Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11471 to 11480 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11471
Serum amyloid A2
SAA, SAA1
Bipolar disorder, Major depressive disorder, Schizophrenia

11472
SAA2-SAA4 readthrough
-
Bipolar disorder, Color vision deficiency, Major depressive disorder, Schizophrenia

11473
Serum amyloid A4, constitutive
C-SAA, CSAA
Color vision deficiency

11474
Serum amyloid A like 1
SPACIA1
Insomnia

11475
SAC3 domain containing 1
HSU79266, SHD1
Melanoma

11476
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

11477
SUMO1 activating enzyme subunit 1
AOS1, HSPC140, SUA1, UBLE1A
Alzheimer disease, Lymphocytic leukemia, Multiple sclerosis

11478
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

11479
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

11480
Spalt like transcription factor 2
COLB, HSAL2, Sal-2, ZNF795, p150(Sal2)
Cleft eyelid, Coloboma, Commissural facial cleft, Congenital iris coloboma, Congenital ocular coloboma