Type |
Details |
Score |
Publication |
First Author: |
Bairoch A |
Year: |
1999 |
Journal: |
Database Release |
Title: |
SWISS-PROT Annotated protein sequence database |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2005 |
|
Title: |
Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics |
Year: |
2010 |
Journal: |
Database Release |
Title: |
Protein Ontology Association Load. |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2005 |
|
Title: |
Obtaining and loading genome assembly coordinates from NCBI annotations |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2009 |
Journal: |
Database Download |
Title: |
Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Meng J |
Year: |
2024 |
Journal: |
Theranostics |
Title: |
The biphasic role of Hspb1 on ferroptotic cell death in Parkinson's disease. |
Volume: |
14 |
Issue: |
12 |
Pages: |
4643-4666 |
|
•
•
•
•
•
|
Publication |
First Author: |
Srivastava AK |
Year: |
2012 |
Journal: |
Neurobiol Dis |
Title: |
Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice. |
Volume: |
47 |
Issue: |
2 |
Pages: |
163-73 |
|
•
•
•
•
•
|
HT Experiment |
|
Experiment Type: |
RNA-Seq |
Study Type: |
WT vs. Mutant |
Source: |
GEO |
|
•
•
•
•
•
|
Allele |
Name: |
heat shock protein 1; endonuclease-mediated mutation 1, Shanghai Model Organisms Center |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Null/knockout |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:7580670 |
Assay Type: |
Immunohistochemistry |
Annotation Date: |
2024-02-07 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1784128 |
Pattern: |
Not Specified |
Stage: |
TS28 |
Assay Id: |
MGI:7580681 |
Age: |
postnatal day 15 |
Image: |
10B/C |
Note: |
Coexpressed with Hspb1 (about 10% of the TDRD7 protein was co-localized with Hspb1 mRNA). |
Specimen Label: |
10B/C |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, mutant strain, endonuclease-mediated mutation |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
209
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Allele |
Name: |
gene trap ROSA 26, Philippe Soriano; endonuclease-mediated mutation 1, Jun Chen |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Conditional ready, Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
175
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
197
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Allele |
Name: |
heat shock protein 1; endonuclease-mediated mutation 1, Michael Wiles |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Humanized sequence |
|
•
•
•
•
•
|
Publication |
First Author: |
d'Ydewalle C |
Year: |
2011 |
Journal: |
Nat Med |
Title: |
HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease. |
Volume: |
17 |
Issue: |
8 |
Pages: |
968-74 |
|
•
•
•
•
•
|
Allele |
Name: |
transgene insertion, Ludo Van Den Bosch |
Allele Type: |
Transgenic |
Attribute String: |
Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Allele |
Name: |
transgene insertion, Ludo Van Den Bosch |
Allele Type: |
Transgenic |
Attribute String: |
Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Thy1-HSPB1*S135F)#Lvdb/? |
Background: |
involves: FVB/N |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Thy1-HSPB1*P182L)#Lvdb/? |
Background: |
involves: FVB/N |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Trichoplein keratin filament-binding protein (TCHP) may act as a 'capping' or 'branching' protein for keratin filaments in the cell periphery. It may regulate K8/K18 filament and desmosome organisation mainly at the apical or peripheral regions of simple epithelial cells []. In human, it acts as a tumor suppressor which has the ability to inhibit cell growth and be pro-apoptotic during cell stress. It inhibits cell growth in bladder and prostate cancer cells by a down-regulation of HSPB1 by inhibiting its phosphorylation []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Nishizawa M |
Year: |
2005 |
Journal: |
J Cell Sci |
Title: |
Identification of trichoplein, a novel keratin filament-binding protein. |
Volume: |
118 |
Issue: |
Pt 5 |
Pages: |
1081-90 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
497
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Vecchione A |
Year: |
2009 |
Journal: |
Oncogene |
Title: |
MITOSTATIN, a putative tumor suppressor on chromosome 12q24.1, is downregulated in human bladder and breast cancer. |
Volume: |
28 |
Issue: |
2 |
Pages: |
257-69 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This entry represents the trichohyalin-plectin-homology domain. This domain can be found in mitostatin (also known as trichoplein keratin filament-binding protein, TCHP) and related proteins [, ]. Trichoplein keratin filament-binding protein (TCHP) may act as a 'capping' or 'branching' protein for keratin filaments in the cell periphery. It may regulate K8/K18 filament and desmosome organisation mainly at the apical or peripheral regions of simple epithelial cells []. In human, it acts as a tumor suppressor which has the ability to inhibit cell growth and be pro-apoptotic during cell stress. It inhibits cell growth in bladder and prostate cancer cells by a down-regulation of HSPB1 by inhibiting its phosphorylation []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Shi Y |
Year: |
2017 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Endothelium-targeted overexpression of heat shock protein 27 ameliorates blood-brain barrier disruption after ischemic brain injury. |
Volume: |
114 |
Issue: |
7 |
Pages: |
E1243-E1252 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
547
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
551
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
491
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
206
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
64
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
219
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
538
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
361
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
This entry includes CFAP53 and TCHP.Cilia- and flagella-associated protein 53 (CFAP53), also known as coiled-coil domain-containing protein 11 (CCDC11), is a novel centriolar satellite protein essential for the assembly and function of motile cilia and establishment of left-right asymmetry [, ]. In zebrafish, it is required for cilia rotation specifically in Kupffer's vesicle, the zebrafish laterality organ [].Trichoplein keratin filament-binding protein (TCHP) may act as a 'capping' or 'branching' protein for keratin filaments in the cell periphery. It may regulate K8/K18 filament and desmosome organisation mainly at the apical or peripheral regions of simple epithelial cells []. In human, it acts as a tumor suppressor which has the ability to inhibit cell growth and be pro-apoptotic during cell stress. It inhibits cell growth in bladder and prostate cancer cells by a down-regulation of HSPB1 by inhibiting its phosphorylation []. |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
514
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
428
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Tang D |
Year: |
2011 |
Journal: |
Cell Metab |
Title: |
High-mobility group box 1 is essential for mitochondrial quality control. |
Volume: |
13 |
Issue: |
6 |
Pages: |
701-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Friedman MJ |
Year: |
2007 |
Journal: |
Nat Neurosci |
Title: |
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration. |
Volume: |
10 |
Issue: |
12 |
Pages: |
1519-28 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sheehan BK |
Year: |
2021 |
Journal: |
iScience |
Title: |
ATG9A regulates proteostasis through reticulophagy receptors FAM134B and SEC62 and folding chaperones CALR and HSPB1. |
Volume: |
24 |
Issue: |
4 |
Pages: |
102315 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
215
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
50
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Noël ES |
Year: |
2016 |
Journal: |
Hum Mutat |
Title: |
A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function. |
Volume: |
37 |
Issue: |
2 |
Pages: |
194-200 |
|
•
•
•
•
•
|
Publication |
First Author: |
Silva E |
Year: |
2016 |
Journal: |
Mol Biol Cell |
Title: |
Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry. |
Volume: |
27 |
Issue: |
1 |
Pages: |
48-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Narasimhan V |
Year: |
2015 |
Journal: |
Hum Mutat |
Title: |
Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer. |
Volume: |
36 |
Issue: |
3 |
Pages: |
307-18 |
|
•
•
•
•
•
|
Publication |
First Author: |
Menon MB |
Year: |
2010 |
Journal: |
J Biol Chem |
Title: |
p38 MAP kinase and MAPKAP kinases MK2/3 cooperatively phosphorylate epithelial keratins. |
Volume: |
285 |
Issue: |
43 |
Pages: |
33242-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhou Y |
Year: |
2016 |
Journal: |
Biochim Biophys Acta |
Title: |
Lens ER-stress response during cataract development in Mip-mutant mice. |
Volume: |
1862 |
Issue: |
8 |
Pages: |
1433-42 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ciocca DR |
Year: |
2012 |
Journal: |
Histochem Cell Biol |
Title: |
Absence of caveolin-1 alters heat shock protein expression in spontaneous mammary tumors driven by Her-2/neu expression. |
Volume: |
137 |
Issue: |
2 |
Pages: |
187-94 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pelaez MC |
Year: |
2024 |
Journal: |
Neurotherapeutics |
Title: |
Reversal of cognitive deficits in FUS(R521G) amyotrophic lateral sclerosis mice by arimoclomol and a class I histone deacetylase inhibitor independent of heat shock protein induction. |
Volume: |
21 |
Issue: |
5 |
Pages: |
e00388 |
|
•
•
•
•
•
|
Publication |
First Author: |
Binet F |
Year: |
2008 |
Journal: |
Br J Haematol |
Title: |
Arsenic trioxide induces de novo protein synthesis of annexin-1 in neutrophils: association with a heat shock-like response and not apoptosis. |
Volume: |
140 |
Issue: |
4 |
Pages: |
454-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yamashita M |
Year: |
2018 |
Journal: |
Development |
Title: |
Uhrf1 is indispensable for normal limb growth by regulating chondrocyte differentiation through specific gene expression. |
Volume: |
145 |
Issue: |
1 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Cui X |
Year: |
2022 |
Journal: |
Dis Model Mech |
Title: |
Exercise suppresses mouse systemic AApoAII amyloidosis through enhancement of the p38 MAPK signaling pathway. |
Volume: |
15 |
Issue: |
3 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Sanbe A |
Year: |
2009 |
Journal: |
PLoS One |
Title: |
Protective effect of geranylgeranylacetone via enhancement of HSPB8 induction in desmin-related cardiomyopathy. |
Volume: |
4 |
Issue: |
4 |
Pages: |
e5351 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sadler E |
Year: |
2020 |
Journal: |
Front Cell Neurosci |
Title: |
Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle Epithelium. |
Volume: |
14 |
|
Pages: |
123 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ninkina N |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein. |
Volume: |
18 |
Issue: |
10 |
Pages: |
1779-94 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tang MK |
Year: |
2013 |
Journal: |
PLoS One |
Title: |
Promyelocytic leukemia (PML) protein plays important roles in regulating cell adhesion, morphology, proliferation and migration. |
Volume: |
8 |
Issue: |
3 |
Pages: |
e59477 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vos MJ |
Year: |
2009 |
Journal: |
Biochim Biophys Acta |
Title: |
HSPB7 is a SC35 speckle resident small heat shock protein. |
Volume: |
1793 |
Issue: |
8 |
Pages: |
1343-53 |
|
•
•
•
•
•
|
Publication |
First Author: |
La Padula V |
Year: |
2016 |
Journal: |
Exp Neurol |
Title: |
HSPB3 protein is expressed in motoneurons and induces their survival after lesion-induced degeneration. |
Volume: |
286 |
|
Pages: |
40-49 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kalmar B |
Year: |
2017 |
Journal: |
Hum Mol Genet |
Title: |
Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease. |
Volume: |
26 |
Issue: |
17 |
Pages: |
3313-3326 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tadros SF |
Year: |
2014 |
Journal: |
PLoS One |
Title: |
Gene expression changes for antioxidants pathways in the mouse cochlea: relations to age-related hearing deficits. |
Volume: |
9 |
Issue: |
2 |
Pages: |
e90279 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang W |
Year: |
2021 |
Journal: |
Front Pharmacol |
Title: |
Paeonol Ameliorates Chronic Itch and Spinal Astrocytic Activation via CXCR3 in an Experimental Dry Skin Model in Mice. |
Volume: |
12 |
|
Pages: |
805222 |
|
•
•
•
•
•
|
Publication |
First Author: |
Singh MK |
Year: |
2017 |
Journal: |
J Therm Biol |
Title: |
The small heat shock protein Hsp27: Present understanding and future prospects. |
Volume: |
69 |
|
Pages: |
149-154 |
|
•
•
•
•
•
|
Publication |
First Author: |
Piotrowicz RS |
Year: |
1997 |
Journal: |
J Biol Chem |
Title: |
Basolateral membrane-associated 27-kDa heat shock protein and microfilament polymerization. |
Volume: |
272 |
Issue: |
41 |
Pages: |
25920-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bektas M |
Year: |
2010 |
Journal: |
J Invest Dermatol |
Title: |
What's in a name?: Heat shock protein 27 and keratinocyte differentiation. |
Volume: |
130 |
Issue: |
1 |
Pages: |
10-2 |
|
•
•
•
•
•
|
Publication |
First Author: |
Arrigo AP |
Year: |
2005 |
Journal: |
Antioxid Redox Signal |
Title: |
Hsp27 consolidates intracellular redox homeostasis by upholding glutathione in its reduced form and by decreasing iron intracellular levels. |
Volume: |
7 |
Issue: |
3-4 |
Pages: |
414-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Perrin V |
Year: |
2007 |
Journal: |
Mol Ther |
Title: |
Neuroprotection by Hsp104 and Hsp27 in lentiviral-based rat models of Huntington's disease. |
Volume: |
15 |
Issue: |
5 |
Pages: |
903-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sinsimer KS |
Year: |
2008 |
Journal: |
Mol Cell Biol |
Title: |
Chaperone Hsp27, a novel subunit of AUF1 protein complexes, functions in AU-rich element-mediated mRNA decay. |
Volume: |
28 |
Issue: |
17 |
Pages: |
5223-37 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hayes D |
Year: |
2009 |
Journal: |
J Biol Chem |
Title: |
Phosphorylation dependence of hsp27 multimeric size and molecular chaperone function. |
Volume: |
284 |
Issue: |
28 |
Pages: |
18801-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sur R |
Year: |
2008 |
Journal: |
J Invest Dermatol |
Title: |
Hsp27 regulates pro-inflammatory mediator release in keratinocytes by modulating NF-kappaB signaling. |
Volume: |
128 |
Issue: |
5 |
Pages: |
1116-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Arrigo AP |
Year: |
2007 |
Journal: |
FEBS Lett |
Title: |
Hsp27 (HspB1) and alphaB-crystallin (HspB5) as therapeutic targets. |
Volume: |
581 |
Issue: |
19 |
Pages: |
3665-74 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This entry represents the alpha crystallin domain (ACD) found in mammalian Hsp27 (also denoted HspB1 in human).Small heat shock proteins (sHsps) are molecular chaperones that suppress protein aggregation and protect against cell stress, and are generally active as large oligomers consisting of multiple subunits [, ]. They are characterised by the presence of an alpha crystallin domain (ACD) [].Hsp27 shows enhanced synthesis in response to stress. It is a molecular chaperone which interacts with a large number of different proteins. It is found in many types of human cells including breast, uterus, cervix, platelets and cancer cells. Hsp27 has diverse cellular functions including chaperoning, regulation of actin polymerization, keratinocyte differentiation, regulation of inflammatory pathways in keratinocytes, and protection from oxidative stress through modulating glutathione levels [, , , ]. It is also a subunit of AUF1-containing protein complexes []. Hsp27 has been linked to several transduction pathways regulating cellular functions including differentiation, cell growth, development, and apoptosis []. Its activity can be regulated by phosphorylation. Its unphosphorylated state is a high molecular weight aggregated form (100-800kDa) composed of up to 24 subunits, which forms as a result of multiple interactions within the ACD, and is required for chaperone function and resistance to oxidative stress. Upon phosphorylation these large aggregates rapidly disassociate to smaller oligomers and chaperone activity is modified [].High constitutive levels of Hsp27 have been detected in various cancer cells, in particular those of carcinoma origin []. Over-expression of Hsp27 has a protective effect against various diseases-processes, including Huntington's disease []. Mutations in Hsp27 have been associated with a form of distal hereditary motor neuropathy type II and Charcot-Marie-Tooth disease type 2 []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Nie X |
Year: |
2018 |
Journal: |
Am J Physiol Renal Physiol |
Title: |
Pharmacological and genetic inhibition of downstream targets of p38 MAPK in experimental nephrotic syndrome. |
Volume: |
314 |
Issue: |
4 |
Pages: |
F602-F613 |
|
•
•
•
•
•
|
Publication |
First Author: |
Qie C |
Year: |
2020 |
Journal: |
Theranostics |
Title: |
Single-cell RNA-Seq reveals the transcriptional landscape and heterogeneity of skin macrophages in Vsir-/- murine psoriasis. |
Volume: |
10 |
Issue: |
23 |
Pages: |
10483-10497 |
|
•
•
•
•
•
|
Publication |
First Author: |
Haslbeck M |
Year: |
2002 |
Journal: |
Cell Mol Life Sci |
Title: |
sHsps and their role in the chaperone network. |
Volume: |
59 |
Issue: |
10 |
Pages: |
1649-57 |
|
•
•
•
•
•
|
Publication |
First Author: |
Haslbeck M |
Year: |
2005 |
Journal: |
Nat Struct Mol Biol |
Title: |
Some like it hot: the structure and function of small heat-shock proteins. |
Volume: |
12 |
Issue: |
10 |
Pages: |
842-6 |
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•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
209
 |
Fragment?: |
false |
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•
•
•
•
•
|
Publication |
First Author: |
Narberhaus F |
Year: |
2002 |
Journal: |
Microbiol Mol Biol Rev |
Title: |
Alpha-crystallin-type heat shock proteins: socializing minichaperones in the context of a multichaperone network. |
Volume: |
66 |
Issue: |
1 |
Pages: |
64-93; table of contents |
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•
•
•
•
|