|
1011
|
|
|
Synaptopodin 2 like |
- |
|
|
1012
|
|
|
Stearoyl-CoA desaturase 5 |
ACOD4, DFNA79, FADS4, HSCD5, SCD2, SCD4 |
|
|
1013
|
|
|
Sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 |
C9orf13, CCP22, POLYDOM, SEL-OB, SELOB |
|
|
1014
|
|
|
STN1 subunit of CST complex |
AAF-44, AAF44, CRMCC2, OBFC1, RPA-32, bA541N10.2 |
Basal cell neoplasm, Bronchiectasis, Carcinoma, Central nervous system neoplasms, Cerebroretinal microangiopathy with calcifications and cysts, Chronic obstructive pulmonary disease, Coats disease, Coronary artery disease, Diffuse interstitial pulmonary fibrosis, Dyskeratosis congenita, Esophageal varix, Gastroesophageal reflux disease, Glioma, Honeycomb lung, Hypertension, Lung neoplasms, Lung cancer, Lung diseases, Malignant melanoma of skin, Melanoma, Osteopenia, Ovarian epithelial carcinoma, Pancytopenia, Portal hypertension, Pulmonary fibrosis, Hamman-rich syndrome, Retinal telangiectasia, Uterine fibroids, Plexiform leiomyomaView all (14 more) |
|
1015
|
|
|
Semaphorin 6D |
- |
|
|
1016
|
|
|
Solute carrier family 66 member 2 |
PQLC1 |
|
|
1017
|
|
|
SplA/ryanodine receptor domain and SOCS box containing 1 |
SSB-1, SSB1 |
|
|
1018
|
|
|
SPG11 vesicle trafficking associated, spatacsin |
ALS5, CMT2X, KIAA1840 |
Agenesis of corpus callosum, Amyotrophic lateral sclerosis, Bipolar disorder, Bowel incontinence, Cerebral cortical atrophy, Charcot-marie-tooth disease, Developmental delay, Distal amyotrophy, Distal peripheral sensory neuropathy, Dysarthria, Dysphagia, Hypoplasia of corpus callosum, Impaired cognition, Leukodystrophy, Age-related macular degeneration, Mental retardation, Nakamura osame syndrome, Nervous system diseases, Nystagmus, Obesity, Peripheral axonal neuropathy, Polyneuropathy, Schizophrenia, Sensory neuropathy, Spastic paraplegia, Specific learning disorderView all (11 more) |
|
1019
|
|
|
Solute carrier family 35 member F5 |
- |
|
|
1020
|
|
|
Signal transducing adaptor molecule |
STAM-1, STAM1 |
|
