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BTBD7P1 BTB domain containing 7 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 441548, updated on 13-May-2022

Summary

Official Symbol
BTBD7P1provided by HGNC
Official Full Name
BTB domain containing 7 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:44875
See related
AllianceGenome:HGNC:44875
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 BTBD7P1 in Genome Data Viewer
Location:
10p13
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (13156683..13158243, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (13171306..13172868, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (13198683..13200243, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene 10p13 OPTN distal Alu-mediated recombination region Neighboring gene 10p13 OPTN proximal Alu-mediated recombination region Neighboring gene optineurin Neighboring gene ribosomal protein L36a pseudogene 36 Neighboring gene minichromosome maintenance 10 replication initiation factor Neighboring gene Sharpr-MPRA regulatory region 2216

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_022140.2 

    Range
    94..1654
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    13156683..13158243 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    13171306..13172868 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)