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ITFG2-AS1 ITFG2 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 283440, updated on 23-Nov-2021

Summary

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Official Symbol
ITFG2-AS1provided by HGNC
Official Full Name
ITFG2 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:53128
See related
Ensembl:ENSG00000256150 Ensembl:ENSG00000258325
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
Low expression observed in reference dataset See more
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Genomic context

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See ITFG2-AS1 in Genome Data Viewer
Location:
12p13.33
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (2742626..2812924, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (2851792..2922090, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene calcium voltage-gated channel subunit alpha1 C Neighboring gene CACNA1C antisense RNA 2 Neighboring gene CACNA1C antisense RNA 1 Neighboring gene calcium voltage-gated channel subunit alpha1 C pseudogene Neighboring gene long intergenic non-protein coding RNA 2371 Neighboring gene IQ motif and Sec7 domain 3 pseudogene 1 Neighboring gene ribosomal protein L23a pseudogene 14 Neighboring gene chromobox 3 pseudogene 4 Neighboring gene FKBP prolyl isomerase 4 Neighboring gene integrin alpha FG-GAP repeat containing 2 Neighboring gene nuclear receptor interacting protein 2 Neighboring gene testis expressed 52

Genomic regions, transcripts, and products

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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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Related articles in PubMed

  1. Identification of antisense long noncoding RNAs that function as SINEUPs in human cells. Schein A, et al. Sci Rep, 2016 Sep 20. PMID 27646849, Free PMC Article
  2. cDNA microarray analysis of altered gene expression in Ara-C-treated leukemia cells. Takagaki K, et al. Biochem Biophys Res Commun, 2003 Sep 19. PMID 12951057
  3. Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. Lowe JK, et al. PLoS Genet, 2009 Feb. PMID 19197348, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

NCBI Reference Sequences (RefSeq)

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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_146317.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC005841, AC092471, BI856634
    Related
    ENST00000540093.2

  2. NR_146318.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AA977050, AC005841, BP430004
    Related
    ENST00000547794.2

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    2742626..2812924 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_033958.1: Suppressed sequence

    Description
    NR_033958.1: This RefSeq was removed because there is currently insufficient evidence that this transcript is complete.
Nucleotide Protein
Heading Accession and Version

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