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3151
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Jumonji domain containing 1C |
KDM3C, TRIP-8, TRIP8 |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion syndrome, Acne, Acrocephaly, Adenocarcinoma, Anxiety disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bowel incontinence, Breast carcinoma, Cataract, Central nervous system germinoma, Choanal atresia, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Conotruncal anomaly face syndrome, Corneal neovascularization, Cryptorchidism, Developmental delay, Digeorge syndrome, Dwarfism, Dysphasia, Gastroesophageal reflux disease, Germinoma of the central nervous system, Glaucoma, Hearing loss, Hirschsprung disease, Hydrocephalus, Hyperthyroidism, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic deficiency syndromes, Imperforate anus, Juvenile arthritis, Laryngomalacia, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Myelomeningocele, Obesity, Optic atrophy, Otitis media, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Polycystic kidney disease, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Shprintzen syndrome, Specific learning disorder, Still disease, Strabismus, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (69 more) |
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3152
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Family with sequence similarity 171 member A1 |
APCN, C10orf38 |
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3153
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Solute carrier family 39 member 12 |
LZT-Hs8, ZIP-12, ZIP12, bA570F3.1 |
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3154
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NOP2/Sun RNA methyltransferase 6 |
4933414E04Rik, ARL5B-AS1, MRT82, NOPD1 |
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3155
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ARF like GTPase 5B |
ARL8 |
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3156
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|
|
Spindle and kinetochore associated complex subunit 3 |
C13orf3, RAMA1 |
|
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3157
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Spermatogenesis associated 13 |
ARHGEF29, ASEF2 |
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3158
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Serine protease 54 |
CT67, KLKBL4 |
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3159
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Fc gamma receptor IIa |
CD32, CD32A, CDw32, FCG2, FCGR2, FCGR2A1, FcGR, FcgammaRIIa, IGFR2 |
Anemia, Ankylosing spondylitis, Arthritis, Asthma, Biliary cirrhosis, Bronchiectasis, Cor pulmonale, Crohn disease, Cystic fibrosis, Cystic fibrosis of pancreas, Exocrine pancreatic insufficiency, Inflammatory bowel disease, Kawasaki disease, Leukopenia, Lung diseases, Lupus erythematosus, Meconium ileus, Nephritis, Nonbacterial verrucal endocardiosis, Pericarditis, Pleuritis, Psychosis, Pulmonary cystic fibrosis, Rectal prolapse, Rheumatoid arthritis, Sjogren`s syndrome, Ulcerative colitisView all (12 more) |
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3160
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Long intergenic non-protein coding RNA 305 |
C18orf20, HsT1235, NCRNA00305 |
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