DHX37
Probable ATP-dependent RNA helicase DHX37
Also known as: DDX37, Dhr1, DHX37_HUMAN, KIAA1517, MGC2695, MGC4322
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IY37
- Gene
- DHX37
- Ensembl
- ENSG00000150990
- Chromosome
- 12
- Canonical length
- 1157 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nuclear membrane
OverviewNCBI Gene
This gene encodes a DEAD box protein. 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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1157 residues, UniProt reviewed canonical sequence.
>Q8IY37|DHX37
1 MGKLRRRYNI KGRQQAGPGP SKGPPEPPPV QLELEDKDTL KGVDASNALV LPGKKKKKTK
61 APPLSKKEKK PLTKKEKKVL QKILEQKEKK SQRAEMLQKL SEVQASEAEM RLFYTTSKLG
121 TGNRMYHTKE KADEVVAPGQ EKISSLSGAH RKRRRWPSAE EEEEEEEESE SELEEESELD
181 EDPAAEPAEA GVGTTVAPLP PAPAPSSQPV PAGMTVPPPP AAAPPLPRAL AKPAVFIPVN
241 RSPEMQEERL KLPILSEEQV IMEAVAEHPI VIVCGETGSG KTTQVPQFLY EAGFSSEDSI
301 IGVTEPRRVA AVAMSQRVAK EMNLSQRVVS YQIRYEGNVT EETRIKFMTD GVLLKEIQKD
361 FLLLRYKVVI IDEAHERSVY TDILIGLLSR IVTLRAKRNL PLKLLIMSAT LRVEDFTQNP
421 RLFAKPPPVI KVESRQFPVT VHFNKRTPLE DYSGECFRKV CKIHRMLPAG GILVFLTGQA
481 EVHALCRRLR KAFPPSRARP QEKDDDQKDS VEEMRKFKKS RARAKKARAE VLPQINLDHY
541 SVLPAGEGDE DREAEVDEEE GALDSDLDLD LGDGGQDGGE QPDASLPLHV LPLYSLLAPE
601 KQAQVFKPPP EGTRLCVVAT NVAETSLTIP GIKYVVDCGK VKKRYYDRVT GVSSFRVTWV
661 SQASADQRAG RAGRTEPGHC YRLYSSAVFG DFEQFPPPEI TRRPVEDLIL QMKALNVEKV
721 INFPFPTPPS VEALLAAEEL LIALGALQPP QKAERVKQLQ ENRLSCPITA LGRTMATFPV
781 APRYAKMLAL SRQHGCLPYA ITIVASMTVR ELFEELDRPA ASDEELTRLK SKRARVAQMK
841 RTWAGQGASL KLGDLMVLLG AVGACEYASC TPQFCEANGL RYKAMMEIRR LRGQLTTAVN
901 AVCPEAELFV DPKMQPPTES QVTYLRQIVT AGLGDHLARR VQSEEMLEDK WRNAYKTPLL
961 DDPVFIHPSS VLFKELPEFV VYQEIVETTK MYMKGVSSVE VQWIPALLPS YCQFDKPLEE
1021 PAPTYCPERG RVLCHRASVF YRVGWPLPAI EVDFPEGIDR YKHFARFLLE GQVFRKLASY
1081 RSCLLSSPGT MLKTWARLQP RTESLLRALV AEKADCHEAL LAAWKKNPKY LLAEYCEWLP
1141 QAMHPDIEKA WPPTTVHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DHX37 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 17 nTPM
- pancreas: 9 nTPM
- bone marrow: 8.3 nTPM
- esophagus: 7.6 nTPM
- spleen: 7.3 nTPM
- lymph node: 6.9 nTPM
Single-cell type
- erythrocyte progenitors: 26 nCPM
- myosatellite cells: 24 nCPM
- megakaryocyte-erythroid progenitors: 24 nCPM
- retinal pigment epithelial cells: 21 nCPM
- megakaryocyte progenitors: 20 nCPM
- monocyte progenitors: 20 nCPM
Immune cell
- memory B-cell: 1.8 nTPM
- intermediate monocyte: 1.7 nTPM
- gdT-cell: 1.6 nTPM
- memory CD8 T-cell: 1.6 nTPM
- classical monocyte: 1.5 nTPM
- MAIT T-cell: 1.4 nTPM
Brain region
- medulla oblongata: 11 nTPM
- white matter: 11 nTPM
- midbrain: 10 nTPM
- cerebral cortex: 10 nTPM
- pons: 9.6 nTPM
- basal ganglia: 9.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DHX37.
Disease | AllUniProt
Conditions DHX37 is implicated in, by any mechanism.
- Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies (NEDBAVC) MIM:618731
- 46,XY sex reversal 11 (SRXY11) MIM:273250
Disease | GeneticClinVar
16 pathogenic / likely-pathogenic of 647 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- 46,XY sex reversal 11
- Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
- Neurodevelopmental disorders
- Male infertility with azoospermia or oligozoospermia due to single gene mutation
- Intellectual disability
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)
- 0.29
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.83
- DepMap mean gene effect
- -1.47
- DepMap dependency class
- pan
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
- brain development
- maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
- positive regulation of male gonad development
- ribosomal small subunit biogenesis
- ribosome assembly
- ribosome biogenesis
Molecular functions
- ATP binding
- ATP hydrolysis activity
- helicase activity
- RNA binding
- RNA helicase activity
- U3 snoRNA binding
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
- ATP-dependent RNA helicase DHX37-like, C-terminal domain
- DEAH helicase DHX37 C-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DHX37 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 DHX37 as an antibody target. Whether an autoantibody or antibody against DHX37 could matter depends on whether native DHX37 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DHX37 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 DHX37 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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