Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
11241 to 11250 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

11241
RAR related orphan receptor B
EIG15, NR1F2, ROR-BETA, RORbeta, RZR-BETA, RZRB, bA133M9.1
Color vision deficiency, Neurodevelopmental disorder, Endometriosis, Epilepsy, Idiopathic generalized epilepsy, Hyperopia, Insomnia, Non-specific syndromic intellectual disability, Schizophrenia

11242
RAR related orphan receptor C
IMD42, NR1F3, RORG, RZR-GAMMA, RZRG, TOR
Ankylosing spondylitis, Asthma, Eczema, Crohn disease, Gout, Immunodeficiency, Inflammatory bowel disease, Insomnia, Non-melanoma skin carcinoma, Psoriasis, Respiratory system disease, Sclerosing cholangitis, Sleep disorder, Ulcerative colitis

11243
ROS proto-oncogene 1, receptor tyrosine kinase
MCF3, ROS, c-ros-1
Breast cancer, Non-small-cell lung carcinoma, Cholangiocarcinoma, Giant cell glioblastoma, Glioma, Male infertility single gene azoospermia, Melanoma, Scoliosis

11244
RP1 axonemal microtubule associated
DCDC4A, ORP1
Leber congenital amaurosis, Retinitis pigmentosa, Biliary atresia, Brain aneurysm, Coronary artery disease, Lung cancer, Multiple myeloma, Optic atrophy, Leber hereditary optic neuropathy, Osteoarthritis, Retinopathy, Schizophrenia, Squamous cell carcinoma

11245
RP1 like 1
DCDC4B, OCMD, RP88
Autism, Retinitis pigmentosa, Barrett esophagus, Brain aneurysm, Cone dystrophy, Epidermolysis bullosa, Esophageal adenocarcinoma, Major depressive disorder, Neurotic disorder, Obesity, Optic atrophy, Osteoarthritis, Psychiatric disorders, Psychotic disorders, Diabetes mellitus type 2
View all (1 more)

11246
RP2 activator of ARL3 GTPase
DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2
Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Polycystic ovary syndrome, Retinitis pigmentosa, Retinopathy, X-linked retinitis pigmentosa

11247
RP9 pre-mRNA splicing factor
PAP-1, PAP1
Optic atrophy, Retinitis pigmentosa

11248
Replication protein A1
HSSB, MST075, PFBMFT6, REPA1, RF-A, RP-A, RPA70
Bipolar disorder, Chloracne, Polycystic ovary syndrome, Prostate cancer, Telomere-related pulmonary fibrosis and/or bone marrow failure

11249
Replication protein A3
REPA3, RP-A p14
Interstitial lung disease, Neurotic disorder, Diabetes mellitus type 2

11250
RPA interacting protein
HRIP, RIP
Schizophrenia