Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11391 to 11400 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11391
Radial spoke head 6 homolog A
RSHL1, RSP4, RSP6, RSPH4B
Alzheimer disease, Obstructive pulmonary disease, Coronary artery disease, Heart failure, Hypertrophic cardiomyopathy, Myocardial infarction

11392
Radial spoke head component 9
C6orf206, CILD12, MRPS18AL1
Brain aneurysm, Ciliary dyskinesia, Congenital nasopharyngeal atresia

11393
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

11394
R-spondin 2
CRISTIN2, HHRRD, TETAMS2
Androgenetic alopecia, Lymphoblastic leukemia, Desbuquois syndrome, Dupuytren contracture, Oligodendroglioma, Prostate cancer, Tetra-amelia syndrome

11395
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)

11396
R-spondin 4
C20orf182, CRISTIN4
Anonychia, Peripheral neuropathy, Hypertension

11397
Ring finger and SPRY domain containing 1
SEMDFA
Desbuquois syndrome, Spondyloepimetaphyseal dysplasia

11398
Arginine and serine rich coiled-coil 1
BM-011, MRT70, SFRS21, SRrp53
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Gout, Hypertension, Intellectual developmental disorder, Lung cancer, Major depressive disorder, Neuroblastoma, Neurotic disorder, Obesity
View all (4 more)

11399
Arginine and serine rich coiled-coil 2
-
Autism, Neurodevelopmental disorder, Global developmental delay, Glomerulonephritis, Myopia, Neurotic disorder, Non-specific syndromic intellectual disability, Obesity, Strabismus

11400
Arginine and serine rich protein 1
C1orf63, NPD014
Rh isoimmunization, Arrhythmogenic right ventricular cardiomyopathy, Hemolytic disease of fetus and newborn