331
|
|
|
Erb-b2 receptor tyrosine kinase 4 |
ALS19, HER4, p180erbB4 |
Alzheimer disease, Amyotrophic lateral sclerosis, Anorexia nervosa, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Bell's palsy, Soft tissue neoplasms, Bipolar disorder, Breast cancer, Central nervous system cancer, Color vision deficiency, Colorectal cancer, Coronary artery disease, Diabetic neuropathy, Peritoneal disease, Endometriosis, Frontotemporal dementia, Gallbladder neoplasms, Gastroesophageal reflux disease, Glioblastoma, Glioma, Gout, Insomnia, Internet addiction disorder, Irritable bowel syndrome, Language development disorders, Lung cancer, Major depressive disorder, Ovarian epithelial cancer, Melanoma, Metabolic syndrome, Migraine, Mood disorder, Neurotic disorder, Obesity, Ovarian cancer, Polycystic ovary syndrome, Psychiatric disorders, Schizophrenia, Skin neoplasms, Squamous cell carcinoma, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus type 2, Urinary bladder cancerView all (32 more) |
332
|
|
|
Erbb2 interacting protein |
ERBB2IP, HEL-S-78, LAP2 |
|
333
|
|
|
ELKS/RAB6-interacting/CAST family member 1 |
Cast2, ELKS, ERC-1, RAB6IP2 |
|
334
|
|
|
ELKS/RAB6-interacting/CAST family member 2 |
CAST, CAST1, ELKSL, SPBC110, Spc110 |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Cannabis abuse, Lymphoblastic leukemia, Obstructive pulmonary disease, Dementia, Gastritis, Gastroesophageal reflux disease, Major depressive disorder, Osteoarthritis, Ovarian serous carcinoma, Periodontitis, Schizophrenia, Scoliosis, Substance abuse, Tourette syndromeView all (2 more) |
335
|
|
|
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, Nasopharyngeal carcinoma, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Stomach neoplasms, Testicular neoplasms, Transient ischemic attack, Uterine neoplasms, Xeroderma pigmentosumView all (9 more) |
336
|
|
|
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, Macular degeneration, Myocardial ischemia, Occupational disease, Prostatic neoplasms, Sarcoma, Senile cataract, Skin abnormalities, Skin disease, Skin neoplasms, Stomach neoplasms, Trichothiodystrophy, Urinary bladder neoplasms, Xeroderma pigmentosum, Xeroderma pigmentosum-cockayne syndromeView all (14 more) |
337
|
|
|
ERCC excision repair 3, TFIIH core complex helicase subunit |
BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2, XPB |
|
338
|
|
|
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, Neurotic disorder, Non-neoplastic peripheral nervous system disease, Obesity, Obsessive-compulsive disorder, Oligodendroglioma, Premature ovarian failure, Peripheral nervous system disease, Peripheral neuropathy, Psychiatric disorders, Schizophrenia, Scoliosis, Spastic ataxia, Substance abuse, Testicular neoplasms, Tourette syndrome, Diabetes mellitus type 2, Urinary bladder neoplasms, Xeroderma pigmentosum, Xeroderma pigmentosum-cockayne syndrome, Xfe progeroid syndromeView all (20 more) |
339
|
|
|
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 |
340
|
|
|
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, Microcephaly, Microphthalmos, Premature ovarian failure, Psychiatric disorders, Uv-sensitive syndromeView all (5 more) |
