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CTAGE11P CTAGE family member 11, pseudogene [ Homo sapiens (human) ]

Gene ID: 647288, updated on 13-May-2022

Summary

Official Symbol
CTAGE11Pprovided by HGNC
Official Full Name
CTAGE family member 11, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:37293
See related
Ensembl:ENSG00000214249 AllianceGenome:HGNC:37293
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See CTAGE11P in Genome Data Viewer
Location:
13q22.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (75237753..75240381, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (74461439..74464067, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (75811889..75814517, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 38, pseudogene Neighboring gene signal sequence receptor subunit 1 pseudogene 2 Neighboring gene long intergenic non-protein coding RNA 1078 Neighboring gene TBC1 domain family member 4

Genomic regions, transcripts, and products

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_027466.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL133018, AL162571
    Related
    ENST00000451540.1

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    75237753..75240381 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    74461439..74464067 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_011533.1: Suppressed sequence

    Description
    NG_011533.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.