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SLC25A5P7 solute carrier family 25 member 5 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 442255, updated on 10-Oct-2023

Summary

Official Symbol
SLC25A5P7provided by HGNC
Official Full Name
solute carrier family 25 member 5 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:513
See related
AllianceGenome:HGNC:513
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ANTP7
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Genomic context

Location:
6q22.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (121653739..121654948)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (122840765..122841973)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (121974885..121976094)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89523 Neighboring gene RNA, U4 small nuclear 76, pseudogene Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121892975-121893482 Neighboring gene RNA, U2 small nuclear 8, pseudogene Neighboring gene ReSE screen-validated silencer GRCh37_chr6:121925900-121926110 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:121940073-121940713 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121941509-121942161 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:121948343-121949542 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89548 Neighboring gene LSM14A, SCD6 homolog A (S. cerevisiae) pseudogene Neighboring gene ribosomal protein L23a pseudogene 48

Genomic regions, transcripts, and products

General gene information

Other Names

  • adenine nucleotide translocator pseudogene 7 (clone 2)
  • solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5 pseudogene 7

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_009280.2 

    Range
    101..1310
    Download
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    121653739..121654948
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    122840765..122841973
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)