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REXO1L1P REXO1 like 1, pseudogene [ Homo sapiens (human) ]

Gene ID: 254958, updated on 23-Nov-2023

Summary

Official Symbol
REXO1L1Pprovided by HGNC
Official Full Name
REXO1 like 1, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:24660
See related
AllianceGenome:HGNC:24660
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
GOR; REXO1L1
Summary
Predicted to enable exonuclease activity. Predicted to be involved in nucleic acid phosphodiester bond hydrolysis. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

Location:
8q21.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (85661256..85662410, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (86204232..86205386, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (86573485..86574639, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene REXO1 like 8, pseudogene Neighboring gene OCT4 hESC enhancer GRCh37_chr8:86560715-86561216 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:86567267-86568134 Neighboring gene REXO1 like 3, pseudogene Neighboring gene OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:86573707-86574476 Neighboring gene REXO1 like 12, pseudogene Neighboring gene putative exonuclease GOR Neighboring gene REXO1 like 11, pseudogene

Genomic regions, transcripts, and products

Bibliography

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • REX1, RNA exonuclease 1 homolog-like 1, pseudogene
  • antigen GOR homolog
  • exonuclease GOR

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables exonuclease activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables nucleic acid binding IEA
Inferred from Electronic Annotation
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Component Evidence Code Pubs
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
 

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_053157.1 

    Range
    101..1255
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    85661256..85662410 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    86204232..86205386 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_172239.4: Suppressed sequence

    Description
    NM_172239.4: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.