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".
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21p13-q11, AUTS12 to 21q21-q22.1, GABPA <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
21p13-q11 AUTS12 Autism, susceptibility to, 12   610838 {Autism, susceptibility to, 12} (2) max lod at D21S1437 Fd  
21p12 RNR4 Ribosomal RNA-4   180453     A  
21p TPTE Transmembrane phosphatase with tensin homology   604336     REc, A  
21q11 NRIP1, RIP140 Nuclear receptor interacting protein 1 (receptor interacting protein 140) 602490     A, REc  
21q11.1 CNN2 Calonin 2   602373     A  
21q11.1 STCH Stress 70 protein chaperone, microsome-associated, p60   601100     A  
21q11.2 ANKRD21, POTE Ankyrin repeat domain 21   607549     REc, A  
21q11.2 CXADR, CAR Coxsackie virus and adenovirus receptor   602621   pseudogenes on chr.15 and chr.18 Psh, A  
21q11.2 LIPI, LPDL, PRED5 Lipase I   609252 {Hypertriglyceridemia, susceptibility to}, 145750 (3)   REc 16(Lipi)
21q11.2 NRCLP3 Narcolepsy 3   609039 Narcolepsy 3 (2) max lod at D21S1245 Fd  
21q11.2 SAMSN1, HACS1 SAM domain, SH3 domain, and nuclear localization signals 1   607978     REc  
21q11.2 TAM, MST Myeloproliferative syndrome, transient (transient abnormal myelopoiesis) 159595 Leukemia, transient, of Down syndrome (2)   Ch  
21q11.2-q21 MRPL39, MRPL5 Mitochondrial ribosomal protein L39   611845     R, REc  
21q11.2-q21.1 BTG3, ANA, TOB5 B-cell translocation gene 3   605674     A  
21q21 APP, AAA, CVAP, AD1 Amyloid beta (A4) precursor protein   104760 Cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arcticvariants, 605714 (3); Alzheimer disease 1, familial, 104300 (3); Dementia, early-onset progressive, autosomal recessive (3) proximal to SOD; very distal q21 or boundary with q22 REa, A, Fd, RE 16(App)
21q21 NCAM2 Cell adhesion molecule, neural, 2   602040     Psh  
21q21 PRSS7, ENTK Protease, serine, 7 (enterokinase)   606635 Enterokinase deficiency, 226200 (3)   A  
21q21 TAK1L, C21orf7 TAK1-like   611110     REc  
21q21 USH1E Usher syndrome-1E, autosomal recessive, severe   602097 Usher syndrome, type 1E (2)   Fd  
21q21-q22 ADAMTS5, ADAMTS11 A disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 5 (aggrecanase 2) 605007     REa, R 16(Adamts5)
21q21-q22.1 GABPA, E4TF1A GA-binding protein transcription factor, alpha subunit, 60kD   600609     A, REn, Psh, REc  
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