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"
201 to 210 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
Lipase C, hepatic type
HDLCQ12, HL, HTGL, LIPH
Alzheimer disease, Amyotrophic lateral sclerosis, Arterial occlusive disease, Atrial fibrillation, Atrophic macular degeneration, Cancer, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Hyperlipidemia, Heart failure, Hepatic lipase deficiency, Hypercholesterolemia
View all (13 more)

202
Lipase E, hormone sensitive type
AOMS4, FPLD6, HSL, LHS, REH
Partial lipodystrophy, Hypertension, Lipodystrophy

203
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

204
Lipase H
AH, ARWH2, HYPT7, LAH2, LPDLR, PLA1B, mPA-PLA1
Hypotrichosis, Hypotrichosis simplex, Diabetes mellitus type 2, Woolly hair

205
Lipase I
CT17, LPDL, PLA1C, PRED5, mPA-PLA1 beta
Hypertriglyceridemia

206
Lipase family member J
LIPL1, bA425M17.2
Kidney disease

207
Lipase family member K
LIPL2, bA186O14.2
Ocular hypertension, Psoriasis, Scoliosis

208
Lipase family member N
ARCI8, LI4, LIPL4, bA186O14.3
Congenital ichthyosis, Lamellar ichthyosis

209
Lipoyltransferase 1
LIPT1D
Hearing impairment, Leigh syndrome, Lipoyltransferase deficiency

210
Lipoyl(octanoyl) transferase 2
-
Brugada syndrome, Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome, Lipoyltransferase deficiency, Mitochondrial disease, Ventricular fibrillation