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TMSB4XP2 TMSB4X pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 7116, updated on 1-Aug-2020

Summary

Official Symbol
TMSB4XP2provided by HGNC
Official Full Name
TMSB4X pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:11884
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TMSL2

Genomic context

See TMSB4XP2 in Genome Data Viewer
Location:
2p25.3
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (3617153..3617757, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (3664728..3665350, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene RNASEH1 antisense RNA 1 Neighboring gene ribosomal protein S7 Neighboring gene collectin subfamily member 11 Neighboring gene allantoicase Neighboring gene glyceraldehyde 3 phosphate dehydrogenase pseudogene 48 Neighboring gene uncharacterized LOC105373393

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • thymosin beta 4, X-linked pseudogene 2
  • thymosin-like 2 (pseudogene)

Clone Names

  • MGC125884, MGC125885

NCBI Reference Sequences (RefSeq)

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_004719.7 

    Range
    101..705
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    3617153..3617757 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_182793.1: Suppressed sequence

    Description
    NM_182793.1: This RefSeq was permanently suppressed because this gene is a pseudogene.
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