|
341
|
|
|
Lipin 1 |
PAP1 |
|
|
342
|
|
|
La ribonucleoprotein 4B |
KIAA0217, LARP5 |
|
|
343
|
|
|
Leucyl-tRNA synthetase 2, mitochondrial |
HLASA, LEURS, PRLTS4, mtLeuRS |
Bipolar disorder, Gonadal dysgenesis, Hydrops, lactic acidosis, and sideroblastic anemia, Hypertension, Patent ductus arteriosus, Perrault syndrome, Physiologic amenorrhea, Premature menopause, Schizophrenia, Sideroblastic anemia, Uterine anomalies, Ventricular septal defect |
|
344
|
|
|
Leptin receptor overlapping transcript like 1 |
HSPC112, Vps55, my047 |
|
|
345
|
|
|
Leukocyte immunoglobulin like receptor A4 |
CD85g, ILT7 |
|
|
346
|
|
|
LEM domain containing 3 |
MAN1 |
12q14 microdeletion syndrome, Arnold-chiari malformation, Arthritis, Buschke-ollendorff syndrome, Camptodactyly of fingers, Congenital malrotation of intestine, Craniosynostosis, Dermatofibrosis lenticularis disseminata, Developmental delay, Diabetes mellitus, Diffuse skin atrophy, Dwarfism, Ectopic kidney, Frontal bossing, Hemangioma, Horseshoe kidney, Hyperostosis, Hypertension, Hypodontia, Isolated osteopoikilosis, Limb muscle atrophy, Melorheostosis, Melorheostosis with osteopoikilosis, Mental retardation, Microcephaly, Micrognathism, Microtia, Mixed sclerosing bone dystrophy, Multiple lipomata, Osteochondrodysplasia, Osteopoikilosis, Palmoplantar keratoderma, Renal hypoplasia, Renal insufficiency, Scleroderma, Scoliosis, Skeletal dysplasia, Specific learning disorder, Strabismus, Syndactyly of fingers, Synophrys, SyringomyeliaView all (27 more) |
|
347
|
|
|
Lymphocyte antigen 96 |
ESOP-1, MD-2, MD2, ly-96 |
|
|
348
|
|
|
LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated |
YER146W |
|
|
349
|
|
|
Long intergenic non-protein coding RNA 315 |
C21orf93, NCRNA00315 |
|
|
350
|
|
|
Lysocardiolipin acyltransferase 1 |
1AGPAT8, AGPAT8, ALCAT1, HSRG1849, LPLAT6, LYCAT, UNQ1849 |
|
