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"
221 to 230 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
Limb development membrane protein 1 like
LIMR
Insomnia

222
LMBR1 domain containing 1
C6orf209, LMBD1, MAHCF, NESI
Cobalamin c disease, Disorders of intracellular cobalamin metabolism, Donnai-barrow syndrome, Metabolic syndrome, Methylmalonic acidemia, Nonalcoholic fatty liver disease, Oligodendroglioma, Diabetes mellitus type 2

223
LMBR1 domain containing 2
DENBA
Developmental delay, Developmental delay with variable neurological abnormalities, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

224
LIM and cysteine rich domains 1
-
Congenital esophageal anomaly, Congenital insufficiency of mitral valve, Diverticular disease, Mitral valve prolapse, Narcolepsy, Tetralogy of fallot

225
Lipase maturation factor 1
C16orf26, HMFN1876, JFP11, TMEM112, TMEM112A
Astrocytoma, Breast cancer, Central nervous system cancer, Dilated cardiomyopathy, Glioblastoma, Glioma, Heart failure, Hypertriglyceridemia, Hypertrophic cardiomyopathy, Malignant glioma, Diabetes mellitus type 2

226
Lipase maturation factor 2
TMEM112B, TMEM153
Hearing loss

227
Lamin A/C
CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1
Cardiac arrhythmias, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrioventricular block, Werner syndrome, Distal hereditary motor neuropathy, Emery-dreifuss muscular dystrophy, Emery dreifuss muscular dystrophy, Severe lipodystrophic laminopathy, Bethlem myopathy, Cardiac conduction disease, Cardiomyopathy, Dilated cardiomyopathy, Cerebrovascular disorder, Charcot-marie-tooth disease
View all (44 more)

228
Lamin B1
ADLD, ADLDAT, LMN, LMN2, LMNB, MCPH26
Demyelinating leukodystrophy, Primary microcephaly, Dyslexia, Microcephaly, Parkinson disease

229
Lamin B2
EPM9, LAMB2, LMN2, MCPH27
Central nervous system malformation, Progressive myoclonic epilepsy, Lipodystrophy, Microcephaly, Neurodevelopmental disorder, Partial lipodystrophy

230
Lamin tail domain containing 1
IFLTD1, LMNARS1, PAS1C1
Lung neoplasms, Non-melanoma skin carcinoma, Oligodendroglioma, Systemic lupus erythematosus, Hypertension