Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11441 to 11450 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11441
Radial spoke head 14 homolog
RTDR1
Bladder calculus, Coronary artery disease, Major depressive disorder, Nephrolithiasis, Ureterolithiasis, Urolithiasis

11442
Radial spoke head 3
CILD32, RSHL2, RSP3, dJ111C20.1
Attention deficit hyperactivity disorder, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Systemic lupus erythematosus

11443
Radial spoke head component 4A
CILD11, RSHL3, RSPH6B, dJ412I7.1
Autism, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia

11444
Radial spoke head 6 homolog A
RSHL1, RSP4, RSP6, RSPH4B
Alzheimer disease, Obstructive pulmonary disease, Coronary artery disease, Heart failure, Hypertrophic cardiomyopathy, Myocardial infarction

11445
Radial spoke head component 9
C6orf206, CILD12, MRPS18AL1
Brain aneurysm, Ciliary dyskinesia, Congenital nasopharyngeal atresia

11446
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

11447
R-spondin 2
CRISTIN2, HHRRD, TETAMS2
Androgenetic alopecia, Lymphoblastic leukemia, Desbuquois syndrome, Dupuytren contracture, Oligodendroglioma, Prostate cancer, Tetra-amelia syndrome

11448
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
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11449
R-spondin 4
C20orf182, CRISTIN4
Anonychia, Peripheral neuropathy, Hypertension

11450
Ring finger and SPRY domain containing 1
SEMDFA
Desbuquois syndrome, Spondyloepimetaphyseal dysplasia