|
311
|
|
|
Denticleless E3 ubiquitin protein ligase adapter |
CDT2, DCAF2, L2DTL, RAMP |
|
|
312
|
|
|
Diphthamide biosynthesis 5 |
AD-018, CGI-30, HSPC143, NEDSFF, NPD015 |
|
|
313
|
|
|
Dynein cytoplasmic 2 light intermediate chain 1 |
CGI-60, D2LIC, LIC3 |
Cubitus valgus, Aortic coarctation, Asphyxiating thoracic dystrophy, Atresia of vagina, Atrial septal defect, Brachydactyly, Congenital epicanthus, Short clavicles, Cryptorchidism, Dwarfism, Ellis-van creveld syndrome, Epispadias, Foot polydactyly, Hamartoma, Horseshoe kidney, Hydrometrocolpos, Hypodontia, Hypospadias, Jeune syndrome, Jeune thoracic dystrophy, Kidney disease, Leukemia, Majewski syndrome, Mental retardation, Microdontia, Micromelia, Nail diseases, Nail dysplasia, Narcolepsy, Nephronophthisis, Osteochondrodysplasia, Patent ductus arteriosus, Polydactyly, Polydactyly of toes, Renal insufficiency, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with or without polydactyly, Situs inversus, Skeletal dysplasia, Strabismus, Syndactyly of the toes, Thoracic hypoplasia, Postaxial hand polydactyly, Ventricular septal defectView all (29 more) |
|
314
|
|
|
Dehydrogenase/reductase 7 |
CGI-86, SDR34C1, retDSR4, retSDR4 |
|
|
315
|
|
|
DnaJ heat shock protein family (Hsp40) member B11 |
ABBP-2, ABBP2, DJ9, Dj-9, EDJ, ERdj3, ERj3, ERj3p, PKD6, PRO1080, UNQ537 |
|
|
316
|
|
|
Defective in cullin neddylation 1 domain containing 1 |
DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3 |
|
|
317
|
|
|
Dolichyl-phosphate mannosyltransferase subunit 3, regulatory |
CDG1O, MDDGB15, MDDGC15 |
|
|
318
|
|
|
DnaJ heat shock protein family (Hsp40) member C10 |
ERdj5, JPDI, MTHr, PDIA19 |
|
|
319
|
|
|
DGCR8 microprocessor complex subunit |
C22orf12, DGCRK6, Gy1, pasha |
Behavior disorders, Blepharophimosis, Conotruncal anomaly face syndrome, Digeorge syndrome, Dwarfism, Mental disorders, Mental retardation, Microcephaly, Mood swings, Nephroblastoma, Nonorganic psychosis, Paranoia, Pierre-robin syndrome, Posterior embryotoxon, Psychosis, Pulmonary dysgenesis, Schizophrenia, Shprintzen syndrome, Specific learning disorder, Velopharyngeal insufficiency, Ventricular septal defect, Wilms tumorView all (7 more) |
|
320
|
|
|
DNA damage inducible transcript 4 |
Dig2, REDD-1, REDD1 |
|
