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BSNDP4 BSND pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 106481726, updated on 27-Nov-2019

Summary

Official Symbol
BSNDP4provided by HGNC
Official Full Name
BSND pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:51539
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See BSNDP4 in Genome Data Viewer
Location:
7p11.2
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (57638725..57639112)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene NCOR1 pseudogene 3 Neighboring gene abhydrolase domain containing 15 pseudogene Neighboring gene uncharacterized LOC105375302 Neighboring gene abhydrolase domain containing 15 pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000007.14 Chromosome 7 Reference GRCh38.p13 Primary Assembly

General gene information

Other Names

  • barttin CLCNK type accessory beta subunit pseudogene 4
  • barttin CLCNK-type chloride channel accessory beta subunit pseudogene 4

NCBI Reference Sequences (RefSeq)

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_043429.1 

    Range
    101..488
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    57638725..57639112
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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