1121
|
|
|
Exosome component 6 |
EAP4, MTR3, Mtr3p, hMtr3p, p11 |
Curated: N/A
Unreviewed: Adrenoleukodystrophy, Anxiety Disorder, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Hematological Disease, Hereditary Liability To Pressure Palsies, Hydrocephalus, Irritable Bowel Syndrome, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mental Depression, Mental Disorders, Motor neuron atrophy, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Parkinson disease, Sarcoma, Schizophrenia, Smith-Magenis Syndrome, Stress Disorder, Thyroid Carcinoma
|
1122
|
|
|
Exosome component 7 |
EAP1, RRP42, Rrp42p, hRrp42p, p8 |
Curated: N/A
Unreviewed: N/A
|
1123
|
|
|
Exosome component 8 |
CIP3, EAP2, OIP2, PCH1C, RRP43, Rrp43p, bA421P11.3, p9 |
Curated: Congenital pontocerebellar hypoplasia, Pontocerebellar hypoplasia, Spastic ataxia
Unreviewed: Central Nervous System Demyelination, Cerebral cortical atrophy, Colorectal Cancer, Contracture, Developmental Delay, Esotropia, Hypoplasia Of Corpus Callosum, Nervous system disease, Nervous System Disorder, Neurodegenerative Disorders, Nystagmus, Pontoneocerebellar hypoplasia, Prostatic neoplasm, Respiratory Failure, Spastic tetraparesis, Spinal Muscular Atrophy
|
1124
|
|
|
EXOSC8 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1125
|
|
|
Exosome component 9 |
PCH1D, PM/Scl-75, PMSCL1, RRP45, Rrp45p, p5, p6 |
Curated: Cerebral atrophy, Congenital pontocerebellar hypoplasia, Osteoarthritis, Pontocerebellar hypoplasia
Unreviewed: Breast neoplasm, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral Atrophy, Congenital Epicanthus, Developmental Delay, Dysphagia, Erythermalgia, High palate, Microcephaly, Motor nerve neuritis, Mucopolysaccharidosis, Nystagmus, Oropharyngeal Dysphagia, Polymyositis, Pontoneocerebellar hypoplasia, Respiratory Failure
|
1126
|
|
|
Exophilin 5 |
EBS4, SLAC2-B, SLAC2B |
Curated: Alzheimer disease, Clear cell renal cell carcinoma, Dementia, Epidermolysis bullosa, Estrogen-receptor negative breast cancer, Orofacial cleft, Prostate cancer, Scoliosis, Uterine fibroid
Unreviewed: Blister, Chronic obstructive pulmonary disease, Epidermolysis Bullosa, Epidermolysis Bullosa Simplex, Epidermolysis Bullosa Simplex With Mottled Pigmentation, Hyperkeratosis, Junctional Epidermolysis Bullosa, Malignant Neoplasm
|
1127
|
|
|
Exostosin glycosyltransferase 1 |
EXT, LGCR, LGS, TRPS2, TTV |
Curated: Atrial fibrillation, Autism, Bone fracture, Breast cancer, Chondrosarcoma, Colorectal cancer, Desbuquois syndrome, Endometrial cancer, Epilepsy, Exostoses, Generalized epilepsy, Gestational diabetes, Insomnia, Major depressive disorder, Metabolic syndrome, Obesity, Partial epilepsy, Psoriasis, Schizophrenia, Trichorhinophalangeal syndrome, Diabetes mellitus type 2, exostoses, multiple, type 1
Unreviewed: Adenocarcinoma, Antisocial Personality Disorder, Arthritis, Astrocytoma, Atrophy, Autoimmune Diseases, Avascular Necrosis Of The Capital Femoral Epiphysis, Blood coagulation disorder, Bone Disease, Bone neoplasms, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Calcinosis, Carcinogenesis, Carcinoma Of The Head And Neck, Cervical Intraepithelial Neoplasia, Cervical myelopathy, Chondroblastoma, Chondroma, Chordoma, Conduct Disorder, Congenital Chromosomal Disease, Contiguous gene syndrome, Cornelia De Lange Syndrome, Cranial Nerve Paralysis, De lange syndrome, Diabetes Mellitus, Dwarfism, Enchondromatosis, End Stage Liver Disease, Endometrial carcinoma, Facial dysmorphism, Frontotemporal dementia, Fulminant Hepatitis, Glioma, Glomerulonephritis, Glycogen storage disease, Hearing Loss, Hemiplegia/hemiparesis, Hepatitis c, Hepatocellular carcinoma, Hypercholesterolemia, Hyperlipoproteinemia, Hyperostosis, Hypogonadism, Hypoxia, Inflammatory Myopathy, Intellectual developmental disorder, Langer-Giedion Syndrome, Legg-Calve-Perthes Disease, Lennox-Gastaut Syndrome, Leukemia, Liver carcinoma, Liver neoplasms, Lupus Nephritis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Madelung deformity, Malignant Neoplasm, Melanoma, Membranous Glomerulonephritis, Mental Disorders, Mental retardation, Metachondromatosis, Microcephaly, Micromelia, Mucopolysaccharidosis, Multiple congenital exostosis, Multiple exostoses, Multiple myeloma, Multiple Osteochondromas, Myoclonic Epilepsy, Neoplasms, Nephrotic Syndrome, Osseous Ankylosis, Osteochondroma, Osteopoikilosis, Osteoporosis, Osteosarcoma, Pelvic bone exostoses, Pica, Pituitary dwarfism, Polydactyly, Prostatic neoplasm, Proteinuria, Rectal Carcinoma, Rheumatoid arthritis, Sarcoma, Scapular exostoses, Scoliosis, Spinal cord compression, Squamous cell carcinoma, Steroid-Sensitive Nephrotic Syndrome, Systemic lupus erythematosus, Talipes, Tibial hemimelia, Transient myeloproliferative disorder, Trichorhinophalangeal Dysplasia, Vasculitis, Vesicoureteral Reflux
|
1128
|
|
|
Exostosin glycosyltransferase 2 |
SOTV, SSMS |
Curated: Androgenetic alopecia, 11p11.2 deletion syndrome, Desbuquois syndrome, Exostoses, Potocki-shaffer syndrome, Seizures, scoliosis, and macrocephaly/microcephaly syndrome, exostoses, multiple, type 2
Unreviewed: 11p11.2 Deletion Syndrome, Anemia, Arthritis, Atrophy, Autism, Autoimmune Diseases, Benign Neoplasm, Bone Disease, Bone neoplasms, Brachycephaly, Breast Carcinoma, Breast disease, Breast neoplasm, Camptodactyly of fingers, Cervical myelopathy, Chondrosarcoma, Colorectal Cancer, Congenital Chromosomal Disease, Congenital disorder of glycosylation, Congenital Epicanthus, Cranial Nerve Paralysis, Cryptorchidism, Defect Of Skull Ossification, Development Disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Dwarfism, Enchondromatosis, Frontotemporal dementia, Gastroesophageal Reflux Disease, Gestational diabetes, Glioblastoma, Glioma, Glomerulonephritis, Glycogen storage disease, Growth disorder, Hemiplegia/hemiparesis, Hereditary Cancer Syndrome, Hypercholesterolemia, Hyperlipoproteinemia, Hyperostosis, Hypertension, Hypothyroidism, Lupus Nephritis, Macrocephaly, Madelung deformity, Membranous Glomerulonephritis, Mental retardation, Metachondromatosis, Microcephaly, Micrognathism, Micromelia, Motor delay, Mucopolysaccharidosis, Multiple congenital exostosis, Multiple exostoses, Multiple Osteochondromas, Nail Diseases, Nail dysplasia, Neoplasms, Nephroblastoma, Neurodegenerative disorder, Nystagmus, Osseous Ankylosis, Osteochondroma, Osteopenia, Osteosarcoma, Parietal Foramina, Pelvic bone exostoses, Penis Agenesis, Pica, Pituitary dwarfism, Potocki-Shaffer Syndrome, Proteinuria, Sarcoma, Scapular exostoses, Scoliosis, Seizures, Scoliosis, And Macrocephaly Syndrome, Squamous cell carcinoma, Stereotyped Behavior, Strabismus, Systemic lupus erythematosus, Ventricular septal defect
|
1129
|
|
|
- |
EXT2 |
Curated: N/A
Unreviewed: Chondrosarcoma, Exostoses, Multiple congenital exostosis
|
1130
|
|
|
Exostosin like glycosyltransferase 1 |
EXTL |
Curated: N/A
Unreviewed: Autoimmune disease, Colorectal neoplasm, Malignant Neoplasm, Neoplasms, Neuroblastoma
|