Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1611 to 1620 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1611
Chromosome 3 open reading frame 85
-
Colorectal cancer

1612
Complement C4A (Chido/Rodgers blood group)
C4, C4A2, C4A3, C4A4, C4A6, C4AD, C4S, CO4, CPAMD2, RG
Systemic lupus erythematosus, Behcet disease, Complement pathway abnormality, Complement component deficiency, Graves disease, Vitiligo

1613
Complement C4B (Chido/Rodgers blood group)
C4B1, C4B12, C4B2, C4B3, C4B5, C4BD, C4B_2, C4F, CH, CO4, CPAMD3
Ankylosing spondylitis, Autism, Autoimmune disease, C1 esterase inhibitor deficiency, Complement pathway abnormality, Complement component deficiency, Graves disease, Systemic lupus erythematosus, Rheumatoid arthritis

1614
Complement component 4 binding protein alpha
C4BP, PRP
Bell's palsy, Venous thromboembolism

1615
Chromosome 4 open reading frame 17
-
Eating disorder, Major depressive disorder

1616
Chromosome 4 open reading frame 36
-
Amyotrophic lateral sclerosis, Hypothyroidism, Schizophrenia

1617
Chromosome 4 open reading frame 50
-
Thyroid gland neoplasms, Color vision deficiency, Coronary artery disease, Oligodendroglioma, Diabetes mellitus type 2

1618
Chromosome 4 open reading frame 54
FOPV
Gout, Stroke

1619
Complement C5
C5D, C5a, C5b, CPAMD4, ECLZB
Asthma, Cold paroxysmal hemoglobinuria, Complement component deficiency, Coronary artery disease, Endometriosis, Hemoglobinuria paroxysmal, Liver cirrhosis, Neutropenia, Paroxysmal nocturnal hemoglobinuria, Peritonitis, Rheumatoid arthritis, Terminal complement component deficiency

1620
Complement C5a receptor 1
C5A, C5AR, C5R1, CD88
Liver cirrhosis, Periodontitis, Toxic shock syndrome