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Gene Gene information from NCBI Gene database.
Entrez ID 10273
Gene name STIP1 homology and U-box containing protein 1
Gene symbol STUB1
Synonyms (NCBI Gene)
CHIPHSPABP2NY-CO-7SCA48SCAR16SDCCAG7UBOX1
Chromosome 16
Chromosome location 16p13.3
Summary This gene encodes a protein containing tetratricopeptide repeat and a U-box that functions as a ubiquitin ligase/cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA polymerase beta (Polb), among other t
miRNA miRNA information provided by mirtarbase database.
77 Show/Hide all (77)
miRTarBase ID miRNA Experiments Reference
MIRT028574 hsa-miR-30a-5p Proteomics 18668040
MIRT029709 hsa-miR-26b-5p Microarray 19088304
MIRT1399920 hsa-miR-1178 CLIP-seq
MIRT1399921 hsa-miR-1275 CLIP-seq
MIRT1399922 hsa-miR-1290 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
119 Show/Hide all (119)
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex IDA 12150907, 16275660, 16307917
GO:0000165 Process MAPK cascade IEA
GO:0000165 Process MAPK cascade ISS
GO:0000209 Process Protein polyubiquitination IBA
GO:0000209 Process Protein polyubiquitination IDA 15781469, 16275660
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607207 11427 ENSG00000103266
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UNE7
Protein name E3 ubiquitin-protein ligase CHIP (EC 2.3.2.27) (Antigen NY-CO-7) (CLL-associated antigen KW-8) (Carboxy terminus of Hsp70-interacting protein) (RING-type E3 ubiquitin transferase CHIP) (STIP1 homology and U box-containing protein 1)
Protein function E3 ubiquitin-protein ligase which targets misfolded chaperone substrates towards proteasomal degradation (PubMed:10330192, PubMed:11146632, PubMed:11557750, PubMed:23990462, PubMed:26265139). Plays a role in the maintenance of mitochondrial morp
PDB 4KBQ , 6EFK , 6NSV , 7TB1 , 8EHZ , 8EI0 , 8F14 , 8F15 , 8F16 , 8F17 , 8FYU , 8GCK , 8SUV , 9DRY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04564 U-box 227 → 299 U-box domain Domain
PF12895 ANAPC3 39 → 120 Domain
PF18391 CHIP_TPR_N 142 → 225 CHIP N-terminal tetratricopeptide repeat domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in differentiated myotubes (at protein level) (PubMed:17369820). Highly expressed in skeletal muscle, heart, pancreas, brain and placenta (PubMed:10330192, PubMed:11435423). Detected in kidney, liver and lung (PubMed:10330192
Sequence
Sequence length 303
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway Reactome Pathway
Ubiquitin mediated proteolysis Downregulation of TGF-beta receptor signaling
Protein processing in endoplasmic reticulum Downregulation of ERBB2 signaling
  Regulation of RUNX2 expression and activity
  Regulation of PTEN stability and activity
  Antigen processing: Ubiquitination & Proteasome degradation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
14
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
Autosomal recessive spinocerebellar ataxia 16 Likely pathogenic; Pathogenic rs760424025, rs1732133553, rs369941408, rs587777340, rs587777341, rs587777342, rs587777344, rs587777345, rs587777346, rs587777347, rs776620952, rs690016544, rs2543803363, rs2543803110, rs1555475283
View all (4 more)
RCV006258536
RCV006258537
RCV006258652
RCV000114998
RCV000114999
View all (15 more)
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Ovarian serous cystadenocarcinoma Likely pathogenic rs760424025 RCV005911068
★★★★★
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Spinocerebellar ataxia 48 Likely pathogenic; Pathogenic rs2151504167, rs2151504209, rs760424025, rs1732133553, rs2151507049, rs780883873, rs2151505158, rs690016544, rs1555475283, rs748984540, rs754446573, rs2039704361, rs770730338, rs2039634238, rs2039691550
View all (1 more)
RCV001647176
RCV001647149
RCV001647174
RCV001647177
RCV001809156
View all (11 more)
★★★★★
★★★★★
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.
Show/Hide Unknown Diseases (11)
Phenotype Name Clinical Significance Source Reference Evidence Score
ATAXIA, SPINOCEREBELLAR — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA DUE TO STIP1 HOMOLOGY AND U-BOX CONTAINING PROTEIN 1 DEFICIENCY — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA DUE TO STUB1 DEFICIENCY — Orphanet 24113144, 24312598, 24742043, 25258038
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Gastric cancer Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (143)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alopecia Alopecia HPO_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Alzheimer disease Pubtator 21220432 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis BEFREE 30669930
★★★★★
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder HPO_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Apraxia of Phonation Apraxia HPO_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Arachnodactyly Arachnodactyly HPO_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Arteriosclerosis Arteriosclerosis BEFREE 30566180
★★★★★
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 35943876 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 37604355 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Ataxia Ataxia Pubtator 24742043, 28193273, 32713943, 33811518, 34070858, 36422518 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only