|
121
|
|
|
Sodium voltage-gated channel alpha subunit 11 |
FEPS3, HSAN7, NAV1.9, NaN, PN5, SCN12A, SNS-2 |
Congenital pain insensitivity, Dysautonomia, Episodic pain syndrome, Erythermalgia, Erythromelalgia, Hereditary motor and sensory neuropathy, Hereditary sensory and autonomic neuropathy, Leukemia, Motor delay, Nervous system diseases, Paroxysmal extreme pain disorder, Sodium channelopathy-related small fiber neuropathy, Vasculitis |
|
122
|
|
|
SAGA complex associated factor 29 |
CCDC101, STAF36, TDRD29 |
|
|
123
|
|
|
Solute carrier organic anion transporter family member 2B1 |
OATP-B, OATP2B1, OATPB, SLC21A9 |
|
|
124
|
|
|
Secretory carrier membrane protein 4 |
SCAMP-4 |
|
|
125
|
|
|
Solute carrier family 46 member 1 |
G21, HCP1, HsPCFT, PCFT, hPCFT |
Anemia, Anorexia, Cheilitis, Congenital defect of folate absorption, Developmental delay, Dyskinetic syndrome, Eosinophilia, Gastroesophageal reflux disease, Glossitis, Hereditary folate malabsorption, Hyperhomocysteinemia, Immunologic deficiency syndromes, Leukopenia, Malabsorption syndrome, Mental retardation, Nervous system diseases, Neutropenia, Oral ulcer, PancytopeniaView all (4 more) |
|
126
|
|
|
Solute carrier family 52 member 3 |
BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2 |
Brown-vialetto-van laere syndrome, Bulbar palsy, Cerebral cortical atrophy, Diabetes insipidus, Dysarthria, Dysautonomia, Dysmorphic features, Dysphagia, Esophagus neoplasm, External ophthalmoplegia, Facial paralysis, Gynecomastia, Hallucinations, Hearing loss, Hypertension, Hypogonadism, Mental retardation, Nervous system diseases, Progressive bulbar palsy, Prostate cancer, Ptosis, Riboflavin transporter deficiency, Scoliosis, Sensorineural hearing loss, Sleep apnea, Vocal cord paralysisView all (11 more) |
|
127
|
|
|
Serine/threonine kinase 38 |
NDR, NDR1 |
|
|
128
|
|
|
Small integral membrane protein 12 |
C1orf212 |
|
|
129
|
|
|
Synaptopodin |
SYNPO1 |
|
|
130
|
|
|
Small integral membrane protein 40 |
- |
|
