Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11791 to 11800 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11791
Seizure related 6 homolog like
SEZ6L1
Bipolar disorder, Central nervous system cancer, Coronary artery disease, Diabetic ketoacidosis, Glioblastoma, Glioma, Oligodendroglioma, Preeclampsia, Diabetes mellitus type 2, Vascular brain injury

11792
Seizure related 6 homolog like 2
BSRPA, PSK-1
Alzheimer disease, Autism, Systemic lupus erythematosus

11793
Splicing factor 1
BBP, D11S636, MBBP, ZCCHC25, ZFM1, ZNF162
Gout, Melanoma, Neurodevelopmental disorder

11794
Splicing factor 3a subunit 2
PRP11, PRPF11, SAP62, SF3a66
Obesity

11795
Splicing factor 3a subunit 3
PRP9, PRPF9, SAP61, SF3a60
Obstructive pulmonary disease, Colorectal adenoma, Colorectal cancer, Coronary artery disease, Thyroiditis

11796
Splicing factor 3b subunit 1
Hsh155, MDS, PRP10, PRPF10, SAP155, SF3b155
Atrial fibrillation, Autism, Bipolar disorder, Neurodevelopmental disorder, Lymphocytic b-cell leukemia, Major depressive disorder, Mesothelioma, Myelodysplastic syndrome, Prostatic neoplasms, Schizophrenia, Uveal melanoma

11797
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

11798
Splicing factor 3b subunit 3
RSE1, SAP130, SF3b130, STAF130
Alzheimer disease

11799
Splicing factor 3b subunit 4
AFD1, Hsh49, SAP49, SF3b49
Acrofacial dysostosis, Congenital hearing disorder, Desbuquois syndrome, Metabolic syndrome, Metaphyseal chondrodysplasia, Diabetes mellitus type 2

11800
SFI1 centrin binding protein
PISD, PPP1R139, hSfi1p
Diabetes mellitus type 2