ERLIN2 / TRP channels
Name: Erlin-2
(ERLIN2)
Official Symbol: ERLIN2
provided by HGNC
Function:
Component of the ERLIN1/ERLIN2 complex which mediates the endoplasmic reticulum-associated degradation (ERAD) of inositol 1,4,5-trisphosphate receptors (IP3Rs). Also involved in ITPR1 degradation by the ERAD pathway.
Source: Reorganizing the protein space at the Universal Protein Resource (UniProt)
Nucleic Acids Res. 40: D71-D75 (2012).
Species |
External DB
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Entrez Gene | UniprotKB | DIP | IntAct | MINT | BioGRID | STRING | IUPHAR-DB | KEGG | OMIM | |
Human
![]() |
11160![]() |
O94905![]() |
MINT-3035811![]() |
116331![]() |
O94905![]() |
hsa:11160![]() |
611605![]() |
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Mouse
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244373![]() |
Q8BFZ9![]() |
DIP-51706N![]() |
Q8BFZ9![]() |
MINT-1846748![]() |
232642![]() |
Q8BFZ9![]() |
mmu:244373![]() |
||
Rat
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290823![]() |
B5DEH2![]() |
253334![]() |
B5DEH2![]() |
rno:290823![]() |
PPI pairs:
Biological Process:
- GO:0008219
: cell death
- GO:0030433
: ER-associated protein catabolic process
Source: The Gene Ontology Consortium. Gene ontology: tool for the unification of biology. Nat. Genet.. May 2000;25(1):25-9.
World Wide Web URL: http://www.geneontology.org/
World Wide Web URL: http://www.geneontology.org/
Disease:
- OMIM:611605
: Spastic paraplegia 18, autosomal recessive (OMIM:611225
)
Source: Online Mendelian Inheritance in Man, OMIM®. McKusick-Nathans Institute of Genetic Medicine,
Johns Hopkins University (Baltimore, MD), May, 2012.
World Wide Web URL: http://omim.org/
World Wide Web URL: http://omim.org/
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Screening
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Experimental screening | Non-experimental screening | Reference | ||||||||
TRP channel construct | Interactor source | |||||||||
TRP channel | Interactor | Method | Species | Region | Species | Organ/tissue | Sample type | |||
TRPP1 |
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ERLIN2 | Affinity purification-mass spectrometry | Mouse | Not specified | Mouse | Vascular smooth muscle | MOVAS lysates | 19879844 |
(
:
click the arrow icon to show interactions only between the corresponding TRP channel and the interactor)
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