|
421
|
|
|
Doublecortin like kinase 3 |
CLR, DCAMKL3, DCDC3C, DCK3 |
|
|
422
|
|
|
Dispatched RND transporter family member 2 |
C15orf36, DISPB, HsT16908, LINC00594 |
|
|
423
|
|
|
DIX domain containing 1 |
CCD1 |
|
|
424
|
|
|
DnaJ heat shock protein family (Hsp40) member C5 beta |
CSP-beta |
|
|
425
|
|
|
Delta 4-desaturase, sphingolipid 1 |
DEGS, DEGS-1, DES1, Des-1, FADS7, HLD18, MIG15, MLD |
|
|
426
|
|
|
Dynein axonemal heavy chain 17 |
DNAHL1, DNEL2, SPGF39 |
|
|
427
|
|
|
Dachsous cadherin-related 1 |
CDH19, CDH25, CDHR6, FIB1, MMVP2, MVP2, PCDH16, VMLDS1 |
Agenesis of corpus callosum, Blepharophimosis, Cerebrofacioarticular syndrome, Choanal atresia, Clinodactyly, Colorectal cancer, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital heart defects, Short clavicles, Developmental delay, Dwarfism, Dysplastic corpus callosum, Hearing loss, High palate, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Hypospadias, Imperforate anus, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Mitral valve prolapse, Narcolepsy, Neuronal heterotopia, Osteochondrodysplasia, Osteopenia, Pachygyria, Periventricular heterotopia, Periventricular gray matter heterotopia, Periventricular nodular heterotopia, Ptosis, Pulmonary stenosis, Renal hypoplasia, Scoliosis, Skeletal dysplasia, Subcortical band heterotopia, Syndactyly, Syndactyly of fingers, TracheomalaciaView all (28 more) |
|
428
|
|
|
DEAD-box helicase 3 Y-linked |
DBY |
|
|
429
|
|
|
Dynein light chain LC8-type 1 |
DLC1, DLC8, DNCL1, DNCLC1, LC8, LC8a, PIN, hdlc1 |
|
|
430
|
|
|
Diacylglycerol O-acyltransferase 1 |
ARAT, ARGP1, DGAT, DIAR7 |
|
