Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1541 to 1550 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1541
Core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
C1GALT, T-synthase
Alzheimer disease, Cardiovascular disease, Obstructive pulmonary disease, Coronary artery disease, Dementia, Hypertension, Insomnia, Metabolic syndrome, Migraine, Multiple sclerosis, Myocardial infarction, Diabetes mellitus type 2

1542
C1GALT1 specific chaperone 1
AHUS8, C1GALT2, C38H2-L1, COSMC, HSPC067, MST143, TNPS
Hemolytic uremic syndrome

1543
Chromosome 1 open reading frame 105
-
Global developmental delay, Glycosylphosphatidylinositol biosynthesis defect, Non-immune hydrops fetalis, Hypertension

1544
Chromosome 1 open reading frame 116
SARG
Oligodendroglioma

1545
Chromosome 1 open reading frame 122
ALAESM
Galloway-mowat syndrome

1546
Chromosome 1 open reading frame 141
-
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Central precocious puberty, Common variable immunodeficiency, Crohn disease, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Juvenile idiopathic arthritis, Psoriasis, Psoriatic arthritis, Rheumatoid arthritis, Sarcoidosis, Sclerosing cholangitis
View all (5 more)

1547
Chromosome 1 open reading frame 146
SCRE, SPO16
Male infertility, Systemic lupus erythematosus

1548
Chromosome 1 open reading frame 167
-
Ischemic heart disease, Coronary artery disease, Hypertension, Myocardial ischemia, Neural tube defect, Schizophrenia

1549
Chromosome 1 open reading frame 185
-
Atrial fibrillation, Obstructive pulmonary disease, Hyperparathyroidism, Parathyroid disease

1550
Chromosome 1 open reading frame 198
-
Major depressive disorder, Venous thromboembolism