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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2pter-p12, ARHB to 2p25, ODC1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
2pter-p12 ARHB, ARH6, RHOH6 RAS homolog gene family, member B (oncogene RHO H6)   165370     REa, A  
2p25.3 COLEC11, CLK1 Collectin 11   612502     REc  
2p25.3 PXDN, D2S448E, KIAA0230, PRG2, PXN Peroxidasin, Drosophila, homolog of   605158     REa, R, A  
2p25.2 CMPK2 Cytidine monophosphate (UMP-CMP) kinase 2, mitochondrial   611787     REc  
2p25.2 ITGB1BP1, ICAP1, ICAP1A, ICAP1B Integrin cytoplasmic domain-associated protein 1 beta   607153     R, REc  
2p25.2 RSAD2, VIPERIN Radical S-adenosyl methionine domain containing 2   607810     R, REc  
2p25.2 TSSC1 Tumor-suppressing subtransferable fragment candidate gene 1   608998   previously assigned to 11p15.5 REc, H 12(Tssc1)
2p25.2-p25.1 YWHAZ Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide 601288     A  
2p25.1 GRHL1, LBP32, MGR Grainyhead-like 1   609786     R, REc  
2p25.1 GREB1 GREB1 protein   611736     R, REc  
2p25.1 HPCAL1 Hippocalcin-like 1   600207     REa, REc  
2p25.1 MBOAT2, LPCAT4 Membrane-bound O-acyltransferase domain-containing 2   611949     R, REc  
2p25.1-p24.3 DFNB47 Deafness, neurosensory, autosomal recessive 47   609946 Deafness, neurosensory, autosomal recessive 47 (2) max lod at D2S1400 and D2S262 Fd  
2p25 ACP1 Acid phosphatase 1, soluble   171500     D, S, A 12(Acp1)
2p25 ADAM17, TACE A disintegrin and metalloproteinase domain 17   603639     R 12(Tace)
2p25 ALLC Allantoicase   612396   nonfunctional in humans Psh, REc  
2p25 ID2 Inhibitor of DNA binding 2, dominant negative   600386     REa, A  
2p25 ITSN2, SH3D1B, SWAP, KIAA1256 Intersectin 2   604464     REc  
2p25 KCNF1, KH1 Potassium voltage-gated channel, subfamily F, member 1   603787     A  
2p25 KLF11, TIEG2, FKLF1, FKLF, MODY7 Kruppel-like factor 11   603301 Maturity-onset diabetes of the young, type VII, 610508 (3)   Psh  
2p25 ODC1 Ornithine decarboxylase-1   165640 {Colonic adenoma recurrence, reduced risk of}, 114500 (3) pseudogene ODCP on 7q31-qter REa, A 12(Odc)
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