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    GPSM1 G protein signaling modulator 1 [ Homo sapiens (human) ]

    Gene ID: 26086, updated on 10-Dec-2024

    Summary

    Official Symbol
    GPSM1provided by HGNC
    Official Full Name
    G protein signaling modulator 1provided by HGNC
    Primary source
    HGNC:HGNC:17858
    See related
    Ensembl:ENSG00000160360 MIM:609491; AllianceGenome:HGNC:17858
    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
    AGS3
    Summary
    G-protein signaling modulators (GPSMs) play diverse functional roles through their interaction with G-protein subunits. This gene encodes a receptor-independent activator of G protein signaling, which is one of several factors that influence the basal activity of G-protein signaling systems. The protein contains seven tetratricopeptide repeats in its N-terminal half and four G-protein regulatory (GPR) motifs in its C-terminal half. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
    Expression
    Broad expression in brain (RPKM 5.1), testis (RPKM 4.7) and 24 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See GPSM1 in Genome Data Viewer
    Location:
    9q34.3
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (136327539..136359601)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (148556955..148588936)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (139221995..139254053)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene coiled-coil domain containing 187 Neighboring gene uncharacterized LOC124902308 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20506 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29304 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20507 Neighboring gene uncharacterized LOC26102 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139218370-139218998 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139218999-139219627 Neighboring gene Sharpr-MPRA regulatory region 1004 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139222157-139222686 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139222687-139223215 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:139227274-139227906 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29305 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139237289-139238070 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139238071-139238852 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139239387-139240040 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139240041-139240694 Neighboring gene Sharpr-MPRA regulatory region 3186 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20508 Neighboring gene uncharacterized LOC124902309 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20509 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20510 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:139258773-139259663 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:139259664-139260553 Neighboring gene Sharpr-MPRA regulatory region 3996 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:139268303-139269016 Neighboring gene DNL-type zinc finger Neighboring gene caspase recruitment domain family member 9 Neighboring gene small nuclear RNA activating complex polypeptide 4 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:139291906-139293105 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20511 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20512

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • DKFZp727I051

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables G-protein alpha-subunit binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables GDP-dissociation inhibitor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables GDP-dissociation inhibitor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    colocalizes_with Golgi membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    colocalizes_with cell cortex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol IEA
    Inferred from Electronic Annotation
    more info
     
    colocalizes_with endoplasmic reticulum membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of protein-containing complex IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    G-protein-signaling modulator 1
    Names
    G-protein signalling modulator 1 (AGS3-like, C. elegans)
    activator of G-protein signaling 3

    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_028088.2 RefSeqGene

      Range
      4996..37058
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001145638.3NP_001139110.2  G-protein-signaling modulator 1 isoform a

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a, also known as AGS3-FL).
      Source sequence(s)
      AY173053, BC009979, BC017257, BQ214873
      Consensus CDS
      CCDS48055.1
      UniProtKB/Swiss-Prot
      A9Z1X4, B1B0W3, Q86SR5, Q86YR5, Q969T1, Q9UFS8
      UniProtKB/TrEMBL
      A0A0A0MSK4
      Related
      ENSP00000392828.1, ENST00000440944.6
      Conserved Domains (6) summary
      smart00390
      Location:596618
      GoLoco; LGN motif, putative GEFs specific for G-alpha GTPases
      sd00006
      Location:250277
      TPR; TPR repeat [structural motif]
      pfam00515
      Location:250278
      TPR_1; Tetratricopeptide repeat
      pfam02188
      Location:496517
      GoLoco; GoLoco motif
      pfam13176
      Location:291325
      TPR_7; Tetratricopeptide repeat
      pfam13424
      Location:210281
      TPR_12; Tetratricopeptide repeat
    2. NM_001145639.2NP_001139111.1  G-protein-signaling modulator 1 isoform c

      See identical proteins and their annotated locations for NP_001139111.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR, lacks multiple 5' coding exons, and initiates translation at a downstream in-frame start codon, compared to variant 1. The encoded isoform (c, also known as AGS3-SHORT) is shorter at the N-terminus, compared to isoform a. Both variants 3 and 4 encode the same isoform (c).
      Source sequence(s)
      AY173053, BC017257, BI766024, BQ214873, BX649589
      Consensus CDS
      CCDS48056.1
      UniProtKB/Swiss-Prot
      Q86YR5
      Related
      ENSP00000390705.1, ENST00000429455.5
      Conserved Domains (1) summary
      pfam02188
      Location:122143
      GoLoco; GoLoco motif
    3. NM_001200003.2NP_001186932.1  G-protein-signaling modulator 1 isoform c

      See identical proteins and their annotated locations for NP_001186932.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR, lacks multiple 5' coding exons, and initiates translation at a downstream in-frame start codon, compared to variant 1. The encoded isoform (c, also known as AGS3-SHORT) is shorter at the N-terminus, compared to isoform a. Both variants 3 and 4 encode the same isoform (c).
      Source sequence(s)
      AL545250, AY173053, BC017257, BC048343, BX649589
      Consensus CDS
      CCDS48056.1
      UniProtKB/Swiss-Prot
      Q86YR5
      Related
      ENSP00000376673.1, ENST00000392944.5
      Conserved Domains (1) summary
      pfam02188
      Location:122143
      GoLoco; GoLoco motif
    4. NM_001412257.1NP_001399186.1  G-protein-signaling modulator 1 isoform d

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) uses the same exon combination as variant 2 but represents the allele encoded by the T2T-CHM13v2.0 genome assembly. The encoded isoform (d) has a frameshifted C-terminus compared to isoform b.
      Source sequence(s)
      CP068269
    5. NM_015597.6NP_056412.5  G-protein-signaling modulator 1 isoform b

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) lacks multiple 3' exons and its transcription extends past a splice site used in variant 1, resulting in a distinct 3' coding region and 3' UTR. This variant represents the allele encoded by the GRCh38 reference genome and encodes isoform b, which has a distinct C-terminus and is shorter than isoform a.
      Source sequence(s)
      AC174065, BC009979
      Consensus CDS
      CCDS6996.2
      UniProtKB/TrEMBL
      A0A087WVF5
      Related
      ENSP00000479405.1, ENST00000616132.4
      Conserved Domains (5) summary
      sd00006
      Location:250277
      TPR; TPR repeat [structural motif]
      pfam00515
      Location:250278
      TPR_1; Tetratricopeptide repeat
      pfam13176
      Location:291325
      TPR_7; Tetratricopeptide repeat
      pfam13424
      Location:210281
      TPR_12; Tetratricopeptide repeat
      cl14649
      Location:73160
      BRO1_Alix_like; Protein-interacting Bro1-like domain of mammalian Alix and related domains

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      136327539..136359601
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      148556955..148588936
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)