Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12951 to 12960 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12951
Syntaxin binding protein 6
HSPC156, amisyn
Alzheimer disease, Autism, Cataract, Central nervous system cancer, Gastroesophageal reflux disease, Glioblastoma, Glioma, Ocular sarcoidosis

12952
Serine/threonine/tyrosine interacting protein
-
Alzheimer disease

12953
Serine/threonine/tyrosine interacting like 2
DUSP27
Atrial fibrillation

12954
SUB1 regulator of transcription
P15, PC4, p14
Breast cancer, Crohn disease

12955
Succinate-CoA ligase ADP-forming subunit beta
A-BETA, A-SCS, LINC00444, MTDPS5, SCS-betaA
Color vision deficiency, Colorectal cancer, Mitochondrial dna depletion syndrome, Peritoneal disease, Eosinophilia, Global developmental delay, Leigh syndrome, Obesity, Oligodendroglioma

12956
Succinate-CoA ligase GDP/ADP-forming subunit alpha
GALPHA, MTDPS9, SUCLA1
Astrocytoma, Mitochondrial dna depletion syndrome, Leigh syndrome, Stomach neoplasms

12957
Succinate-CoA ligase GDP-forming subunit beta
G-SCS, GBETA, GTPSCS
Corneal astigmatism, Diabetic neuropathy, Endometriosis, Methylmalonic acidemia, Obesity, Pelvic organ prolapse, Prostate cancer

12958
SUN domain containing ossification factor
C1orf9, CH1, OPT, SLP1
Dementia, Temporal lobe epilepsy, Osteogenesis imperfecta, Hypertension

12959
SIN3A corepressor complex component SDS3
SAP45, SDS3
Alzheimer disease, Major depressive disorder, Neurotic disorder

12960
SUFU negative regulator of hedgehog signaling
BCNS2, JBTS32, PRO1280, SUFUH, SUFUXL
Apraxia, Atrial fibrillation, Basal cell nevus syndrome, Bipolar disorder, Basal cell carcinoma, Ciliopathy, Crohn disease, Medulloblastoma, Aplasia of the vermis, Meningioma, Gastrointestinal stromal tumor, Gorlin syndrome, Heart failure, Inflammatory bowel disease, Joubert syndrome
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