DHX34
Probable ATP-dependent RNA helicase DHX34
Also known as: DDX34, DHX34_HUMAN, KIAA0134
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14147
- Gene
- DHX34
- Ensembl
- ENSG00000134815
- Chromosome
- 19
- Canonical length
- 1143 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
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 DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. It is mapped to the glioma 19q tumor suppressor region and is a tumor suppressor candidate gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1143 residues, UniProt reviewed canonical sequence.
>Q14147|DHX34
1 MPPPRTREGR DRRDHHRAPS EEEALEKWDW NCPETRRLLE DAFFREEDYI RQGSEECQKF
61 WTFFERLQRF QNLKTSRKEE KDPGQPKHSI PALADLPRTY DPRYRINLSV LGPATRGSQG
121 LGRHLPAERV AEFRRALLHY LDFGQKQAFG RLAKLQRERA ALPIAQYGNR ILQTLKEHQV
181 VVVAGDTGCG KSTQVPQYLL AAGFSHVACT QPRRIACISL AKRVGFESLS QYGSQVGYQI
241 RFESTRSAAT KIVFLTVGLL LRQIQREPSL PQYEVLIVDE VHERHLHNDF LLGVLQRLLP
301 TRPDLKVILM SATINISLFS SYFSNAPVVQ VPGRLFPITV VYQPQEAEPT TSKSEKLDPR
361 PFLRVLESID HKYPPEERGD LLVFLSGMAE ISAVLEAAQT YASHTQRWVV LPLHSALSVA
421 DQDKVFDVAP PGVRKCILST NIAETSVTID GIRFVVDSGK VKEMSYDPQA KLQRLQEFWI
481 SQASAEQRKG RAGRTGPGVC FRLYAESDYD AFAPYPVPEI RRVALDSLVL QMKSMSVGDP
541 RTFPFIEPPP PASLETAILY LRDQGALDSS EALTPIGSLL AQLPVDVVIG KMLILGSMFS
601 LVEPVLTIAA ALSVQSPFTR SAQSSPECAA ARRPLESDQG DPFTLFNVFN AWVQVKSERS
661 RNSRKWCRRR GIEEHRLYEM ANLRRQFKEL LEDHGLLAGA QAAQVGDSYS RLQQRRERRA
721 LHQLKRQHEE GAGRRRKVLR LQEEQDGGSS DEDRAGPAPP GASDGVDIQD VKFKLRHDLA
781 QLQAAASSAQ DLSREQLALL KLVLGRGLYP QLAVPDAFNS SRKDSDQIFH TQAKQGAVLH
841 PTCVFAGSPE VLHAQELEAS NCDGSRDDKD KMSSKHQLLS FVSLLETNKP YLVNCVRIPA
901 LQSLLLFSRS LDTNGDCSRL VADGWLELQL ADSESAIRLL AASLRLRARW ESALDRQLAH
961 QAQQQLEEEE EDTPVSPKEV ATLSKELLQF TASKIPYSLR RLTGLEVQNM YVGPQTIPAT
1021 PHLPGLFGSS TLSPHPTKGG YAVTDFLTYN CLTNDTDLYS DCLRTFWTCP HCGLHAPLTP
1081 LERIAHENTC PQAPQDGPPG AEEAALETLQ KTSVLQRPYH CEACGKDFLF TPTEVLRHRK
1141 QHVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DHX34 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- testis: 21 nTPM
- spleen: 12 nTPM
- bone marrow: 11 nTPM
- ovary: 10 nTPM
- liver: 9.7 nTPM
- cerebellum: 9.2 nTPM
Single-cell type
- neutrophils: 423 nCPM
- monocytes: 114 nCPM
- late spermatids: 107 nCPM
- early primary spermatocytes: 93 nCPM
- neutrophil progenitors: 53 nCPM
- macrophages: 48 nCPM
Immune cell
- neutrophil: 12 nTPM
- classical monocyte: 1.8 nTPM
- intermediate monocyte: 1.8 nTPM
- myeloid DC: 1.7 nTPM
- memory CD8 T-cell: 1.5 nTPM
- non-classical monocyte: 1.5 nTPM
Brain region
- cerebral cortex: 21 nTPM
- white matter: 15 nTPM
- medulla oblongata: 13 nTPM
- cerebellum: 13 nTPM
- thalamus: 12 nTPM
- basal ganglia: 12 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DHX34.
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 335 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.77
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.08
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
- nuclear-transcribed mRNA catabolic process
- nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
- positive regulation of phosphorylation
Molecular functions
- ATP binding
- ATP hydrolysis activity
- helicase activity
- protein-containing complex binding
- RNA binding
- RNA helicase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Helicase, C-terminal domain-like
- Helicase-associated domain
- DEAD/DEAH-box helicase domain
- DEAD-box helicase, OB fold
- Helicase superfamily 1/2, ATP-binding domain
- P-loop containing nucleoside triphosphate hydrolase
- Helicase associated domain (HA2), winged-helix domain
- DEAD/DEAH box helicase
- Helicase conserved C-terminal domain
- Helicase associated domain (HA2), winged-helix
- Oligonucleotide/oligosaccharide-binding (OB)-fold
- Helicase associated domain (HA2), ratchet-like
- DHX34-like, C2H2-type zinc finger
- DHX34-like, C2H2-type zinc finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DHX34 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DHX34 as an antibody target. Whether an autoantibody or antibody against DHX34 could matter depends on whether native DHX34 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DHX34 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label DHX34 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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