Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5021 to 5030 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5021
Guanidinoacetate N-methyltransferase
CCDS2, HEL-S-20, PIG2, TP53I2
Amino acid metabolism disorder, Cerebral creatine deficiency syndrome, Congenital neurologic anomalies, Creatine deficiency syndrome, Guanidinoacetate methyltransferase deficiency, Intellectual developmental disorder, Hereditary parkinson disease, Seizures

5022
Gigaxonin
GAN1, GIG, KLHL16
Arthritis, Charcot-marie-tooth disease, Giant axonal neuropathy, Intellectual developmental disorder, Metabolic syndrome, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Diabetes mellitus type 2

5023
Glucosidase II alpha subunit
G2AN, GIIA, GIIalpha, GLUII, PKD3
Polycystic kidney disease, Kidney disease, Irritable bowel syndrome, Polycystic liver disease

5024
Growth associated protein 43
B-50, GAP-43, PP46
Bipolar disorder, Colonic neoplasms, Major depressive disorder, Dysthymic disorder, Metabolic syndrome, Mood disorder, Proliferative diabetic retinopathy, Schizophrenia, Status epilepticus, Diabetes mellitus type 1, Diabetes mellitus type 2

5025
Glyceraldehyde-3-phosphate dehydrogenase
G3PD, GAPD, HEL-S-162eP
Alzheimer disease, Hepatocellular carcinoma, Squamous cell carcinoma, Colorectal neoplasms, Esophageal neoplasms, Hypoxia, Microcephaly, Mouth neoplasms, Necrosis, Osteoarthritis, Osteoporosis, Parkinson disease

5026
Glyceraldehyde-3-phosphate dehydrogenase, spermatogenic
GAPD2, GAPDH-2, GAPDS, HEL-S-278, HSD-35
Alzheimer disease, Liver disease

5027
GRB2 binding adaptor protein, transmembrane
C5orf29
Major depressive disorder, Hypertension

5028
GTPase activating protein and VPS9 domains 1
GAPEX5, GAPex-5, RAP6
Attention deficit hyperactivity disorder, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Hypothyroidism, Obstructive sleep apnea syndrome, Substance abuse

5029
GAR1 ribonucleoprotein
NOLA1
Dyskeratosis congenita, Hematologic disease

5030
GRB2 associated regulator of MAPK1 subtype 1
C18orf11, FAM59A, GAREM, Gm944
Breast cancer, Estrogen-receptor negative breast cancer, Lung cancer, Metabolic syndrome, Osteoarthritis, Hypertension