|
441
|
|
|
Ts translation elongation factor, mitochondrial |
EFTS, EFTSMT |
Cardiomyopathy, Combined oxidative phosphorylation deficiency, Concentric hypertrophic cardiomyopathy, Developmental delay, Epileptic encephalopathy, Fatal mitochondrial disease, Impaired cognition, Multiple sclerosis, Hypotonia, Optic atrophy, Patent ductus arteriosus, Patent foramen ovale, Respiratory failure |
|
442
|
|
|
Peptidylprolyl isomerase F |
CYP3, CyP-M, Cyp-D, CypD |
|
|
443
|
|
|
OVCH1 antisense RNA 1 |
- |
|
|
444
|
|
|
FOXP4 antisense RNA 1 |
- |
|
|
445
|
|
|
NUTM2B antisense RNA 1 |
OPML1 |
|
|
446
|
|
|
Tripartite motif containing 10 |
HERF1, RFB30, RNF9 |
|
|
447
|
|
|
- |
FNZ127, MKRN3-AS, MKRN3AS, NCRNA00009, ZNF127-AS, ZNF127AS |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (7 more) |
|
448
|
|
|
Actin related protein 2/3 complex subunit 2 |
ARC34, PNAS-139, PRO2446, p34-Arc |
|
|
449
|
|
|
Serum/glucocorticoid regulated kinase 2 |
H-SGK2, dJ138B7.2 |
|
|
450
|
|
|
HELLP associated long non-coding RNA |
LINC-HELLP, lncHELLP |
|
