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INE1 inactivation escape 1 [ Homo sapiens (human) ]

Gene ID: 8552, updated on 1-Jun-2020

Summary

Official Symbol
INE1provided by HGNC
Official Full Name
inactivation escape 1provided by HGNC
Primary source
HGNC:HGNC:6060
See related
Ensembl:ENSG00000224975 MIM:300164
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NCRNA00010
Summary
X chromosome inactivation provides dosage compensation for the expression level of X-linked genes from the single X in males and the two in females. This X chromosome gene is intronless and was identified because its transcription escapes X inactivation in females. This gene does not make a protein.[provided by RefSeq, May 2010]

Genomic context

See INE1 in Genome Data Viewer
Location:
Xp11.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (47204848..47205861)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (47064247..47065260)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene NADH:ubiquinone oxidoreductase subunit B11 Neighboring gene RNA binding motif protein 10 Neighboring gene ITPK1 pseudogene 1 Neighboring gene ubiquitin like modifier activating enzyme 1 Neighboring gene uncharacterized LOC105373194 Neighboring gene cyclin dependent kinase 16 Neighboring gene ubiquitin specific peptidase 11

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • inactivation escape 1 (non-protein coding)

Clone Names

  • MGC97326, MGC97335, MGC97386

NCBI Reference Sequences (RefSeq)

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.

Genomic

  1. NG_021353.1 RefSeqGene

    Range
    5001..6014
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_024616.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC069772, DA439607, Y10696
    Related
    ENST00000456273.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    47204848..47205861
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_003669.1: Suppressed sequence

    Description
    NM_003669.1: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
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