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IMPA1P1 inositol monophosphatase 1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 650747, updated on 10-Oct-2023

Summary

Official Symbol
IMPA1P1provided by HGNC
Official Full Name
inositol monophosphatase 1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:33956
See related
AllianceGenome:HGNC:33956
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
IMPA1P
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Genomic context

Location:
8q21.13
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (81603884..81631277, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (82035475..82062868, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (82516119..82543512, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101927118 Neighboring gene ferritin heavy chain 1 pseudogene 11 Neighboring gene fatty acid binding protein 12 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:82512159-82512934 Neighboring gene Sharpr-MPRA regulatory region 11945 Neighboring gene NIPA2 pseudogene 4 Neighboring gene ribosomal protein S26 pseudogene 34 Neighboring gene SLC10A5 pseudogene 1 Neighboring gene inositol monophosphatase 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:82598306-82598806

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

General gene information

Markers

Other Names

  • inositol(myo)-1(or 4)-monophosphatase 1 pseudogene

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_146081.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC090255

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    81603884..81631277 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    82035475..82062868 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_007612.3: Suppressed sequence

    Description
    NG_007612.3: This RefSeq was removed because it is now thought that this locus is transcribed.