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SORD2P sorbitol dehydrogenase 2, pseudogene [ Homo sapiens (human) ]

Gene ID: 653381, updated on 23-Nov-2021

Summary

Official Symbol
SORD2Pprovided by HGNC
Official Full Name
sorbitol dehydrogenase 2, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:49919
See related
Ensembl:ENSG00000259479
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
SORD2
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Genomic context

See SORD2P in Genome Data Viewer
Location:
15q21.1
Exon count:
11
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (44825747..44884694, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (45117945..45176892, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene ring finger protein 4 pseudogene Neighboring gene tripartite motif containing 69 Neighboring gene uncharacterized LOC105370798 Neighboring gene RNA, U1 small nuclear 119, pseudogene Neighboring gene telomere repeat binding bouquet formation protein 2 pseudogene Neighboring gene 5-azacytidine induced 2 pseudogene Neighboring gene RNA, U6 small nuclear 1108, pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • SORD pseudogene

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_146393.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC120778, AC122108
  2. NR_146394.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC122108, BU151661, DT218022
    Related
    ENST00000561384.3

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    44825747..44884694 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NT_187605.1 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    150087..216558 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_008173.3: Suppressed sequence

    Description
    NG_008173.3: This RefSeq was removed because it is now thought that this locus is transcribed.
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