|
381
|
|
|
Dysbindin domain containing 1 |
- |
|
|
382
|
|
|
DET1 and DDB1 associated 1 |
C19orf58, PCIA1 |
|
|
383
|
|
|
DEAD-box helicase 54 |
DP97 |
|
|
384
|
|
|
DEK proto-oncogene |
D6S231E |
|
|
385
|
|
|
DExH-box helicase 58 |
D11LGP2, D11lgp2e, LGP2, RLR-3 |
|
|
386
|
|
|
Derlin 1 |
DER-1, DER1, derlin-1 |
|
|
387
|
|
|
DExD-box helicase 39B |
BAT1, D6S81E, UAP56 |
|
|
388
|
|
|
Dynein cytoplasmic 2 heavy chain 1 |
ATD3, DHC1b, DHC2, DNCH2, DYH1B, SRPS2B, SRTD3, hdhc11 |
Agenesis of corpus callosum, Ambiguous genitalia, Asphyxiating thoracic dystrophy, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Cataract, Cerebellar hypoplasia, Ciliopathies, Congenital duplication of uterus, Congenital epicanthus, Congenital hepatic fibrosis, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Diastrophic dysplasia, Dwarfism, Ectopic anus, Esophageal atresia, Foot polydactyly, Frontal bossing, Hydronephrosis, Hydrops fetalis, Imperforate anus, Jeune syndrome, Jeune thoracic dystrophy, Keratosis follicularis, Kidney disease, Macrocephaly, Majewski syndrome, Marfan syndrome, Micrognathism, Micromelia, Nephronophthisis, Osteochondrodysplasia, Polycystic kidney disease, Polydactyly, Renal cyst, Renal dysplasia, Renal hypoplasia, Renal insufficiency, Scoliosis, Short rib-polydactyly syndrome, Skeletal dysplasia, Syndactyly of the toes, Thoracic hypoplasia, Postaxial hand polydactylyView all (35 more) |
|
389
|
|
|
DEAH-box helicase 40 |
ARG147, DDX40, PAD |
|
|
390
|
|
|
Divergent protein kinase domain 2B |
4930578C19Rik, CXorf36, DIA1R, EPQL1862, PRO3743, bA435K1.1 |
|
