Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11711 to 11720 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11711
SUMO specific peptidase 7
-
Alzheimer disease, Arthrogryposis multiplex congenita, Asthma, Myeloproliferative disorder, Skin disease

11712
Selenophosphate synthetase 1
SELD, SPS, SPS1
Neurodevelopmental disorder, Schizophrenia, Ververi-brady syndrome

11713
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
LP, PCH2D, SLA, SLA-p35, SLA/LP, SecS
Arthrogryposis multiplex congenita, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital brain malformation, Congenital hypoplasia of part of brain, Dysarthria, Hydranencephaly, Lissencephaly, Littles disease, Macrogyria, Metabolic syndrome, Microgyria, Pontocerebellar hypoplasia, Spastic ataxia, Diabetes mellitus type 2

11714
Septin 1
DIFF6, LARP, PNUTL3, SEP1, SEPT1, Septin-1
Color vision deficiency

11715
Septin 10
SEPT10, Septin-10
Astrocytoma, Color vision deficiency, Schizophrenia

11716
Septin 11
SEPT11, Septin-11
Cerebellar ataxia, Bipolar disorder, Differentiated thyroid carcinoma, Methylmalonic acidemia, Thyroid carcinoma, Schizophrenia

11717
Septin 12
SEPT12, SPGF10
Congenital impairment of spermatozoa motility, Spermatogenic failure

11718
Septin 14
SEPT14, Septin-14
Alzheimer disease, Giant cell glioblastoma, Glioblastoma, Gliosarcoma, Parkinson disease

11719
Septin 2
DIFF6, NEDD-5, NEDD5, Pnutl3, SEPT2, Septin-2, hNedd5
Androgenetic alopecia, Lymphocytic leukemia, Methylmalonic acidemia, Non-organic psychosis, Prostate cancer, Psychotic disorders, Diabetes mellitus type 1, Diabetes mellitus type 2

11720
Septin 3
SEP3, SEPT3, bK250D10.3
Attention deficit hyperactivity disorder, Autism, Major depressive disorder, Schizophrenia