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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3p21.3, FLU to 3p21.3, LIMD1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3p21.3 FLU BLU gene   607070     REc  
3p21.3 CACNA2D2, KIAA0558 Calcium channel, voltage-dependent, alpha-2/delta subunit 2   607082     R, REc  
3p21.3 CAMP, FALL39 Cathelicidin antimicrobial peptide   600474     A  
3p21.3 CISH Cytokine inducible SH2-containing protein   602441     Ch 9(Cish)
3p21.3 CCR3, CKR3, CMKBR3 Chemokine (C-C) receptor 3   601268     R, REc  
3p21.3 CCR9 Chemokine, CC motif, receptor 9   604738     R, A  
3p21.3 CCBP2, CMKBR9, D6, CCR9, CCR10 Chemokine binding protein 2 (chemokine, C-C, receptor 9)   602648     R  
3p21.3 COL7A1 Collagen VII, alpha-1 polypeptide   120120 Epidermolysis bullosa dystrophica, AD, 131750 (3); Epidermolysisbullosa dystrophica, AR, 226600 (3); Epidermolysis bullosa, pretibial, 131850 (3); EBD, Bart type, 132000 (3); EBD, localisata variant (3); Transient bullousof the newborn, 131705 (3); Epidermolysis bullosa pruriginosa, 604129 (3); Toenail dystrophy, isolated, 607523 (3); EBD inversa, 226600 (3)   REa, A  
3p21.3 CYB561D2, 101F6 Cytochrome b-561 domain containing 2   607068     REc  
3p21.3 DNAH1, HL11, DNAHC1, HDHC7 Dynein, axonemal, heavy chain-1   603332     Psh, A 14(Dnah1)
3p21.3 ENTPD3, CD39L3 Ectonucleoside triphosphate diphosphohydrolase 3   603161     R, Psh  
3p21.3 FUS2 FUS2 gene   607073     REc  
3p21.3 GPX1 Glutathione peroxidase-1   138320 Hemolytic anemia due to glutathione peroxidase deficiency (1) ?pseudogene on 3p11-p12 S, REa, Psh, A  
3p21.3 HYAL2, LUCA2 Hyaluronoglucosaminidase 2   603551     REc, H 9(Hyal2)
3p21.3 HYAL3, LUCA3 Hyaluronoglucosaminidase 3   604038     REn  
3p21.3 IBD12 Inflammatory bowel disease 12   612241 {Inflammatory bowel disease 12} (2)   Fd  
3p21.3 IFRD2 Interferon-related developmental regulator-2   602725     REc  
3p21.3 ITGA9 Integrin, alpha-9   603963     REn  
3p21.3 LAMR1, LAMBR Laminin receptor-1, 67kD   150370 ?Arrhythmogenic right ventricular dysplasia 5, 604400 (1)   A 9(Lamr1)
3p21.3 LARS2 Leucyl-tRNA synthetase, mitochondrial   604544     REc  
3p21.3 LIMD1 LIM domain-containing protein 1   604543     REc 9(Limd1)
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