Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5201 to 5210 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5201
GLI pathogenesis related 2
C9orf19, GAPR-1, GAPR1, gliPR 2
Squamous cell carcinoma

5202
GLIS family zinc finger 1
-
Androgenetic alopecia, Mitral valve prolapse, Open angle glaucoma, Osteoarthritis, Tetralogy of fallot

5203
GLIS family zinc finger 2
NKL, NPHP7
Gastrointestinal stromal tumor, Nephronophthisis, Kidney disease, Diabetes mellitus type 2

5204
GLIS family zinc finger 3
NDH, ZNF515
Alzheimer disease, Androgenetic alopecia, Angle closure glaucoma, Asthma, Biliary atresia, Cardiac embolism, Cardioembolic stroke, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Dementia, Dental caries, Diabetes mellitus, Diabetes mellitus type 1, Neonatal diabetes mellitus with congenital hypothyroidism
View all (25 more)

5205
Glomulin, FKBP associated protein
FAP, FAP48, FAP68, FKBPAP, GLML, GVM, VMGLOM
Arteriovenous hemangioma, Blue rubber bleb nevus syndrome, Congenital venous anomaly

5206
Glyoxalase I
GLOD1, GLYI, HEL-S-74
Anxiety disorder, Autism, Bipolar disorder, Major depressive disorder, Diabetes mellitus type 2, Diabetic retinopathy, Esophageal squamous cell carcinoma, Insomnia, Kidney failure, Melanoma, Schizophrenia, Vascular disease

5207
Glucagon like peptide 1 receptor
GLP-1, GLP-1-R, GLP-1R
Colorectal cancer, Diabetes mellitus, Diabetes mellitus type 2, Heart failure, Hyperplasia, Hypertension, Obesity, Diabetes mellitus type 1

5208
Glucagon like peptide 2 receptor
-
Metabolic syndrome, Diabetes mellitus type 2

5209
Glycine receptor alpha 1
HKPX1, STHE
Central nervous system cancer, Dystonia, Glioblastoma, Glioma, Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary, Scoliosis, Diabetes mellitus type 2

5210
Glycine receptor alpha 2
GLR, MRXSP
Intellectual developmental disorder, x-linked