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MIR222HG miR222/221 cluster host gene [ Homo sapiens (human) ]

Gene ID: 104457406, updated on 23-Nov-2021

Summary

Official Symbol
MIR222HGprovided by HGNC
Official Full Name
miR222/221 cluster host geneprovided by HGNC
Primary source
HGNC:HGNC:49555
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
Lnc-Ang362
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Genomic context

See MIR222HG in Genome Data Viewer
Location:
Xp11.3
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (45745214..45770267, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (45604642..45629670, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene keratin 8 pseudogene 14 Neighboring gene MFF pseudogene 3 Neighboring gene microRNA 221 Neighboring gene microRNA 222 Neighboring gene long intergenic non-protein coding RNA 2595 Neighboring gene SRSF6 pseudogene 1

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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_170290.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC234772

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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    45745214..45770267 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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