|
2591
|
|
|
Dynein assembly factor with WD repeats 1 |
CILD52, DNAAF18, ODA16, WDR69 |
|
|
2592
|
|
|
LON peptidase N-terminal domain and ring finger 2 |
RNF192 |
|
|
2593
|
|
|
DNA damage inducible transcript 3 |
AltDDIT3, C/EBPzeta, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 |
Arthritis, Asbestosis, Autoimmune diabetes, Breast cancer, Mammary neoplasms, Breast carcinoma, Colorectal cancer, Dermatitis, Diabetes mellitus, Brittle diabetes mellitus, Fatty liver, Glaucoma, Intestinal diseases, Juvenile arthritis, Liposarcoma, Marfan syndrome, Myocardial infarction, Myxoid liposarcoma, Nephrosis, Obesity, Ocular hypertension, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still diseaseView all (9 more) |
|
2594
|
|
|
AE binding protein 1 |
ACLP |
Arthritis, Bursitis, Carpal tunnel syndrome, Classical-like ehlers-danlos syndrome, Congenital exomphalos, Cryptorchidism, High palate, Macrotia, Micrognathism, Mitral valve prolapse, Neck webbing, Osteoporosis |
|
2595
|
|
|
Dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit |
AGER1, CDG1R, GATD6, OKSWcl45, OST, OST48, WBP1 |
Blood coagulation disorders, Congenital disorder of glycosylation, Developmental delay, Dwarfism, Esotropia, Fatty liver, Gastroesophageal reflux disease, Hypothyroidism, Lipodystrophy, Oromotor apraxia, Osteopenia, Speech disorders, Strabismus |
|
2596
|
|
|
TOG array regulator of axonemal microtubules 2 |
FAM179A |
|
|
2597
|
|
|
Family with sequence similarity 171 member B |
KIAA1946 |
|
|
2598
|
|
|
DEAD-box helicase 1 |
DBP-RB, UKVH5d |
|
|
2599
|
|
|
DEAD-box helicase 3 X-linked |
CAP-Rf, DBX, DDX14, DDX3, HLP2, MRX102, MRXSSB |
Aphasia, Arthritis, Attention deficit hyperactivity disorder, Autism, Breast cancer, Renal agenesis, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dysmorphic features, Epilepsy, Esotropia, Glaucoma, Hypoplasia of corpus callosum, Mental retardation, Intellectual disability-hypotonia-movement disorder syndrome, x-linked, Lymphoblastic leukemia, Macrotia, Malignant mesothelioma, Mental retardation, x-linked, Microcephaly, Micrognathism, Movement disorders, Multiple congenital anomalies, Neurodevelopmental disorders, Oral cleft, Osteoarthrosis deformans, Polymicrogyria, Precocious puberty, Scoliosis, Speech disorders, T-cell lymphoma, Toriello-carey syndrome, Vesicoureteral refluxView all (19 more) |
|
2600
|
|
|
DEAD-box helicase 5 |
G17P1, HLR1, HUMP68, p68 |
|
