Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7191 to 7200 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7191
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

7192
Lipase H
AH, ARWH2, HYPT7, LAH2, LPDLR, PLA1B, mPA-PLA1
Hypotrichosis, Hypotrichosis simplex, Diabetes mellitus type 2, Woolly hair

7193
Lipase I
CT17, LPDL, PLA1C, PRED5, mPA-PLA1 beta
Hypertriglyceridemia

7194
Lipase family member J
LIPL1, bA425M17.2
Kidney disease

7195
Lipase family member K
LIPL2, bA186O14.2
Ocular hypertension, Psoriasis, Scoliosis

7196
Lipase family member N
ARCI8, LI4, LIPL4, bA186O14.3
Congenital ichthyosis, Lamellar ichthyosis

7197
Lipoyltransferase 1
LIPT1D
Hearing impairment, Leigh syndrome, Lipoyltransferase deficiency

7198
Lipoyl(octanoyl) transferase 2
-
Brugada syndrome, Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome, Lipoyltransferase deficiency, Mitochondrial disease, Ventricular fibrillation

7199
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)

7200
LKAAEAR motif containing 1
C20orf201
Metabolic syndrome, Diabetes mellitus type 2