Genes | GeDiPNet - Gene Disease Pathway & Associations

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4211 to 4220 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
4211	2067	ERCC1	ERCC excision repair 1, endonuclease non-catalytic subunit	COFS4, RAD10, UV20	Alzheimer disease, Anemia, Azoospermia, Non-small-cell lung carcinoma, Cerebrooculofacioskeletal syndrome, Cholestasis, Cockayne syndrome, Cerebro-oculo-facio-skeletal syndrome, Hyperlipidemia, Gastroesophageal reflux disease, Genetic predisposition to disease, Kidney failure, Lung neoplasms, Melanoma, Myopathy View all (9 more)
4212	2068	ERCC2	ERCC excision repair 2, TFIIH core complex helicase subunit	COFS2, CXPD, EM9, TFIIH, TTD, TTD1, XPD	Alzheimer disease, Squamous cell carcinoma, Cerebrooculofacioskeletal syndrome, Ischemic heart disease, Cerebro-oculo-facio-skeletal syndrome, Colorectal neoplasms, Congenital skin anomaly, Congenital nonbullous ichthyosiform erythroderma, Coronary artery disease, Crohn disease, Dermatologic disorder, Gastroesophageal reflux disease, Hypotrichosis simplex, Leukodystrophy, Lung cancer View all (14 more)
4213	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
4214	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)
4215	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
4216	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)
4217	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
4218	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
4219	2069	EREG	Epiregulin	EPR, ER, Ep	Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Erythropoietic protoporphyria, Ovarian neoplasms, Creutzfeldt-jakob disease
4220	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

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