Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "L"
201 to 210 of 462 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
Lipase E, hormone sensitive type
AOMS4, FPLD6, HSL, LHS, REH
Partial lipodystrophy, Hypertension, Lipodystrophy

202
Lipase G, endothelial type
EDL, EL, PRO719
Alzheimer disease, Cardiovascular disease, Ischemic stroke, Ischemic heart disease, Coronary artery disease, Metabolic syndrome, Multiple sclerosis, Myocardial infarction, Myocardial ischemia, Obesity, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

203
Lipase H
AH, ARWH2, HYPT7, LAH2, LPDLR, PLA1B, mPA-PLA1
Hypotrichosis, Hypotrichosis simplex, Diabetes mellitus type 2, Woolly hair

204
Lipase I
CT17, LPDL, PLA1C, PRED5, mPA-PLA1 beta
Hypertriglyceridemia

205
Lipase family member J
LIPL1, bA425M17.2
Kidney disease

206
Lipase family member K
LIPL2, bA186O14.2
Ocular hypertension, Psoriasis, Scoliosis

207
Lipase family member N
ARCI8, LI4, LIPL4, bA186O14.3
Congenital ichthyosis, Lamellar ichthyosis

208
Lipoyltransferase 1
LIPT1D
Hearing impairment, Leigh syndrome, Lipoyltransferase deficiency

209
Lipoyl(octanoyl) transferase 2
-
Brugada syndrome, Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome, Lipoyltransferase deficiency, Mitochondrial disease, Ventricular fibrillation

210
Lipopolysaccharide induced TNF factor
PIG7, SIMPLE, TP53I7
Androgenetic alopecia, Ankylosing spondylitis, Asthma, Basal cell carcinoma, Charcot-marie-tooth disease, Cholecystolithiasis, Color vision deficiency, Colorectal cancer, Crohn disease, Distal spinal muscular atrophy, Endometrial neoplasms, Gallstones, Hereditary motor and sensory neuropathies, Inflammatory bowel disease, Multiple sclerosis
View all (6 more)