Gene

dhx9

ID
ZDB-GENE-070912-171
Name
DEAH (Asp-Glu-Ala-His) box helicase 9
Symbol
dhx9 Nomenclature History
Previous Names
  • si:ch211-194i4.1
  • wu:fe02c10
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to enable ATP hydrolysis activity; RNA binding activity; and helicase activity. Acts upstream of or within response to virus. Predicted to be located in centrosome and nucleoplasm. Predicted to be part of ribonucleoprotein complex. Predicted to be active in nucleolus. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 75. Orthologous to human DHX9 (DExH-box helicase 9).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
sa8582Allele with one point mutationUnknownSplice SiteENU
sa13148Allele with one point mutationUnknownPremature StopENU
sa18641Allele with one point mutationUnknownSplice SiteENU
sa19813Allele with one point mutationUnknownPremature StopENU
sa32962Allele with one point mutationUnknownSplice SiteENU
sa39873Allele with one point mutationUnknownPremature StopENU
sa39874Allele with one point mutationUnknownSplice SiteENU
sa39875Allele with one point mutationUnknownSplice SiteENU
sa45108Allele with one point mutationUnknownSplice SiteENU
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Sequence Targeting Reagents
Targeting Reagent Created Alleles Citations
MO1-dhx9N/AGe et al., 2015
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Human Disease
Associated With dhx9 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant intellectual developmental disorder 75 Alliance Intellectual developmental disorder, autosomal dominant 75 620988
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Associated With dhx9 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR002464 DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site
Domain IPR001650 Helicase, C-terminal domain-like
Domain IPR007502 Helicase-associated domain
Domain IPR011545 DEAD/DEAH box helicase domain
Domain IPR011709 DEAD-box helicase, OB fold
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Domain Details Per Protein
Protein Additional Resources Length DEAD-box helicase, OB fold DEAD/DEAH box helicase domain DHX9, DEXH-box helicase domain DHX9, first double-stranded RNA binding domain DHX9, second double-stranded RNA binding domain DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site Double-stranded RNA-binding domain Helicase-associated domain Helicase associated domain (HA2), winged-helix domain Helicase, C-terminal domain-like Helicase superfamily 1/2, ATP-binding domain P-loop containing nucleoside triphosphate hydrolase
UniProtKB:A0A8F5CC50 InterPro
UniProtKB:A0A8M3AQB4 InterPro 1062
UniProtKB:A0A8M1P3F9 InterPro 1270
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 2
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA dhx9-201 (1) Ensembl 4,118 nt
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Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-194I4ZFIN Curated Data
EncodesESTfe02c10
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanDHX91
Amino acid sequence comparison (1)
Conserved genome location (synteny) (1)
MouseDhx91
Conserved genome location (synteny) (1)
Amino acid sequence comparison (1)
Citations
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