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17769 Mthfr

17769

Mthfr

methylenetetrahydrofolate reductase

protein-coding

Mus musculus

基因描述

Type Description
Definition methylenetetrahydrofolate reductase

研究结论

Date Results Publications
2019-03-23 12:21:00 Maternal and offspring Mthfr genotypes interact in a mouse model to induce autism spectrum disorder-like behavior. 30552741
2019-03-09 10:21:00 The data suggest that MTHFR deficiency decreases recovery after stroke by reducing neuronal and astrocyte viability. 30055159
2019-02-02 12:04:00 data provide evidence for a similar cross-species response to high dose folic acid supplementation, of sperm DNA hypomethylation, and implicate MTHFR downregulation as a possible mechanism. 29360980
2018-02-17 10:32:00 findings indicate that the loss of folate as a methyl donor is a modifier of allergic airway disease, and that epigenetic and expression changes correlate with this modification. 29329322
2017-07-01 11:33:00 Ganglion cell loss and vasculopathy observed in Mthfr+/- and Cbs+/- mouse retinas may be milder than expected, not because of compensatory increases of enzymes in remethylation/transsulfuration pathways, but because downstream transsulfuration pathway products GSH, taurine, and H2S are maintained at robust levels. 28384716

名称对应

Type IDs
Synonymous AI323986
Gene
UniProtKB-ID: MTHR_MOUSE, A2A7F7_MOUSE, Q3UDB2_MOUSE, Q497H7_MOUSE
UniprotKB: Q9WU20, A2A7F7, Q3UDB2, Q497H7
UniParc: UPI00005AC982, UPI000059E219, UPI00005904EA, UPI000002308A
EMBL: AL606929, AF105990, AF105996, CH466594, AF105993, AF105992, AF105988, BC100550, AF105997, AK030192, AK150159, AF105995, AF105998, BC052466, AF105991, AF105994, BC051017, AF105989
Ensembl: ENSMUSG00000029009
KO: mmu:17769
Nucleutide sequences
EMBL-CDS: EDL14796.1, AAH52466.1, AAD20313.1, EDL14797.1, EDL14794.1, AAH51017.1, BAC26832.1, BAE29349.1, AAI00551.1
Ensembl_TRS: ENSMUST00000097788, ENSMUST00000069604
Protein sequencees
Ensembl_PRO: ENSMUSP00000095395, ENSMUSP00000069774
RefSeq: NP_034970.2, NP_001155270.1
Others
UniRef100: UniRef100_Q9WU20, UniRef100_Q3UDB2
UniRef90: UniRef90_Q9WU20
UniRef50: UniRef50_P42898
UniGene: Mm.89959
CCDS: CCDS18929.1

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