Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4331 to 4340 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4331
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

4332
Exocyst complex component 5
HSEC10, PRO1912, SEC10, SEC10L1, SEC10P
Color vision deficiency

4333
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
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4334
Exocyst complex component 6B
SEC15B, SEC15L2, SEMDJL3
Desbuquois syndrome, Neuroblastoma, Schizophrenia, Spondyloepimetaphyseal dysplasia, Diabetes mellitus type 2

4335
Exocyst complex component 7
2-5-3p, BLOM4, EX070, EXO70, EXOC1, Exo70p, NEDSEBA, YJL085W
Neurodevelopmental disorder, Alzheimer disease, Non-specific syndromic intellectual disability

4336
Exocyst complex component 8
EXO84, Exo84p, NEDMISB, SEC84
Aplasia of the vermis, Neurodevelopmental disorder

4337
Exo/endonuclease G
ENDOGL1, ENDOGL2, ENGL, ENGL-a, ENGL-b, ENGLA, ENGLB
Brugada syndrome

4338
Exosome component 1
CGI-108, CSL4, Csl4p, PCH1F, SKI4, Ski4p, p13
Pontocerebellar hypoplasia, Vascular brain injury

4339
Exosome component 2
RRP4, Rrp4p, SHRF, hRrp4p, p7
Color vision deficiency, Liver neoplasms, Retinitis pigmentosa, Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome, Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

4340
Exosome component 3
CGI-102, PCH1B, RRP40, Rrp40p, bA3J10.7, hRrp-40, p10
Congenital myopathy, Congenital neurologic anomalies, Congenital pontocerebellar hypoplasia, Lissencephaly, Pena-shokeir syndrome , Pontocerebellar hypoplasia