Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5211 to 5220 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5211
Galactosidase alpha
GALA
Angiokeratoma, Cardiomyopathy, Fabry disease, Hypertrophic cardiomyopathy, Intellectual developmental disorder, x-linked, Nephrotic syndrome

5212
Galactosidase beta 1
EBP, ELNR1, MPS4B
Asthma, Eczema, Bone disease, Celiac disease, Obstructive pulmonary disease, Congenital cartilage disorder, Contact dermatitis, Corneal opacity, Atopic dermatitis, Desbuquois syndrome, Gm1 gangliosidosis, Hepatocellular carcinoma, Mucopolysaccharidosis, Multiple sclerosis, Osteochondrodysplasias
View all (7 more)

5213
Galactosidase beta 1 like 2
MST114, MSTP114
Schizophrenia

5214
Galactosidase beta 1 like 3
-
Alzheimer disease, Obesity

5215
Glucocorticoid induced 1
FAM117C, GCTR, GIG18, TSSN1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Rotator cuff tear, Schizophrenia, Uterine fibroid

5216
Glucuronic acid epimerase
HSEPI
Cerebrovascular disorder, Hypertension

5217
Glycine decarboxylase
GCE, GCE1, GCSP, HYGN1
Asthma, Astrocytoma, Glycine encephalopathy, Generalized epilepsy, Global developmental delay, Hyperglycemia, Neurodevelopmental disorder, Obesity, Osteosarcoma, Retinitis pigmentosa

5218
Gliomedin
CLOM, COLM, CRG-L2, CRGL2, LCCS11, UNC-112, UNC-122
Arthrogryposis multiplex congenita, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital joint contractures, Contracture of multiple joints, Fetal akinesia deformation sequence, Lethal congenital contracture syndrome, Pena-shokeir syndrome , Pericarditis, Primary aldosteronism
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5219
GLE1 RNA export mediator
CAAHC, CAAHD, GLE1L, LCCS, LCCS1, hGLE1
Amyotrophic lateral sclerosis, Arthrogryposis with anterior horn cell disease, Congenital arthrogryposis with anterior horn cell disease, Hypertension, Lethal congenital contracture syndrome, Oligodendroglioma

5220
Golgi glycoprotein 1
CFR-1, ESL-1, MG-160, MG160
Amyotrophic lateral sclerosis, Celiac disease, Color vision deficiency, Schizophrenia