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Aliases for USP17L8 Gene

Aliases for USP17L8 Gene

  • Ubiquitin Specific Peptidase 17-Like Family Member 8 2 3 5
  • Ubiquitin Specific Peptidase 17-Like 8 2 3
  • Inactive Ubiquitin Carboxyl-Terminal Hydrolase 17-Like Protein 8 3
  • EC 3.1.2.15 61
  • USP17L10 3

External Ids for USP17L8 Gene

Previous GeneCards Identifiers for USP17L8 Gene

  • GC08M007870
  • GC08M007874
  • GC08M007831

Summaries for USP17L8 Gene

GeneCards Summary for USP17L8 Gene

USP17L8 (Ubiquitin Specific Peptidase 17-Like Family Member 8) is a Protein Coding gene. Among its related pathways are Deubiquitination and Metabolism of proteins. GO annotations related to this gene include thiol-dependent ubiquitinyl hydrolase activity. An important paralog of this gene is USP17L2.

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for USP17L8 Gene

Genomics for USP17L8 Gene

Regulatory Elements for USP17L8 Gene


Genomic Location for USP17L8 Gene

Chromosome:
8
Start:
7,971,661 bp from pter
End:
7,973,253 bp from pter
Size:
1,593 bases
Orientation:
Minus strand

Genomic View for USP17L8 Gene

Genes around USP17L8 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
USP17L8 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for USP17L8 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for USP17L8 Gene

Proteins for USP17L8 Gene

  • Protein details for USP17L8 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P0C7I0-U17L8_HUMAN
    Recommended name:
    Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 8
    Protein Accession:
    P0C7I0

    Protein attributes for USP17L8 Gene

    Size:
    530 amino acids
    Molecular mass:
    59635 Da
    Quaternary structure:
    No Data Available

neXtProt entry for USP17L8 Gene

Selected DME Specific Peptides for USP17L8 Gene

P0C7I0:
  • AQSVKQAL
  • SDTFDPYLDI
  • WRSQIKCL
  • VYVLYAVLVH
  • HEFLMFTVDAMKKACLPGHKQVDHH
  • QCLTYTPPLANY
  • SVLSQQAYVLFYI
  • CTMQAHIT
  • RVDLCDDLAPVARQLAPR
  • GFHRGKQED

Post-translational modifications for USP17L8 Gene

  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

Other Protein References for USP17L8 Gene

ENSEMBL proteins:
REFSEQ proteins:

Domains & Families for USP17L8 Gene

Protein Domains for USP17L8 Gene

Suggested Antigen Peptide Sequences for USP17L8 Gene

Graphical View of Domain Structure for InterPro Entry

P0C7I0

UniProtKB/Swiss-Prot:

U17L8_HUMAN :
  • Belongs to the peptidase C19 family. USP17 subfamily.
Family:
  • Belongs to the peptidase C19 family. USP17 subfamily.
genes like me logo Genes that share domains with USP17L8: view

No data available for Gene Families for USP17L8 Gene

Function for USP17L8 Gene

Enzyme Numbers (IUBMB) for USP17L8 Gene

Gene Ontology (GO) - Molecular Function for USP17L8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0036459 thiol-dependent ubiquitinyl hydrolase activity IEA --
genes like me logo Genes that share ontologies with USP17L8: view

Phenotypes for USP17L8 Gene

genes like me logo Genes that share phenotypes with USP17L8: view

Animal Model Products

CRISPR Products

Clone Products

Flow Cytometry Products

No data available for Molecular function , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for USP17L8 Gene

Localization for USP17L8 Gene

Subcellular locations from UniProtKB/Swiss-Prot for USP17L8 Gene

Nucleus. Endoplasmic reticulum.

Gene Ontology (GO) - Cellular Components for USP17L8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus IEA --
GO:0005783 endoplasmic reticulum IEA --
genes like me logo Genes that share ontologies with USP17L8: view

No data available for Subcellular locations from COMPARTMENTS for USP17L8 Gene

Pathways & Interactions for USP17L8 Gene

genes like me logo Genes that share pathways with USP17L8: view

Pathways by source for USP17L8 Gene

Interacting Proteins for USP17L8 Gene

Selected Interacting proteins: P0C7I0-U17L8_HUMAN for USP17L8 Gene via IID

Gene Ontology (GO) - Biological Process for USP17L8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006511 ubiquitin-dependent protein catabolic process IEA --
GO:0016579 protein deubiquitination IEA --
genes like me logo Genes that share ontologies with USP17L8: view

No data available for SIGNOR curated interactions for USP17L8 Gene

Transcripts for USP17L8 Gene

mRNA/cDNA for USP17L8 Gene

(1) REFSEQ mRNAs :
(1) Ensembl transcripts including schematic representations, and UCSC links where relevant :

CRISPR Products

Clone Products

Flow Cytometry Products

Alternative Splicing Database (ASD) splice patterns (SP) for USP17L8 Gene

No ASD Table

Relevant External Links for USP17L8 Gene

GeneLoc Exon Structure for
USP17L8
ECgene alternative splicing isoforms for
USP17L8

Expression for USP17L8 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for USP17L8 Gene

NURSA nuclear receptor signaling pathways regulating expression of USP17L8 Gene:

USP17L8

SOURCE GeneReport for Unigene cluster for USP17L8 Gene:

Hs.741135
genes like me logo Genes that share expression patterns with USP17L8: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for USP17L8 Gene

Orthologs for USP17L8 Gene

Evolution for USP17L8 Gene

ENSEMBL:
Gene Tree for USP17L8 (if available)
TreeFam:
Gene Tree for USP17L8 (if available)

No data available for Orthologs for USP17L8 Gene

Paralogs for USP17L8 Gene

Variants for USP17L8 Gene

Sequence variations from dbSNP and Humsavar for USP17L8 Gene

SNP ID Clin Chr 08 pos Sequence Context AA Info Type
rs1005031588 -- 7,972,799(+) GGAAG(C/T)CAGCA intron-variant, reference, missense
rs1015450215 -- 7,972,939(+) TAGTT(C/G)GCAAG intron-variant, reference, synonymous-codon
rs1028912527 -- 7,974,190(+) GAGTG(A/G)TTTCG intron-variant, upstream-variant-2KB
rs1051025708 -- 7,973,669(+) TGTCT(C/G)TGTGT intron-variant, upstream-variant-2KB
rs1053870155 -- 7,975,176(+) TGTGC(A/T)TTCAT intron-variant, upstream-variant-2KB

Structural Variations from Database of Genomic Variants (DGV) for USP17L8 Gene

Variant ID Type Subtype PubMed ID
dgv11914n54 CNV gain 21841781
dgv11928n54 CNV gain 21841781
dgv11931n54 CNV loss 21841781
dgv1265e199 CNV deletion 23128226
dgv13n29 CNV gain+loss 16826518
dgv2035e212 CNV gain 25503493
dgv262n111 CNV deletion 26073780
dgv3764n106 CNV deletion 24896259
dgv6882n100 CNV gain 25217958
dgv6887n100 CNV loss 25217958
dgv6890n100 CNV gain 25217958
dgv6895n100 CNV loss 25217958
dgv6896n100 CNV gain+loss 25217958
dgv6909n100 CNV gain 25217958
dgv6910n100 CNV gain+loss 25217958
dgv6911n100 CNV loss 25217958
dgv6912n100 CNV loss 25217958
dgv6915n100 CNV gain 25217958
dgv6936n100 CNV gain+loss 25217958
dgv6940n100 CNV loss 25217958
dgv6949n100 CNV gain 25217958
dgv6950n100 CNV loss 25217958
dgv6955n100 CNV gain 25217958
dgv6962n100 CNV gain 25217958
dgv6963n100 CNV loss 25217958
dgv6964n100 CNV gain 25217958
dgv6970n100 CNV gain 25217958
dgv6976n100 CNV loss 25217958
dgv6978n100 CNV loss 25217958
dgv6980n100 CNV gain 25217958
dgv6983n100 CNV loss 25217958
dgv6984n100 CNV gain+loss 25217958
dgv6986n100 CNV loss 25217958
dgv6987n100 CNV loss 25217958
dgv6988n100 CNV loss 25217958
dgv6989n100 CNV gain 25217958
dgv6990n100 CNV loss 25217958
dgv6991n100 CNV loss 25217958
esv1000987 CNV gain 20482838
esv2422039 CNV deletion 20811451
esv25631 CNV gain+loss 19812545
esv2752265 CNV gain 17911159
esv2752266 CNV loss 17911159
esv2759589 CNV gain+loss 17122850
esv2761169 CNV gain+loss 21179565
esv2764098 CNV gain+loss 21179565
esv3891318 CNV gain 25118596
esv3891321 CNV gain+loss 25118596
nsv1015205 CNV gain+loss 25217958
nsv1017081 CNV gain 25217958
nsv1018143 CNV gain+loss 25217958
nsv1020728 CNV gain+loss 25217958
nsv1030619 CNV loss 25217958
nsv1031577 CNV gain 25217958
nsv1075524 CNV deletion 25765185
nsv428194 CNV gain+loss 18775914
nsv433398 CNV gain 18776910
nsv471650 CNV gain+loss 15918152
nsv471651 CNV gain+loss 15918152
nsv510977 OTHER complex 20534489
nsv515968 CNV gain+loss 19592680
nsv610137 CNV loss 21841781
nsv821327 CNV deletion 20802225
nsv821656 CNV gain 15273396
nsv8281 CNV gain+loss 18304495
nsv951093 CNV deletion 24416366
nsv967561 CNV duplication 23825009

Relevant External Links for USP17L8 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
USP17L8

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot and Variation tolerance for USP17L8 Gene

Disorders for USP17L8 Gene

Relevant External Links for USP17L8

Atlas of Genetics and Cytogenetics in Oncology and Haematology:
USP17L8

No disorders were found for USP17L8 Gene.

No data available for MalaCards , UniProtKB/Swiss-Prot and Genatlas for USP17L8 Gene

Publications for USP17L8 Gene

  1. Hyaluronan- and RNA-binding deubiquitinating enzymes of USP17 family members associated with cell viability. (PMID: 17109758) Shin J.-M. … Baek K.-H. (BMC Genomics 2006) 2 3 4 64
  2. The DUB/USP17 deubiquitinating enzymes, a multigene family within a tandemly repeated sequence. (PMID: 15780755) Burrows J.F. … Johnston J.A. (Genomics 2005) 2 3 4 64
  3. DNA sequence and analysis of human chromosome 8. (PMID: 16421571) Nusbaum C. … Lander E.S. (Nature 2006) 3 4 64
  4. Lys-63-specific deubiquitination of SDS3 by USP17 regulates HDAC activity. (PMID: 21239494) Ramakrishna S. … Baek K.H. (J. Biol. Chem. 2011) 3 64
  5. The deubiquitinating enzyme USP17 is essential for GTPase subcellular localization and cell motility. (PMID: 21448158) de la Vega M. … Johnston J.A. (Nat. Commun. 2011) 3 64

Products for USP17L8 Gene

Sources for USP17L8 Gene

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