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ID2B inhibitor of DNA binding 2B (pseudogene) [ Homo sapiens (human) ]

Gene ID: 84099, updated on 18-Aug-2022

Summary

Official Symbol
ID2Bprovided by HGNC
Official Full Name
inhibitor of DNA binding 2B (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:30656
See related
AllianceGenome:HGNC:30656
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
Predicted to be involved in negative regulation of transcription, DNA-templated. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See ID2B in Genome Data Viewer
Location:
3p14.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (62123426..62124718, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (62166918..62168192, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (62109100..62110392, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene protein tyrosine phosphatase receptor type G Neighboring gene Sharpr-MPRA regulatory region 14465 Neighboring gene RNA, U2 small nuclear 10, pseudogene Neighboring gene Sharpr-MPRA regulatory region 11400 Neighboring gene uncharacterized LOC124909389

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
EBI GWAS Catalog

General gene information

Markers

Other Names

  • inhibitor of DNA binding 2B, HLH protein (pseudogene)
  • inhibitor of DNA binding 2B, dominant negative helix-loop-helix protein (pseudogene)
  • inhibitor of differentiation 2B
  • striated muscle contraction regulatory protein

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_000937.3 

    Range
    101..1393
    Download
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    62123426..62124718 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    62166918..62168192 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001039082.1: Suppressed sequence

    Description
    NM_001039082.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
  2. NR_026582.1: Suppressed sequence

    Description
    NR_026582.1: This RefSeq was permanently suppressed because there is insufficient evidence that this locus is transcribed.