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.
Xq28, HMS1 to Xq28, MAGEA8 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
Xq28 HMS1, GAY1 Homosexuality, male   306995 [?Homosexuality, male] (2)   Fd  
Xq28 OPN1MW, GCP, CBD, CBBM Green cone pigment (opsin 1, medium-wave-sensitive)   303800 Colorblindness, deutan (3); Blue-cone monochromacy, 303700 (3) linked to G6PD; multiple genes F, RE, A, Fd X(Rsvp)
Xq28 GPR50 G protein-coupled receptor 50   300207     R X(Gpr50)
Xq28 HCFC1, HCF1 Host cell factor C1 (VP16-accessory protein)   300019   50kb distal to V2R REn, REa, A X(Hcfc1)
Xq28 HMGB3, HMG4, HMG2A High-mobility group box 3 (high mobility group protein 4) 300193     REc  
Xq28 IDH3G Isocitrate dehydrogenase 3 (NAD+), gamma   300089     REc  
Xq28 IDS, MPS2, SIDS Iduronate 2-sulfatase (Hunter syndrome)   309900 Mucopolysaccharidosis II (3) telomeric IDS2 source of inversion in IDS X/A, Fd, F, RE X(Ids)
Xq28 IKBKG, NEMO, FIP3, IP2, IPD2, AMCBX1 Inhibitor of kappa light polypeptide gene enhancer in B cells, kinase of, gamma (NF-kappa-B essential modulator) 300248 Incontinentia pigmenti, type II, 308300 (3); Ectodermal dysplasia,hypohidrotic, with immune deficiency, 300291 (3); Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301 (3); Immunodeficiency,isolated, 300584 (3); {Atypical mycobacteriosis, familial}, 300636 (3); Invasive pneumococcal disease, recurrent isolated, 2, 300640 (3)   Fd, REn X(Ikbkg)
Xq28 IL9R Interleukin-9 receptor   300007   in PAR2 pseudoautosomal region A, REc  
Xq28 IRAK1 Interleukin 1 receptor-associated kinase 1   300283     R X(Irak1)
Xq28 IPOX, CIIPX Intestinal pseudoobstruction, neuronal, primary idiopathic   300048 Intestinal pseudoobstruction, neuronal, X-linked (2)   Fd  
Xq28 ITBA1 ITBA1 gene   300059     RE  
Xq28 ITBA2 ITBA2 gene   300060     RE  
Xq28 L1CAM, CAML1, HSAS1 L1 cell adhesion molecule   308840 Hydrocephalus due to aqueductal stenosis, 307000 (3); MASA syndrome,303350 (3); CRASH syndrome, 303350 (3); Hydrocephalus with Hirschsprung disease and cleft palate, 142623 (3); Hydrocephalus with congenital idiopathicintestinal pseudoobstruction, 307000 (3); Corpus callosum, partial agenesis of, 304100 (3) between RCP/GCP cluster and G6PD A, RE, H, Fd X(L1cam)
Xq28 MAFD2, MDX Major affective disorder 2   309200 {?Major affective disorder 2} (2) linkage to G6PD,CB in non-Ashkenazi Jews F  
Xq28 MAGE1 Melanoma antigen 1 (directs expression of antigen MZ2-E)   300016   cluster of 12 genes REa, A  
Xq28 MAGEA2, MAGE2 Melanoma antigen, family A, 2   300173     RE, REn  
Xq28 MAGEA3, MAGE3 Melanoma antigen, family A, 3   300174     RE, REn  
Xq28 MAGEA4, MAGE4A, MAGE4B Melanoma antigen, family A, 4   300175     RE, REn  
Xq28 MAGEA5, MAGE5 Melanoma antigen, family A, 5   300340     REa, REc X(Mage5)
Xq28 MAGEA8, MAGE8 Melanoma antigen, family A, 8   300341     REa, REc X(Mage8)
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