Functions and Diseases

RBP Type Non-canonical_RBPs
Diseases Disease
Drug N.A.
Main interacting RNAs N.A.
Moonlighting functions N.A.
Localizations Stress granucleNucleoli
BulkPerturb-seq

Description

Ensembl ID ENSG00000013573 Gene ID 1663 Accession 2736
Symbol DDX11 Alias CHL1;KRG2;WABS;CHLR1 Full Name DEAD/H-box helicase 11
Status Confidence Length 30940 bases Strand Plus strand
Position 12 : 31073860 - 31104799 RNA binding domain N.A.
Summary DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an enzyme that possesses both ATPase and DNA helicase activities. This gene is a homolog of the yeast CHL1 gene, and may function to maintain chromosome transmission fidelity and genome stability. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

RNA binding domains (RBDs)

Protein Domain Pfam ID E-value Domain number

RNA binding proteomes (RBPomes)

Pubmed ID Full Name Cell Author Time Doi

Literatures on RNA binding capacity

Pubmed ID Title Author Time Journal
30469382 Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11. M Francesca Pisani 2018-11-21 Genes
33669056 Role of the DDX11 DNA Helicase in Warsaw Breakage Syndrome Etiology. Diana Santos 2021-02-25 International journal of molecular sciences
31824187 Spotlight on Warsaw Breakage Syndrome. M Francesca Pisani 2019-01-01 The application of clinical genetics
34281459 Long non-coding RNA DDX11-AS1 promotes esophageal carcinoma cell proliferation and migration through regulating the miR-514b-3p/RBX1 axis. Chao Wu 2021-12-01 Bioengineered

Transcripts

Name Transcript ID bp Protein Translation ID
DDX11-218 ENST00000542129 1561 304aa ENSP00000442466
DDX11-201 ENST00000228264 3717 880aa ENSP00000228264
DDX11-223 ENST00000542838 3920 906aa ENSP00000443426
DDX11-205 ENST00000438391 1135 302aa ENSP00000407646
DDX11-204 ENST00000435753 4182 288aa ENSP00000406799
DDX11-217 ENST00000540935 1210 288aa ENSP00000443578
DDX11-213 ENST00000539049 3471 297aa ENSP00000445568
DDX11-208 ENST00000536265 3603 No protein -
DDX11-203 ENST00000415475 883 224aa ENSP00000406457
DDX11-229 ENST00000545668 3751 970aa ENSP00000440402
DDX11-202 ENST00000350437 3724 856aa ENSP00000309965
DDX11-206 ENST00000535158 1718 No protein -
DDX11-226 ENST00000543756 613 78aa ENSP00000439298
DDX11-220 ENST00000542244 1193 171aa ENSP00000441425
DDX11-207 ENST00000535317 879 191aa ENSP00000440171
DDX11-227 ENST00000544652 400 91aa ENSP00000473610
DDX11-211 ENST00000538345 498 31aa ENSP00000445219
DDX11-219 ENST00000542242 795 No protein -
DDX11-224 ENST00000543026 2066 No protein -
DDX11-230 ENST00000545717 617 No protein -
DDX11-209 ENST00000536580 838 No protein -
DDX11-214 ENST00000539673 652 No protein -
DDX11-225 ENST00000543511 571 No protein -
DDX11-215 ENST00000539699 569 No protein -
DDX11-221 ENST00000542661 562 No protein -
DDX11-212 ENST00000538740 750 No protein -
DDX11-222 ENST00000542777 489 No protein -
DDX11-210 ENST00000537136 482 No protein -
DDX11-228 ENST00000545115 545 76aa ENSP00000443750
DDX11-216 ENST00000539702 951 172aa ENSP00000441015

Pathways

Pathway ID Pathway Name Source

Phenotypes

ensgID Trait pValue Pubmed ID
49342Child Development Disorders, Pervasive1.6160000E-005-
49345Child Development Disorders, Pervasive2.2221000E-005-
49349Child Development Disorders, Pervasive2.2221000E-005-
49354Child Development Disorders, Pervasive2.2221000E-005-
50070Child Development Disorders, Pervasive4.0257000E-006-
50073Child Development Disorders, Pervasive5.8312000E-006-
50078Child Development Disorders, Pervasive5.8312000E-006-
50081Child Development Disorders, Pervasive5.8312000E-006-

GWAS

ensgIDSNPChromosomePosition TraitPubmedIDOr or BEAT EFO ID

Protein-Protein Interaction (PPI)

Paralogs

Ensembl ID Source Target
Species Protein ID Perc_pos Perc_id Species Protein ID Perc_pos Perc_id

Orthologs

Ensembl ID Source Target
Species Protein ID Perc_pos Perc_id Species Protein ID Perc_pos Perc_id

Gene Ontology

Go ID Go term No. evidence Entries Species Category
GO:0000785part_of chromatin1IDAHomo_sapiens(9606)Component
GO:0000922located_in spindle pole1IDAHomo_sapiens(9606)Component
GO:0003677enables DNA binding1IDAHomo_sapiens(9606)Function
GO:0003678enables DNA helicase activity2IBA,IDAHomo_sapiens(9606)Function
GO:0003682enables chromatin binding2IDA,IMPHomo_sapiens(9606)Function
GO:0003688enables DNA replication origin binding1IMPHomo_sapiens(9606)Function
GO:0003690enables double-stranded DNA binding1IDAHomo_sapiens(9606)Function
GO:0003697enables single-stranded DNA binding1IDAHomo_sapiens(9606)Function
GO:0003727enables single-stranded RNA binding1IDAHomo_sapiens(9606)Function
GO:0004386enables helicase activity1IDAHomo_sapiens(9606)Function
GO:0005515enables protein binding1IPIHomo_sapiens(9606)Function
GO:0005524enables ATP binding1IEAHomo_sapiens(9606)Function
GO:0005634colocalizes_with nucleus1IDAHomo_sapiens(9606)Component
GO:0005654located_in nucleoplasm2IDA,TASHomo_sapiens(9606)Component
GO:0005730located_in nucleolus1IDAHomo_sapiens(9606)Component
GO:0005737located_in cytoplasm1IEAHomo_sapiens(9606)Component
GO:0005813located_in centrosome1IDAHomo_sapiens(9606)Component
GO:0006281involved_in DNA repair1IEAHomo_sapiens(9606)Process
GO:0006974involved_in DNA damage response1IMPHomo_sapiens(9606)Process
GO:0007062involved_in sister chromatid cohesion1IDAHomo_sapiens(9606)Process
GO:0008094enables ATP-dependent activity, acting on DNA2IDA,IMPHomo_sapiens(9606)Function
GO:0008186enables ATP-dependent activity, acting on RNA1IDAHomo_sapiens(9606)Function
GO:0016887enables ATP hydrolysis activity1IEAHomo_sapiens(9606)Function
GO:0030496located_in midbody1IDAHomo_sapiens(9606)Component
GO:0031297involved_in replication fork processing1IMPHomo_sapiens(9606)Process
GO:0032079involved_in positive regulation of endodeoxyribonuclease activity1IDAHomo_sapiens(9606)Process
GO:0032091involved_in negative regulation of protein binding1IMPHomo_sapiens(9606)Process
GO:0032508involved_in DNA duplex unwinding2IBA,IDAHomo_sapiens(9606)Process
GO:0034085involved_in establishment of sister chromatid cohesion1IBAHomo_sapiens(9606)Process
GO:0035563involved_in positive regulation of chromatin binding1IDAHomo_sapiens(9606)Process
GO:0043139enables 5-3 DNA helicase activity1IDAHomo_sapiens(9606)Function
GO:0044806involved_in G-quadruplex DNA unwinding1IDAHomo_sapiens(9606)Process
GO:0045142enables triplex DNA binding1IDAHomo_sapiens(9606)Function
GO:0045876involved_in positive regulation of sister chromatid cohesion1IMPHomo_sapiens(9606)Process
GO:0046872enables metal ion binding1IEAHomo_sapiens(9606)Function
GO:0051539enables 4 iron, 4 sulfur cluster binding1IEAHomo_sapiens(9606)Function
GO:0051880enables G-quadruplex DNA binding1IDAHomo_sapiens(9606)Function
GO:0070062located_in extracellular exosome1HDAHomo_sapiens(9606)Component
GO:0072711involved_in cellular response to hydroxyurea1IMPHomo_sapiens(9606)Process
GO:0072719involved_in cellular response to cisplatin1IMPHomo_sapiens(9606)Process
GO:1901838involved_in positive regulation of transcription of nucleolar large rRNA by RNA polymerase I1IMPHomo_sapiens(9606)Process
GO:1904976involved_in cellular response to bleomycin1IMPHomo_sapiens(9606)Process
GO:1990700involved_in nucleolar chromatin organization1IMPHomo_sapiens(9606)Process
GO:2000781involved_in positive regulation of double-strand break repair1IMPHomo_sapiens(9606)Process

Expression