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
11671 to 11680 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

11671
Syndecan 3
SDCN, SYND3
Obesity, Prostate cancer

11672
Syndecan 4
SYND4
Non-small-cell lung carcinoma, Psoriasis

11673
Syndecan binding protein
MDA-9, MDA9, SDCBP1, ST1, SYCL, TACIP18
Osteoarthritis

11674
Syndecan binding protein 2
SITAC, SITAC18, ST-2, ST2
Bipolar disorder, Major depressive disorder, Schizophrenia

11675
SHH signaling and ciliogenesis regulator SDCCAG8
BBS16, CCCAP, CCCAP SLSN7, HSPC085, NPHP10, NY-CO-8, SLSN7, hCCCAP
Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Bipolar disorder, Kidney disease, Ciliopathy, Cystic kidney disease, Focal glomerulosclerosis, Metabolic syndrome, Nephronophthisis, Obesity, Parkinson disease, Retinitis pigmentosa, Schizoaffective disorder, Schizophrenia, Senior-loken syndrome
View all (1 more)

11676
Stromal cell derived factor 2 like 1
-
Atrial fibrillation, Crohn disease, Prostatic neoplasms, Rheumatoid arthritis

11677
Stromal cell derived factor 4
Cab45, SDF-4
Ankylosing spondylitis, Crohn disease, Hypothyroidism, Psoriasis, Schizophrenia, Sclerosing cholangitis, Ulcerative colitis

11678
Succinate dehydrogenase complex flavoprotein subunit A
CMD1GG, FP, MC2DN1, NDAXOA, PGL5, PPGL5, SDH1, SDH2, SDHF
Dilated cardiomyopathy, Carney complex, Carney-stratakis syndrome, Congenital pulmonary artery atresia, Disorder of skeletal muscle, Gastrointestinal stromal tumor, Leigh syndrome, Mitochondrial complex deficiency, Osteoarthritis, Paraganglioma, Pheochromocytoma/paraganglioma syndrome, Schizophrenia

11679
Succinate dehydrogenase complex assembly factor 1
LYRM8, MC2DN2
Central nervous system cancer, Vascular dementia, Glioblastoma, Glioma, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

11680
Succinate dehydrogenase complex assembly factor 2
C11orf79, PGL2, PPGL2, SDH5, hSDH5
Hepatolenticular degeneration, Paraganglioma, Pheochromocytoma/paraganglioma syndrome, Diabetes mellitus type 2