U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

BTF3P11 basic transcription factor 3 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 690, updated on 13-May-2022

Summary

Official Symbol
BTF3P11provided by HGNC
Official Full Name
basic transcription factor 3 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:1126
See related
MIM:602543; AllianceGenome:HGNC:1126
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
OPG; OCIF; BRF3L1; BTF3L1; HUMBTFB; TNFRSF11B
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See BTF3P11 in Genome Data Viewer
Location:
13q22.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (76928451..76929090)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (76152120..76152759)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (77502585..77503224)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984587 Neighboring gene potassium channel tetramerization domain containing 12 Neighboring gene uncharacterized LOC105370269 Neighboring gene aconitate decarboxylase 1 Neighboring gene ribosomal protein L7 pseudogene 44

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD.
EBI GWAS Catalog
Multiple genetic loci for bone mineral density and fractures.
EBI GWAS Catalog
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.
EBI GWAS Catalog

General gene information

Markers

Other Names

  • BTF3 homologue
  • basic transcription factor 3, like 1
  • basic transcription factor 3-like 1, pseudogene
  • lambda h27A

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

RNA

  1. NR_026983.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC000403

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    76928451..76929090
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    76152120..76152759
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_004671.3: Suppressed sequence

    Description
    NG_004671.3: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.
  2. NM_001208.1: Suppressed sequence

    Description
    NM_001208.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.