Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11381 to 11390 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11381
Round spermatid basic protein 1
KDM9, ROSBIN
Ankylosing spondylitis, Anti-neutrophil antibody associated vasculitis, Asthma, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Coronary artery disease, Crohn disease, Diabetic ketoacidosis, Hyperthyroidism, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis
View all (18 more)

11382
Round spermatid basic protein 1 like
-
Atrial fibrillation, Kidney disease, Hypothyroidism

11383
Remodeling and spacing factor 1
HBXAP, RSF-1, XAP8, p325
Breast cancer

11384
Ribosomal protein S6 kinase related
SGK494
Pharyngeal disorder, Insomnia

11385
Ribosomal L1 domain containing 1
CSIG, L12, PBK1, UTP30
Scoliosis, Uterine fibroid

11386
Ribosomal L24 domain containing 1
C15orf15, HRP-L30-iso, L30, RLP24, RPL24, RPL24L, TVAS3
Eczema, Attention deficit hyperactivity disorder, Breast cancer, Coronary artery disease, Estrogen-receptor negative breast cancer, Inflammatory skin disease, Psoriasis

11387
Radial spoke head component 1
CT79, RSP44, RSPH10A, TSA2, TSGA2
Ciliary dyskinesia, Congenital nasopharyngeal atresia

11388
Radial spoke head 14 homolog
RTDR1
Bladder calculus, Coronary artery disease, Major depressive disorder, Nephrolithiasis, Ureterolithiasis, Urolithiasis

11389
Radial spoke head 3
CILD32, RSHL2, RSP3, dJ111C20.1
Attention deficit hyperactivity disorder, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Systemic lupus erythematosus

11390
Radial spoke head component 4A
CILD11, RSHL3, RSPH6B, dJ412I7.1
Autism, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia