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
1551 to 1560 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1551
Chromosome 1 open reading frame 202
-
Myocardial infarction

1552
Chromosome 1 open reading frame 21
PIG13
Systemic lupus erythematosus

1553
Chromosome 1 open reading frame 210
TEMP
Color vision deficiency

1554
Chromosome 1 open reading frame 52
gm117
Metabolic syndrome, Multiple sclerosis, Diabetes mellitus type 2

1555
Chromosome 1 open reading frame 53
-
Attention deficit hyperactivity disorder, Biliary cirrhosis, Bipolar disorder, Color vision deficiency, Endometriosis, Insomnia, Major depressive disorder, Myocardial infarction, Neurotic disorder, Biliary cholangitis, Psoriasis, Substance abuse

1556
Chromosome 1 open reading frame 54
-
Eczema

1557
Chromosome 1 open reading frame 87
CREF
Central nervous system cancer, Dyskinesia, Glioma, Migraine

1558
Chromosome 1 open reading frame 94
-
Central nervous system cancer, Epilepsy, Generalized epilepsy, Glioblastoma, Glioma, Lung cancer, Nonalcoholic fatty liver disease, Peripheral arterial disease, Proliferative diabetic retinopathy, Seborrheic dermatitis, Squamous cell carcinoma

1559
Complement C1q A chain
C1QD1
Systemic lupus erythematosus, C1q deficiency, Basal cell carcinoma, Complement pathway abnormality, Exanthema, Glomerulonephritis, Iga nephropathy, Stevens-johnson syndrome

1560
Complement C1q B chain
C1QD2
C1q deficiency, Complement pathway abnormality, Color vision deficiency, Iga nephropathy, Liver cirrhosis, Myocardial ischemia, Ovarian cysts, Schizophrenia, Diabetes mellitus type 2