|
131
|
|
|
Outer dynein arm docking complex subunit 4 |
TTC25 |
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Kartagener syndrome, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (3 more) |
|
132
|
|
|
Olfactory receptor family 1 subfamily E member 2 |
OR17-135, OR17-136, OR17-93, OR1E4, OR1E7, OST529 |
|
|
133
|
|
|
Obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF |
ARHGEF30, RHABDO1, UNC89 |
|
|
134
|
|
|
O-linked N-acetylglucosamine (GlcNAc) transferase |
HINCUT-1, HRNT1, MRX106, O-GLCNAC, OGT1, XLID106 |
|
|
135
|
|
|
OFD1 centriole and centriolar satellite protein |
71-7A, CXorf5, JBTS10, RP23, SGBS2 |
Acquired porencephaly, Agenesis of corpus callosum, Alopecia, Anodontia, Arachnoid cyst, Asthenozoospermia, Asthma, Brachydactyly, Bronchiectasis, Camptodactyly of fingers, Cataract, Cerebellar vermis agenesis, Choanal atresia, Ciliary dyskinesia, Ciliopathies, Clinodactyly, Asplenia, Congenital clubfoot, Developmental dysplasia of the hip, Congenital epicanthus, Congenital heart defects, Congenital hypoplasia of penis, Congenital pectus excavatum, Corneal dystrophy, Cryptorchidism, Dandy-walker syndrome, Dental enamel hypoplasia, Developmental delay, Diabetes mellitus, Disorder of eye, Dolichocephaly, Dwarfism, Esotropia, Exocrine pancreatic insufficiency, Frontal bossing, Bronchitis, Glaucoma, Hearing loss, High palate, Hydrocephalus, Hydronephrosis, Hyperinsulinism, Hypertension, Hypodontia, Hypogonadism, Hypothalamic hamartomas, Mental retardation, Joubert syndrome, Kartagener syndrome, Keratoconus, Liver cyst, Liver fibrosis, Lung diseases, Macrocephaly, Macrostomia, Malformation of cortical development, Microcephaly, Micrognathism, Movement disorders, Multicystic renal dysplasia, Nasal polyposis, Neuronal heterotopia, Nystagmus, Obesity, Odontogenic tumor, Optic atrophy, Orofaciodigital syndrome, Otitis media, Oto-palato-digital syndrome, Ovarian cysts, Pancreatic cyst, Penis agenesis, Polycystic kidney disease, Polydactyly, Polydactyly of toes, Porencephalic cyst, Posteriorly rotated ear, Radial polydactyly, Renal agenesis, Renal insufficiency, Retinitis pigmentosa, Rhinitis, Rod-cone dystrophy, Scaphocephaly, Scoliosis, Simpson-golabi-behmel syndrome, Sinusitis, Situs inversus, Spade-like hand, Syndactyly, Syndactyly of fingers, Tarsal coalition, Postaxial hand polydactylyView all (78 more) |
|
136
|
|
|
ORAI calcium release-activated calcium modulator 1 |
CRACM1, IMD9, ORAT1, TAM2, TMEM142A |
Amelogenesis imperfecta, Anemia, Aphthous ulcer, Centronuclear myopathy, Centronuclear myopathy, x-linked, Asplenia, Congenital myopathy with fiber type disproportion, Congenital structural myopathy, Dwarfism, Ectodermal dysplasia, Hypertension, Ichthyosis, Immune dysfunction with t-cell inactivation, Immunologic deficiency syndromes, Mental depression, Miosis disorder, Myopathy, Severe combined immunodeficiency disease, Speech disorders, Stomatitis, Stormorken syndrome, Stormorken-sjaastad-langslet syndrome, Tubular aggregate myopathyView all (8 more) |
|
137
|
|
|
2'-5'-oligoadenylate synthetase like |
OASL1, OASLd, TRIP-14, TRIP14, p59 OASL, p59-OASL, p59OASL |
|
|
138
|
|
|
OTU deubiquitinase with linear linkage specificity |
AIPDS, AIPDSA, FAM105B, GUM, IMD107 |
|
|
139
|
|
|
Oncostatin M receptor |
IL-31R-beta, IL-31RB, OSMRB, OSMRbeta, PLCA1 |
Amyloidosis, Ankylosing spondylitis, Cholangitis, Crohn disease, Cutis laxa, Amyloid polyneuropathy, Inflammatory bowel disease, Lichen amyloidosis, Liver carcinoma, Lung carcinoma, Malignant mesothelioma, Localized cutaneous amyloidosis, Psoriasis, Ulcerative colitis |
|
140
|
|
|
Otopetrin 2 |
- |
|
