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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19q12-q13.11, DYRK1B to 19q13, HAMP <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
19q12-q13.11 DYRK1B, MIRK Dual-specificity tyrosine phosphorylation-regulated kinase 1B   604556     R, REc  
19q12-q13.2 ATP1A3, DYT12, RDP ATPase, Na+K+ transporting, alpha-3 polypeptide   182350 Dystonia-12, 128235 (3)   REa, H, Fd 7(Atpla3)
19q12-q13.2 LRP3 Low density lipoprotein receptor related protein 3   603159     Psh, A  
19q13 ACTN4, FSGS1, FSGS Actinin, alpha-4   604638 Glomerulosclerosis, focal segmental, 1, 603278 (3)   Fd, REc 7(Actn4)
19q13 ACPT Acid phosphatase, testicular   606362     REc  
19q13 ANIB2 Aneurysm, intracranial berry, 2   608542 Aneurysm, intracranial berry, 2 (2) between D19S245 and D19S246 Fd  
19q13 BCAT2, BCT2 Branched chain aminotransferase-2, mitochondrial   113530 ?Hypervalinemia or hyperleucine-isoleucinemia (1)   S, H 7(Bcat2)
19q13 BCL3 B-cell CLL/lymphoma-3   109560 Leukemia/lymphoma, B-cell, 3 (2)   Ch, S, H 7(Bcl3)
19q13 BLOC1S3, BLOS3, HPS8 Biogenesis of lysosome-related organelles complex 1, subunit 3   609762 Hermansky-Pudlak syndrome 8, 203300 (3)   R, Fd 7(rp)
19q13 CAPN12 Calpain 12   608839     REc 7(Capn12)
19q13 CATCN1 Cataract, congenital nuclear, 1   609376 Cataract, congenital nuclear, 1 (2) max lod at D19S416 Fd  
19q13 CKM, CKMM Creatine kinase, muscle type   123310     REa, A 7(Ckmm)
19q13 CLIPR59 Cytoplasmic linker protein 170-related protein, 59kD   607382     R  
19q13 CNFN Cornifelin   611764     REc, H 7(Cnfn)
19q13 DLL3, SCDO1 Delta, Drosophila, homolog of   602768 Spondylocostal dysostosis, autosomal recessive, 1, 277300 (3)   Fd, REc 7(Dll3)
19q13 EA7 Episodic ataxia, type 7   611907 Episodic ataxia, type 7 (2) between rs1366444 and rs952108 Fd  
19q13 ECH1 Enoyl Coenzyme A hydratase 1, peroxisomal   600696     REc, REa  
19q13 EPN1 Epsin 1   607262     REc  
19q13 FGF21 Fibroblast growth factor 21   609436     REc  
19q13 FUZ Fuzzy, Drosophila, homolog of   610622     REc  
19q13 HAMP, LEAP1, HEPC, HFE2 Hepcidin antimicrobial peptide   606464 Hemochromatosis, juvenile, 602390 (3); Hemochromatosis, juvenile,digenic, 602390 (3)   REc, Fd 7(Hepc1)
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