|
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 |
Asthma, Cardiomyopathy, Central nervous system cancer, Dental caries, Gallstones, Glioblastoma, Glioma, Major depressive disorder, Kawasaki disease, Small vessel stroke, Stroke, Diabetes mellitus, type 2 |
|
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 |
Isolated sensorineural deafness, Nonsyndromic hearing loss, Basal cell carcinoma, Central nervous system cancer, Color vision deficiency, Deafness, Glioblastoma, Glioma, Hearing impairment, Hearing loss, Obesity, Oligodendroglioma, Schizophrenia, Scoliosis, Squamous cell carcinoma |
|
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 |
Congenital anomalies of the kidney and urinary tract, Colobomatous microphthalmia, Desbuquois syndrome, Diverticular disease, Klippel-feil syndrome, Leber congenital amaurosis, Microphthalmia, Microphthalmos, Multiple synostoses syndrome, Parkinson disease, Retinitis pigmentosa, Diabetes mellitus, type 2 |
|
369
|
|
|
Grid2 interacting protein |
DELPHILIN |
|
|
370
|
|
|
GATA3 antisense RNA 1 |
- |
|
