|
2181
|
|
|
Casein beta |
CASB, PDC213 |
|
|
2182
|
|
|
PH domain containing endocytic trafficking adaptor 1 |
FAM109A, IPIP27A, SES1 |
|
|
2183
|
|
|
Casein kappa |
CNS10, CSN10, CSNK, KCA |
|
|
2184
|
|
|
Laccase domain containing 1 |
C13orf31, FAMIN, JUVAR |
Arthritis, Asthma, Crohn disease, Inflammatory bowel disease, Leprosy, Multiple sclerosis, Pericarditis, Pleural effusion, Rheumatoid arthritis, Still disease, Uveitis |
|
2185
|
|
|
Long intergenic non-protein coding RNA 343 |
LINC00344, NCRNA00343, NCRNA00344 |
|
|
2186
|
|
|
Beta 3-glucosyltransferase |
B3GALTL, B3GTL, B3Glc-T, Gal-T, beta3Glc-T |
Accessory kidney, Agenesis of corpus callosum, Anomalous pulmonary artery, Anterior segment dysgenesis, Atrial septal defect, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebral atrophy, Cerebral cortical atrophy, Chamber synechiae, Congenital coloboma of iris, Congenital exomphalos, Congenital hypothyroidism, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Disorder of eye, Double ureter, Exudative macular degeneration, Frontal bossing, Fundus coloboma, Geographic atrophy, Glaucoma, Hearing loss, Heart septal defects, Hydrocephalus, Hydronephrosis, Hypopituitarism, Hypoplasia of the maxilla, Hypoplasia of vagina, Hypoplastic left heart syndrome, Hypospadias, Imperforate anus, Krause-kivlin syndrome, Macrocephaly, Macrostomia, Age-related macular degeneration, Mental depression, Mental retardation, Microcephaly, Microcornea, Micrognathism, Micromelia, Multicystic renal dysplasia, Myopia, Neck webbing, Nystagmus, Optic atrophy, Patent ductus arteriosus, Peters plus syndrome, Posteriorly rotated ear, Ptosis, Pulmonary stenosis, Renal hypoplasia, Retinal coloboma, Rhizomelia, Scoliosis, Spade-like hand, Spina bifida occulta, Stenosis of external auditory canal, Syndactyly, Syndactyly of the toes, Talipes transversoplanus, Ventricular septal defectView all (52 more) |
|
2187
|
|
|
Casein kinase 1 alpha 1 |
CK1, CK1a, CKIa, HEL-S-77p, HLCDGP1, PRO2975 |
|
|
2188
|
|
|
PPP1R13B divergent transcript |
HITT, LINC00637 |
|
|
2189
|
|
|
Retinol dehydrogenase 12 |
LCA13, RP53, SDR7C2 |
Cataract, Ciliopathies, Cone-rod dystrophy, Congenital cerebral hernia, Congenital hypoplasia of penis, Developmental delay, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosaView all (7 more) |
|
2190
|
|
|
Goosecoid homeobox |
GSC1, SAMS |
Congenital clubfoot, Dislocated radial head, Cryptorchidism, Dwarfism, Hearing loss, High palate, Micrognathism, Microstomia, Microtia, Rhizomelia, Short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities(sams), Short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities |
