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TBC1D3P2 TBC1 domain family member 3 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 440452, updated on 17-Sep-2024

Summary

Official Symbol
TBC1D3P2provided by HGNC
Official Full Name
TBC1 domain family member 3 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:27783
See related
Ensembl:ENSG00000290800 AllianceGenome:HGNC:27783
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 9.0), skin (RPKM 1.7) and 12 other tissues See more
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Genomic context

See TBC1D3P2 in Genome Data Viewer
Location:
17q23.2
Exon count:
14
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (62264702..62275655, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (63134633..63145601, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (60342063..60353016, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene RNA polymerase mitochondrial pseudogene 1 Neighboring gene ribosomal protein S6 kinase B1 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:60340887-60341386 Neighboring gene uncharacterized LOC105371853 Neighboring gene ubiquitin specific peptidase 32 pseudogene 4

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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.

RNA

  1. NR_027486.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC053481
  2. NR_174974.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC053481
    Related
    ENST00000581291.5

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    62264702..62275655 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    63134633..63145601 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_005460.3: Suppressed sequence

    Description
    NG_005460.3: This RefSeq was permanently suppressed because it was based on sequence from the wrong location.
  2. NM_001024654.1: Suppressed sequence

    Description
    NM_001024654.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.