|
391
|
|
|
USH1 protein network component harmonin |
AIE-75, DFNB18, DFNB18A, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1cpst |
Anxiety disorder, Cataract, Cerebral cortical atrophy, Ciliopathies, Congenital sensorineural hearing loss, Deafness, Developmental delay, Disorder of eye, Hallucinations, Hearing loss, Hemianopsia, Hereditary retinal dystrophy, Leukemia, Mental depression, Mental retardation, Motor delay, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Nyctalopia, Retinitis pigmentosa, Rod-cone dystrophy, Schizophrenia, Subcortical cerebral atrophy, Usher syndromeView all (9 more) |
|
392
|
|
|
Polyglutamine binding protein 1 |
MRX2, MRX55, MRXS3, MRXS8, NPW38, RENS1, SHS |
Anxiety disorder, Arachnodactyly, Atrial septal defect, Brachycephaly, Camptodactyly of fingers, Cataract, Cerebral atrophy, Charcot-marie-tooth disease, Colorectal cancer, Congenital camptodactyly, Congenital epicanthus, Congenital microcephaly, Congenital ocular coloboma, Congenital pectus excavatum, Developmental delay, Dwarfism, Dysmorphic features, Hamel cerebro-palato-cardiac syndrome, High palate, Hyperopia, Hypospadias, Imperforate anus, Spastic diplegia, Macroglossia, Macrotia, Malocclusion, Mental retardation, Mental retardation, x-linked, Microcephaly, Micrognathism, Microlissencephaly, Microstomia, Nail dystrophy, Partial agenesis of corpus callosum, Persistent ostium primum, Renpenning syndrome, Scoliosis, Secundum atrial septal defect, Situs inversus, Spastic paraplegia, Strabismus, Tetralogy of fallot, Ventricular septal defect, Hereditary spastic paraplegia, x-linkedView all (29 more) |
|
393
|
|
|
MicroRNA 5094 |
- |
|
|
394
|
|
|
EGF like repeats and discoidin domains 3 |
DEL1 |
|
|
395
|
|
|
Fibrinogen silencer binding protein |
- |
|
|
396
|
|
|
CYP3A7-CYP3A51P readthrough |
CYP3A7, CYP3A7-3AP1, CYP3A7-CYP3AP1, CYP3A7.1L, CYPIIIA7 |
|
|
397
|
|
|
Long intergenic non-protein coding RNA 558 |
- |
|
|
398
|
|
|
SCA7/ATXN7 antisense RNA 1 |
ATXN7-AS1 |
|
|
399
|
|
|
Ceramide transporter 1 |
CERT, CERTL, COL4A3BP, GPBP, MRD34, NEDHSF, STARD11 |
Atrial fibrillation, Cardiovascular diseases, Central visual impairment, Congenital epicanthus, Coronary heart disease, Developmental delay, Diabetes, Diabetes mellitus, Epilepsy, Heart failure, Lung carcinoma, Malignant neoplasm, Mental retardation, Neurodevelopmental disorders, Seizure, Stereotyped behavior, Stroke, Syndactyly of the toes, SynophrysView all (4 more) |
|
400
|
|
|
PTCHD1 and PHEX antisense RNA |
DDX53-AS1, PHEX-AS1, PTCHD1AS1, PTCHD1AS2 |
|
