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

Gene ID: 105375591, updated on 23-Nov-2021

Summary

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Official Symbol
INSIG1-DTprovided by HGNC
Official Full Name
INSIG1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:55155
Gene type
ncRNA
RefSeq status
MODEL
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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Genomic context

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See INSIG1-DT in Genome Data Viewer
Location:
7q36.3
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (155288609..155297724, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375587 Neighboring gene uncharacterized LOC105375588 Neighboring gene uncharacterized LOC105375589 Neighboring gene CRISPRi-validated cis-regulatory element chr7.5881 Neighboring gene insulin induced gene 1 Neighboring gene uncharacterized LOC105375592

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000007.14 Chromosome 7 Reference GRCh38.p13 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

Genotypes

General gene information

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Clone Names

  • AC144652.1

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    155288609..155297724 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_928234.3 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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