Homo sapiens Gene: PLSCR2
Summary
InnateDB Gene IDBG-60151.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PLSCR2
Gene Name phospholipid scramblase 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000163746
Encoded Proteins
phospholipid scramblase 2
phospholipid scramblase 2
phospholipid scramblase 2
phospholipid scramblase 2
phospholipid scramblase 2
phospholipid scramblase 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the phospholipid scramblase family. Phospholipid scramblases are membrane proteins that mediate calcium-dependent, non-specific movement of plasma membrane phospholipids and phosphatidylserine exposure. The encoded protein contains a low affinity calcium binding motif and may play a role in blood coagulation and apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:146391421-146495991
Strand Reverse strand
Band q24
Transcripts
ENST00000336685 ENSP00000338707
ENST00000463633 ENSP00000419669
ENST00000497985 ENSP00000420132
ENST00000489015 ENSP00000418444
ENST00000474418
ENST00000613069 ENSP00000478902
ENST00000610787 ENSP00000478044
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005509 calcium ion binding
GO:0017128 phospholipid scramblase activity
Biological Process
GO:0017121 phospholipid scrambling
Cellular Component
GO:0005634 nucleus
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL C9J636
UniProt Splice Variant
Entrez Gene 57047
UniGene Hs.177968
RefSeq NM_001199978 NM_001199979 NM_020359
HUGO HGNC:16494
OMIM 607610
CCDS CCDS3134 CCDS56284 CCDS75029
HPRD 09621
IMGT
EMBL AC069528
GenPept
RNA Seq Atlas 57047