Genes | GeDiPNet - Gene Disease Pathway & Associations

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4231 to 4240 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
4231	2071	ERCC3	ERCC excision repair 3, TFIIH core complex helicase subunit	BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2, XPB	Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Trichothiodystrophy, Venous thromboembolism, Xeroderma pigmentosum, Xeroderma pigmentosum-cockayne syndrome
4232	2072	ERCC4	ERCC excision repair 4, endonuclease catalytic subunit	ERCC11, FANCQ, RAD1, XFEPS, XPF	Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autism, Cerebellar ataxia, Bipolar disorder, Cockayne syndrome, Color vision deficiency, Conduct disorder, Dental caries, Fanconi anemia, Genetic predisposition to disease, Major depressive disorder, Metabolic syndrome, Mitral valve prolapse View all (20 more)
4233	2073	ERCC5	ERCC excision repair 5, endonuclease	COFS3, ERCC5-201, ERCM2, UVDR, XPG, XPGC	Cerebellar atrophy, Cerebrooculofacioskeletal syndrome, Cerebro-oculo-facio-skeletal syndrome, Colorectal neoplasms, Congenital pes cavus, Dysarthria, Genetic predisposition to disease, Polyneuropathy, Spastic paraplegia, Xeroderma pigmentosum, Xeroderma pigmentosum-cockayne syndrome
4234	2074	ERCC6	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)
4235	375748	ERCC6L2	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
4236	1161	ERCC8	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
4237	2069	EREG	Epiregulin	EPR, ER, Ep	Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Erythropoietic protoporphyria, Ovarian neoplasms, Creutzfeldt-jakob disease, Tuberculoma
4238	2077	ERF	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
4239	2078	ERG	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)
4240	57222	ERGIC1	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

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