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TRIM51CP tripartite motif-containing 51C, pseudogene [ Homo sapiens (human) ]

Gene ID: 100130105, updated on 10-Oct-2023

Summary

Official Symbol
TRIM51CPprovided by HGNC
Official Full Name
tripartite motif-containing 51C, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:43968
See related
Ensembl:ENSG00000249910 AllianceGenome:HGNC:43968
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

Location:
11p11.12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (48945684..48952068)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (49122175..49128560)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (48967236..48973620)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ANKRD33B pseudogene 2 Neighboring gene tripartite motif containing 48 pseudogene Neighboring gene tripartite motif-containing 51G Neighboring gene tripartite motif containing 53C, pseudogene

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_028918.2 

    Range
    101..6485
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    48945684..48952068
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    49122175..49128560
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)