Gene Gene information from NCBI Gene database.
Entrez ID 55760
Gene name DEAH-box helicase 32 (putative)
Gene symbol DHX32
Synonyms (NCBI Gene)
DDX32DHLP1
Chromosome 10
Chromosome location 10q26.2
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 m
miRNA miRNA information provided by mirtarbase database.
114
miRTarBase ID miRNA Experiments Reference
MIRT018169 hsa-miR-335-5p Microarray 18185580
MIRT2212244 hsa-miR-1302 CLIP-seq
MIRT2212245 hsa-miR-3122 CLIP-seq
MIRT2212246 hsa-miR-3157-5p CLIP-seq
MIRT2212247 hsa-miR-338-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003723 Function RNA binding IBA
GO:0003724 Function RNA helicase activity IEA
GO:0004386 Function Helicase activity IBA
GO:0004386 Function Helicase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607960 16717 ENSG00000089876
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7L7V1
Protein name Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 (EC 3.6.4.13) (DEAD/H box 32) (DEAD/H helicase-like protein 1) (DHLP1) (DEAH box protein 32) (HuDDX32)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04408 HA2 458 547 Helicase associated domain (HA2) Domain
PF07717 OB_NTP_bind 616 696 Oligonucleotide/oligosaccharide-binding (OB)-fold Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in lymphoid tissues (at protein level). Expressed in brain, heart, skeletal muscle, colon, thymus, spleen, kidney, liver, small intestine, placenta, lung, lymphoid tissues and blood leukocytes. {ECO:0000269|PubMed:12163057, E
Sequence
MEEEGLECPNSSSEKRYFPESLDSSDGDEEEVLACEDLELNPFDGLPYSSRYYKLLKERE
DLPIWKEKYSFMENLLQNQIVIVSGDAKCGKSAQVPQWCAEYCLSIHYQHGGVICTQVHK
QTVVQLALRVADEMDVNIGHEVGYVIPFENCCTNETILRYCTDDMLQREMMSNPFLGSYG
VIILDDIHERSIATDVLLGLLKDVLLARPELKLIINSSPHLISKLNSYYGNVPVIEVKNK
HPVEVVYLSEAQKDSFESILRLIFEIHHSGEKGDIVVFLACEQDIEKVCETVYQGSNLNP
DLGELVVVPLYPKEKCSLFKPLDETEKRCQVYQRRVVLTTSSGEFLIWSNSVRFVIDVGV
ERRKVYNPRIRANSLVMQPISQSQAEIRKQILGSSSSGKFFCLYTEEFASKDMTPLKPAE
MQEANLTSMVLFMKRIDIAGLGHCDFMNRPAPESLMQALEDLDYLAALDNDGNLSEFGII
MSEFPLDPQLSKSILASCEFDCVDEVLTIAAMVTAPNCFSHVPHGAEEAALTCWKTFLHP
EGDHFTL
ISIYKAYQDTTLNSSSEYCVEKWCRDYFLNCSALRMADVIRAELLEIIKRIEL
PYAEPAFGSKENTLNIKKALLSGYFMQIARDVDGSGNYLMLTHKQVAQLHPLSGYSITKK
MPEWVLFHKFSISENNYIRITSEISPELFMQLVPQY
YFSNLPPSESKDILQQVVDHLSPV
STMNKEQQMCETCPETEQRCTLQ
Sequence length 743
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
8
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormal circulating immunoglobulin concentration Uncertain significance rs2134053537 RCV001849811
Cervical cancer Benign rs140070899 RCV005921032
Clear cell carcinoma of kidney Benign rs140070899 RCV005921033
Familial cancer of breast Benign rs140070899 RCV005921030
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 25848939
Carcinoma Hepatocellular Stimulate 33729094
Colorectal Neoplasms Associate 19161603
Colorectal Neoplasms Stimulate 25782664
Leukemia Myeloid Acute Associate 30760869
Lymphatic Metastasis Associate 19161603
Neoplasm Metastasis Associate 25782664
Neoplasms Associate 19161603
Neoplasms Stimulate 33729094
Precursor Cell Lymphoblastic Leukemia Lymphoma Inhibit 16080506