|
2001
|
|
|
Trace amine associated receptor 1 |
TA1, TAR1, TRAR1 |
|
|
2002
|
|
|
Cytochrome c oxidase subunit 7B |
APLCC, LSDMCA2 |
Absence of septum pellucidum, Agenesis of corpus callosum, Ambiguous genitalia, Aphasia, Aplasia cutis congenita, Atrial septal defect, Cardiomyopathy, Cataract, Colpocephaly, Mandibular aplasia, Congenital anomaly of rectum, Congenital coloboma of iris, Congenital diaphragmatic hernia, Developmental delay, Dwarfism, Dysphasia, Epispadias, Glaucoma, Heart septal defects, Histiocytoid cardiomyopathy, Hydrocephalus, Hypertrophic cardiomyopathy, Hypertrophy of clitoris, Hypospadias, Imperforate anus, Linear skin defects with multiple congenital anomalies, Male pseudohermaphroditism, Mental retardation, Microcephaly, Micrognathism, Microphthalmia with linear skin defects syndrome, Syndromic microphthalmia, Microphthalmos, Mitral valve prolapse, Overriding aorta, Ovotestis, Penis agenesis, Posterior embryotoxon, Respiratory failure, Retinal dysplasia, Retinal dystrophy, Retinitis pigmentosa, Sclerocornea, Specific learning disorder, Status epilepticus, Tricuspid valve insufficiency, Tricuspid valve prolapse, True hermaphroditism, Ventricular septal defect, VitritisView all (35 more) |
|
2003
|
|
|
Adenosine A2a receptor |
A2aR, ADORA2, RDC8 |
Anxiety disorder, Cardiomyopathy, Clonic seizures, Encephalopathy with biphasic seizures and diffusion, Hypotonic seizures, Insomnia, Jacksonian seizure, Melancholia, Mental depression, Mood disorder, Movement disorders, Myocardial diseases, Nonorganic insomnia, Panic disorder, Psychophysiological insomnia, Rheumatoid arthritis, Schizophrenia, Seizure, Septicemia, Sleep disorders, Status marmoratusView all (6 more) |
|
2004
|
|
|
Cytochrome c oxidase subunit 7C |
- |
|
|
2005
|
|
|
Cytochrome c oxidase subunit 8A |
COX, COX8, COX8-2, COX8L, MC4DN15, VIII, VIII-L |
Anemia, Cytochrome-c oxidase deficiency, Developmental delay, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Isolated cytochrome c oxidase deficiency, Leukoencephalopathy, Mental retardation, Motor delay, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (1 more) |
|
2006
|
|
|
Nuclear receptor coactivator 7 |
ERAP140, ESNA1, NCOA7-AS, Nbla00052, Nbla10993, TLDC4, dJ187J11.3 |
|
|
2007
|
|
|
Histidine triad nucleotide binding protein 3 |
HINT4 |
|
|
2008
|
|
|
Parkin coregulated |
BUG21, GLUP, HAK005771, PACRG2.1, PARK2CRG, pf12 |
|
|
2009
|
|
|
Beta-1,3-glucuronyltransferase 2 |
GLCATS |
|
|
2010
|
|
|
Succinate dehydrogenase complex assembly factor 4 |
C6orf57, Sdh8 |
|
