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108037 Shmt2

108037

Shmt2

serine hydroxymethyltransferase 2 (mitochondrial)

protein-coding

Mus musculus

基因描述

Type Description
Definition serine hydroxymethyltransferase 2 (mitochondrial)

研究结论

Date Results Publications
2020-10-31 13:13:00 Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders. 31690790
2020-10-10 13:00:00 Loss of PYCR2 Causes Neurodegeneration by Increasing Cerebral Glycine Levels via SHMT2. 32330411
2020-06-06 13:19:00 SHMT2 can contribute to liver regeneration after partial hepatectomy, and this is likely related to the activation of Akt/mTOR signaling pathway by its metabolic product, glycine, in hepatocytes. 30964837
2020-04-25 11:00:00 Knockdown of SHMT2 worsens IR injury through the signaling pathway. 31828098
2010-01-21 00:00:00 SHMT1 and SHMT2 are functionally redundant in nuclear de novo thymidylate biosynthesis 19513116

名称对应

Type IDs
Synonymous 2700043D08Rik, AA408223, AA986903, SHMT
Gene
UniProtKB-ID: GLYM_MOUSE
UniprotKB: Q9CZN7
UniParc: UPI0000022602, UPI00005B2538
EMBL: AK162421, BC051396, BC004825, AK051207, AK037339, AK169192, AK012355, AC167719
Ensembl: ENSMUSG00000025403
KO: mmu:108037
Nucleutide sequences
EMBL-CDS: BAE36907.1, BAE40968.1, AAH51396.1, BAC34556.1, BAB28184.1, BAC29790.1, AAH04825.1
Ensembl_TRS: ENSMUST00000026470, ENSMUST00000219239
Protein sequencees
Ensembl_PRO: ENSMUSP00000151616, ENSMUSP00000026470
RefSeq: NP_082506.1, NP_001239245.1
Others
UniRef100: UniRef100_Q9CZN7
UniRef90: UniRef90_P34897
UniRef50: UniRef50_P34897
UniGene: Mm.29890, Mm.452356
CCDS: CCDS88105.1, CCDS24244.1

全选

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研究热度

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