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 "E"
441 to 450 of 463 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

441
Exocyst complex component 7
2-5-3p, BLOM4, EX070, EXO70, EXOC1, Exo70p, NEDSEBA, YJL085W
Neurodevelopmental disorder, Alzheimer disease, Non-specific syndromic intellectual disability

442
Exocyst complex component 8
EXO84, Exo84p, NEDMISB, SEC84
Aplasia of the vermis, Neurodevelopmental disorder

443
Exo/endonuclease G
ENDOGL1, ENDOGL2, ENGL, ENGL-a, ENGL-b, ENGLA, ENGLB
Brugada syndrome

444
Exosome component 1
CGI-108, CSL4, Csl4p, PCH1F, SKI4, Ski4p, p13
Pontocerebellar hypoplasia, Vascular brain injury

445
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

446
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

447
Exosome component 4
RRP41, RRP41A, Rrp41p, SKI6, Ski6p, hRrp41p, p12A
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

448
Exosome component 5
CABAC, RRP41B, RRP46, Rrp46p, hRrp46p, p12B
Atrial fibrillation, Cerebellar ataxia, brain abnormalities, and cardiac conduction defects, Desbuquois syndrome, Neurodevelopmental disorder, Stomach neoplasms

449
Exosome component 8
CIP3, EAP2, OIP2, PCH1C, RRP43, Rrp43p, bA421P11.3, p9
Congenital pontocerebellar hypoplasia, Pontocerebellar hypoplasia, Spastic ataxia

450
Exosome component 9
PCH1D, PM/Scl-75, PMSCL1, RRP45, Rrp45p, p5, p6
Cerebral atrophy, Congenital pontocerebellar hypoplasia, Osteoarthritis, Pontocerebellar hypoplasia