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TCP10L3 t-complex 10 like 3, pseudogene [ Homo sapiens (human) ]

Gene ID: 6953, updated on 25-Oct-2022

Summary

Official Symbol
TCP10L3provided by HGNC
Official Full Name
t-complex 10 like 3, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:11656
See related
Ensembl:ENSG00000290751 MIM:187020; AllianceGenome:HGNC:11656
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
TCP10; TCP10A
Annotation information
Annotation category: suggests misassembly
Expression
Restricted expression toward testis (RPKM 4.5) See more
Orthologs
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Genomic context

See TCP10L3 in Genome Data Viewer
Location:
6q27
Exon count:
9
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (167373090..167384510, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (168755727..168767109, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (167786578..167797998, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene mitotic arrest deficient 2 like 1 pseudogene Neighboring gene Sharpr-MPRA regulatory region 6086 Neighboring gene Sharpr-MPRA regulatory region 8873 Neighboring gene Sharpr-MPRA regulatory region 3778

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Other Names

  • T-complex protein 10A homolog
  • t-complex 10 (a murine tcp homolog)
  • t-complex 10 homolog

Clone Names

  • MGC34049

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_163193.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL592444
    Related
    ENST00000674952.1
  2. NR_163194.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL592444
  3. NR_163195.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL592444
  4. NR_163196.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL592444
    Related
    ENST00000617120.5

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    167373090..167384510 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    168755727..168767109 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001366311.1: Suppressed sequence

    Description
    NM_001366311.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  2. NM_001366312.1: Suppressed sequence

    Description
    NM_001366312.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  3. NM_001366313.1: Suppressed sequence

    Description
    NM_001366313.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  4. NM_001366317.1: Suppressed sequence

    Description
    NM_001366317.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  5. NM_004610.3: Suppressed sequence

    Description
    NM_004610.3: This RefSeq was removed because it is now thought that this gene is a pseudogene.