Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7131 to 7140 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7131
Legumain
AEP, LGMN1, PRSC1
Alzheimer disease, Myopia

7132
Leucine rich repeat containing G protein-coupled receptor 4
BNMD17, DPSL, GPR48
Androgenetic alopecia, Bone mineral density quantitative trait locus, Metabolic syndrome, Diabetes mellitus type 2

7133
Leucine rich repeat containing G protein-coupled receptor 5
FEX, GPR49, GPR67, GRP49, HG38
Basal cell carcinoma, Colonic neoplasms, Colorectal neoplasms

7134
Leucine rich repeat containing G protein-coupled receptor 6
GPCR, VTS20631
Breast cancer, Breast neoplasms, Squamous cell carcinoma, Colorectal neoplasms, Estrogen-receptor negative breast cancer, Myelodysplastic syndrome, Pernicious anemia, Post-traumatic stress disorder, Willis-ekbom disease, Triple negative breast cancer

7135
Lengsin, lens protein with glutamine synthetase domain
GLULD1, LGS
Asthma, Autoimmune musculoskeletal system disorder, Major depressive disorder, Schizophrenia, Diabetes mellitus type 2

7136
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

7137
Luteinizing hormone/choriogonadotropin receptor
HHG, LCGR, LGR2, LH/CG-R, LH/CGR, LHR, LHRHR, LSH-R, ULG5
46, xy disorder of sex development, Disorders of sex development, Testotoxicosis, Male infertility, Metabolic syndrome, Polycystic ovary syndrome, Hypogonadism, Diabetes mellitus type 2

7138
LHFPL tetraspan subfamily member 2
-
Cardiovascular disease, Iga nephropathy, Parkinson disease, Stroke

7139
LHFPL tetraspan subfamily member 3
LHFPL4
Lymphocytic leukemia, Diverticular disease, Endometrial cancer, Endometrial neoplasms, Eosinophilia, Gout, Insomnia, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

7140
LHFPL tetraspan subfamily member 5
DFNB67, TMHS, dJ510O8.8
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Nonsyndromic hearing loss, Diabetes mellitus type 1, Diabetes mellitus type 2