U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

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

Gene ID: 104457406, updated on 10-Mar-2024

Summary

Official Symbol
MIR222HGprovided by HGNC
Official Full Name
miR222/221 cluster host geneprovided by HGNC
Primary source
HGNC:HGNC:49555
See related
AllianceGenome: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
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See MIR222HG in Genome Data Viewer
Location:
Xp11.3
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (45745214..45770267, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (45154669..45179732, complement)
105.20220307 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 Sharpr-MPRA regulatory region 11747 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29569 Neighboring gene Sharpr-MPRA regulatory region 14703 Neighboring gene MFF pseudogene 3 Neighboring gene microRNA 221 Neighboring gene microRNA 222 Neighboring gene NANOG hESC enhancer GRCh37_chrX:45645628-45646174 Neighboring gene NANOG hESC enhancer GRCh37_chrX:45661291-45661869 Neighboring gene MED14-independent group 3 enhancer GRCh37_chrX:45662536-45663735 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20789 Neighboring gene long intergenic non-protein coding RNA 2595 Neighboring gene small nucleolar RNA SNORD77

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    45154669..45179732 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)