Gene Gene information from NCBI Gene database.
Entrez ID 55593
Gene name OTU deubiquitinase 5
Gene symbol OTUD5
Synonyms (NCBI Gene)
DUBAMCAND
Chromosome X
Chromosome location Xp11.23
Summary This gene encodes a member of the OTU (ovarian tumor) domain-containing cysteine protease superfamily. The OTU domain confers deubiquitinase activity and the encoded protein has been shown to suppress the type I interferon-dependent innate immune response
miRNA miRNA information provided by mirtarbase database.
169
miRTarBase ID miRNA Experiments Reference
MIRT051503 hsa-let-7e-5p CLASH 23622248
MIRT043793 hsa-miR-328-3p CLASH 23622248
MIRT042795 hsa-miR-339-5p CLASH 23622248
MIRT041070 hsa-miR-505-3p CLASH 23622248
MIRT052692 hsa-miR-1260b CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
37
GO ID Ontology Definition Evidence Reference
GO:0001818 Process Negative regulation of cytokine production IEA
GO:0004843 Function Cysteine-type deubiquitinase activity IBA
GO:0004843 Function Cysteine-type deubiquitinase activity IDA 22245969, 23827681, 33110214
GO:0004843 Function Cysteine-type deubiquitinase activity IEA
GO:0005634 Component Nucleus IDA 33523931
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300713 25402 ENSG00000068308
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96G74
Protein name OTU domain-containing protein 5 (EC 3.4.19.12) (Deubiquitinating enzyme A) (DUBA)
Protein function Deubiquitinating enzyme that functions as a negative regulator of the innate immune system (PubMed:17991829, PubMed:22245969, PubMed:23827681, PubMed:33523931). Has peptidase activity towards 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains (P
PDB 3PFY , 3TMO , 3TMP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02338 OTU 219 338 OTU-like cysteine protease Family
Tissue specificity TISSUE SPECIFICITY: Expressed in various tissues, including the liver and placenta, as well as in peripheral blood leukocytes. {ECO:0000269|PubMed:17991829}.
Sequence
MTILPKKKPPPPDADPANEPPPPGPMPPAPRRGGGVGVGGGGTGVGGGDRDRDSGVVGAR
PRASPPPQGPLPGPPGALHRWALAVPPGAVAGPRPQQASPPPCGGPGGPGGGPGDALGAA
AAGVGAAGVVVGVGGAVGVGGCCSGPGHSKRRRQAPGVGAVGGGSPEREEVGAGYNSEDE
YEAAAARIEAMDPATVEQQEHWFEKALRDKKGFIIKQMKEDGACLFRAVADQVYGDQDMH
EVVRKHCMDYLMKNADYFSNYVTEDFTTYINRKRKNNCHGNHIEMQAMAEMYNRPVEVYQ
YSTGTSAVEPINTFHGIHQNEDEPIRVSYHRNIHYNSV
VNPNKATIGVGLGLPSFKPGFA
EQSLMKNAIKTSEESWIEQQMLEDKKRATDWEATNEAIEEQVARESYLQWLRDQEKQARQ
VRGPSQPRKASATCSSATAAASSGLEEWTSRSPRQRSSASSPEHPELHAELGMKPPSPGT
VLALAKPPSPCAPGTSSQFSAGADRATSPLVSLYPALECRALIQQMSPSAFGLNDWDDDE
ILASVLAVSQQEYLDSMKKNKVHRDPPPDKS
Sequence length 571
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  RIG-I-like receptor signaling pathway   Ovarian tumor domain proteases
Negative regulators of DDX58/IFIH1 signaling
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Multiple congenital anomalies-neurodevelopmental syndrome, X-linked Pathogenic; Likely pathogenic rs2147523033, rs2519708540, rs2063984022, rs2063620799, rs2063801903, rs2063659512 RCV001528131
RCV003152813
RCV001290731
RCV001290732
RCV001290733
RCV001290735
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
OTUD5-related disorder Likely pathogenic rs2519728724 RCV003399964
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Abnormal cerebral cortex morphology Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DYSGENESIS OF CORPUS CALLOSUM Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Dysplastic corpus callosum Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Ependymoma Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Anemia Congenital Hypoplastic with Multiple Congenital Anomalies Mental Retardation Syndrome Associate 38037881
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Inhibit 32248621, 35765958
★☆☆☆☆
Found in Text Mining only
Congenital Abnormalities Associate 33523931
★☆☆☆☆
Found in Text Mining only
Contracture Associate 38037881
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Associate 38037881
★☆☆☆☆
Found in Text Mining only
Down Syndrome Associate 29049012
★☆☆☆☆
Found in Text Mining only
Fanconi Anemia Associate 37713620
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Associate 38037881
★☆☆☆☆
Found in Text Mining only
Kidney Diseases Associate 38037881
★☆☆☆☆
Found in Text Mining only
Liver Cirrhosis Biliary Associate 33675743
★☆☆☆☆
Found in Text Mining only