Gene Gene information from NCBI Gene database.
Entrez ID 161725
Gene name OTU deubiquitinase 7A
Gene symbol OTUD7A
Synonyms (NCBI Gene)
C15orf16C16ORF15CEZANNE2NEDHSOTUD7
Chromosome 15
Chromosome location 15q13.3
Summary The protein encoded by this gene is a deubiquitinizing enzyme and possible tumor suppressor. The encoded protein acts on TNF receptor associated factor 6 (TRAF6) to control nuclear factor kappa B expression. However, this gene is downregulated by SNAIL1 i
miRNA miRNA information provided by mirtarbase database.
69
miRTarBase ID miRNA Experiments Reference
MIRT047999 hsa-miR-30c-5p CLASH 23622248
MIRT616944 hsa-miR-670-3p HITS-CLIP 23824327
MIRT622957 hsa-miR-1197 HITS-CLIP 23824327
MIRT622956 hsa-miR-8080 HITS-CLIP 23824327
MIRT616943 hsa-miR-153-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0004843 Function Cysteine-type deubiquitinase activity IBA
GO:0004843 Function Cysteine-type deubiquitinase activity IDA 23827681
GO:0004843 Function Cysteine-type deubiquitinase activity IEA
GO:0004843 Function Cysteine-type deubiquitinase activity TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612024 20718 ENSG00000169918
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TE49
Protein name OTU domain-containing protein 7A (EC 3.4.19.12) (Zinc finger protein Cezanne 2)
Protein function Deubiquitinase, which cleaves 'Lys-11'-linked polyubiquitin chains. Might be required for PA28-20S proteasome assembly (Probable).
PDB 2L2D
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14555 UBA_4 28 63 Domain
PF02338 OTU 205 368 OTU-like cysteine protease Family
PF01754 zf-A20 888 912 A20-like zinc finger Family
Sequence
MVSSVLPNPTSAECWAALLHDPMTLDMDAVLSDFVRSTGAEPGLARDLLEGKNWDLTAAL
SDY
EQLRQVHTANLPHVFNEGRGPKQPEREPQPGHKVERPCLQRQDDIAQEKRLSRGISH
ASSAIVSLARSHVASECNNEQFPLEMPIYTFQLPDLSVYSEDFRSFIERDLIEQATMVAL
EQAGRLNWWSTVCTSCKRLLPLATTGDGNCLLHAASLGMWGFHDRDLVLRKALYTMMRTG
AEREALKRRWRWQQTQQNKEEEWEREWTELLKLASSEPRTHFSKNGGTGGGVDNSEDPVY
ESLEEFHVFVLAHILRRPIVVVADTMLRDSGGEAFAPIPFGGIYLPLEVPPNRCHCSPLV
LAYDQAHF
SALVSMEQRDQQREQAVIPLTDSEHKLLPLHFAVDPGKDWEWGKDDNDNARL
AHLILSLEAKLNLLHSYMNVTWIRIPSETRAPLAQPESPTASAGEDVQSLADSLDSDRDS
VCSNSNSNNGKNGKDKEKEKQRKEKDKTRADSVANKLGSFSKTLGIKLKKNMGGLGGLVH
GKMGRANSANGKNGDSAERGKEKKAKSRKGSKEESGASASTSPSEKTTPSPTDKAAGASP
AEKGGGPRGDAWKYSTDVKLSLNILRAAMQGERKFIFAGLLLTSHRHQFHEEMIGYYLTS
AQERFSAEQEQRRRDAATAAAAAAAAAAATAKRPPRRPETEGVPVPERASPGPPTQLVLK
LKERPSPGPAAGRAARAAAGGTASPGGGARRASASGPVPGRSPPAPARQSVIHVQASGAR
DEACAPAVGALRPCATYPQQNRSLSSQSYSPARAAALRTVNTVESLARAVPGALPGAAGT
AGAAEHKSQTYTNGFGALRDGLEFADADAPTARSNGECGRGGPGPVQRRCQRENCAFYGR
AETEHYCSYCYR
EELRRRREARGARP
Sequence length 926
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Ovarian tumor domain proteases
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
27
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Epileptic encephalopathy Pathogenic rs1162953058 RCV001263452
Language disorder Pathogenic rs1162953058 RCV001263452
Neurodevelopmental disorder Likely pathogenic rs1428047310 RCV003592054
Neurodevelopmental disorder with hypotonia and seizures Pathogenic rs2504476908, rs1162953058 RCV004525824
RCV004526099
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Non-syndromic intellectual disability no classifications from unflagged records rs1194968943 RCV002466346
OTUD7A-related disorder Benign; Uncertain significance; Likely benign rs2338682, rs2338681, rs144509293, rs750664811, rs2504425756, rs2504429029, rs2504428618, rs867747505, rs777418666, rs77376353, rs78774681, rs749384931, rs199744400, rs1398694572, rs749890600
View all (3 more)
RCV003980778
RCV003968417
RCV003906585
RCV003399733
RCV003400060
RCV003400162
RCV003404562
RCV003906754
RCV003919728
RCV003973887
RCV003897288
RCV003909772
RCV003952079
RCV003941418
RCV003941668
RCV003949781
RCV003932119
RCV003952309
See cases Uncertain significance rs2141058802 RCV001591679
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Venous Thromboembolism Associate 23650146