|
1441
|
|
|
A-kinase anchoring protein 13 |
AKAP-13, AKAP-Lbc, ARHGEF13, BRX, HA-3, Ht31, LBC, PRKA13, PROTO-LB, PROTO-LBC, c-lbc, p47 |
|
|
1442
|
|
|
A-kinase anchoring protein 10 |
AKAP-10, D-AKAP-2, D-AKAP2, PRKA10 |
|
|
1443
|
|
|
Mitochondrial ribosomal protein L3 |
COXPD9, MRL3, RPML3, uL3m |
|
|
1444
|
|
|
Ribosomal protein L35 |
DBA19, L35, uL29 |
|
|
1445
|
|
|
Long intergenic non-protein coding RNA 2814 |
LINC02815 |
|
|
1446
|
|
|
Polypeptide N-acetylgalactosaminyltransferase 5 |
GALNAC-T5, GALNACT5 |
|
|
1447
|
|
|
Ras association domain family member 8 |
C12orf2, HOJ1 |
|
|
1448
|
|
|
Chimerin 1 |
ARHGAP2, CHN, DURS2, NC, RHOGAP2 |
Aniridia, Arachnodactyly, Blepharophimosis, Blepharospasm, Brachydactyly, Congenital camptodactyly, Congenital clubfoot, Congenital coloboma of iris, Congenital hypoplasia of radius, Dandy-walker syndrome, Developmental delay, Diaphragmatic eventration, Duane retraction syndrome, Duane syndrome, Duane-radial ray syndrome, Dysphagia, Ectopic kidney, Fundus coloboma, Hearing loss, Hydronephrosis, Hypoplasia of optic disc, Laryngomalacia, Microcephaly, Microcornea, Microglossia, Micrognathism, Neck webbing, Nyctalopia, Nystagmus, Oculomotor nerve palsy, Plagiocephaly, Polydactyly, Ptosis, Retinal coloboma, Spina bifida occulta, Stenosis of external auditory canal, Strabismus, UranostaphyloschisisView all (23 more) |
|
1449
|
|
|
SEC63 protein translocation regulator |
DNAJC23, ERdj2, PCLD2, PRO2507, SEC63L |
|
|
1450
|
|
|
DNA polymerase gamma 2, accessory subunit |
HP55, MTDPS16, MTDPS16A, MTDPS16B, MTPOLB, PEOA4, POLB, POLG-BETA, POLGB |
Anxiety disorder, Atrial fibrillation, Bipolar disorder, Cardiomyopathy, Cataract, Central visual impairment, Cerebellar atrophy, Diabetes mellitus, Dysarthria, Dysphagia, External ophthalmoplegia, Facial paralysis, Gastroesophageal reflux disease, Gastroparesis, Hyperthyroidism, Hypoplasia of corpus callosum, Hypothyroidism, Impaired cognition, Ketosis, Left ventricular hypertrophy, Liver failure, Major affective disorder, Mental depression, Migraine, Mitochondrial myopathy, Nocturia, Osteoporosis, Peripheral axonal neuropathy, Progressive external ophthalmoplegia, Progressive external ophthalmoplegia with mitochondrial dna deletions, Ptosis, Ventricular arrhythmiaView all (17 more) |