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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17q25, SEPT9 to 17q25.1-q25.2, NPTX1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q25 SEPT9, MSF, MSF1, NAPB Septin 9   604061 Leukemia, acute myeloid, therapy-related (1); Ovarian carcinoma (1);Amyotrophy, hereditary neuralgic, 162100 (3)   Ch, REa, Fd  
17q25 SFRS2 Splicing factor, arginine/serine-rich 2   600813     H, REc 11(Sfrs2)
17q25 TBCD Tubulin-specific chaperone D   604649     REc  
17q25 TIMP2 Tissue inhibitor of metalloproteinase-2   188825     H, REa, A 11(Timp2)
17q25 SYNGR2 Synaptogyrin 2   603926   pseudogene on 15q11; near EV1, EV2, TK1 A, REc  
17q25 TOC, TEC Tylosis with esophageal cancer   148500 Tylosis with esophageal cancer (2) distal to type I keratin cluster Fd  
17q25 WBP2 WW domain-binding protein 2   606962     A  
17q25-qter MRPL12, RPML12 Ribosomal protein, mitochondrial, L12   602375     A  
17q25.1 C17orf28, DMC1 Downregulated in multiple cancers-1   605752     REc  
17q25.1 CD300LB, TREM5, IREM3 CD300 antigen-like family, member B   610705     REc 11(Cd300lb)
17q25.1 CASKIN2, KIAA1139 CASK-interacting protein 2   612185     R, REc  
17q25.1 CD300LE, IREM2, CLM2 CD300 antigen-like family, member E   609801     REc  
17q25.1 CD300LF, IGSF13, IREM1, CLM1 CD300 antigen-like family, member F   609807     REc  
17q25.1 COG1, LDLB, KIAA1381, CDG2G Component of oligomeric golgi complex 1   606973 Congenital disorder of glycosylation, type IIg, 611209 (3)   R, REc  
17q25.1 EXOC1, EX070, KIAA1067 Exocyst complex component 7   608163     R, REc  
17q25.1 MIF4GD, SLIP1 MIF4G domain-containing protein   612072     REc  
17q25.1 RAB37 Pas-associated protein RAB37   609956     R, REc  
17q25.1 SLC9A3R1, EBP50, NHERF1, NPHLOP2 Solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 regulatory factor 1 604990 Nephrolithiasis/osteoporosis, hypophosphatemic, 2, 612287 (3)   R, REc  
17q25.1 SRP68 Signal recognition particle, 68kD   604858     R, A  
17q25.1 UNC13D, MUNC13-4, HPLH3, HLH3, FHL3 UNC13, C. elegans, homolog of, D   608897 Hemophagocytic lymphohistiocytosis, familial, 3, 608898 (3)   Fd, REc  
17q25.1-q25.2 NPTX1, NP1 Pentraxin I, neuronal   602367     A 11(Nptx1)
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