OMIM Gene/Loci: 1 - 10 of 1,023 on Chromosome 19 (All Entries)
| Location (from NCBI, GRCh38) |
Gene/Locus | Gene/Locus name | Gene/Locus MIM number |
Phenotype | Phenotype MIM number |
Inheritance | Pheno map key |
Comments | Mouse symbol (from MGI) |
|---|---|---|---|---|---|---|---|---|---|
|
19:0-12,600,000
19p13.3-p13.2 |
ATHS, ALP | Atherosclerosis susceptibility (lipoprotein associated) | 108725 | {Atherosclerosis, susceptibility to} | 108725 | Autosomal dominant | 2 | closely linked to LDLR; may be LDLR | |
|
19:0-58,617,616
19pter-q13 |
CXB3S | Coxsackie virus B3 sensitivity | 120050 | ||||||
|
19:0-26,200,000
19p |
EXT3 | Exostoses, multiple, 3 | 600209 | Exostoses, multiple, type 3 | 600209 | Autosomal dominant | 2 | ||
|
19:0-6,900,000
19p13.3 |
FEB2 | Febrile seizures, familial, 2 | 602477 | Febrile seizures, familial, 2 | 602477 | Autosomal dominant | 2 | ||
|
19:0-19,900,000
19pter-p13.1 |
FPH1, MUH, HPP | Hyperpigmentation, familial progressive, 1 | 614233 | Hyperpigmentation, familial progressive, 1 | 614233 | 2 | |||
|
19:0-19,900,000
19p13 |
IBD6 | Inflammatory bowel disease 6 | 606674 | {Inflammatory bowel disease 6} | 606674 | 2 | |||
|
19:0-6,900,000
19p13.3 |
IS1, AIS | Adolescent idiopathic scoliosis | 181800 | Scoliosis, idiopathic 1 | 181800 | Autosomal dominant | 2 | ||
|
19:0-6,900,000
19p13.3 |
KIR2DL5A, KIR2DL5 | Killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A | 605305 | ||||||
|
19:0-6,900,000
19p13.3 |
MDRV | Muscular dystrophy with rimmed vacuoles | 601846 | Muscular dystrophy with rimmed vacuoles | 601846 | Autosomal dominant | 2 | ||
|
19:0-19,900,000
19p13 |
MGR5 | Migraine with or without aura, susceptibility to, 5 | 607508 | {Migraine with or without aura, susceptibility to, 5} | 607508 | Autosomal dominant | 2 |