|
421
|
|
|
Golgi associated PDZ and coiled-coil motif containing |
CAL, FIG, GOPC1, PIST, dJ94G16.2 |
|
|
422
|
|
|
Gap junction protein gamma 2 |
CX46.6, Cx47, GJA12, HLD2, LMPH1C, LMPHM3, PMLDAR, SPG44 |
Cerebellar ataxia, Cerebral atrophy, Choreoathetosis, Congenital epicanthus, Developmental delay, Dysarthria, Dysmorphic features, Erysipelas, Facial paralysis, Hearing loss, Hemangiosarcoma, Hyperkeratosis, Hypoplasia of corpus callosum, Impaired cognition, Leukodystrophy, Leukoencephalopathy, Lymphatic malformation, Milroy disease, Motor delay, Movement disorders, Myopia, Optic atrophy, Pelizaeus-merzbacher disease, Pendular nystagmus, Rotary nystagmus, Scoliosis, Skin neoplasms, Ataxia, spastic with optic atrophy and mental retardation, Spastic paraplegia, Specific learning disorder, Strabismus, Testicular hydrocele, Vulval varicesView all (18 more) |
|
423
|
|
|
Gap junction protein delta 2 |
CX36, GJA9 |
|
|
424
|
|
|
Polypeptide N-acetylgalactosaminyltransferase 16 |
GALNACT16, GALNTL1, GalNAc-T16 |
|
|
425
|
|
|
GATA zinc finger domain containing 2B |
GANDS, MRD18, P66beta, p68 |
Apraxia, Autism, Blepharophimosis, Bowel incontinence, Congenital epicanthus, Developmental delay, Dyssomnia, Esotropia, Exotropia, Frontal bossing, Tourette syndrome, High palate, Hyperopia, Hyperopic astigmatism, Hypoplasia of the optic nerve, Hypospadias, Mental retardation, Intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome, Language disorders, Macrostomia, Micrognathism, Microstomia, Movement disorders, Hypoglycemia, Hypotonia, Sleep disorders, Strabismus, Vitamin d deficiencyView all (13 more) |
|
426
|
|
|
GRAM domain containing 1B |
LINC01059 |
B-cell neoplasm, Bipolar disorder, Breast carcinoma, Development disorder, Erectile dysfunction, Hodgkin disease, Lymphocytic leukemia, Lymphoma, Multiple myeloma, Nasopharyngeal carcinoma, Schizophrenia |
|
427
|
|
|
G protein-coupled receptor 158 |
mGlyR |
|
|
428
|
|
|
Glycerol-3-phosphate acyltransferase, mitochondrial |
GPAT, GPAT1 |
|
|
429
|
|
|
Glucosylceramidase beta 2 |
AD035, NLGase, SPG46 |
Asthenozoospermia, Atrophy of corpus callosum, Cataract, Cerebellar ataxia, Cerebellar ataxia with spasticity, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Dementia, Distal amyotrophy, Dysarthria, Dysphagia, Hearing loss, Hypoplasia of corpus callosum, Mental retardation, Nystagmus, Peripheral axonal neuropathy, Scoliosis, Sensorimotor neuropathy, Spastic paraplegiaView all (5 more) |
|
430
|
|
|
Glucosylceramidase beta 3 (gene/pseudogene) |
CBG, CBGL1, GLUC, KLRP |
|
