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LGALS9DP galectin 9D, pseudogene [ Homo sapiens (human) ]

Gene ID: 645754, updated on 23-Nov-2021

Summary

Official Symbol
LGALS9DPprovided by HGNC
Official Full Name
galectin 9D, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:49896
Gene type
pseudo
RefSeq status
INFERRED
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 LGALS9DP in Genome Data Viewer
Location:
17q11.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (27746040..27755279)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (26073066..26082305)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene TBC1 domain family member 29, pseudogene pseudogene Neighboring gene carboxypeptidase D pseudogene 1 Neighboring gene nitric oxide synthase 2 Neighboring gene NOS2 5' regulatory region Neighboring gene LYR motif containing 9

Genomic regions, transcripts, and products

General gene information

Other Names

  • lectin, galactoside-binding, soluble, 9 pseudogene
  • lectin, galactoside-binding, soluble, 9D, 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.

Genomic

  1. NG_005629.4 

    Range
    9..9248
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    27746040..27755279
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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