571
|
|
|
Dynactin associated protein |
C18orf26 |
|
572
|
|
|
Dynein cytoplasmic 1 heavy chain 1 |
CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22 |
Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Autism, Cerebellar ataxia, Charcot-marie-tooth disease, Childhood-onset spinal muscular atrophy, Distal hereditary motor neuropathy, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Congenital pes cavus, Cortical dysplasia with other brain malformations, Dejerine-sottas disease, Distal spinal muscular atrophy, Spinal muscular atrophy, Global developmental delay, Gross motor development delay, Hereditary motor and sensory neuropathies, Motor neuron disease, Hypertrophic neuropathy, Intellectual developmental disorder, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Myopathy, Neurodevelopmental disorder, Pena-shokeir syndrome , Peripheral neuropathy, Peroneal muscle atrophy, Polymicrogyria, Polyneuropathy, Rhizomelic chondrodysplasia punctata, Roussy-levy syndrome, Saldino-noonan syndrome, Seizures, Papillary thyroid cancer, Tonic-clonic epilepsyView all (23 more) |
573
|
|
|
Dynein cytoplasmic 1 intermediate chain 1 |
DNCI1, DNCIC1 |
|
574
|
|
|
Dynein cytoplasmic 1 intermediate chain 2 |
DIC74, DNCI2, IC2, NEDMIBA |
|
575
|
|
|
Dynein cytoplasmic 2 heavy chain 1 |
ATD3, DHC1b, DHC2, DNCH2, DYH1B, SRPS2B, SRTD3, hdhc11 |
Jeune syndrome, Asthma, Polycystic kidney disease, Retinitis pigmentosa, Bowed long bones, Breast neoplasms, Ciliopathy, Clinodactyly, Congenital heart defects, Desbuquois syndrome, Gout, Hypertension, Intellectual developmental disorder, Jeune thoracic dystrophy, Majewski syndrome, Metabolic syndrome, Micrognathism, Oligodendroglioma, Optic atrophy, Saldino-noonan syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia, Skeletal dysplasia, Small cell lung carcinoma, Diabetes mellitus type 2View all (10 more) |
576
|
|
|
Dynein 2 intermediate chain 1 |
CFAP163, DIC6, FAP163, SRPS6, SRTD8, WDR60 |
|
577
|
|
|
Dynein 2 intermediate chain 2 |
CFAP133, DIC5, FAP133, SRTD11, WDR34, bA216B9.3 |
|
578
|
|
|
Dynein cytoplasmic 2 light intermediate chain 1 |
CGI-60, D2LIC, LIC3 |
Jeune syndrome, Cholecystolithiasis, Kidney disease, Desbuquois syndrome, Ellis-van creveld syndrome, Jeune thoracic dystrophy, Kidney failure, Majewski syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia, Sitosterolemia, Thrombocytopenia |
579
|
|
|
Dynein light chain LC8-type 1 |
DLC1, DLC8, DNCL1, DNCLC1, LC8, LC8a, PIN, hdlc1 |
|
580
|
|
|
Dynein light chain roadblock-type 1 |
BITH, BLP, DNCL2A, DNLC2A, ROBLD1 |
|
