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TRIM53CP tripartite motif containing 53C, pseudogene [ Homo sapiens (human) ]

Gene ID: 340970, updated on 17-Sep-2024

Summary

Official Symbol
TRIM53CPprovided by HGNC
Official Full Name
tripartite motif containing 53C, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:43979
See related
Ensembl:ENSG00000254764 AllianceGenome:HGNC:43979
Gene type
pseudo
RefSeq status
INFERRED
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 TRIM53CP in Genome Data Viewer
Location:
11p11.12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (48985753..48991881, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (49162855..49168989, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (49007305..49013433, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene tripartite motif-containing 51C, pseudogene Neighboring gene tripartite motif-containing 51G Neighboring gene tripartite motif containing 64B pseudogene Neighboring gene tripartite motif containing 49B

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.

Genomic

  1. NG_021782.3 

    Range
    101..6229
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    48985753..48991881 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    49162855..49168989 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)