|
361
|
|
|
AAR2 splicing factor |
C20orf4, CGI-23 |
|
|
362
|
|
|
Amine oxidase copper containing 1 |
ABP, ABP1, DAO, DAO1, KAO, KDAO |
|
|
363
|
|
|
Acyl-CoA thioesterase 11 |
BFIT, STARD14, THEA, THEM1 |
|
|
364
|
|
|
Attractin like 1 |
ALP, bA338L11.1, bA454H24.1 |
|
|
365
|
|
|
Activator of transcription and developmental regulator AUTS2 |
FBRSL2, MRD26 |
Achoo syndrome, Agenesis of corpus callosum, Alopecia, Apraxia, Arthrogryposis multiplex congenita, Astigmatism, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Autism spectrum disorder, Brachycephaly, Burkitt`s lymphoma, Cerebral palsy, Congenital epicanthus, Congenital exomphalos, Cryptorchidism, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Eczema, Epilepsy, Esotropia, Hypoplasia of the optic nerve, Leukemia, Lymphoblastic leukemia, Maternal hypertension, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Motion sickness, Multiple congenital anomalies, Obsessive-compulsive disorder, Oligodontia, Periauricular skin pits, Proptosis, Ptosis, Receptive language delay, Repetitive compulsive behavior, Schizophrenia, Scoliosis, Sleep apnea, Specific learning disorder, Strabismus, Syndactyly of the toesView all (33 more) |
|
366
|
|
|
Ankyrin repeat domain 17 |
CAGS, GTAR, MASK2, NY-BR-16 |
|
|
367
|
|
|
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 |
APPL, DIP13alpha, MODY14 |
Breast cancer, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Diabetes, Diabetes mellitus, Exocrine pancreatic insufficiency, Hepatocellular adenoma, Hyperglycemia, Hypoinsulinemia, Kidney disease, Mason type diabetes, Hypoglycemia, Obesity, Renal cyst, Retinal diseases |
|
368
|
|
|
Rho guanine nucleotide exchange factor 26 |
CSGEF, HMFN1864, SGEF |
|
|
369
|
|
|
Abhydrolase domain containing 12, lysophospholipase |
ABHD12A, BEM46L2, C20orf22, PHARC, dJ965G21.2, hABHD12 |
Ataxia, Cataract, Cerebellar atrophy, Cone dystrophy, Congenital pes cavus, Demyelinating neuropathy, Disorder of eye, Distal amyotrophy, Dysarthria, Hearing loss, Methylmalonic acidemia with homocystinuria, Nystagmus, Optic atrophy, Polyneuropathy, Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Sensorimotor neuropathy, Subcapsular cataractView all (5 more) |
|
370
|
|
|
ATP binding cassette subfamily A member 12 |
ARCI4A, ARCI4B, ICR2B, LI2 |
Alopecia, Cataract, Colorectal cancer, Colorectal neoplasms, Congenital ichthyosis, Congenital nonbullous ichthyosiform erythroderma, Corneal erosion, Drachtman weinblatt sitarz syndrome, Dwarfism, Ectropion, Exfoliative dermatitis, Gangrene, Harlequin ichthyosis, Hyperkeratosis, Hypohidrosis, Hypotrichosis, Ichthyosis, Ichthyosis congenita, Impaired cognition, Keratitis, Lamellar ichthyosis, Otitis media, Palmoplantar keratoderma, Pancreatic adenocarcinoma, Polydactyly of toes, Proptosis, Renal insufficiencyView all (12 more) |
