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 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1571
Complement C1r
EDS8, EDSPD1
Systemic lupus erythematosus, Complement pathway abnormality, Vascular dementia, Ehlers-danlos syndrome, Endometriosis, Periodontal ehlers-danlos syndrome

1572
Complement C1r subcomponent like
C1RL1, C1RLP, C1r-LP, CLSPa
Ehlers-danlos syndrome

1573
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

1574
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)

1575
Chromosome 20 open reading frame 202
-
Multiple sclerosis, Oligodendroglioma

1576
Chromosome 20 open reading frame 203
-
Cardiovascular disease, Hypertension, Insomnia, Willis-ekbom disease, Diabetes mellitus type 2

1577
Chromosome 20 open reading frame 204
LINC00176, NCRNA00176, PRR17
Insomnia

1578
Chromosome 22 open reading frame 31
HS747E2A, bK747E2.1
Cardiovascular disease, Kidney disease, Metabolic syndrome, Diabetes mellitus type 2, Uterine fibroid

1579
Chromosome 22 open reading frame 39
Pants
Central nervous system cancer, Glioblastoma, Glioma

1580
Chromosome 22 open reading frame 42
dJ90G24.6
Polycystic ovary syndrome, Selective iga deficiency disease, Diabetes mellitus type 2