971
|
|
|
SLC25A24 pseudogene 1 |
- |
|
972
|
|
|
Surfactant protein A2 |
COLEC5, ILD2, PSAP, PSP-A, PSPA, SFTP1, SFTPA2B, SP-2A, SP-A, SPA2, SPAII |
|
973
|
|
|
Shisa family member 9 |
CKAMP44 |
|
974
|
|
|
SEC14 like lipid binding 6 |
- |
|
975
|
|
|
Small ubiquitin like modifier 1 |
DAP1, GMP1, OFC10, PIC1, SENP2, SMT3, SMT3C, SMT3H3, UBL1 |
|
976
|
|
|
Solute carrier family 35 member A2 |
CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL |
Anisometropia, Brainstem atrophy, Breast cancer, Central visual impairment, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral atrophy, Congenital clubfoot, Congenital disorder of glycosylation, Cortical dysplasia, Craniosynostosis, Dandy-walker syndrome, Developmental delay, Dwarfism, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Esotropia, Exotropia, Gastroesophageal reflux disease, Hearing loss, High palate, Hyperopia, Hypoalbuminemia, Hypoglycemia, Hypopigmentation disorder, Hypoplasia of corpus callosum, Hypoplastic hippocampus, Infantile spasms, Mental retardation, Isolated focal cortical dysplasia, Microcephaly, Monocytosis, Nystagmus, Osteopenia, Precocious puberty, Premature adrenarche, Rod-cone dystrophy, Salaam seizures, Scoliosis, Sleep apnea, Spastic tetraparesis, Strabismus, Tetralogy of fallot, Transient nephrotic syndrome, West syndromeView all (31 more) |
977
|
|
|
Secretoglobin family 1A member 1 |
CC10, CC16, CCPBP, CCSP, UGB, UP-1, UP1 |
|
978
|
|
|
Splicing factor 1 |
BBP, D11S636, MBBP, ZCCHC25, ZFM1, ZNF162 |
|
979
|
|
|
Solute carrier family 30 member 1 |
ZNT1, ZRC1 |
|
980
|
|
|
Solute carrier family 30 member 2 |
PP12488, TNZD, ZNT2, ZnT-2 |
|