|
21
|
|
|
DDB1 and CUL4 associated factor 7 |
AN11, HAN11, SWAN-1, WDR68 |
|
|
22
|
|
|
DENN domain containing 4A |
IRLB, MYCPBP |
|
|
23
|
|
|
Deleted in lymphocytic leukemia 1 |
BCMS, BCMS1, DLB1, DLEU2, LEU1, LEU2, LINC00021, NCRNA00021, XTP6 |
Autoimmune diseases, Benign prostatic hyperplasia, Cardiovascular diseases, Celiac disease, Diabetes mellitus, Diffuse lymphoma, Diabetic maculopathy, Eczema, Hypothyroidism, Lymphocytic leukemia, Multiple sclerosis, Biliary cirrhosis |
|
24
|
|
|
DLC1 Rho GTPase activating protein |
ARHGAP7, HP, STARD12, p122-RhoGAP |
Benign neoplasm, Colorectal cancer, Colorectal neoplasms, Gastric cancer, Hereditary nonpolyposis colorectal cancer, Leiomyosarcoma of uterus, Liver carcinoma, Malignant neoplasm, Meningomyelocele, Myelocele, Neoplasms, Ovarian neoplasm, Ovarian cancer, Renal carcinoma, Schizophrenia, Spina bifida occulta, Stomach neoplasms, Bladder carcinomaView all (3 more) |
|
25
|
|
|
DLX2 divergent transcript |
DLX2-AS1, TCONS_00003049 |
|
|
26
|
|
|
DEAF1 transcription factor |
MRD24, NEDHELS, NUDR, SPN, VSVS, ZMYND5 |
Anxiety disorder, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Developmental dysplasia of the hip, Developmental delay, Developmental regression, Dwarfism, Dyskinesia, seizures, and intellectual developmental disorder, Dyskinetic syndrome, Dysmorphic features, Dyssomnia, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hypercholesterolemia, Hypothyroidism, Mental retardation, Intellectual disability-epilepsy-extrapyramidal syndrome, Low-frequency hearing loss, Macrocephaly, Malocclusion, Mental depression, Microcephaly, Microcornea, Micrognathism, Mood swings, Myopia, Non-syndromic intellectual disability, Obesity, Otitis media, Pica, Precocious puberty, Repetitive compulsive behavior, Retinal detachment, Scoliosis, Sleep disorders, Smith-magenis syndrome, Speech disorders, Status epilepticus, Stereotyped behavior, Strabismus, Syndactyly of the toes, Synophrys, TaurodontismView all (33 more) |
|
27
|
|
|
DR1 associated protein 1 |
NC2-alpha |
|
|
28
|
|
|
Delta like canonical Notch ligand 3 |
SCDO1 |
Abnormal spinal segmentation, Acquired kyphoscoliosis, Anaplastic astrocytoma, Astrocytoma, Chondrodystrophic myotonia, Congenital diaphragmatic hernia, Congenital exomphalos, Rib fusion, Congenital kyphoscoliosis, Congenital meningocele, Cryptorchidism, Dwarfism, Dyschondroplasias, Fibrillary astrocytoma, Gemistocytic astrocytoma, Grade i astrocytoma, Hypospadias, Intracranial astrocytoma, Jarcho-levin syndrome, Leukodystrophy and acquired microcephaly with or without dystonia, Macrocephaly, Melnick-needles syndrome, Mental retardation, Microcephaly, Multiple epiphyseal dysplasia, Oligoastrocytoma, Osteochondrodysplasia, Protoplasmic astrocytoma, Pulmonary venous return anomaly, Schwartz-jampel syndrome, Scoliosis, Spina bifida occulta, Spondylocostal dysostosis, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Syndactyly of fingers, Van buchem diseaseView all (22 more) |
|
29
|
|
|
DIAPH2 antisense RNA 1 |
EPAG |
|
|
30
|
|
|
Damage induced long noncoding RNA |
DINO |
|
