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. Author manuscript; available in PMC: 2022 Jul 1.
Published in final edited form as: Expert Opin Drug Metab Toxicol. 2021 Jun 30;17(7):767–784. doi: 10.1080/17425255.2021.1940952

Table 3.

Summary of potential diseases related to human SULT genetic polymorphisms.

SULT Polymorphism Related diseases References
1A1 Arg213His brain tumor 69
breast cancer 82, 84
esophageal cancer 83
gastric cancer 85
lung cancer 86, 87, 88
colorectal cancer (reduced risk) 82
bladder cancer (reduced risk) 94
endometrial cancer 148, 149
Met223Val endometrial cancer 149
3’-UTR variant (rs6839, rs1042157) endometrial cancer 148
1A3 low copy number alzheimer’s disease 120
chromosomal mutation in SULT1A3/SULT1A4 gene area (16p11.2)* autism 115119, 121, 122
obesity 123
schizophrenia 124
attention deficit hyperactivity disorder 125
1C4 Asp5Glu higher post-treatment relapse rate in acute myeloblastic leukemia 133
1E1 His224Gln breast cancer 152
5’-UTR variant (rs3736599) endometrial cancer 148, 149
ischemic stroke in young adults 150
intron variant (rs3775778) breast cancer 103
reduced bone mineral density 151
intron variant (rs3775775) breast cancer 103
intron variant (rs1238574) poor survival rate of colorectal cancer 153
intron variant (rs3822172) poor survival rate of colorectal cancer 153
2A1 intron variant (rs182420) prostate cancer, polycystic ovary syndrome 168, 169
intron variant (rs2547238) prostate cancer 168
2B1 Arg274Gln autosomal recessive ichthyosis 189
Arg100Trp congenital ichthyosiform erythroderma 190
Glu78Lys congenital ichthyosiform erythroderma 190
intron variant (rs4149455) esophageal squamous cell carcinoma 191
intron variant (rs3760806) colorectal cancer 153
4A1 5’-UTR variant (D22s1749e) schizophrenia 48
intron variant (rs138060) schizophrenia 49
intron variant (rs138097) schizophrenia 49
*

These mutations (deletion and duplication) occur in the 16p11.2 at which SULT1A3/SULT1A4 genes are located in. No potential SULT allozymes have been identified in these studies.