Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11851 to 11860 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11851
Splicing factor 3b subunit 2
CFM, Cus1, HFM, SAP145, SF3B145, SF3b1, SF3b150
Craniofacial microsomia, Goldenhar syndrome, Hemifacial microsomia, Metabolic syndrome, Retinitis pigmentosa, Diabetes mellitus type 2

11852
Splicing factor 3b subunit 3
RSE1, SAP130, SF3b130, STAF130
Alzheimer disease

11853
Splicing factor 3b subunit 4
AFD1, Hsh49, SAP49, SF3b49
Acrofacial dysostosis, Congenital hearing disorder, Desbuquois syndrome, Metabolic syndrome, Metaphyseal chondrodysplasia, Diabetes mellitus type 2

11854
Splicing factor 3b subunit 5
SF3b10, Ysf3
Leprosy

11855
SFI1 centrin binding protein
PISD, PPP1R139, hSfi1p
Diabetes mellitus type 2

11856
Scm like with four mbt domains 1
RU1, SFMBT, hSFMBT
Kidney disease, Clear cell renal cell carcinoma, Colorectal cancer, Gout, Hemorrhoid, Hypertrophic cardiomyopathy, Hyperuricemia, Kidney cancer, Major depressive disorder, Obsessive-compulsive disorder, Willis-ekbom disease, Schizophrenia, Ulcerative colitis

11857
Scm like with four mbt domains 2
-
Immune system disease, Insomnia, Myasthenia gravis, Nephrotic syndrome, Periprosthetic osteolysis, Urinary bladder cancer

11858
Stratifin
YWHAS
Hepatocellular carcinoma, Squamous cell carcinoma, Esophageal neoplasms, Esophageal squamous cell carcinoma, Lymphatic metastasis, Mouth neoplasms

11859
Splicing factor proline and glutamine rich
POMP100, PPP1R140, PSF
Dermatologic disorder, Schizophrenia, Skin disease

11860
SWI5 dependent homologous recombination repair protein 1
C10orf78, MEI5, MEIR5, bA373N18.1
Preeclampsia, Uterine fibroid