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 463 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

341
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

342
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

343
Epiregulin
EPR, ER, Ep
Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Erythropoietic protoporphyria, Ovarian neoplasms, Creutzfeldt-jakob disease

344
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

345
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)

346
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

347
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

348
ERH mRNA splicing and mitosis factor
DROER
Intrahepatic cholestasis of pregnancy

349
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

350
ERI1 exoribonuclease family member 2
EXOD1, ZGRF5
Hodgkin lymphoma