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"
211 to 220 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
Lipopolysaccharide induced TNF factor
PIG7, SIMPLE, TP53I7
Androgenetic alopecia, Ankylosing spondylitis, Asthma, Basal cell carcinoma, Charcot-marie-tooth disease, Cholecystolithiasis, Color vision deficiency, Colorectal cancer, Crohn disease, Distal spinal muscular atrophy, Endometrial neoplasms, Gallstones, Hereditary motor and sensory neuropathies, Inflammatory bowel disease, Multiple sclerosis
View all (6 more)

212
LKAAEAR motif containing 1
C20orf201
Metabolic syndrome, Diabetes mellitus type 2

213
LLGL scribble cell polarity complex component 1
DLG4, HUGL, HUGL-1, HUGL1, LLGL, Lgl1, Mgl1
Breast cancer, Breast neoplasms, Obstructive pulmonary disease, Tourette syndrome

214
LLGL scribble cell polarity complex component 2
HGL, Hugl-2, LGL2
Breast neoplasms

215
LLP homolog, long-term synaptic facilitation factor
C12orf31, hLLP
Dementia

216
Lectin, mannose binding 1
ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58
Basal cell carcinoma, Combined deficiency of factor v and factor viii, Combined factor v and factor viii deficiency, Factor v deficiency, Hearing loss, Hemophilia a

217
Lectin, mannose binding 1 like
ERGIC-53L, ERGL
Celiac disease, Osteoarthritis, Squamous cell carcinoma

218
Lectin, mannose binding 2
C5orf8, GP36B, VIP36
Asthma, Eczema, Color vision deficiency, Gout, Metabolic syndrome, Multiple sclerosis, Psoriasis, Respiratory system disease, Small vessel stroke, Diabetes mellitus type 2

219
Lectin, mannose binding 2 like
MRD69, MRT52, VIPL
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Bipolar disorder, Renal cell carcinoma, Neurodevelopmental disorder, Bipolar depression, Intellectual developmental disorder, Major depressive disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

220
Limb development membrane protein 1
ACHP, C7orf2, DIF14, LSS, PPD2, THYP, TPT, TPTPS, ZRS
Acheiropody, Color vision deficiency, Desbuquois syndrome, Holoprosencephaly, Patterson stevenson fontaine syndrome, Polydactyly, Schizophrenia, Syndactyly, Triphalangeal thumb-polysyndactyly syndrome