Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
21 to 30 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

21
Serum amyloid A2
SAA, SAA1
Bipolar disorder, Major depressive disorder, Schizophrenia

22
SAA2-SAA4 readthrough
-
Bipolar disorder, Color vision deficiency, Major depressive disorder, Schizophrenia

23
Serum amyloid A4, constitutive
C-SAA, CSAA
Color vision deficiency

24
Serum amyloid A like 1
SPACIA1
Insomnia

25
SAC3 domain containing 1
HSU79266, SHD1
Melanoma

26
Sacsin molecular chaperone
ARSACS, DNAJC29, PPP1R138, SPAX6
Ataxia, spastic, autosomal recessive with optic atrophy and impaired intellect, Spastic ataxia of charlevoix-saguenay, Bipolar disorder, Charcot-marie-tooth disease, x-linked, Hereditary ataxia, Pelvic organ prolapse, Spastic ataxia, Spastic paraplegia, Hereditary spastic paraplegia, Diabetes mellitus type 2

27
SUMO1 activating enzyme subunit 1
AOS1, HSPC140, SUA1, UBLE1A
Alzheimer disease, Lymphocytic leukemia, Multiple sclerosis

28
S-antigen visual arrestin
RP47, RP96, S-AG
Cone dystrophy, Crohn disease, Inflammatory bowel disease, Nephrolithiasis, Night blindness, congenital stationary, Oguchi disease, Pancreatic cancer, Retinitis pigmentosa, Diabetes mellitus type 2, Uveitis

29
Spalt like transcription factor 1
HEL-S-89, HSAL1, Sal-1, TBS, ZNF794
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Congenital abnormalities, Dental caries, Desbuquois syndrome, Diabetes mellitus, Gastroesophageal reflux disease, Insomnia, Congenital anomaly of limb, Middle lobe syndrome, Post-traumatic stress disorder, Scoliosis, Townes-brocks syndrome, Vacterl association

30
Spalt like transcription factor 2
COLB, HSAL2, Sal-2, ZNF795, p150(Sal2)
Cleft eyelid, Coloboma, Commissural facial cleft, Congenital iris coloboma, Congenital ocular coloboma