Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11841 to 11850 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11841
SET and mariner transposase domain methyltransferase
METNASE, Mar1
Spondylosis

11842
SET like protein
SETP18
Intellectual developmental disorder

11843
Senataxin
ALS4, AOA2, SCAN2, SCAR1, STEX, Sen1, bA479K20.2
Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia with oculomotor apraxia, Distal hereditary motor neuropathy, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Charcot-marie-tooth disease, Dementia, Distal spinal muscular atrophy, Frontotemporal dementia, Hereditary motor and sensory neuropathies, Motor neuron disease, Nystagmus, Proximal spinal muscular atrophy
View all (5 more)

11844
Seizure related 6 homolog
BSRPC
Gout, Liver cirrhosis, Schizophrenia

11845
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

11846
Seizure related 6 homolog like 2
BSRPA, PSK-1
Alzheimer disease, Autism, Systemic lupus erythematosus

11847
Splicing factor 1
BBP, D11S636, MBBP, ZCCHC25, ZFM1, ZNF162
Gout, Melanoma, Neurodevelopmental disorder

11848
Splicing factor 3a subunit 2
PRP11, PRPF11, SAP62, SF3a66
Obesity

11849
Splicing factor 3a subunit 3
PRP9, PRPF9, SAP61, SF3a60
Obstructive pulmonary disease, Colorectal adenoma, Colorectal cancer, Coronary artery disease, Thyroiditis

11850
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