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.
Search for: (from the current location)    
  • 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.
15q21.1, FBN1 to 15q21.3, SCG3 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
15q21.1 FBN1, MFS1, WMS Fibrillin-1   134797 Marfan syndrome, 154700 (3); Shprintzen-Goldberg syndrome,182212 (3); Ectopia lentis, familial, 129600 (3); MASS syndrome, 604308 (3); Weill-Marchesani syndrome, dominant, 608328 (3); Aortic aneurysm, ascending,and dissection (3)   A, Fd 2(Fbn1)
15q21.1 NMES1 Normal mucosa of esophagus-specific gene 1   608409     R  
15q21.1 SLC24A5, NCKX5, SHEP4 Solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 609802 [Skin/hair/eye pigmentation 4, fair/dark skin], 113750 (3)   REc, R  
15q21.1 SLC30A4, ZNT4 Solute carrier family 30 (zinc transporter), member 4   602095     A, REc, H 2(lm, Slc30a4)
15q21.1 SPG11, KIAA1840, FLJ21439 Spastascin   610844 Spastic paraplegia-11, 604360 (3)   Fd, R  
15q21.1-q21.2 CRI1, C15orf3, EID1 CREBBP/EP300 inhibitory protein 1   605894     R  
15q21.1-q21.2 ONECUT1, HNF6A, HNF6 One cut domain, family member 1 (hepatocyte nuclear factor 6-alpha)   604164     A  
15q21.1-q21.2 TMOD2 Tropomodulin 2, neuronal   602928     R 9(Tmod2)
15q21.1-q21.2 TMOD3 Tropomodulin 3   605112     R, REc 9(Tmod3)
15q21.2 AP4E1 Adaptor-related protein complex 4, epsilon-1 subunit   607244     REc  
15q21.2 DMXL2, RC3, KIAA0856 DMX-like 2   612186     R, REc  
15q21.2 GLDN, CRGL2 Gliomedin   608603     REc  
15q21.2 SLC27A2, FACVL1, VLACS Solute carrier family 27 (fatty acid transporter), member 2 (fatty acid CoA ligase, very long-chain 1) 603247     A  
15q21.2 GABPB, BABPB2, GABPB1, E4TF1B, NRF2B1 GA-binding protein transcription factor, beta subunit   600610     A  
15q21.2 TRIP15, SGN2, COPS2 Thyroid hormone receptor interactor-15   604508     REc 2(Cops2)
15q21.2-q21.3 CGNL1, FLJ14957, KIAA1749 Cingulin-like 1   607856     REc, REn  
15q21.3 GCNT3 Glucosaminyl (N-acetyl) transferase 3, mucin-type   606836     Psh, R, A  
15q21.3 MNS1, FLJ11222 Meiosis-specific nuclear structural protein 1   610766     REc  
15q21.3 NARG2 NMDA receptor-regulated 2   610835   pseudogenes on chr.4 and chr.3 REc, H 9(narg2)
15q21.3 RFX7, RFXDC2 Regulatory factor X, 7   612660     REc  
15q21.3 SCG3 Secretogranin III   611796     REc  
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

Disclaimer | Write to the Help Desk | Privacy Policy
NCBI | NLM | NIH