Type | Description |
---|---|
Definition | serine hydroxymethyltransferase 2 (mitochondrial) |
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 |
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
|
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Refseq |
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