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BPIFB9P BPI fold containing family B member 9, pseudogene [ Homo sapiens (human) ]

Gene ID: 402016, updated on 23-Nov-2021

Summary

Official Symbol
BPIFB9Pprovided by HGNC
Official Full Name
BPI fold containing family B member 9, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:16109
See related
Ensembl:ENSG00000125997
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
C20orf115; dJ1187J4.2; dJ1187J4.3
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Genomic context

See BPIFB9P in Genome Data Viewer
Location:
20q11.21
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (33347120..33355044)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (31934926..31942850)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene BPI fold containing family B member 1 Neighboring gene uncharacterized LOC105372594 Neighboring gene BPI fold containing family B member 5, pseudogene Neighboring gene CDK5 regulatory subunit associated protein 1 Neighboring gene VISTA enhancer hs2173 Neighboring gene syntrophin alpha 1

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_029803.1 

    Range
    101..8025
    Download
    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_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    33347120..33355044
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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