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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". You must capitalize X and Y to search for those chromosomes.
16p13.2, SOCS1 to 16p13, EIM <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
16p13.2 SOCS1, SSI1, CIS1, CISH1 Suppressor of cytokine signaling 1   603597     REc  
16p13.13-p13.12 MYH11, AAT4, FAA4 Myosin, heavy polypeptide-11, smooth muscle   160745 Aortic aneurysm, familial thoracic 4, 132900 (3) fused with CBFB by inversion in acute myelomonocytic leukemia REa, A, Ch, Fd 16(Myh11)
16p13.11 ACSM3, SAH Acyl-CoA synthetase medium-chain family member 3   145505 {?Hypertension, essential} (1)   REa, A  
16p13.11-p12.3 CRYM, DFNA40 Crystallin, mu   123740 Deafness, autosomal dominant 40 (3)   Psh  
16p13.1 ABCC1, MRP1, MRP ATP-binding cassette, subfamily C, member 1 (multidrug resistance-associated protein 1) 158343     A  
16p13.1 ABCC6, ARA, ABC34, MLP1, PXE ATP-binding cassette, subfamily C, member 6   603234 Pseudoxanthoma elasticum, 264800 (3); Pseudoxanthoma elasticum,forme fruste, 177850 (3)   A, Fd, LD  
16p13.1 GSPT1 G1 to S phase transition-1   139259     REa, A  
16p13.1 NDE1, NUDE Nude, A. nidulans, homolog of, 1   609449     R, REc  
16p13.1 NPIP Nuclear pore complex-interacting protein   606406     A  
16p13.1 NUBP1, NBP Nucleotide-binding protein 1   600280     R, H 16(Nubp1)
16p13.1 TNFRSF17, BCMA Tumor necrosis factor receptor superfamily, member 17 (B-cell maturation factor) 109545     Ch  
16p13.1 XYLT1, XT1 Xylosyltransferase 1   608124 {Pseudoxanthoma elasticum, modifier of severity of}, 264800 (3)   R  
16p13.1-p12 CACNG3 Calcium channel, voltage-dependent, gamma-3 subunit   606403     REc  
16p13.1-p12 CDR2 Cerebellar degeneration-related antigen-2, 62kD   117340     REa, A 7(Cdr2)
16p13.1-p12 COQ7, CLK1 COQ7, S. cerevisiae, homolog of   601683     Psh, A, R  
16p13.1-p12 PLA2G10, SPLA2, GXSPLA2 Phospholipase A2, group X   603603     A  
16p13.1-p11.2 MVP, LRP Major vault protein, rat, homolog of   605088     A  
16p13 A2BP1, FOX1, HRNBP1 Ataxin 2-binding protein 1   605104     Ch, A, REc  
16p13 ADHD1 Attention deficit-hyperactivity disorder, susceptibility to, 1   608903 {Attention deficit-hyperactivity disorder}, 143465 (2) max lod at D16S3114 Fd  
16p13 BMIQ5 Body mass index quantitative trait locus 5   608558 [Body mass index QTL5] (2) near D16S404 and D16S764 Fd  
16p13 EIM Infantile myoclonic epilepsy   605021 Epilepsy, myoclonic, infantile (2)   Fd  
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