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PGBP pepsinogen B, pseudogene [ Homo sapiens (human) ]

Gene ID: 441897, updated on 26-Oct-2024

Summary

Official Symbol
PGBPprovided by HGNC
Official Full Name
pepsinogen B, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:39503
See related
AllianceGenome:HGNC:39503
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
PGCP1
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See PGBP in Genome Data Viewer
Location:
1p13.2
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (111384519..111389851, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (111399203..111404533, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (111927141..111932473, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378904 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr1:111906935-111908134 Neighboring gene HIG1 hypoxia inducible domain family member 1A pseudogene 12 Neighboring gene uncharacterized LOC124904309 Neighboring gene NANOG hESC enhancer GRCh37_chr1:111958109-111958610 Neighboring gene oviductal glycoprotein 1 Neighboring gene UBE2F pseudogene 3

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

General gene information

Markers

Other Names

  • progastricsin (pepsinogen C) pseudogene 1
  • progastricsin pseudogene 1

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_029429.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL356387, DV080281, DV080282

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
    111384519..111389851 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    111399203..111404533 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)