Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7211 to 7220 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7211
LMBR1 domain containing 2
DENBA
Developmental delay, Developmental delay with variable neurological abnormalities, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

7212
LIM and cysteine rich domains 1
-
Congenital esophageal anomaly, Congenital insufficiency of mitral valve, Diverticular disease, Mitral valve prolapse, Narcolepsy, Tetralogy of fallot

7213
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

7214
Lipase maturation factor 2
TMEM112B, TMEM153
Hearing loss

7215
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 (43 more)

7216
Lamin B1
ADLD, ADLDAT, LMN, LMN2, LMNB, MCPH26
Demyelinating leukodystrophy, Primary microcephaly, Dyslexia, Microcephaly, Parkinson disease

7217
Lamin B2
EPM9, LAMB2, LMN2, MCPH27
Central nervous system malformation, Progressive myoclonic epilepsy, Lipodystrophy, Microcephaly, Neurodevelopmental disorder, Partial lipodystrophy

7218
Lamin tail domain containing 1
IFLTD1, LMNARS1, PAS1C1
Lung neoplasms, Non-melanoma skin carcinoma, Oligodendroglioma, Systemic lupus erythematosus, Hypertension

7219
LIM domain only 1
RBTN1, RHOM1, TTG1
T-cell leukemia-lymphoma, Movement disorder, Neuroblastoma, Periodic limb movement disorder, Willis-ekbom disease, Diabetes mellitus type 2

7220
LIM domain only 2
LMO-2, RBTN2, RBTNL1, RHOM2, TTG2
T-cell leukemia-lymphoma, Major depressive disorder, Post-operative acute kidney injury