Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "L"
41 to 50 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
LARGE xylosyl- and glucuronyltransferase 1
LARGE, MDC1D, MDDGA6, MDDGB6
Amphetamine or sympathomimetic abuse, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myopathy, Liver neoplasms, Major depressive disorder, Metabolic syndrome, Muscle eye brain disease, Muscular dystrophy, Neurotic disorder, Oligodendroglioma, Retinitis pigmentosa, Schizophrenia, Scoliosis, Diabetes mellitus type 2
View all (1 more)

42
La ribonucleoprotein 1, translational regulator
LARP, Lar1, Lhp1
Cholecystitis, Cholecystolithiasis, Diffuse gastric adenocarcinoma, Gastric cancer, Polycystic ovary syndrome

43
La ribonucleoprotein 1B
LARP2
Periodontal disease, Periodontitis, Diabetes mellitus type 2

44
La ribonucleoprotein 4
PP13296
Alzheimer disease, Androgenetic alopecia, Polycystic ovary syndrome, Diabetes mellitus type 2

45
La ribonucleoprotein 4B
KIAA0217, LARP5
Atypical femoral fracture, Autism, Kidney disease, Colorectal cancer, Migraine, Prostate cancer

46
La ribonucleoprotein 7, transcriptional regulator
ALAZS, HDCMA18P, PIP7S, hLARP7
Developmental and epileptic encephalopathy, Intellectual developmental disorder, Thyroid cancer

47
Leucyl-tRNA synthetase 1
HSPC192, ILFS1, LARS, LEURS, LEUS, LFIS, LRS, PIG44, RNTLS, cLRS, hr025Cl
Alzheimer disease, Seizure, Global developmental delay, Liver failure, Microcytic anemia, Hearing loss

48
Leucyl-tRNA synthetase 2, mitochondrial
HLASA, LEURS, PRLTS4, mtLeuRS
Eczema, Bipolar disorder, Gonadal dysgenesis, Hydrops with lactic acidosis and sideroblastic anemia, Inflammatory skin disease, Major depressive disorder, Metabolic syndrome, Mitochondrial myopathy, Premature ovarian failure, Perrault syndrome, Psoriasis, Schizophrenia, Scoliosis, Diabetes mellitus type 2, Xx gonadal dysgenesis syndrome

49
LAS1 like ribosome biogenesis factor
Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2
Autism, Global developmental delay, Hypogonadism, Insomnia, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, Partington syndrome, Spinal muscular atrophy, Wilson-turner syndrome, X-linked intellectual disability

50
LIM and SH3 protein 1
Lasp-1, MLN50
Autism, Endometrial neoplasms, Schizophrenia