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79890 RIN3

79890

RIN3

Ras and Rab interactor 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition Ras and Rab interactor 3

研究结论

Date Results Publications
2020-08-29 12:44:00 Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of Onset. 30726512
2017-10-07 13:02:00 RIN3 may be involved in endolysosomal transport-a process known to be important to development of early onset AD. 28738127
2016-02-20 11:55:00 RIN3 may contribute to Paget's disease of bone susceptibility by affecting osteoclast function. 25701875
2016-02-13 10:07:00 discovered novel interaction candidates for CD2AP and characterized subtle yet significant differences in the recognition preferences of its three SH3 domains for c-CBL, ALIX, and RIN3 26296892
2015-06-27 14:26:00 The study reports a novel association between a variant within RIN3 and lower limb-bone mineral density and note its previous association with risk of Paget's disease. 24945404

名称对应

Type IDs
Gene
UniProtKB-ID: RIN3_HUMAN, Q86U22_HUMAN, Q6ZRC2_HUMAN, Q6NSK7_HUMAN
UniprotKB: Q8TB24, Q86U22, Q6ZRC2, Q6NSK7
UniParc: UPI00001AAC57, UPI000035EC91, UPI00001C1C97, UPI00001C0FBC, UPI000000CBE8
EMBL: AK074176, AK021762, BC070062, AL159141, AL136332, BX248258, AB060338, BC025248, AB081753, AK026092, AK128338, AK090451
Ensembl: ENSG00000100599
KO: hsa:79890
Nucleutide sequences
EMBL-CDS: BAB15357.1, BAC16513.1, BAB13888.1, BAC03432.1, BAB85002.1, AAH25248.2, BAB84316.1, CAD62586.1, BAC87390.1, AAH70062.1
Ensembl_TRS: ENST00000216487
Protein sequencees
Ensembl_PRO: ENSP00000216487
RefSeq: NP_079108.3, XP_016877143.1, XP_016877140.1, NP_001306916.1, XP_011535466.1, XP_016877141.1, XP_011535467.1, XP_016877142.1
Others
UniRef100: UniRef100_Q6NSK7, UniRef100_Q8TB24, UniRef100_Q6ZRC2, UniRef100_Q86U22
UniRef90: UniRef90_A0A2I3NDL3, UniRef90_Q8TB24
UniRef50: UniRef50_P59729, UniRef50_Q8TB24
UniGene: Hs.326822
CCDS: CCDS32144.1

全选

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