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LOC102724738 solute carrier family 25 member 1 pseudogene [ Homo sapiens (human) ]

Gene ID: 102724738, updated on 17-Sep-2024

Summary

Gene symbol
LOC102724738
Gene description
solute carrier family 25 member 1 pseudogene
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 LOC102724738 in Genome Data Viewer
Location:
7q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (63346800..63350066, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (64545542..64548808, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (62807178..62810444, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene ARAF pseudogene 3 Neighboring gene uncharacterized LOC100287704 Neighboring gene vomeronasal 1 receptor 30 pseudogene Neighboring gene long intergenic non-protein coding RNA 3075 Neighboring gene vomeronasal 1 receptor 31 pseudogene Neighboring gene uncharacterized LOC101929050 Neighboring gene vomeronasal 1 receptor 32 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.

RNA

  1. NR_136256.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC006455

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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    63346800..63350066 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    64545542..64548808 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)