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    RGS20 regulator of G protein signaling 20 [ Homo sapiens (human) ]

    Gene ID: 8601, updated on 27-Nov-2024

    Summary

    Official Symbol
    RGS20provided by HGNC
    Official Full Name
    regulator of G protein signaling 20provided by HGNC
    Primary source
    HGNC:HGNC:14600
    See related
    Ensembl:ENSG00000147509 MIM:607193; AllianceGenome:HGNC:14600
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    RGSZ1; ZGAP1; gz-GAP; g(z)GAP
    Summary
    The protein encoded by this gene belongs to the family of regulator of G protein signaling (RGS) proteins, which are regulatory and structural components of G protein-coupled receptor complexes. RGS proteins inhibit signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound forms. This protein selectively binds to G(z)-alpha and G(alpha)-i2 subunits, and regulates their signaling activities. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
    Expression
    Biased expression in brain (RPKM 2.5), thyroid (RPKM 0.6) and 3 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See RGS20 in Genome Data Viewer
    Location:
    8q11.23
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (53851795..53959303)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (54229188..54336699)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (54764355..54871863)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene chromosome 5 open reading frame 13 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27358 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:54640179-54641378 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27359 Neighboring gene ATPase H+ transporting V1 subunit H Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27360 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19193 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27361 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:54789287-54789787 Neighboring gene Sharpr-MPRA regulatory region 5984 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19194 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19195 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:54793331-54793962 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:54793963-54794594 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27362 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27363 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27364 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27365 Neighboring gene RPS27A pseudogene 13 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27366 Neighboring gene RNA, U6 small nuclear 1331, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:54856969-54858168 Neighboring gene LYPLA1-TCEA1 readthrough Neighboring gene ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae) pseudogene Neighboring gene transcription elongation factor A1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19197 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19198 Neighboring gene Uncharacterized LOC133039971 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:54934747-54935540 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:54935541-54936332 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:54942814-54943544 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:54943545-54944276 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:54958280-54958473 Neighboring gene lysophospholipase 1

    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?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables GTPase activator activity TAS
    Traceable Author Statement
    more info
    PubMed 
    enables GTPase activity TAS
    Traceable Author Statement
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    located_in nucleus IEA
    Inferred from Electronic Annotation
    more info
     
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     
    located_in trans-Golgi network IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 

    General protein information

    Preferred Names
    regulator of G-protein signaling 20
    Names
    gz-selective GTPase-activating protein
    regulator of G-protein signaling Z1
    regulator of G-protein signalling 20
    regulator of Gz-selective protein signaling 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.

    mRNA and Protein(s)

    1. NM_001286673.2NP_001273602.1  regulator of G-protein signaling 20 isoform c

      See identical proteins and their annotated locations for NP_001273602.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) lacks an in-frame exon in the 5' coding region comapred to variant 1. The encoded isoform (c) is shorter than isoform a.
      Source sequence(s)
      AC100821, AC113194, AF366054
      Consensus CDS
      CCDS69482.1
      UniProtKB/Swiss-Prot
      O76081
      Related
      ENSP00000344630.6, ENST00000344277.10
      Conserved Domains (1) summary
      cd08746
      Location:106261
      RGS_RGS20; Regulator of G protein signaling (RGS) domain found in the RGS20 protein
    2. NM_001286674.2NP_001273603.1  regulator of G-protein signaling 20 isoform d

      See identical proteins and their annotated locations for NP_001273603.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) lacks three in-frame exons in the central coding region which results in the use of an alternate start codon compared to variant 1. The encoded isoform (d) is shorter and has a distinct N-terminus compared to isoform a.
      Source sequence(s)
      AC100821, AC113194, AF366056
      UniProtKB/Swiss-Prot
      O76081
      Conserved Domains (1) summary
      cl02565
      Location:12140
      RGS; Regulator of G protein signaling (RGS) domain superfamily
    3. NM_001286675.2NP_001273604.1  regulator of G-protein signaling 20 isoform e

      See identical proteins and their annotated locations for NP_001273604.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) lacks two in-frame exons in the central coding region which results in the use of an alternate start codon compared to variant 1. The encoded isoform (e) is shorter than isoform a.
      Source sequence(s)
      AC100821, AC113194, AF366055
      UniProtKB/Swiss-Prot
      O76081
      Conserved Domains (1) summary
      cl02565
      Location:11168
      RGS; Regulator of G protein signaling (RGS) domain superfamily
    4. NM_003702.5NP_003693.2  regulator of G-protein signaling 20 isoform b

      See identical proteins and their annotated locations for NP_003693.2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and 5' coding region compared to variant 1. The resulting isoform (b) has a shorter and distinct N-terminus compared to isoform a.
      Source sequence(s)
      AC100821, AC113194
      Consensus CDS
      CCDS6156.1
      UniProtKB/TrEMBL
      H9NIM5
      Related
      ENSP00000276500.4, ENST00000276500.5
      Conserved Domains (1) summary
      cd08746
      Location:74229
      RGS_RGS20; Regulator of G protein signaling (RGS) domain found in the RGS20 protein
    5. NM_170587.4NP_733466.1  regulator of G-protein signaling 20 isoform a

      See identical proteins and their annotated locations for NP_733466.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a).
      Source sequence(s)
      AC100821, AC113194, AY046538
      Consensus CDS
      CCDS6155.1
      UniProtKB/Swiss-Prot
      O76081, Q96BG9
      Related
      ENSP00000297313.3, ENST00000297313.8
      Conserved Domains (1) summary
      cd08746
      Location:221376
      RGS_RGS20; Regulator of G protein signaling (RGS) domain found in the RGS20 protein

    RNA

    1. NR_104578.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) uses an alternate exon structure compared to variant 1 but does share exon structure with variant 2. This variant is represented as non-coding because it lacks the entire coding region found in variant 1.
      Source sequence(s)
      BC054867
      Related
      ENST00000523064.1
    2. NR_104579.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7) has multiple differences compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AC100821, AC113194, AK094503
      Related
      ENST00000522225.5

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      53851795..53959303
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      54229188..54336699
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)