Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1561 to 1570 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1561
Complement C1q binding protein
COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R, gC1qR, p32
Breast neoplasms, Combined oxidative phosphorylation deficiency, Mitochondrial disease

1562
Complement C1q C chain
C1Q-C, C1QD3, C1QG
C1q deficiency, Complement pathway abnormality, Fatty liver, alcoholic, Nonalcoholic fatty liver disease, Stevens-johnson syndrome

1563
Complement C1q like 1
C1QRF, C1QTNF14, CRF, CTRP14
Dry eye syndrome, Sjogren syndrome

1564
C1q and TNF related 1
CTRP1, GIP, ZSIG37
Basal cell carcinoma

1565
C1q and TNF related 12
C1QDC2, CTRP12, FAM132A
Fatty liver, Hypothyroidism, Schizophrenia, Systemic lupus erythematosus

1566
C1q and TNF related 4
CTRP4, ZACRP4
Cardiovascular disease

1567
C1q and TNF related 5
CTRP5, MFRP
Macular degeneration, Microphthalmia, Microphthalmia with retinitis pigmentosa and ocular anomalies, Nanophthalmos, Optic atrophy, Retinitis pigmentosa

1568
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

1569
C1q and TNF related 7
CTRP7, ZACRP7
Bell's palsy, Conduct disorder, Diverticular disease

1570
C1q and TNF related 8
CTRP8, UNQ5829
Osteoarthritis