Version 5.4
Homo sapiens Protein: TMEM88
Summary
InnateDB Protein IDBP-26949.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TMEM88
Protein Name transmembrane protein 88
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000301599
InnateDB Gene IDBG-26947 (TMEM88)
Protein Structure
UniProt Annotation
Function Inhibits the Wnt/beta-catenin signaling pathway. Crucial for heart development and acts downstream of GATA factors in the pre-cardiac mesoderm to specify lineage commitment of cardiomyocyte development. {ECO:0000269PubMed:23924634}.
Subcellular Localization Cell membrane {ECO:0000269PubMed:21044957}; Multi-pass membrane protein {ECO:0000269PubMed:21044957}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0007275 multicellular organismal development
GO:0016055 Wnt signaling pathway
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q6PEY1
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 92162
UniGene
RefSeq NP_981956
HUGO HGNC:32371
OMIM
CCDS CCDS11121
HPRD 17438
IMGT
EMBL BC057812
GenPept AAH57812

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca