Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
7201 to 7210 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7201
LLGL scribble cell polarity complex component 1
DLG4, HUGL, HUGL-1, HUGL1, LLGL, Lgl1, Mgl1
Breast cancer, Breast neoplasms, Obstructive pulmonary disease, Tourette syndrome

7202
LLGL scribble cell polarity complex component 2
HGL, Hugl-2, LGL2
Breast neoplasms

7203
LLP homolog, long-term synaptic facilitation factor
C12orf31, hLLP
Dementia

7204
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

7205
Lectin, mannose binding 1 like
ERGIC-53L, ERGL
Celiac disease, Osteoarthritis, Squamous cell carcinoma

7206
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

7207
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

7208
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

7209
Limb development membrane protein 1 like
LIMR
Insomnia

7210
LMBR1 domain containing 1
C6orf209, LMBD1, MAHCF, NESI
Cobalamin c disease, Intracellular cobalamin metabolism disorder, Donnai-barrow syndrome, Metabolic syndrome, Methylmalonic acidemia, Nonalcoholic fatty liver disease, Oligodendroglioma, Diabetes mellitus type 2