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DDX11L8 DEAD/H-box helicase 11 like 8 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 100302090, updated on 23-Nov-2023

Summary

Official Symbol
DDX11L8provided by HGNC
Official Full Name
DEAD/H-box helicase 11 like 8 (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:37101
See related
AllianceGenome:HGNC:37101
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
Predicted to enable DNA helicase activity. Predicted to be involved in DNA duplex unwinding and establishment of sister chromatid cohesion. Predicted to be located in nucleolus. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
Annotation information
Note: The name of this locus was changed from DDX11L11 to DDX11L8 in collaboration with HGNC and based on the definition of the location provided in PMID: 19476624. [31 Aug 2011]
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Genomic context

Location:
12p13.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (12310..14526)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (91214..93430, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene WAS protein family homolog 8, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:86703-87203 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:81477-82356 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:78811-79310 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:78309-78810 Neighboring gene OCT4-H3K27ac hESC enhancer GRCh37_chr12:73943-74609 Neighboring gene uncharacterized LOC107987170 Neighboring gene family with sequence similarity 138 member D

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11 like 8
  • DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 like 8

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables ATP binding IEA
Inferred from Electronic Annotation
more info
 
enables ATP hydrolysis activity IEA
Inferred from Electronic Annotation
more info
 
enables DNA binding IEA
Inferred from Electronic Annotation
more info
 
enables DNA helicase activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables RNA binding IEA
Inferred from Electronic Annotation
more info
 
enables RNA helicase activity IEA
Inferred from Electronic Annotation
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
involved_in DNA duplex unwinding IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in establishment of sister chromatid cohesion IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in nucleobase-containing compound metabolic process IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in nucleolus 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_029416.2 

    Range
    101..2317
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    12310..14526
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NW_003571049.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    2310..4526
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)