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Plek2 pleckstrin 2 [ Rattus norvegicus (Norway rat) ]

Gene ID: 314260, updated on 11-Apr-2024

Summary

Official Symbol
Plek2provided by RGD
Official Full Name
pleckstrin 2provided by RGD
Primary source
RGD:1305786
See related
Ensembl:ENSRNOG00000010098 AllianceGenome:RGD:1305786
Gene type
protein coding
RefSeq status
PROVISIONAL
Organism
Rattus norvegicus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Summary
Predicted to enable phosphatidylinositol-3,4-bisphosphate binding activity; phosphatidylinositol-3,5-bisphosphate binding activity; and phosphatidylinositol-3-phosphate binding activity. Predicted to be involved in actin cytoskeleton reorganization and positive regulation of plasma membrane bounded cell projection assembly. Predicted to act upstream of or within actin cytoskeleton organization and positive regulation of cell projection organization. Predicted to be located in membrane. Predicted to be active in plasma membrane. Orthologous to human PLEK2 (pleckstrin 2). [provided by Alliance of Genome Resources, Apr 2022]
Expression
Biased expression in Spleen (RPKM 61.3), Kidney (RPKM 15.9) and 5 other tissues See more
Orthologs
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Genomic context

Location:
6q24
Exon count:
9
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCr8 (GCF_036323735.1) 6 NC_086024.1 (103434156..103452457, complement)
RS_2023_06 previous assembly mRatBN7.2 (GCF_015227675.2) 6 NC_051341.1 (97700123..97719417, complement)
106 previous assembly Rnor_6.0 (GCF_000001895.5) 6 NC_005105.4 (102076736..102095002, complement)

Chromosome 6 - NC_086024.1Genomic Context describing neighboring genes Neighboring gene ATPase H+ transporting V1 subunit D Neighboring gene eukaryotic translation initiation factor 2 subunit alpha Neighboring gene uncharacterized LOC102547797 Neighboring gene transmembrane protein 229B

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001114180.1NP_001107652.1  pleckstrin-2

    See identical proteins and their annotated locations for NP_001107652.1

    Status: PROVISIONAL

    Source sequence(s)
    CH473947
    UniProtKB/TrEMBL
    A6HCF5, D4ACD5
    Related
    ENSRNOP00000014125.3, ENSRNOT00000014125.6
    Conserved Domains (4) summary
    cd04444
    Location:128236
    DEP_PLEK2; DEP (Dishevelled, Egl-10, and Pleckstrin) domain found in pleckstrin 2-like proteins. Pleckstrin 2 is found in a wide variety of cell types, which suggest a more general role in signaling than pleckstrin 1. Pleckstrin-like proteins contain a central ...
    cd13301
    Location:3113
    PH1_Pleckstrin_2; Pleckstrin 2 Pleckstrin homology (PH) domain, repeat 1
    cd13302
    Location:243353
    PH2_Pleckstrin_2; Pleckstrin 2 Pleckstrin homology (PH) domain, repeat 2
    pfam00169
    Location:595
    PH; PH domain

RefSeqs of Annotated Genomes: GCF_036323735.1-RS_2024_02

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCr8

Genomic

  1. NC_086024.1 Reference GRCr8

    Range
    103434156..103452457 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_063261929.1XP_063117999.1  pleckstrin-2 isoform X1

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001108035.1: Suppressed sequence

    Description
    NM_001108035.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.