|
301
|
|
|
Integrator complex subunit 2 |
INT2, KIAA1287 |
|
|
302
|
|
|
Intraflagellar transport 80 |
ATD2, CFAP167, FAP167, SRTD2, WDR56 |
Agenesis of corpus callosum, Ambiguous genitalia, Asphyxiating thoracic dystrophy, Bone disease, Brachydactyly, Cataract, Cerebellar hypoplasia, Ciliopathies, Congenital duplication of uterus, Congenital epicanthus, Congenital hepatic fibrosis, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Cryptorchidism, Cystic kidney disease, Dandy-walker syndrome, Dwarfism, Ectopic anus, Esophageal atresia, Foot polydactyly, Frontal bossing, Hydronephrosis, Hydrops fetalis, Imperforate anus, Jeune syndrome, Jeune thoracic dystrophy, Kidney disease, Macrocephaly, Majewski syndrome, Mesomelia, Micrognathism, Micromelia, Nephronophthisis, Oral ulcer, Osteochondrodysplasia, Polydactyly, Renal cyst, Renal hypoplasia, Renal insufficiency, Respiratory failure, Rhizomelia, Short rib-polydactyly syndrome, Skeletal dysplasia, Spade-like hand, Syndactyly of the toes, Thoracic diseases, Postaxial hand polydactylyView all (33 more) |
|
303
|
|
|
INTS3 and NABP interacting protein |
C9orf80, HSPC043, MISE, SOSSC, SSBIP1, hSSBIP1 |
|
|
304
|
|
|
Interleukin 21 |
CVID11, IL-21, Za11 |
|
|
305
|
|
|
Interferon induced with helicase C domain 1 |
AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5, RLR-2, SGMRT1 |
Acquired porencephaly, Acrosteolysis, Aicardi goutieres syndrome, Anemia, Ankylosing spondylitis, Aortic aneurysm, Aortic valve calcification, Aortic valve sclerosis, Arrhinencephaly, Arthritis, Autoinflammatory disease, Brain atrophy, Cerebral atrophy, Chilblain lesions, Cholangitis, Congenital clubfoot, Congestive heart failure, Crohn disease, Cutis marmorata, Degeneration of the striatum, Demyelinating neuropathy, Dermatitis, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Enchondroma, Glaucoma, Glaucoma, congenital, Graves disease, Hemiplegia/hemiparesis, Hypertension, Hypertrophic cardiomyopathy, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Hypothyroidism, Congenital hypothyroidism, nongoitrous, Immunoglobulin a deficiency, Inflammatory bowel disease, Lenticulostriate vasculopathy, Lymphocytic leukemia, Leukodystrophy, Lipoatrophy, Lipodystrophy, Lupus erythematosus, Mental retardation, Microcephaly, Multiple sclerosis, Myopia, Myositis, Alloimmune thrombocytopenia, Hypotonia, Nonbacterial verrucal endocardiosis, Nystagmus, Onycholysis, Osteoporosis, Palmoplantar pustules, Panniculitis, Penis agenesis, Petechiae, Plagiocephaly, Porencephalic cyst, Pseudo-torch syndrome, Psoriasis, Ptosis, Pulmonary arterial hypertension, Raynaud phenomenon, Scoliosis, Selective immunoglobulin a deficiency, Singleton merten syndrome, Spastic quadriplegia, Spastic tetraparesis, Strabismus, Subaortic stenosis, Ulcerative colitis, Vasculitis, VitiligoView all (62 more) |
|
306
|
|
|
Interferon regulatory factor 2 binding protein like |
C14orf4, EAP1, NEDAMSS |
Abducens palsy, Atrial fibrillation, Atrophy of corpus callosum, Bowel incontinence, Cerebellar ataxia, Cerebellar atrophy, Cerebral atrophy, Cerebral palsy, Choreoathetosis, Congenital dermal melanocytosis, Dementia, Developmental delay, Developmental regression, Dysarthria, Dysmorphic features, Dysphagia, Elbow flexion contracture, Esotropia, Exotropia, Flexion contracture of wrist, Gastroparesis, Hypertrichosis, Impaired cognition, Infantile spasms, Mental retardation, Micrognathism, Multiple congenital anomalies, Myopathy, Myopia, Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures, Nystagmus, Paroxysmal atrial fibrillation, Quadriplegia, Spastic quadriplegia, TrismusView all (20 more) |
|
307
|
|
|
IKAROS family zinc finger 4 |
EOS, ZNFN1A4 |
|
|
308
|
|
|
IKAROS family zinc finger 5 |
PEGASUS, THC7, ZNFN1A5 |
|
|
309
|
|
|
Inverted formin 2 |
C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 |
Charcot-marie-tooth disease, Distal lower limb amyotrophy, Distal upper limb amyotrophy, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulosclerosis, Hypertension, Hypertensive nephropathy, Kidney failure, Nephritis, Nephrotic syndrome, Renal glomerular disease, Renal insufficiency |
|
310
|
|
|
Intersectin 1 |
ITSN, SH3D1A, SH3P17 |
|
