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INSIG1-DT INSIG1 divergent transcript [ Homo sapiens (human) ]

Gene ID: 105375591, updated on 9-Jun-2025
Official Symbol
INSIG1-DTprovided by HGNC
Official Full Name
INSIG1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:55155
See related
Ensembl:ENSG00000273117 AllianceGenome:HGNC:55155
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Broad expression in brain (RPKM 1.9), testis (RPKM 1.8) and 25 other tissues See more
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See INSIG1-DT in Genome Data Viewer
Location:
7q36.3
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (155288596..155298980, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (156464151..156474533, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (155080306..155090690, complement)

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 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 insulin induced gene 1 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

Go to nucleotide: Graphics FASTA GenBank

  • 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

GeneRIFs: Gene References Into Functions

Review eQTL and phenotype association data in this region using PheGenI

See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

Clone Names

  • AC144652.1

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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.

RNA

  1. NR_183446.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC144652
    Related
    ENST00000743985.1

  2. NR_183447.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC144652

  3. NR_183448.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC144652

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
    155288596..155298980 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    156464151..156474533 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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