Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4311 to 4320 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4311
Exocyst complex component 3 like 2
BMRS, XTP7
Alzheimer disease, Atrophic macular degeneration, Brain malformations, Coronary artery disease, Meckel-gruber syndrome, Myocardial infarction, Peptic ulcer disease, Diabetes mellitus type 2, Age-related macular degeneration

4312
Exocyst complex component 3 like 4
C14orf73
Biliary cirrhosis, Nonalcoholic fatty liver disease, Biliary cholangitis, Diabetes mellitus type 1, Diabetes mellitus type 2

4313
Exocyst complex component 4
SEC8, SEC8L1, Sec8p
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Cervical cancer, Facial dysmorphism syndrome, Major depressive disorder, Meckel-gruber syndrome, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

4314
Exocyst complex component 5
HSEC10, PRO1912, SEC10, SEC10L1, SEC10P
Color vision deficiency

4315
Exocyst complex component 6
EXOC6A, SEC15, SEC15L, SEC15L1, SEC15L3, Sec15p
Lymphocytic leukemia, Coronary artery disease, Crohn disease, Diabetic neuropathy, Diabetic retinopathy, Diffuse large b-cell lymphoma, Follicular lymphoma, Hearing loss, Inflammatory bowel disease, Metabolic syndrome, Multiple sclerosis, Open angle glaucoma, Willis-ekbom disease, Stroke, Diabetes mellitus type 2
View all (2 more)

4316
Exocyst complex component 6B
SEC15B, SEC15L2, SEMDJL3
Desbuquois syndrome, Neuroblastoma, Schizophrenia, Spondyloepimetaphyseal dysplasia, Diabetes mellitus type 2

4317
Exocyst complex component 7
2-5-3p, BLOM4, EX070, EXO70, EXOC1, Exo70p, NEDSEBA, YJL085W
Neurodevelopmental disorder, Alzheimer disease, Non-specific syndromic intellectual disability

4318
Exocyst complex component 8
EXO84, Exo84p, NEDMISB, SEC84
Aplasia of the vermis, Neurodevelopmental disorder

4319
Exo/endonuclease G
ENDOGL1, ENDOGL2, ENGL, ENGL-a, ENGL-b, ENGLA, ENGLB
Brugada syndrome

4320
Exosome component 1
CGI-108, CSL4, Csl4p, PCH1F, SKI4, Ski4p, p13
Pontocerebellar hypoplasia, Vascular brain injury