MIM Gene map (via Mowser)

PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM

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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)