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
12511 to 12520 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12511
Stannin
-
Ankylosing spondylitis, Crohn disease, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

12512
Secondary ossification center associated regulator of chondrocyte maturation
ASCL830, C2orf82, UNQ830
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Schizophrenia, Tourette syndrome

12513
Syntaphilin
-
Autoimmune thrombocytopenic purpura, Color vision deficiency

12514
SNF related kinase
HSNFRK
Asthma, Attention deficit hyperactivity disorder, Bipolar disorder, Colorectal cancer, Gastroesophageal reflux disease, Insomnia, Major depressive disorder, Obesity, Oligodendroglioma, Post-traumatic stress disorder, Schizophrenia, Substance abuse

12515
Small nuclear ribonucleoprotein U5 subunit 200
ASCC3L1, BRR2, HELIC2, RP33, U5-200KD
Retinitis pigmentosa, Major depressive disorder, Rod-cone dystrophy, Schizophrenia, Stargardt disease

12516
Small nuclear ribonucleoprotein U11/U12 subunit 25
C16orf33
Metabolic syndrome, Pancreatic cancer

12517
Small nuclear ribonucleoprotein U4/U6.U5 subunit 27
27K, RY1
Atrial fibrillation, Breast cancer

12518
Small nuclear ribonucleoprotein U11/U12 subunit 35
HM-1, HM1, U1SNRNPBP
Osteoarthritis

12519
Small nuclear ribonucleoprotein U1 subunit 70
RNPU1Z, RPU1, SNRP70, Snp1, U1-70K, U170K, U1AP, U1RNP
Global developmental delay, Hypertension, Systemic lupus erythematosus

12520
Small nuclear ribonucleoprotein polypeptide A
Mud1, U1-A, U1A
Neurodevelopmental disorder, Connective tissue disease, Non-specific syndromic intellectual disability, Stomach disease