U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

MIR663AHG MIR663A host gene [ Homo sapiens (human) ]

Gene ID: 284801, updated on 13-May-2022

Summary

Official Symbol
MIR663AHGprovided by HGNC
Official Full Name
MIR663A host geneprovided by HGNC
Primary source
HGNC:HGNC:27662
See related
Ensembl:ENSG00000227195 AllianceGenome:HGNC:27662
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
Restricted expression toward testis (RPKM 13.0) See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See MIR663AHG in Genome Data Viewer
Location:
20p11.1
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (26187019..26209233, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (26190769..26212983, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (26167655..26189869, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene family with sequence similarity 182 member A Neighboring gene uncharacterized LOC124904967 Neighboring gene BSND pseudogene 3 Neighboring gene NCOR1 pseudogene 1 Neighboring gene microRNA 663a Neighboring gene FSHD region gene 1 family member C, pseudogene

Genomic regions, transcripts, and products

Expression

  • 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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_040095.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL121904, BC036544
    Related
    ENST00000427348.5

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    26187019..26209233 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    26190769..26212983 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)