|
361
|
|
|
Glycosyltransferase 6 domain containing 1 |
GLTDC1, GT6M7 |
|
|
362
|
|
|
Glutathione S-transferase kappa 1 |
GST, GST 13-13, GST13, GST13-13, GSTK1-1, hGSTK1 |
|
|
363
|
|
|
Polypeptide N-acetylgalactosaminyltransferase 18 |
GALNACT18, GALNT15, GALNTL4, GalNAc-T15, GalNAc-T18 |
|
|
364
|
|
|
GUSB pseudogene 2 |
GUSBL1, GUSBP4, SMA3-L, SMAC3L, SMAC3L2, b55C20.1, bA239L20.1, bA239L20.5, bGLU-Lp |
|
|
365
|
|
|
G protein-coupled receptor 153 |
PGR1 |
|
|
366
|
|
|
Glutaredoxin and cysteine rich domain containing 1 |
DFNB25, PPP1R88 |
|
|
367
|
|
|
GDNF family receptor alpha like |
C6orf144, GRAL, UNQ9356, bA360D14.1 |
|
|
368
|
|
|
Growth differentiation factor 6 |
BMP-13, BMP13, CDMP2, KFM, KFS, KFS1, KFSL, SGM1, SYNS4 |
Cataract, Microphthalmia with coloboma, Congenital cerebral hernia, Congenital ocular coloboma, Congenital torticollis, Developmental delay, Ectopic anus, Hemiplegia/hemiparesis, Hypoplasia of optic disc, Impaired cognition, Imperforate anus, Isolated klippel-feil syndrome, Keratoconus, Klippel feil syndrome, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Microphthalmia, Microphthalmos, Microtia, Multiple synostoses syndrome, Neck webbing, Nystagmus, Otosclerosis, Sacral agenesis, Scoliosis, Spina bifida, Sprengel deformity, Talipes transversoplanus, Tarsal coalition, Ventricular septal defectView all (16 more) |
|
369
|
|
|
Grid2 interacting protein |
DELPHILIN |
|
|
370
|
|
|
GATA3 antisense RNA 1 |
- |
|
