|
61
|
|
|
Dishevelled binding antagonist of beta catenin 3 |
DAPPER3, RRR1 |
|
|
62
|
|
|
Dpy-19 like C-mannosyltransferase 3 |
- |
|
|
63
|
|
|
Deltex E3 ubiquitin ligase 3L |
BBAP, RNF143 |
|
|
64
|
|
|
DAB2 interacting protein |
AF9Q34, AIP-1, AIP1, DIP1/2 |
|
|
65
|
|
|
Deuterosome assembly protein 1 |
CCDC67 |
|
|
66
|
|
|
DAB adaptor protein 1 |
SCA37 |
Autism, Cerebellar atrophy, Coronary artery disease, Dysarthria, Hearing loss, Horizontal nystagmus, Ischemic stroke, Kawasaki disease, Leukemia, Lung carcinoma, Spinocerebellar ataxia |
|
67
|
|
|
DAB adaptor protein 2 |
DOC-2, DOC2 |
|
|
68
|
|
|
Dachshund family transcription factor 1 |
DACH |
|
|
69
|
|
|
Dystroglycan 1 |
156DAG, A3a, AGRNR, DAG, LGMDR16, MDDGA9, MDDGC7, MDDGC9 |
Absence of septum pellucidum, Agenesis of corpus callosum, Agyria, Alpha-dystroglycanopathy, Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Cataract, Celiac disease, Cerebellar hypoplasia, Common variable immunodeficiency, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital muscular dystrophy, Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, Crohn disease, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Diabetes mellitus, Fukuyama type congenital muscular dystrophy, Glaucoma, Glaucoma, congenital, Hydrocephalus, Hypoplasia of corpus callosum, Mental retardation, Leukodystrophy, Limb-girdle muscular dystrophy, Limb-girdle muscular dystrophy-dystroglycanopathy, Lupus erythematosus, Macrocephaly, Mental depression, Microcephaly, Microcornea, Microphthalmos, Mood disorder, Motor delay, Muscle eye brain disease, Muscle-eye-brain disease with bilateral multicystic leucodystrophy, Muscular dystrophy, Muscular dystrophy-dystroglycanopathy, Myopia, Optic atrophy, Pachygyria, Polymicrogyria, Posteriorly rotated ear, Prostatic neoplasms, Prostate cancer, Psoriasis, Respiratory failure, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Specific learning disorder, Submucosal cleft palate, Syndromic microphthalmia, Ulcerative colitis, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (45 more) |
|
70
|
|
|
DENN domain containing 5B |
- |
|
