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BAG1P1 BAG1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 392442, updated on 10-Oct-2023

Summary

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Official Symbol
BAG1P1provided by HGNC
Official Full Name
BAG1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54932
See related
AllianceGenome:HGNC:54932
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
Xp11.4
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (38479249..38481055)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (37882849..37884655)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (38338502..38340308)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene retinitis pigmentosa GTPase regulator Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20735 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:38191193-38191385 Neighboring gene HNF4 motif-containing MPRA enhancer 122 Neighboring gene ornithine transcarbamylase Neighboring gene CRIPTO pseudogene 1 Neighboring gene ferritin light chain pseudogene 16 Neighboring gene UBTF like 11 (pseudogene)

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

Other Names

  • BAG cochaperone 1 pseudogene
  • BCL2 associated athanogene 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.

Genomic

  1. NG_016482.2 

    Range
    101..1907
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    38479249..38481055
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    37882849..37884655
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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