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
1561 to 1570 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1561
Chromosome 1 open reading frame 54
-
Eczema

1562
Chromosome 1 open reading frame 87
CREF
Central nervous system cancer, Dyskinesia, Glioma, Migraine

1563
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

1564
Complement C1q A chain
C1QD1
Systemic lupus erythematosus, C1q deficiency, Basal cell carcinoma, Complement pathway abnormality, Exanthema, Glomerulonephritis, Iga nephropathy, Liver cirrhosis, Stevens-johnson syndrome

1565
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

1566
Complement C1q binding protein
COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R, gC1qR, p32
Breast neoplasms, Combined oxidative phosphorylation deficiency, Mitochondrial disease

1567
Complement C1q C chain
C1Q-C, C1QD3, C1QG
C1q deficiency, Complement pathway abnormality, Fatty liver, alcoholic, Hepatitis c, Liver cirrhosis, Nonalcoholic fatty liver disease, Stevens-johnson syndrome

1568
Complement C1q like 1
C1QRF, C1QTNF14, CRF, CTRP14
Dry eye syndrome, Sjogren syndrome

1569
C1q and TNF related 1
CTRP1, GIP, ZSIG37
Basal cell carcinoma

1570
C1q and TNF related 12
C1QDC2, CTRP12, FAM132A
Fatty liver, Hypothyroidism, Schizophrenia, Systemic lupus erythematosus