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MSTO2P misato family member 2, pseudogene [ Homo sapiens (human) ]

Gene ID: 100129405, updated on 17-Sep-2024

Summary

Official Symbol
MSTO2Pprovided by HGNC
Official Full Name
misato family member 2, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:26329
See related
AllianceGenome:HGNC:26329
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MSTO2
Expression
Ubiquitous expression in testis (RPKM 23.7), thyroid (RPKM 14.3) and 25 other tissues See more
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Genomic context

See MSTO2P in Genome Data Viewer
Location:
1q22
Exon count:
13
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (155745768..155750688)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (154884637..154889558)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (155715559..155720479)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene YY1 associated protein 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:155657971-155658605 Neighboring gene translation initiation factor IF-2-like Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1818 Neighboring gene uncharacterized LOC124904431 Neighboring gene death associated protein 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1819 Neighboring gene gon-4 like Neighboring gene small Cajal body-specific RNA 26B Neighboring gene Sharpr-MPRA regulatory region 7686 Neighboring gene proteasome 26S subunit, non-ATPase 7 pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues 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

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_024117.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC099909, BF508805, CX784525, DC387604

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    155745768..155750688
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    154884637..154889558
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)