|
1141
|
|
|
Solute carrier family 16 member 7 |
MCT2 |
|
|
1142
|
|
|
Solute carrier family 33 member 1 |
ACATN, AT-1, AT1, CCHLND, HPBDS, SPG42 |
Cataract, Cerebellar atrophy, Cerebral atrophy, Colorectal cancer, Congenital cataract-hearing loss-developmental delay syndrome, Congenital cataracts, hearing loss, and neurodegeneration, Development disorder, Developmental delay, Epilepsy, Nystagmus, Spastic paraplegia |
|
1143
|
|
|
Solute carrier family 25 member 51 |
CG7943, MCART1 |
|
|
1144
|
|
|
Sorting nexin 29 |
A-388D4.1, RUNDC2A |
|
|
1145
|
|
|
Secretoglobin family 3A member 1 |
HIN-1, HIN1, LU105, PnSP-2, UGRP2 |
|
|
1146
|
|
|
STE20 related adaptor alpha |
LYK5, NY-BR-96, PMSE, STRAD, STRAD alpha, Stlk |
Alzheimer disease, Developmental delay, Epilepsy, Macrocephaly, Macrostomia, Medulloblastoma, Medullomyoblastoma, Mental retardation, Polyhydramnios, megalencephaly, and symptomatic epilepsy, Strabismus |
|
1147
|
|
|
SplA/ryanodine receptor domain and SOCS box containing 4 |
SSB-4, SSB4 |
|
|
1148
|
|
|
Sperm antigen with calponin homology and coiled-coil domains 1 |
CYTSB, HCMOGT-1, HCMOGT1, NSP, NSP5 |
|
|
1149
|
|
|
SH3KBP1 binding protein 1 |
PP203, Sb1 |
|
|
1150
|
|
|
Sphingosine-1-phosphate receptor 2 |
AGR16, DFNB68, EDG-5, EDG5, Gpcr13, H218, LPB2, S1P2 |
|
