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BTF3P13 basic transcription factor 3 pseudogene 13 [ Homo sapiens (human) ]

Gene ID: 132556, updated on 12-Oct-2019

Summary

Official Symbol
BTF3P13provided by HGNC
Official Full Name
basic transcription factor 3 pseudogene 13provided by HGNC
Primary source
HGNC:HGNC:1128
See related
MIM:603739
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
BTF3L3; HUMBTFD
Summary
This locus defines a putative member of the BTF3 family of transcription factors and is thought to represent a pseudogene. [provided by RefSeq, Jul 2008]

Genomic context

See BTF3P13 in Genome Data Viewer
Location:
4q23
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 4 NC_000004.12 (98740625..98741496)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (99661776..99662647)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC112267901 Neighboring gene uncharacterized LOC105377342 Neighboring gene mitochondrial import receptor subunit TOM7 homolog pseudogene Neighboring gene uncharacterized LOC105377343 Neighboring gene eukaryotic translation initiation factor 4E Neighboring gene tubulin folding cofactor A pseudogene 3

Genomic regions, transcripts, and products

General gene information

Other Names

  • basic transcription factor 3, like 3
  • basic transcription factor 3, pseudogene
  • basic transcription factor 3-like 3, pseudogene
  • lambda h33

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_006070.4 

    Range
    101..972
    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_000004.12 Reference GRCh38.p13 Primary Assembly

    Range
    98740625..98741496
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001210.2: Suppressed sequence

    Description
    NM_001210.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
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