Live briefing
Everything about DNAJB11
Protein-coding gene in the species Homo sapiens
DnaJ homolog subfamily B member 11 is a protein that in humans is encoded by the DNAJB11 gene. Wikipedia →
🧭 Start here: a 6-step reading path
- Read the overview: DNAJB11A 5-minute orientation
- Skim a recent paper: The role of the co‐chaperone DNAJB11 in polycystic kidney disease: Molecular mechanisms and cellular origin of cyst formationInfluential work since 2022
- Read the landmark paper: Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney DiseaseCited 295 times
- Go sideways: DNAJB9A closely related topic
- Go sideways: DNAJB2A closely related topic
📖 Definitions
No dictionary entry for this exact phrase.
🗂️ The subject at a glance
No outline available.
🏆 Landmark papers (most cited)
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease
Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
The endoplasmic reticulum HSP40 co‐chaperone ERdj3/DNAJB11 assembles and functions as a tetramer
Exosomal DNAJB11 promotes the development of pancreatic cancer by modulating the EGFR/MAPK pathway
Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renal-hepatic-pancreatic dysplasia
More dissimilarities than affinities between DNAJB11-PKD and ADPKD
The Endoplasmic Reticulum Co-Chaperone ERdj3/DNAJB11 Promotes Hepatocellular Carcinoma Progression through Suppressing AATZ Degradation
Dnajb11-Kidney Disease Develops from Reduced Polycystin-1 Dosage but not Unfolded Protein Response in Mice
🆕 Influential since 2022
The role of the co‐chaperone DNAJB11 in polycystic kidney disease: Molecular mechanisms and cellular origin of cyst formation
ATM-mediated co-chaperone DNAJB11 phosphorylation facilitates α-synuclein folding upon DNA double-stranded breaks
DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort
Uromodulin processing in DNAJB11-kidney disease
Quantitative Proteomic Analysis Reveals JMJD6 and DNAJB11 as Endogenous Substrates of E3 Ligase RFFL
📚 Books worth reading
Open Library didn't respond; try again in a moment.
🔗 Related topics
- DNAJB9 DnaJ homolog subfamily B member 9 is a protein that in humans is encoded by the DNAJB9 gene. GRCh38: Ensembl release 89: ENSG00000128590 – Ensembl, May…
- DNAJB2 DnaJ homolog subfamily B member 2 is a protein that in humans is encoded by the DNAJB2 gene. GRCh38: Ensembl release 89: ENSG00000135924 – Ensembl, May…
- DNAJA1 DnaJ homolog subfamily A member 1 is a protein that in humans is encoded by the DNAJA1 gene. DNAJA1 has been shown to interact with PTTG1. GRCh38: Ensembl…
- DNAJC7 DnaJ homolog subfamily C member 7 is a protein that in humans is encoded by the DNAJC7 gene. DNAJC7 has been shown to interact with RAD9A. GRCh38: Ensembl…
- DNAJC10 DnaJ homolog subfamily C member 10 is a protein that in humans is encoded by the DNAJC10 gene. GRCh38: Ensembl release 89: ENSG00000077232 – Ensembl, May…
- SIL1 Nucleotide exchange factor SIL1 is a protein encoded in humans by the SIL1 gene. This gene encodes a resident endoplasmic reticulum (ER) N-linked glycoprotein…
- DNAJA2 DnaJ homolog subfamily A member 2 is a protein that in humans is encoded by the DNAJA2 gene. The protein encoded by this gene shares sequence similarity…
- DNAJB4 DnaJ homolog subfamily B member 4 is a protein that in humans is encoded by the DNAJB4 gene. GRCh38: Ensembl release 89: ENSG00000162616 – Ensembl, May…