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    RRAS2 RAS related 2 [ Homo sapiens (human) ]

    Gene ID: 22800, updated on 4-Jul-2021

    Summary

    Official Symbol
    RRAS2provided by HGNC
    Official Full Name
    RAS related 2provided by HGNC
    Primary source
    HGNC:HGNC:17271
    See related
    Ensembl:ENSG00000133818 MIM:600098
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    NS12; TC21
    Summary
    This gene encodes a member of the R-Ras subfamily of Ras-like small GTPases. The encoded protein associates with the plasma membrane and may function as a signal transducer. This protein may play an important role in activating signal transduction pathways that control cell proliferation. Mutations in this gene are associated with the growth of certain tumors. Pseudogenes of this gene are found on chromosomes 1 and 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]
    Expression
    Ubiquitous expression in small intestine (RPKM 12.4), kidney (RPKM 11.9) and 25 other tissues See more
    Orthologs
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    Genomic context

    See RRAS2 in Genome Data Viewer
    Location:
    11p15.2
    Exon count:
    9
    Annotation release Status Assembly Chr Location
    109.20210514 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (14277920..14364506, complement)
    105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (14299466..14386052, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2683 Neighboring gene spondin 1 Neighboring gene RNA, 5S ribosomal pseudogene 332 Neighboring gene Sharpr-MPRA regulatory region 800 Neighboring gene 60S ribosomal protein L13a-like

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.
    GeneReviews: Not available
    Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
    GeneReviews: Not available
    Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study.
    GeneReviews: Not available
    Noonan syndrome 12
    MedGen: C5231432 OMIM: 618624 GeneReviews: Not available
    Compare labs

    HIV-1 interactions

    Replication interactions

    Interaction Pubs
    Knockdown of related RAS viral (r-ras) oncogene homolog 2 (RRAS2) by shRNA library screening inhibits HIV-1 replication in cultured Jurkat T-cells PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Homology

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables GDP binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    enables GTP binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    enables GTPase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 

    General protein information

    Preferred Names
    ras-related protein R-Ras2
    Names
    ras-like protein TC21
    related RAS viral (r-ras) oncogene homolog 2
    teratocarcinoma oncogene
    NP_001096139.1
    NP_001170785.1
    NP_001170786.1
    NP_036382.2
    XP_016872852.1

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    Genomic

    1. NG_017058.1 RefSeqGene

      Range
      5001..91587
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001102669.2NP_001096139.1  ras-related protein R-Ras2 isoform b

      See identical proteins and their annotated locations for NP_001096139.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and 5' coding region, compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a. Both variants 2 and 4 encode the same isoform (b).
      Source sequence(s)
      AA873016, AC011084, AK309683, BG428983, BQ020351, BQ023701
      Consensus CDS
      CCDS44544.1
      UniProtKB/Swiss-Prot
      P62070
      Related
      ENSP00000434104.1, ENST00000526063.5
      Conserved Domains (1) summary
      cl38936
      Location:199
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    2. NM_001177314.2NP_001170785.1  ras-related protein R-Ras2 isoform c

      See identical proteins and their annotated locations for NP_001170785.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR and 5' coding region and initiates translation at an alternate start codon, compared to variant 1. The resulting isoform (b) is shorter and has a distinct N-terminus compared to isoform a.
      Source sequence(s)
      AA873016, AK300103, BQ020351, BQ023701
      Consensus CDS
      CCDS53603.1
      UniProtKB/Swiss-Prot
      P62070
      Related
      ENSP00000437547.1, ENST00000537760.5
      Conserved Domains (1) summary
      cl38936
      Location:2141
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    3. NM_001177315.1NP_001170786.1  ras-related protein R-Ras2 isoform b

      See identical proteins and their annotated locations for NP_001170786.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR and 5' coding region, compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a. Both variants 2 and 4 encode the same isoform (b).
      Source sequence(s)
      AA873016, AK309550, BQ020351, BQ023701
      Consensus CDS
      CCDS44544.1
      UniProtKB/Swiss-Prot
      P62070
      Related
      ENSP00000431954.1, ENST00000532814.5
      Conserved Domains (1) summary
      cl38936
      Location:199
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    4. NM_012250.6NP_036382.2  ras-related protein R-Ras2 isoform a

      See identical proteins and their annotated locations for NP_036382.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a).
      Source sequence(s)
      AA873016, AK309683, AK313976, BQ020351, BQ023701
      Consensus CDS
      CCDS7814.1
      UniProtKB/Swiss-Prot
      P62070
      Related
      ENSP00000256196.4, ENST00000256196.9
      Conserved Domains (1) summary
      cd04145
      Location:13176
      M_R_Ras_like; R-Ras2/TC21, M-Ras/R-Ras3

    RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

      Range
      14277920..14364506 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_017017363.1XP_016872852.1  ras-related protein R-Ras2 isoform X1

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