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MPHOSPH10P1 MPHOSPH10 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 643802, updated on 13-May-2022

Summary

Official Symbol
MPHOSPH10P1provided by HGNC
Official Full Name
MPHOSPH10 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:55687
See related
Ensembl:ENSG00000260078 AllianceGenome:HGNC:55687
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in bone marrow (RPKM 3.5), spleen (RPKM 1.2) and 5 other tissues See more
Orthologs
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Genomic context

See MPHOSPH10P1 in Genome Data Viewer
Location:
16q12.2
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (53365391..53370993, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (59163205..59168821, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (53399303..53404905, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene RNA, 5S ribosomal pseudogene 427 Neighboring gene golgin subfamily A member 6-like protein 1 Neighboring gene uncharacterized LOC102723373 Neighboring gene RNA, U6 small nuclear 1153, pseudogene Neighboring gene RB transcriptional corepressor like 2

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

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_171055.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC007342
    Related
    ENST00000693362.1

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    53365391..53370993 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    59163205..59168821 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001207030.1: Suppressed sequence

    Description
    NM_001207030.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.
  2. NM_001347693.1: Suppressed sequence

    Description
    NM_001347693.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.