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"
341 to 350 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

341
ERCC excision repair 6, chromatin remodeling factor
ARMD5, CKN2, COFS, COFS1, CSB, CSB-PGBD3, POF11, RAD26, UVSS1
Arthrogryposis, Arthrogryposis multiplex congenita, Cataract, Cerebrooculofacioskeletal syndrome, Cockayne syndrome, Cerebro-oculo-facio-skeletal syndrome, Craniofacial abnormalities, De sanctis-cacchione syndrome, Growth disorder, Hearing impairment, Hearing loss, Lung cancer, Lung neoplasms, Macular degeneration, Age-related macular degeneration
View all (5 more)

342
ERCC excision repair 6 like 2
BMFS2, C9orf102, HEBO, RAD26L, SR278
Amyotrophic lateral sclerosis, Bone marrow failure syndromes, Obstructive pulmonary disease, Congenital bone marrow failure syndrome, Growth hormone insensitivity syndrome with immune dysregulation, Pancytopenia, Thrombocytopenia

343
ERCC excision repair 8, CSA ubiquitin ligase complex subunit
CKN1, CSA, UVSS2
Alzheimer disease, Cockayne syndrome, Congenital neurologic anomalies, Deafness, Mitochondrial complex deficiency, Schizophrenia, Uv-sensitive syndrome

344
Epiregulin
EPR, ER, Ep
Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Erythropoietic protoporphyria, Ovarian neoplasms, Creutzfeldt-jakob disease, Tuberculoma

345
ETS2 repressor factor
CHYTS, CRS4, PE-2, PE2
Craniofacial abnormalities, Craniofacial dysostosis, Craniosynostosis, Crouzon syndrome, Desbuquois syndrome, Language development disorders, Neurodevelopmental disorder, Noonan syndrome, Ocular hypotension, Parieto-occipital craniosynostosis, Prostatic neoplasms

346
ETS transcription factor ERG
LMPHM14, erg-3, p55
Alzheimer disease, Eczema, B-cell acute lymphoblastic leukemia, Central nervous system cancer, Coronary artery disease, Dental caries, Dupuytren contracture, Extraskeletal ewing sarcoma, Gastroesophageal reflux disease, Glioblastoma, Glioma, Leukemia, Myeloid leukemia, Lymphatic malformation, Major depressive disorder
View all (12 more)

347
Endoplasmic reticulum-golgi intermediate compartment 1
AMC2, AMCN, ERGIC-32, ERGIC32, NET24
Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Colorectal cancer, Crohn disease, Frontotemporal dementia, Inflammatory bowel disease, Periodontitis, Ulcerative colitis

348
ERGIC and golgi 3
C20orf47, C2orf47, CGI-54, Erv46, NY-BR-84, PRO0989, SDBCAG84, dJ477O4.2
Non-small-cell lung carcinoma, Developmental disability, Lung neoplasms

349
ERH mRNA splicing and mitosis factor
DROER
Intrahepatic cholestasis of pregnancy

350
Exoribonuclease 1
3'HEXO, HEXO, HXAL, SEMDGC, SEMDGS, THEX1
Asthma, Atrial fibrillation, Bipolar disorder, Global developmental delay, Hoxha-aliu syndrome, Neurotic disorder, Obesity, Spondyloepimetaphyseal dysplasia, Systemic lupus erythematosus, Diabetes mellitus type 2