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Yip1 domain family member 2 (YIPF2)

Target
YIPF2
Molecular classification
Other (Golgi-associated multi-span transmembrane protein, Yip1 domain family)
01

Overview

Yip1 domain family member 2 (YIPF2) is a multi-span transmembrane protein localized primarily in the medial to trans-Golgi apparatus and partially in the trans-Golgi network[2][3]. This protein is part of the Yip1 domain family, which has a role in vesicular trafficking within the Golgi, and between the endoplasmic reticulum (ER) and Golgi compartments[1][2][3]. YIPF2 forms stable complexes with related YIPF proteins such as YIPF1 and YIPF6, which is essential for Golgi apparatus reassembly after stress, and normal glycan synthesis[2][3]. Structurally, YIPF2 is predicted to traverse the membrane five times, with a cytosolic N-terminus and a luminal C-terminus[4]. Recent studies also demonstrate that YIPF2 can interact with several Rab GTPases (Rab5, Rab22a, Rab8), and likely regulates their recruitment and cycling at the Golgi and ER, implicating YIPF2 in membrane trafficking and protein sorting pathways[4]. Depletion of YIPF2 disrupts normal Golgi functions and hinders homologous recombination repair of DNA, thus contributing to genome instability and suggesting a broader implication in maintaining cellular homeostasis and possibly influencing disease states where intracellular trafficking or genome maintenance is compromised[1][2][3]. There are currently no known drugs directly targeting YIPF2, and it is not considered a current therapeutic target or clinical biomarker. There is also no literature describing specific safety concerns or adverse effects related to modulation or loss of YIPF2 in humans.

Other names
Protein YIPF2MGC3262FinGER2Yip5CYIPFbeta3BYIP1 family member 2
02

Biological functions

Golgi apparatus organization and maintenanceVesicle trafficking (intra-Golgi and ER-Golgi transport)Support of normal glycan synthesisMaintenance of genome stability (by affecting homologous recombination repair)Regulation of membrane protein recruitment (e.g., Rab GTPases)
03

Disease associations

Genome instability (due to impaired homologous recombination upon depletion)Possible contribution to inflammatory disease (evidence from related Yip1 family member, YipF6, in mouse models)Other (no direct evidence for other specific disease roles in current literature)

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