Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "R"
691 to 700 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

691
Radial spoke head component 1
CT79, RSP44, RSPH10A, TSA2, TSGA2
Ciliary dyskinesia, Congenital nasopharyngeal atresia

692
Radial spoke head 14 homolog
RTDR1
Bladder calculus, Coronary artery disease, Major depressive disorder, Nephrolithiasis, Ureterolithiasis, Urolithiasis

693
Radial spoke head 3
CILD32, RSHL2, RSP3, dJ111C20.1
Attention deficit hyperactivity disorder, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Systemic lupus erythematosus

694
Radial spoke head component 4A
CILD11, RSHL3, RSPH6B, dJ412I7.1
Autism, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia

695
Radial spoke head 6 homolog A
RSHL1, RSP4, RSP6, RSPH4B
Alzheimer disease, Obstructive pulmonary disease, Coronary artery disease, Heart failure, Hypertrophic cardiomyopathy, Myocardial infarction

696
Radial spoke head component 9
C6orf206, CILD12, MRPS18AL1
Brain aneurysm, Ciliary dyskinesia, Congenital nasopharyngeal atresia

697
R-spondin 1
CRISTIN3, RSPO
Androgenetic alopecia, Epithelial ovarian carcinoma, Endometrial cancer, Endometrial neoplasms, Ovarian epithelial cancer, Open angle glaucoma, Ovarian cancer, Ovarian serous carcinoma, Scoliosis

698
R-spondin 2
CRISTIN2, HHRRD, TETAMS2
Androgenetic alopecia, Lymphoblastic leukemia, Desbuquois syndrome, Dupuytren contracture, Oligodendroglioma, Prostate cancer, Tetra-amelia syndrome

699
R-spondin 3
CRISTIN1, PWTSR, THSD2
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Bone disease, Bone fracture, Breast neoplasms, Hepatocellular carcinoma, Cardiovascular disease, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Coronary artery disease, Crohn disease, Endometriosis
View all (10 more)

700
R-spondin 4
C20orf182, CRISTIN4
Anonychia, Peripheral neuropathy, Hypertension