Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11761 to 11770 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11761
SUMO specific peptidase 2
AXAM2, SMT3IP2
Atrioventricular block, Color vision deficiency, Gout, Liver cirrhosis, Seborrheic dermatitis, Seizures, Diabetes mellitus type 2

11762
SUMO specific peptidase 3
SMT3IP1, SSP3, Ulp1
Metabolic syndrome, Diabetes mellitus type 2

11763
SUMO specific peptidase 5
-
Alzheimer disease, Schizophrenia

11764
SUMO specific peptidase 6
SSP1, SUSP1
Cutaneous lupus erythematosus, Migraine, Osteoarthritis, Prostatic neoplasms, Diabetes mellitus type 2

11765
SUMO specific peptidase 7
-
Alzheimer disease, Arthrogryposis multiplex congenita, Asthma, Myeloproliferative disorder, Skin disease

11766
Selenophosphate synthetase 1
SELD, SPS, SPS1
Neurodevelopmental disorder, Schizophrenia, Ververi-brady syndrome

11767
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

11768
Septin 1
DIFF6, LARP, PNUTL3, SEP1, SEPT1, Septin-1
Color vision deficiency

11769
Septin 10
SEPT10, Septin-10
Astrocytoma, Color vision deficiency, Schizophrenia

11770
Septin 11
SEPT11, Septin-11
Cerebellar ataxia, Bipolar disorder, Differentiated thyroid carcinoma, Methylmalonic acidemia, Thyroid carcinoma, Schizophrenia