|
1121
|
|
|
SH2 domain containing 2A |
F2771, SCAP, TSAD, VRAP |
|
|
1122
|
|
|
Sperm tail PG-rich repeat containing 1 |
C1orf201, MAPO2 |
|
|
1123
|
|
|
Solute carrier family 7 member 7 |
LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1 |
Alveolar proteinosis, Amyloid nephropathy, Anemia, Breast cancer, Cirrhosis, Complement component deficiency, Congenital heart defects, Cutis laxa, Disorder of amino acid metabolism, Dwarfism, Fibrinogen deficiency, Hepatic amyloidosis, Histiocytosis haematophagic, Hypercholesterolemia, Hyperprolinemia, Hypofibrinogenemia, Impaired cognition, Inherited errors of amino acid metabolism, Isolated somatotropin deficiency, Kidney disease, Leukopenia, Liver failure, Lysinuric protein intolerance, Malnutrition, Membranous glomerulonephritis, Mental retardation, Nephritis, Oral aversion, Osteopenia, Osteoporosis, Pancreatitis, Renal fibrosis, Somatotropin deficiencyView all (18 more) |
|
1124
|
|
|
Solute carrier family 7 member 6 |
LAT-2, LAT3, y+LAT-2 |
|
|
1125
|
|
|
StAR related lipid transfer domain containing 13 |
ARHGAP37, DLC2, GT650, LINC00464 |
|
|
1126
|
|
|
SPOC domain containing 1 |
PPP1R146 |
|
|
1127
|
|
|
Solute carrier family 25 member 46 |
HMSN6B, PCH1E |
Charcot-marie-tooth disease, Developmental delay, Dysautonomia, Exotropia, Hereditary motor and sensory neuropathy, Hereditary motor and sensory neuropathy with optic atrophy, Neuropathy, Nystagmus, Optic atrophy, Roussy-levy syndrome, Scoliosis |
|
1128
|
|
|
Scavenger receptor class F member 2 |
NSR1, SREC-II, SREC2, SRECRP-1, VDEGS |
Arachnodactyly, Blepharophimosis, Breast cancer, Congenital clubfoot, Dislocated radial head, Congenital pectus excavatum, Craniosynostosis, Elbow flexion contracture, High palate, Hypoplasia of the maxilla, Laryngomalacia, Marden walker like syndrome, Van den ende-gupta syndrome |
|
1129
|
|
|
Solute carrier family 16 member 6 |
MCT6, MCT7 |
|
|
1130
|
|
|
Solute carrier family 16 member 3 |
MCT 3, MCT 4, MCT-3, MCT-4, MCT3, MCT4 |
|
