|
741
|
|
|
ASB15 antisense RNA 1 |
- |
|
|
742
|
|
|
Long intergenic non-protein coding RNA 1414 |
- |
|
|
743
|
|
|
Long intergenic non-protein coding RNA 1645 |
- |
|
|
744
|
|
|
Long intergenic non-protein coding RNA 1905 |
- |
|
|
745
|
|
|
Long intergenic non-protein coding RNA 2040 |
- |
|
|
746
|
|
|
Long intergenic non-protein coding RNA 1594 |
TCONS_l2_00015893 |
|
|
747
|
|
|
Long intergenic non-protein coding RNA 2822 |
- |
|
|
748
|
|
|
NOVA1 divergent transcript |
C14orf22, LINC02588, NOVA1-AS1 |
|
|
749
|
|
|
STIP1 homology and U-box containing protein 1 |
CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1 |
Alopecia, Anxiety disorder, Apraxia, Arachnodactyly, Spinocerebellar ataxia, Atrophy of corpus callosum, Cerebellar ataxia, Cerebellar atrophy, Cerebellar hypoplasia, Delayed menarche, Developmental delay, Diabetes mellitus, Distal amyotrophy, Dysarthria, Dysphagia, Glaucoma, Horizontal nystagmus, Hypogonadism, Hypothyroidism, Iridocyclitis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Pancreatitis, Physiologic amenorrheaView all (10 more) |
|
750
|
|
|
STAG1 cohesin complex component |
MRD47, SA1, SCC3A |
Coronary artery disease, Cryptorchidism, Development disorder, Developmental delay, Dysmorphic features, Gastroesophageal reflux disease, Mental retardation, Intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome, Macrostomia, Multiple congenital anomalies, Rheumatoid arthritis, Schizophrenia |
