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BCAS2P2 BCAS2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100421045, updated on 23-Nov-2021

Summary

Official Symbol
BCAS2P2provided by HGNC
Official Full Name
BCAS2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39595
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

See BCAS2P2 in Genome Data Viewer
Location:
1p21.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (100392836..100393658, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (100858392..100859214, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 14415 Neighboring gene RNA 3'-terminal phosphate cyclase Neighboring gene chromosome 5 open reading frame 15 pseudogene Neighboring gene cell division cycle 14A Neighboring gene uncharacterized LOC105379827 Neighboring gene Sharpr-MPRA regulatory region 2368

Genomic regions, transcripts, and products

General gene information

Other Names

  • BCAS2, pre-mRNA processing factor pseudogene 2
  • breast carcinoma amplified sequence 2 pseudogene 2

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_026962.2 

    Range
    101..923
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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_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    100392836..100393658 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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