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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3p21, CCR1 to 3p21, TCTA <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3p21 CCR1, CMKBR1, CKR1, HM145 Chemokine (C-C) receptor 1   601159     A 9(Cmkbr1)
3p21 CCR2, CMKBR2 Chemokine (C-C) receptor 2   601267 {HIV infection, susceptibility/resistance to} (3)   REn  
3p21 CCRL2 Chemokine, CC motif, receptor-like protein 2   608379     REc  
3p21 CHBL Chilblain lupus   610448 Chilblain lupus (2) between dbSNP rs704920 and D3S1300 Fd  
3p21 CCR5, CMKBR5, CCCKR5, IDDM22 Chemokine (C-C) receptor 5   601373 {HIV infection, susceptibility/resistance to} (3); {West nile virus,susceptibility to}, 610379 (3); {Hepatitis C virus, resistance to}, 609532 (3); {Diabetes mellitus, insulin-dependent, 22}, 612522 (3)   REc, R  
3p21 CXCR6, STRL33, BONZO Chemokine, CXC motif, receptor 6   605163     REa, Psh  
3p21 DAG1, DAG Dystrophin-associated glycoprotein-1   128239     REa, A 9(Dag1)
3p21 DUSP7, MKPX, PYST2 Dual-specificity phosphatase-7   602749     Psh, A 9(Dusp7)
3p21 FBXW12, FBW12, FBXO35, FBXO12 F-box and WD40 domain protein 12   609075     REc  
3p21 GLYCTK, GLYCTK1 Glycerate kinase   610516     REc  
3p21 GNAI2, GNAI2B, GIP Guanine nucleotide-binding protein (G protein), alpha-inhibiting activity polypeptide-2 139360 Pituitary ACTH-secreting adenoma (3); Ventricular tachycardia,idiopathic, 192605 (3) on 12p13-p12, GNAI2L REa, A 9(Gnai2)
3p21 GNAT1 Guanine nucleotide-binding protein (G protein), alpha-transducing (transducin) activity polypeptide-1 139330 Night blindness, congenital stationary (3)   REa, A 9(Gnat1)
3p21 HSCRS2 Hirschsprung disease, short-segment, 2   606874 {Hirschsprung disease, short-segment, 2} (2)   Fd  
3p21 IHPK2, IP6K2 Inositol hexaphosphate kinase 2   606992     REc  
3p21 LAMB2, LAMS Laminin, beta-2 (laminin S)   150325 Nephrosis, congenital, with or without ocular abnormalities, 609049(3); Pierson syndrome, 609049 (3)   REa, A  
3p21 MAP4 Microtubule-associated protein 4   157132     A 9(Map4)
3p21 MST1, HGFL Macrophage-stimulating-1 (hepatocyte growth factor-like)   142408     REn, H 9(Hgfl)
3p21 PPP2R5C Protein phosphatase-2, regulatory subunit B (B56), gamma isoform   601645     A  
3p21 SCN5A, LQT3, IVF, HB1, SSS1, CMD1E, CDCD2 Sodium channel, voltage-gated, type V, alpha polypeptide   600163 Long QT syndrome-3, 603830 (3); Brugada syndrome 1, 601144 (3); Heartblock, progressive, type IA, 113900 (3); Heart block, nonprogressive, 113900 (3); Ventricular fibrillation, idiopathic, 603829 (3); Sick sinussyndrome 1, 608567 (3); Cardiomyopathy, dilated, 1E, 601154 (3); {Sudden infant death syndrome, susceptibility to}, 272120 (3)   Fd, A  
3p21 SS18L2 SS18-like gene 2   606473     A  
3p21 TCTA T-cell leukemia translocation altered gene   600690     Ch  
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