Format

Send to:

Choose Destination
    • Showing Current items.

    SLC9A3P2 solute carrier family 9 member 3 pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 128997, updated on 17-Jun-2019

    Summary

    Official Symbol
    SLC9A3P2provided by HGNC
    Official Full Name
    solute carrier family 9 member 3 pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:19325
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

    See SLC9A3P2 in Genome Data Viewer
    Location:
    22q11.21
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 22 NC_000022.11 (20652644..20654727)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (21007121..21009014)

    Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene immunoglobulin lambda like polypeptide 4, pseudogene Neighboring gene small G protein signaling modulator 1 pseudogene Neighboring gene abhydrolase domain containing 17A pseudogene P4 Neighboring gene POM121 transmembrane nucleoporin like 4, pseudogene

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 pseudogene 2
    • solute carrier family 9 (sodium/hydrogen exchanger), member 3 pseudogene 2
    • solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 pseudogene 2

    NCBI Reference Sequences (RefSeq)

    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_005203.4 

      Range
      11..2094
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000022.11 Reference GRCh38.p13 Primary Assembly

      Range
      20652644..20654727
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Support Center