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TBC1D29P TBC1 domain family member 29, pseudogene [ Homo sapiens (human) ]

Gene ID: 26083, updated on 25-Oct-2022

Summary

Official Symbol
TBC1D29Pprovided by HGNC
Official Full Name
TBC1 domain family member 29, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:24509
See related
Ensembl:ENSG00000290404 AllianceGenome:HGNC:24509
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TBC1D29
Expression
Restricted expression toward testis (RPKM 3.5) See more
Orthologs
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Genomic context

See TBC1D29P in Genome Data Viewer
Location:
17q11.2
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (30559566..30563493)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (31504207..31508135)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (28886584..28890511)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene arachidonate 12-lipoxygenase pseudogene 1 Neighboring gene TBC1 domain family member 3 pseudogene Neighboring gene SMURF2P1-LRRC37BP1 readthrough transcribed pseudogene Neighboring gene uncharacterized LOC101927093 Neighboring gene keratin 17 pseudogene 3

Genomic regions, transcripts, and products

Expression

  • Project title: 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

General gene information

Markers

Homology

Other Names

  • TBC1 domain family, member 29
  • putative TBC1 domain family member 29

Clone Names

  • DKFZp434O047

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_172920.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC011840
    Related
    ENST00000649411.1

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    30559566..30563493
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    31504207..31508135
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_015594.2: Suppressed sequence

    Description
    NM_015594.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.