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Gene and Protein Information ![]() |
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Species | TM | AA | Chromosomal Location | Gene Symbol | Gene Name | Reference |
Human | 5 | 413 | 10q11.23 | SGMS1 | sphingomyelin synthase 1 | |
Mouse | 5 | 419 | 19 C1 | Sgms1 | sphingomyelin synthase 1 | |
Rat | 5 | 419 | 1q52 | Sgms1 | sphingomyelin synthase 1 |
Previous and Unofficial Names ![]() |
Phosphatidylcholine:ceramide cholinephosphotransferase 1 | Protein Mob | SMS1 | TMEM23 | transmembrane protein 23 |
Database Links ![]() |
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Alphafold | Q86VZ5 (Hs), Q8VCQ6 (Mm), Q7TSX5 (Rn) |
BRENDA | 2.7.8.27 |
ChEMBL Target | CHEMBL3611965 (Hs), CHEMBL4523408 (Mm) |
Ensembl Gene | ENSG00000198964 (Hs), ENSMUSG00000040451 (Mm), ENSRNOG00000012536 (Rn) |
Entrez Gene | 259230 (Hs), 208449 (Mm), 353229 (Rn) |
Human Protein Atlas | ENSG00000198964 (Hs) |
KEGG Enzyme | 2.7.8.27 |
KEGG Gene | hsa:259230 (Hs), mmu:208449 (Mm), rno:353229 (Rn) |
OMIM | 611573 (Hs) |
Pharos | Q86VZ5 (Hs) |
RefSeq Nucleotide | NM_147156 (Hs), NM_144792 (Mm), NM_001168526 (Mm), NM_001168525 (Mm), NM_181386 (Rn) |
RefSeq Protein | NP_671512 (Hs), NP_001161997 (Mm), NP_001161998 (Mm), NP_659041 (Mm), NP_852051 (Rn) |
UniProtKB | Q86VZ5 (Hs), Q8VCQ6 (Mm), Q7TSX5 (Rn) |
Wikipedia | SGMS1 (Hs) |
Enzyme Reaction ![]() |
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Download all structure-activity data for this target as a CSV file
Inhibitors | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Key to terms and symbols | View all chemical structures | Click column headers to sort | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Immuno Process Associations | ||
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1. Li YL, Qi XY, Jiang H, Deng XD, Dong YP, Ding TB, Zhou L, Men P, Chu Y, Wang RX et al.. (2015) Discovery, synthesis and biological evaluation of 2-(4-(N-phenethylsulfamoyl)phenoxy)acetamides (SAPAs) as novel sphingomyelin synthase 1 inhibitors. Bioorg Med Chem, 23 (18): 6173-84. [PMID:26314925]
2. Mo M, Yang J, Jiang XC, Cao Y, Fei J, Chen Y, Qi X, Chu Y, Zhou L, Ye D. (2018) Discovery of 4-Benzyloxybenzo[ d]isoxazole-3-amine Derivatives as Highly Selective and Orally Efficacious Human Sphingomyelin Synthase 2 Inhibitors that Reduce Chronic Inflammation in db/ db Mice. J Med Chem, 61 (18): 8241-8254. [PMID:30074791]