SCZD12 Schizophrenia 12   608543 {Schizophrenia 12}, 181500 (2) max lod at D1S1612 Fd  
1p36.2 SLC2A5, GLUT5 Solute carrier family 2 (facilitated glucose transporter), member 5   138230     REa, A, REc, R  
1p36.2 SLC2A7, GLUT7 Solute carrier family 2 (facilitated glucose transporter), member 7   610371     REc  
1p36.2 TARDBP, TDP43, ALS10 TAR DNA-binding protein   605078 Amyotrophic lateral sclerosis 10, 612069 (3) pseudogenes on 2, 6, 8, 13, 20 R, REc 4(Tardbp)
1p36.2-p36.13 PGD 6-phosphogluconate dehydrogenase   172200     F, S 4(Pgd)
1p36.2-p36.12 PAX7 Paired box homeotic gene-7   167410 Rhabdomyosarcoma, alveolar, 268220 (3) fused with FKHR in rhabdomyosarcoma Psh, H, REa, A 4(Pax7)
1p36.2-p36.1 FGR, SRC2 Oncogene FGR   164940   same as SRC2 A, REb, REa, Fd 4(Fgr)
1p36.2-p36.1 GLC3B Glaucoma 3, primary infantile, B   600975 Glaucoma 3, primary infantile, B (2)   Fd  
1p36.2-p36.1 RERE RE repeats-encoding gene   605226     REc, Ch  
1p36.2-p36.1 SLC45A1, DNB5 Solute carrier family 45, member 1   605763     REc  
1p36.2-p36.1 ZNF151 Zinc finger protein-151   604084     A  
1p36.2-p35 CDA Cytidine deaminase   123920     A, Psh  
1p36.2-p34 EPB41, EL1 Erythrocyte surface protein band 4.1   130500 Elliptocytosis-1, 611804 (3)   F, REb 4(Elp1)
1p36.2-p34 RHCE Rhesus system C and E polypeptides   111700 [Blood group, Rhesus] (3); Rh-null disease, amorph type (3) ?order: C-E-D F, D, Fd  
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