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BORCS8P1 BORCS8 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100128109, updated on 23-Nov-2021

Summary

Official Symbol
BORCS8P1provided by HGNC
Official Full Name
BORCS8 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:49883
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MEF2BNBP1
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Genomic context

See BORCS8P1 in Genome Data Viewer
Location:
12p12.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (19107743..19108196, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (19260677..19261130, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984527 Neighboring gene ribosomal protein L7 pseudogene 6 Neighboring gene pleckstrin homology domain containing A5 Neighboring gene RNA, 7SL, cytoplasmic 459, pseudogene Neighboring gene uncharacterized LOC112268092 Neighboring gene RNA, 7SL, cytoplasmic 67, pseudogene

Genomic regions, transcripts, and products

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_011617.3 

    Range
    101..554
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    19107743..19108196 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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