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CTAGE7P CTAGE family member 7, pseudogene [ Homo sapiens (human) ]

Gene ID: 119437, updated on 13-May-2022

Summary

Official Symbol
CTAGE7Pprovided by HGNC
Official Full Name
CTAGE family member 7, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:25111
See related
Ensembl:ENSG00000233122 AllianceGenome:HGNC:25111
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
CTAGE7; CTAGEP; rcCTAGE5; bA500G10.2
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Genomic context

See CTAGE7P in Genome Data Viewer
Location:
10q26.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (130106009..130108838)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (131035000..131037829)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (131904273..131907102)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene EBF transcription factor 3 Neighboring gene EBF3 antisense RNA 1 Neighboring gene VISTA enhancer hs232 Neighboring gene chromosome 10 open reading frame 143 Neighboring gene uncharacterized LOC102724883 Neighboring gene uncharacterized LOC124902560 Neighboring gene uncharacterized LOC105378561

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • CTAGE family pseudogene
  • CTAGE family, member 5 pseudogene
  • meningioma expressed antigen 6 (coiled-coil proline-rich) pseudogene

Clone Names

  • MGC33437

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_044994.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL139123
    Related
    ENST00000435712.1

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    130106009..130108838
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    131035000..131037829
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_006026.3: Suppressed sequence

    Description
    NG_006026.3: This RefSeq was permanently suppressed because it did not represent the correct sequence for the pseudogene (GeneID 119437). A new NG record is provided to represent the genomic region defined by alignment of BC03652
  2. NG_006973.3: Suppressed sequence

    Description
    NG_006973.3: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.