Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "L"
451 to 460 of 673 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

451
Galectin 3 binding protein
90K, BTBD17B, CyCAP, M2BP, MAC-2-BP, TANGO10B, gp90
Central nervous system cancer, Glioblastoma, Glioma, Liver cirrhosis

452
Galectin 7
GAL7, LGALS7A
Carcinoma, Squamous cell carcinoma, Mouth neoplasm

453
Galectin 9
HUAT, LGALS9A
Autism, Epilepsy, Oligodendroglioma, Squamous cell carcinoma

454
Luteinizing hormone subunit beta
CGB4, HH23, LSH-B, LSH-beta
Bradycardia, Chiari-frommel syndrome, Hyperproinsulinemia, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Female infertility, Male infertility, Male pseudohypopituitarism, Polycystic ovary syndrome

455
Luteinizing hormone/choriogonadotropin receptor
HHG, LCGR, LGR2, LH/CG-R, LH/CGR, LHR, LHRHR, LSH-R, ULG5
Male infertility, Metabolic syndrome, Polycystic ovary syndrome, Hypogonadism, Diabetes mellitus, type 2

456
LIM homeobox 1
LIM-1, LIM1
17q12 microdeletion syndrome, Female infertility

457
LIF interleukin 6 family cytokine
CDF, DIA, HILDA, MLPLI
Cardiomegaly, Delirium, Major depressive disorder, Female infertility, Depression, Nonalcoholic fatty liver disease, Polycystic ovary syndrome

458
LIF receptor subunit alpha
CD118, LIF-R, SJS2, STWS, SWS
Bone fragility with contractures, arterial rupture, and deafness, Congenital anomalies of the kidney and urinary tract, Hepatocellular carcinoma, Color vision deficiency, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Developmental regression, Developmental and epileptic encephalopathy, Global developmental delay, Osteoarthritis, Osteochondrodysplasias, Osteoporosis-pseudoglioma syndrome, Paranoia, Polycystic ovary syndrome
View all (3 more)

459
DNA ligase 1
IMD96, LIGI, hLig1
Immunodeficiency, Urinary bladder cancer

460
DNA ligase 3
LIG2, LIG3alpha, MTDPS20
Mitochondrial dna depletion syndrome, Willis-ekbom disease, Scoliosis