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976 ADGRE5

976

ADGRE5

adhesion G protein-coupled receptor E5

protein-coding

Homo sapiens

基因描述

Type Description
Definition adhesion G protein-coupled receptor E5

研究结论

Date Results Publications
2021-03-20 13:35:00 Tethered agonist exposure in intact adhesion/class B2 GPCRs through intrinsic structural flexibility of the GAIN domain. 33497605
2020-12-19 13:41:00 CD97 Is Decreased in Preeclamptic Placentas and Promotes Human Trophoblast Invasion Through PI3K/Akt/mTOR Signaling Pathway. 32430705
2020-11-21 13:31:00 G Protein-Coupling of Adhesion GPCRs ADGRE2/EMR2 and ADGRE5/CD97, and Activation of G Protein Signalling by an Anti-EMR2 Antibody. 31969668
2020-07-25 10:22:00 CD97 stimulates tumor angiogenesis through RGD motif-independent mechanism.CD97 promotes tumor angiogenesis by overexpressing MMP-9. 31594642
2020-06-13 10:10:00 High levels of CD97 correlate with poor prognosis, and silencing of CD97 reduces disease aggressiveness in vivo. These phenotypes are due to CD97's ability to promote proliferation, survival, and the maintenance of the undifferentiated state in leukemic blasts. 31371381

名称对应

Type IDs
Synonymous CD97, TM7LN1
Gene
UniProtKB-ID: AGRE5_HUMAN
UniprotKB: P48960
UniParc: UPI000006D0B6, UPI0000203564, UPI0000161C9A
EMBL: X94641, X94631, Z99830, AB065966, X94640, U76764, X94630, CH471106, X94647, X94643, AK292159, X94645, X94642, X94637, X94638, X94635, X84700, AK314697, X94646, AC005327, X94632, X94633, X94639, Z99831, X94644, BC026690, X94634, X94636
Ensembl: ENSG00000123146
KO: hsa:976
Nucleutide sequences
EMBL-CDS: AAB36682.1, EAW84413.1, CAA64333.1, EAW84412.1, AAH26690.1, BAG37246.1, BAC06178.1, CAA59173.1, AAC27673.1, BAF84848.1
Ensembl_TRS: ENST00000242786, ENST00000358600, ENST00000357355
Protein sequencees
Ensembl_PRO: ENSP00000349918, ENSP00000351413, ENSP00000242786
RefSeq: XP_011526753.1, NP_001775.2, NP_001020331.1, NP_510966.1
Others
UniRef100: UniRef100_P48960
UniRef90: UniRef90_P48960
UniRef50: UniRef50_P48960
UniGene: Hs.466039
CCDS: CCDS32929.1, CCDS32931.1, CCDS32930.1

全选

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