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SLC25A51P1 SLC25A51 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 442229, updated on 29-Mar-2023

Summary

Official Symbol
SLC25A51P1provided by HGNC
Official Full Name
SLC25A51 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:23325
See related
AllianceGenome:HGNC:23325
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
MCART3P; bA707M13.1
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Genomic context

See SLC25A51P1 in Genome Data Viewer
Location:
6q12
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (65787879..65789483)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (66940192..66941796)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (66497772..66499376)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:66481227-66481728 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:66481729-66482228 Neighboring gene ADH5 pseudogene 4 Neighboring gene NANOG hESC enhancer GRCh37_chr6:66681097-66681598

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrial carrier triple repeat 3 pseudogene
  • solute carrier family 25 member 51 pseudogene 1

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_026540.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL391500, AW665607, BC024198

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    65787879..65789483
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187555.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    13066..14670
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    66940192..66941796
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_025947.1: Suppressed sequence

    Description
    NG_025947.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.