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3421
|
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Zinc finger protein 423 |
Ebfaz, JBTS19, NPHP14, OAZ, Roaz, ZFP423, Zfp104, hOAZ |
Arima syndrome, Autism, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Disorder of eye, Fundus coloboma, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Joubert syndrome with oculorenal defect, Kidney disease, Malformation of cortical development, Mental retardation, Nephronophthisis, Nystagmus, Ovarian neoplasm, Polycystic kidney disease, Polydactyly of toes, Ptosis, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Scoliosis, StrabismusView all (11 more) |
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3422
|
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Rho GTPase activating protein 26 |
GRAF, GRAF1, OPHN1L, OPHN1L1 |
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3423
|
|
|
Tubulin tyrosine ligase like 5 |
CORD19, KIAA0998, STAMP |
Arthritis, Carpal tunnel syndrome, Cone-rod dystrophy, Juvenile arthritis, Leukemia, Nyctalopia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, Retinal dystrophy, Retinitis pigmentosa, Still disease |
|
3424
|
|
|
Signal induced proliferation associated 1 like 3 |
CTRCT45, SPAL3, SPAR3 |
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3425
|
|
|
Kinesin family member 1B |
CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1 |
Adrenal gland pheochromocytoma, Anemia, Aniridia, Capillary hemangioma of retina, Charcot-marie-tooth disease, Congestive heart failure, Cranial nerve compression, Distal amyotrophy, Episodic paroxysmal anxiety, Extra-adrenal pheochromocytoma, Ganglioneuroblastoma, Ganglioneuroma, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hemangioma, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, Horner syndrome, Hypercalcemia, Hypertension, Hypertensive retinopathy, Liver carcinoma, Multiple sclerosis, Neoplasms, Nervous system diseases, Neuroblastoma, Opsoclonus, Panic disorder, Paraganglioma of head and neck, Paroxysmal hypertension, Peripheral axonal atrophy, Pheochromocytoma, Pulsatile tinnitus, Renal artery stenosis, Renal carcinoma, Sinus tachycardia, Spinal cord compression, Vocal cord paralysisView all (24 more) |
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3426
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|
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IQ motif and Sec7 domain ArfGEF 2 |
BRAG1, IQ-ArfGEF, MRX1, MRX18, MRX78, XLID1 |
Anxiety disorder, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Developmental delay, Developmental regression, Dwarfism, Dyssomnia, Epilepsy, Facial paralysis, Frontal bossing, Gastroesophageal reflux disease, Neurosensory hearing impairment, Hearing loss, Horizontal nystagmus, Hypercholesterolemia, Hyperopia, Hypothyroidism, Mental retardation, Intellectual disability microcephaly-midline stereotypic hand movements syndrome, Learning disorders, Macrocephaly, Macrotia, Malocclusion, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Microcornea, Microduplication xp11.22p11.23 syndrome, Micrognathism, Myopia, Neurodevelopmental disorders, Non-syndromic intellectual disability, x-linked, Obesity, Otitis media, Precocious puberty, Retinal detachment, Scoliosis, Seizure, Sleep disorders, Smith-magenis syndrome, Social communication disorder, Speech disorders, Stereotyped behavior, Stereotypy, Strabismus, Syndactyly of the toes, Synophrys, Taurodontism, Xp11.23-p11.22 duplication syndromeView all (38 more) |
|
3427
|
|
|
Cyclin dependent kinase 19 |
CDC2L6, CDK11, DEE87, EIEE87, bA346C16.3 |
|
|
3428
|
|
|
Sterile alpha and TIR motif containing 1 |
HsTIR, MyD88-5, SAMD2, SARM, hSARM1 |
|
|
3429
|
|
|
Aldo-keto reductase family 1 member B |
ADR, ALDR1, ALR2, AR |
|
|
3430
|
|
|
MCF.2 cell line derived transforming sequence-like 2 |
ARHGEF22 |
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