Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1571 to 1580 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1571
C1q and TNF related 4
CTRP4, ZACRP4
Cardiovascular disease

1572
C1q and TNF related 5
CTRP5, MFRP
Macular degeneration, Microphthalmia, Microphthalmia with retinitis pigmentosa and ocular anomalies, Nanophthalmos, Optic atrophy, Retinitis pigmentosa

1573
C1q and TNF related 6
CTFP6, CTRP6, ZACRP6
Autoimmune disease, Autoimmune thyroid disease, Breast cancer, Diabetes mellitus type 1, Graves disease, Hypothyroidism, Systemic lupus erythematosus, Thyroid disease, Diabetes mellitus type 2, Vitiligo

1574
C1q and TNF related 7
CTRP7, ZACRP7
Bell's palsy, Conduct disorder, Diverticular disease

1575
C1q and TNF related 8
CTRP8, UNQ5829
Osteoarthritis

1576
Complement C1r
EDS8, EDSPD1
Systemic lupus erythematosus, Complement pathway abnormality, Vascular dementia, Ehlers-danlos syndrome, Endometriosis, Periodontal ehlers-danlos syndrome

1577
Complement C1r subcomponent like
C1RL1, C1RLP, C1r-LP, CLSPa
Ehlers-danlos syndrome

1578
Complement C1s
EDSPD2
Alzheimer disease, Ankylosing spondylitis, Autoimmune hepatitis, Autoimmune disease, Complement pathway abnormality, Complement component deficiency, Coronary artery disease, Ehlers-danlos syndrome, Hashimoto disease, Hereditary angioedema, Lung cancer, Periodontal ehlers-danlos syndrome

1579
Complement C2
ARMD14, CO2
Alzheimer disease, Atrophic macular degeneration, Autism, C1 esterase inhibitor deficiency, Cancer, Interstitial cystitis, Complement pathway abnormality, Complement component deficiency, Coronary artery disease, Irritant dermatitis, Dermatomyositis, Endometriosis, Glaucoma, Hepatocellular carcinoma, Hypertension
View all (17 more)

1580
Chromosome 20 open reading frame 202
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Multiple sclerosis, Oligodendroglioma