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    INSIG1 insulin induced gene 1 [ Homo sapiens (human) ]

    Gene ID: 3638, updated on 10-Dec-2024

    Summary

    Official Symbol
    INSIG1provided by HGNC
    Official Full Name
    insulin induced gene 1provided by HGNC
    Primary source
    HGNC:HGNC:6083
    See related
    Ensembl:ENSG00000186480 MIM:602055; AllianceGenome:HGNC:6083
    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
    CL6
    Summary
    This gene encodes an endoplasmic reticulum membrane protein that regulates cholesterol metabolism, lipogenesis, and glucose homeostasis. The encoded protein has six transmembrane helices which contain an effector protein binding site. It binds the sterol-sensing domains of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP) and 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), and is essential for the sterol-mediated trafficking of these two proteins. It promotes the endoplasmic reticulum retention of SCAP and the ubiquitin-mediated degradation of HMG-CoA reductase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]
    Expression
    Ubiquitous expression in liver (RPKM 104.0), fat (RPKM 35.8) and 24 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See INSIG1 in Genome Data Viewer
    Location:
    7q36.3
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (155297878..155310235)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (156473431..156485788)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (155089588..155101945)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375588 Neighboring gene uncharacterized LOC105375589 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:155061691-155062191 Neighboring gene CRISPRi-validated cis-regulatory element chr7.5881 Neighboring gene INSIG1 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26895 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18844 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26896 Neighboring gene uncharacterized LOC105375592 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18845 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:155141824-155142690 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:155142691-155143555 Neighboring gene uncharacterized LOC105375593 Neighboring gene B cell acute lymphoblastic leukemia expressed Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:155164583-155165094 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18846 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:155166119-155166630 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:155170781-155171281 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:155174017-155174828 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:155174829-155175640 Neighboring gene long intergenic non-protein coding RNA 3010

    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?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide interaction study of smoking and bladder cancer risk.
    EBI GWAS Catalog
    PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Vif vif HIV-1 Vif upregulates the expression of insulin induced gene 1 (INSIG1) in Vif-expression 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

    Clone Names

    • MGC1405

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables oxysterol binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables protein sequestering activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in SREBP signaling pathway IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in SREBP signaling pathway IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in SREBP-SCAP complex retention in endoplasmic reticulum IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in SREBP-SCAP complex retention in endoplasmic reticulum IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in cellular response to insulin stimulus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cellular response to sterol IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in cholesterol biosynthetic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cholesterol biosynthetic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in cholesterol homeostasis IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in cranial suture morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in inner ear morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in middle ear morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in negative regulation of cargo loading into COPII-coated vesicle IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in negative regulation of cholesterol biosynthetic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of fat cell differentiation IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in negative regulation of fatty acid biosynthetic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in negative regulation of protein exit from endoplasmic reticulum IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in roof of mouth development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in triglyceride metabolic process IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    part_of SREBP-SCAP-Insig complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of SREBP-SCAP-Insig complex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in endoplasmic reticulum IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in endoplasmic reticulum IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in endoplasmic reticulum membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum membrane TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    insulin-induced gene 1 protein
    Names
    INSIG-1 membrane protein

    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_001346590.2NP_001333519.1  insulin-induced gene 1 protein isoform 4

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) contains an alternate exon in the 3' coding region which results in a frameshift, compared to variant 1. The encoded isoform (4) has a distinct C-terminus and is longer than isoform 1. Variants 4 and 5 encode the same protein.
      Source sequence(s)
      AC231970, AK095977, BC001880, BM995866, DA590854
      UniProtKB/TrEMBL
      A0A2Z2EKN2, A4D2M9
    2. NM_001346591.2NP_001333520.1  insulin-induced gene 1 protein isoform 4

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) differs in the 5' UTR and contains an alternate exon in the 3' coding region which results in a frameshift, compared to variant 1. The encoded isoform (4) has a distinct C-terminus and is longer than isoform 1. Variants 4 and 5 encode the same protein.
      Source sequence(s)
      AC231970, AK095977, BC001880, BM995866, DA590854, DB034358, HY070608
      UniProtKB/TrEMBL
      A0A2Z2EKN2, A4D2M9
    3. NM_001346592.2NP_001333521.1  insulin-induced gene 1 protein isoform 1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6) differs in the 5' UTR, compared to variant 1. Variants 1 and 6 encode the same protein.
      Source sequence(s)
      AC144652, AC231970, AK095977, BC001880, BM995866, BT007227, HY070608
      Consensus CDS
      CCDS5938.1
      UniProtKB/Swiss-Prot
      A4D2N1, A8K6L0, O15503, Q53XW8, Q9BUV5
      UniProtKB/TrEMBL
      A0A2Z2EKN2
      Conserved Domains (1) summary
      pfam07281
      Location:87267
      INSIG; Insulin-induced protein (INSIG)
    4. NM_001346593.2NP_001333522.1  insulin-induced gene 1 protein isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7) differs in the 5' UTR, and lacks two exons in the coding region which results in a frameshift and an early stop codon, compared to variant 1. The encoded isoform (3) has a distinct C-terminus and is shorter than isoform 1. Variants 3 and 7 encode the same protein.
      Source sequence(s)
      AC144652, AC231970, AK095977, BC001880, BM995866, BT007227, BU177114, HY070608
      Consensus CDS
      CCDS5939.1
      UniProtKB/Swiss-Prot
      O15503
    5. NM_001346594.2NP_001333523.1  insulin-induced gene 1 protein isoform 5

      Status: REVIEWED

      Description
      Transcript Variant: This variant (8) uses an alternate in-frame splice site in the coding region, compared to variant 1. The encoded isoform (5) is longer than isoform 1.
      Source sequence(s)
      AC144652, AC231970, AK095977, BC001880, BI460711, BM995866
      UniProtKB/TrEMBL
      A0A2Z2EKN2
    6. NM_005542.6NP_005533.2  insulin-induced gene 1 protein isoform 1

      See identical proteins and their annotated locations for NP_005533.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes isoform 1. Variants 1 and 6 encode the same protein.
      Source sequence(s)
      AC231970, AK095977, BC001880, BM995866
      Consensus CDS
      CCDS5938.1
      UniProtKB/Swiss-Prot
      A4D2N1, A8K6L0, O15503, Q53XW8, Q9BUV5
      UniProtKB/TrEMBL
      A0A2Z2EKN2
      Related
      ENSP00000344741.4, ENST00000340368.9
      Conserved Domains (1) summary
      pfam07281
      Location:87267
      INSIG; Insulin-induced protein (INSIG)
    7. NM_198336.4NP_938150.2  insulin-induced gene 1 protein isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) has multiple coding region differences, compared to variant 1, one of which results in a frameshift. The encoded isoform (2) has a distinct C-terminus and is shorter than isoform 1.
      Source sequence(s)
      AC144652, AC231970, AK095977, BC001880, BM995866, DA590854, DA775024
      Consensus CDS
      CCDS94240.1
      UniProtKB/TrEMBL
      F5H6P3
      Related
      ENSP00000340010.4, ENST00000344756.8
      Conserved Domains (1) summary
      pfam07281
      Location:25115
      INSIG; Insulin-induced protein (INSIG)
    8. NM_198337.4NP_938151.1  insulin-induced gene 1 protein isoform 3

      See identical proteins and their annotated locations for NP_938151.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) lacks two exons in the coding region which results in a frameshift and an early stop codon, compared to variant 1. The encoded isoform (3) has a distinct C-terminus and is shorter than isoform 1. Variants 3 and 7 encode the same protein.
      Source sequence(s)
      AC231970, AK095977, BC001880, BM995866, DA738378, DN996424
      Consensus CDS
      CCDS5939.1
      UniProtKB/Swiss-Prot
      O15503
      Related
      ENSP00000344035.5, ENST00000342407.5

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      155297878..155310235
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      156473431..156485788
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)