541
|
|
|
Leucine rich repeat containing 37 member A2 |
LRRC37 |
|
542
|
|
|
Leucine rich repeat containing 18 |
UNQ933, UNQ9338, VKGE9338 |
|
543
|
|
|
Leucine aminopeptidase 3 |
HEL-S-106, LAP, LAPEP, PEPS |
|
544
|
|
|
Lymphoid enhancer binding factor 1 |
ECTD1, ECTD17, LEF-1, TCF10, TCF1ALPHA, TCF7L3 |
|
545
|
|
|
LIM domain and actin binding 1 |
EPLIN, LDLCQ8, SREBP3 |
|
546
|
|
|
Leucyl-tRNA synthetase 1 |
HSPC192, ILFS1, LARS, LEURS, LEUS, LFIS, LRS, PIG44, RNTLS, cLRS, hr025Cl |
|
547
|
|
|
La ribonucleoprotein 7, transcriptional regulator |
ALAZS, HDCMA18P, PIP7S, hLARP7 |
Alazami syndrome, Anxiety disorder, Atrial septal defect, Cutis marmorata, Developmental delay, Dwarfism, Mental retardation, Macrostomia, Microcephalic primordial dwarfism, Microcephaly, Pituitary dwarfism, Scoliosis, Sleep apnea, Stereotypy, Strabismus |
548
|
|
|
Lipolysis stimulated lipoprotein receptor |
ILDR3, LISCH7 |
|
549
|
|
|
Lipoyltransferase 1 |
LIPT1D |
Anemia, Cerebellar ataxia, Cerebellar atrophy, Developmental delay, Dysarthria, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome with leukodystrophy, Leukodystrophy, Lipoyltransferase deficiency, Mood swings, Nervous system diseases, Nystagmus, Optic atrophy, Ptosis, Pulmonary arterial hypertension, Retinitis pigmentosa, Spastic tetraparesis, Strabismus, Ventricular septal defectView all (6 more) |
550
|
|
|
LUC7 like 2, pre-mRNA splicing factor |
CGI-59, CGI-74, LUC7B2 |
|