|
51
|
|
|
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) |
|
52
|
|
|
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 |
|
53
|
|
|
Sigma non-opioid intracellular receptor 1 |
ALS16, DSMA2, HMNR2, OPRS1, SIG-1R, SR-BP, SR-BP1, SRBP, hSigmaR1, sigma1R |
Amnesia, Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Clonic seizures, Distal amyotrophy, Distal hereditary motor neuronopathy, Dysarthria, Frontotemporal dementia, Hypotonic seizures, Jacksonian seizure, Learning disorders, Memory disorders, Age-related memory disorders, Mood disorder, Schizophrenia, Seizure, Sensory neuropathy, Spinal muscular atrophyView all (3 more) |
|
54
|
|
|
Striated muscle enriched protein kinase |
APEG-1, APEG1, BPEG, CNM5, MYLK6, SPEGalpha, SPEGbeta |
Amyotrophy, Cardiomyopathy, Centronuclear myopathy, Congenital clubfoot, Dysarthria, Facial paralysis, Gastric cancer, High palate, Hip contracture, Left ventricular hypertrophy, Mental retardation, Micrognathism, Microstomia, Motor delay, Myopathy, Ovarian adenocarcinomaView all (1 more) |
|
55
|
|
|
Splicing factor 3a subunit 1 |
PRP21, PRPF21, SAP114, SF3A120 |
|
|
56
|
|
|
Small nuclear RNA activating complex polypeptide 5 |
SNAP19 |
|
|
57
|
|
|
Small nucleolar RNA host gene 22 |
SCARNA17, SCARNA17HG |
|
|
58
|
|
|
Signal regulatory protein beta 1 |
CD172b, SIRB1, SIRP-BETA-1 |
|
|
59
|
|
|
Semaphorin 3A |
COLL1, HH16, Hsema-I, Hsema-III, SEMA1, SEMAD, SEMAIII, SEMAL, SemD, coll-1 |
Azoospermia, Breast cancer, Brugada syndrome, Breast hypoplasia, Cryptorchidism, Dysarthria, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Nystagmus, Obesity, Osteochondrodysplasia, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Schizophrenia, Skeletal dysplasiaView all (10 more) |
|
60
|
|
|
Scm polycomb group protein like 2 |
- |
|
