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GXYLT1P2 GXYLT1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 441958, updated on 10-Oct-2023

Summary

Official Symbol
GXYLT1P2provided by HGNC
Official Full Name
GXYLT1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39677
See related
AllianceGenome:HGNC:39677
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

Location:
21q11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (13823471..13825700, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (12167778..12170007, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (15195792..15198021, complement)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene family with sequence similarity 207 member C, pseudogene Neighboring gene brain cytoplasmic RNA 1 (non-protein coding) pseudogene Neighboring gene calponin 2 pseudogene 7 Neighboring gene zinc finger protein 114 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • glucoside xylosyltransferase 1 pseudogene 2
  • glycosyltransferase 8 domain containing 3 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_006139.2 

    Range
    101..2330
    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_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    13823471..13825700 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    12167778..12170007 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)