U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

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

Gene ID: 3638, updated on 5-Mar-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

Location:
7q36.3
Exon count:
7
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (155297878..155310235)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (156473431..156485788)
105.20220307 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: 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

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 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 negative regulation of steroid biosynthetic process IEA
Inferred from Electronic Annotation
more info
 
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_2023_10

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)