Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7361 to 7370 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7361
Leucine rich repeat transmembrane neuronal 1
-
Schizophrenia

7362
Leucine rich repeat transmembrane neuronal 3
-
Arrhythmogenic right ventricular cardiomyopathy, Autism, Essential tremor, Scoliosis, Ulcerative colitis

7363
Leucine rich repeat transmembrane neuronal 4
-
Attention deficit hyperactivity disorder, Cerebrovascular disorder, Colorectal cancer, Exostoses, Hypotension, Insomnia, Major depressive disorder, Peripheral arterial disease, Polycystic ovary syndrome, Willis-ekbom disease, Schizophrenia, Substance abuse, Venous thromboembolism

7364
Leucine rich repeat and sterile alpha motif containing 1
CMT2P, RIFLE, TAL
Charcot-marie-tooth disease, Dejerine-sottas disease, Dementia, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome

7365
Leucine rich repeat transmembrane protein 1
HT017
Central nervous system cancer, Glioblastoma, Glioma

7366
Leucine rich transmembrane and O-methyltransferase domain containing
CFAP111, DFNB63, LRRC51, LRRC51-TOMT, TOMT
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Nonsyndromic hearing loss

7367
Limbic system associated membrane protein
IGLON3, LAMP
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Cannabis abuse, Central nervous system cancer, Kidney disease, Colorectal cancer, Crohn disease, Dementia, Diabetic neuropathy, Endometrial neoplasms, Essential tremor, Estrogen-receptor negative breast cancer, Glioma
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7368
Large 60S subunit nuclear export GTPase 1
-
Brain injuries

7369
LSM1 homolog, mRNA degradation associated
CASM, FICUS, YJL124C
Bicuspid aortic valve, Congenital hemivertebra, Cryptorchidism, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Patent ductus arteriosus, Penile hypospadia, Schizophrenia, Strabismus

7370
LSM10, U7 small nuclear RNA associated
MST074, MSTP074
Diverticulitis, Fraser syndrome