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79751 SLC25A22

79751

SLC25A22

solute carrier family 25 member 22

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 25 member 22

研究结论

Date Results Publications
2021-04-17 13:16:00 In Colorectal With Mutant KRAS, SLC25A22-Mediated Glutaminolysis Reduces DNA Demethylation to Increase WNT Signaling, Stemness, and Drug Resistance. 32814111
2021-03-20 13:30:00 Hsa_circ_0007534 knockdown represses the development of colorectal cancer cells through regulating miR-613/SLC25A22 axis. 32271418
2020-07-25 10:35:00 EIEE type 3 is caused by variants affecting function, in SLC25A22, which is also responsible for epilepsy of infancy with migrating focal seizures (EIMFS). 31285529
2019-05-18 10:10:00 SLC25A22 is highly expressed in osteosarcoma, promoting osteosarcoma cell proliferation and invasion by inhibiting the phosphatase and tensin homolog signaling pathway 30482097
2017-08-26 10:29:00 SLC25A22 is an important mitochondrial glutamate transporter. 28255779

名称对应

Type IDs
Synonymous EIEE3, GC-1, GC1, NET44
Gene
UniProtKB-ID: GHC1_HUMAN
UniprotKB: Q9H936
UniParc: UPI0000073CD3
EMBL: BC019033, BC023545, AK290481, AP006621, AJ428202, BC024212, AK023106
Ensembl: ENSG00000177542
KO: hsa:79751
Nucleutide sequences
EMBL-CDS: BAF83170.1, AAH23545.1, CAD21007.1, AAH24212.2, AAH19033.1, BAB14407.1
Ensembl_TRS: ENST00000320230, ENST00000628067, ENST00000531214
Protein sequencees
Ensembl_PRO: ENSP00000322020, ENSP00000437236, ENSP00000486058
RefSeq: XP_011518671.1, XP_024304455.1, XP_024304456.1, NP_078974.1, NP_001177989.1, NP_001177990.1, XP_011518673.1, XP_011518672.1, XP_024304457.1
Others
UniRef100: UniRef100_Q9H936
UniRef90: UniRef90_Q9H936
UniRef50: UniRef50_Q9H936
UniGene: Hs.99486
CCDS: CCDS7715.1

全选

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研究热度

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