31
|
|
|
WASH complex subunit 1 |
FAM39E, WASH, WASH1 |
Curated: N/A
Unreviewed: Anemia, Borderline personality disorder, Bronchopulmonary Dysplasia, Diabetes Mellitus, Malignant Neoplasm, Malnutrition, Mammary Neoplasms, Mood Disorder, Neurodevelopmental Disorders, Parkinson disease, Schizophrenia
|
32
|
|
|
WASH complex subunit 2A |
FAM21A, FAM21B, bA56A21.1, bA98I6.1 |
Curated: N/A
Unreviewed: N/A
|
33
|
|
|
WASH complex subunit 2C |
FAM21A, FAM21C, VPEF |
Curated: N/A
Unreviewed: N/A
|
34
|
|
|
WASH complex subunit 3 |
CCDC53, CGI-116 |
Curated: Prostate cancer
Unreviewed: N/A
|
35
|
|
|
WASHC3 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
36
|
|
|
WASH complex subunit 4 |
KIAA1033, MRT43, SWIP |
Curated: Nonsyndromic intellectual disability, Intellectual developmental disorder, Schizophrenia
Unreviewed: Absence Of Septum Pellucidum, Alzheimer disease, Autism, Central Visual Impairment, Cerebral Atrophy, Cortical Dysplasia, Developmental Delay, Dwarfism, Dyskinetic Syndrome, Dyssomnia, Hypoplasia Of Corpus Callosum, Mental Depression, Mental retardation, Microcephaly, Motor delay, Myopathy, Non-Syndromic Intellectual Disability, Penile neoplasm, Polymicrogyria, Salaam Seizures, Seizure, Sleep Disorders, Stereotyped Behavior
|
37
|
|
|
WASH complex subunit 5 |
KIAA0196, RTSC, RTSC1, SPG8 |
Curated: Amyotrophic lateral sclerosis, Spastic paraplegia, Frontotemporal dementia, Ritscher-schinzler syndrome, Hereditary spastic paraplegia, Stress urinary incontinence, hereditary spastic paraplegia 8
Unreviewed: 3C syndrome, Amyotrophic Lateral Sclerosis, Aortic Valve Sclerosis, Atrial Septal Defect, Atrioventricular block, Atrophy, Atrophy of the spinal cord, Brachycephaly, Brachydactyly, Carcinoma, Charcot-Marie-Tooth Disease, CHARGE Syndrome, Colorectal neoplasm, Congenital Coloboma Of Iris, Congenital Hypoplasia Of Penis, Congenital malrotation of intestine, Congenital ocular coloboma, Dandy-Walker Syndrome, Developmental Delay, Double Outlet Right Ventricle, Dwarfism, Ectopic anus, Eichsfeld type congenital muscular dystrophy, Frontal bossing, Fundus Coloboma, Gastroesophageal Reflux Disease, Glaucoma, Henoch-Schonlein Nephritis, Huntington Disease, Hydrocephalus, Hydronephrosis, Hypercholesterolemia, Hypertension, Hypoplastic Left Heart Syndrome, Hypospadias, Imperforate anus, Isolated Somatotropin Deficiency, Macrocephaly, Malformation of cortical development, Mental retardation, Micrognathism, Myofibrillar myopathy, Myopathy, Neoplasms, Neuroblastoma, Optic Atrophy, Paget disease, Peroneal muscle atrophy, Pica, Prostate cancer, Pulmonary Stenosis, Retinal coloboma, RITSCHER-SCHINZEL SYNDROME, Russell-Silver Syndrome, Scoliosis, Somatotropin Deficiency, Speech Disorders, Spinocerebellar ataxia, Stomach neoplasms, Syndactyly, Syndactyly of fingers, Tetralogy of Fallot, Ventricular septal defect
|
38
|
|
|
WASHC5 antisense RNA 1 |
KIAA0196-AS1 |
Curated: N/A
Unreviewed: N/A
|
39
|
|
|
WASH and IL9R antisense RNA 1 |
NCRNA00286B |
Curated: N/A
Unreviewed: N/A
|
40
|
|
|
WASH and IL9R antisense RNA 2 |
NCRNA00286A |
Curated: N/A
Unreviewed: Lung adenocarcinoma
|