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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". You must capitalize X and Y to search for those chromosomes.
12pter-p12, CD4 to 12p13.3, CACNA1C <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
12pter-p12 CD4 CD4 antigen (p55)   186940 [CD4+ lymphocyte deficiency] (2); {Lupus erythematosus,susceptibility to} (2) CD = \`cluster of differentiation\' = nomenclatureof leukocyte differentiation antigens REa, A 6(Ly4)
12p13.33 DCP1B, DCP1 Decapping enzyme 1, S. cerevisiae, homolog of   609843     REc, R  
12p13.33 HSN2 HSN2 gene   608620 Neuropathy, hereditary sensory, type II, 201300 (3)   REn  
12p13.33 IQSEC3, KIAA1110 IQ motif- and SEC7 domain-containing protein 3   612118     R, REc  
12p13.32 LAG3 Lymphocyte activation gene-3   153337     A  
12p13.31 A2ML1 Alpha-2-macroglobulin-like 1   610627     REc  
12p13.31 C1RL, CLSPA, C1RLP Complement component C1r-like protein   608974     REc  
12p13.31 CLEC9A, DNGR1 C-type lectin domain family 9, member A   612252     REc  
12p13.31 DPPA3 Developmental pluripotency-associated gene 3   608408     REc, H 6(Dppa3)
12p13.31 DRPLA Atrophin 1   607462 Dentatorubro-pallidoluysian atrophy, 125370 (3)   Fd, D, A 6(Drpla)
12p13.31 ING4 Inhibitor of growth-4   608524     R, REc, D  
12p13.31 MIRN141, MIR141 Micro RNA 141   612093     REc  
12p13.31 MIRN200C, MIR200C Micro RNA 200C   612092     REc  
12p13.31 NECAP1 NECAP endocytosis-associated protein 1   611623     REc  
12p13.31 PLEKHG6, MYOGEF Pleckstrin homology domain-containing protein, family G, member 6   611743     REc  
12p13.31 RBP5, CRBP3 Retinol-binding protein 5   611866     REc  
12p13.31 SPSB2, SSB2 SPRY domain- and SOCS box-containing 2   611658     REc  
12p13.31-p13.1 GAPDH, GAPD Glyceraldehyde-3-phosphate dehydrogenase   138400   pseudogene on Xp21-q11 S, D, R 6(Gapd)
12p13.3 B4GALNT3 Beta-1,4-N-acetylgalactosaminyltransferase 3   612220     REc  
12p13.3 BWCNS Bowen-Conradi syndrome   211180 Bowen-Conradi syndrome (2) between F8VWF and D12S397 Fd  
12p13.3 CACNA1C, CACNL1A1, CCHL1A1, TS Calcium channel, voltage-dependent, L type, alpha 1C subunit   114205 Timothy syndrome, 601005 (3); Brugada syndrome 3, 611875 (3)   Psh, Fd, REa, A  
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