Type |
Details |
Score |
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
zebrafish |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
macaque, rhesus |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
dog, domestic |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chimpanzee |
|
•
•
•
•
•
|
Gene |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
cattle |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
frog, western clawed |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chicken |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Publication |
First Author: |
Huang S |
Year: |
2000 |
Journal: |
Nucleic Acids Res |
Title: |
Characterization of the human and mouse WRN 3'-->5' exonuclease. |
Volume: |
28 |
Issue: |
12 |
Pages: |
2396-405 |
|
•
•
•
•
•
|
Publication |
First Author: |
Moser R |
Year: |
2012 |
Journal: |
Mol Cancer Res |
Title: |
MYC-driven tumorigenesis is inhibited by WRN syndrome gene deficiency. |
Volume: |
10 |
Issue: |
4 |
Pages: |
535-45 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lombard DB |
Year: |
2000 |
Journal: |
Mol Cell Biol |
Title: |
Mutations in the WRN gene in mice accelerate mortality in a p53-null background. |
Volume: |
20 |
Issue: |
9 |
Pages: |
3286-91 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kang SM |
Year: |
2021 |
Journal: |
Sci Rep |
Title: |
Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A. |
Volume: |
11 |
Issue: |
1 |
Pages: |
9122 |
|
•
•
•
•
•
|
Publication |
First Author: |
Aumailley L |
Year: |
2015 |
Journal: |
PLoS One |
Title: |
Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice. |
Volume: |
10 |
Issue: |
10 |
Pages: |
e0140292 |
|
•
•
•
•
•
|
Publication |
First Author: |
Xue Y |
Year: |
2002 |
Journal: |
Biochemistry |
Title: |
A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3'- 5' exonuclease and 5'-protruding strand endonuclease activities. |
Volume: |
41 |
Issue: |
9 |
Pages: |
2901-12 |
|
•
•
•
•
•
|
Publication |
First Author: |
Aumailley L |
Year: |
2018 |
Journal: |
FASEB J |
Title: |
Serum vitamin C levels modulate the lifespan and endoplasmic reticulum stress response pathways in mice synthesizing a nonfunctional mutant WRN protein. |
Volume: |
32 |
Issue: |
7 |
Pages: |
3623-3640 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
643
|
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Massip L |
Year: |
2006 |
Journal: |
Exp Gerontol |
Title: |
Increased insulin, triglycerides, reactive oxygen species, and cardiac fibrosis in mice with a mutation in the helicase domain of the Werner syndrome gene homologue. |
Volume: |
41 |
Issue: |
2 |
Pages: |
157-68 |
|
•
•
•
•
•
|
Publication |
First Author: |
Laud PR |
Year: |
2005 |
Journal: |
Genes Dev |
Title: |
Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway. |
Volume: |
19 |
Issue: |
21 |
Pages: |
2560-70 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shen JC |
Year: |
2000 |
Journal: |
Trends Genet |
Title: |
The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases. |
Volume: |
16 |
Issue: |
5 |
Pages: |
213-20 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chang S |
Year: |
2005 |
Journal: |
Int J Biochem Cell Biol |
Title: |
A mouse model of Werner Syndrome: what can it tell us about aging and cancer? |
Volume: |
37 |
Issue: |
5 |
Pages: |
991-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kahyo T |
Year: |
2008 |
Journal: |
FEBS Lett |
Title: |
Sirtuin-mediated deacetylation pathway stabilizes Werner syndrome protein. |
Volume: |
582 |
Issue: |
17 |
Pages: |
2479-83 |
|
•
•
•
•
•
|
Publication |
First Author: |
Aumailley L |
Year: |
2018 |
Journal: |
PLoS One |
Title: |
Vitamin C alters the amount of specific endoplasmic reticulum associated proteins involved in lipid metabolism in the liver of mice synthesizing a nonfunctional Werner syndrome (Wrn) mutant protein. |
Volume: |
13 |
Issue: |
3 |
Pages: |
e0193170 |
|
•
•
•
•
•
|
Publication |
First Author: |
Aumailley L |
Year: |
2015 |
Journal: |
Exp Gerontol |
Title: |
Impact of vitamin C on the cardiometabolic and inflammatory profiles of mice lacking a functional Werner syndrome protein helicase. |
Volume: |
72 |
|
Pages: |
192-203 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chang S |
Year: |
2004 |
Journal: |
Nat Genet |
Title: |
Essential role of limiting telomeres in the pathogenesis of Werner syndrome. |
Volume: |
36 |
Issue: |
8 |
Pages: |
877-82 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu J |
Year: |
1998 |
Journal: |
Mech Ageing Dev |
Title: |
Effect of age and apoptosis on the mouse homologue of the huWRN gene. |
Volume: |
103 |
Issue: |
1 |
Pages: |
27-44 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kawabe Yi |
Year: |
2001 |
Journal: |
J Biol Chem |
Title: |
A novel protein interacts with the Werner's syndrome gene product physically and functionally. |
Volume: |
276 |
Issue: |
23 |
Pages: |
20364-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kanagaraj R |
Year: |
2012 |
Journal: |
Nucleic Acids Res |
Title: |
Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage. |
Volume: |
40 |
Issue: |
17 |
Pages: |
8449-59 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bachrati CZ |
Year: |
2003 |
Journal: |
Biochem J |
Title: |
RecQ helicases: suppressors of tumorigenesis and premature aging. |
Volume: |
374 |
Issue: |
Pt 3 |
Pages: |
577-606 |
|
•
•
•
•
•
|
Publication |
First Author: |
Du X |
Year: |
2004 |
Journal: |
Mol Cell Biol |
Title: |
Telomere shortening exposes functions for the mouse Werner and Bloom syndrome genes. |
Volume: |
24 |
Issue: |
19 |
Pages: |
8437-46 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lebel M |
Year: |
1998 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. |
Volume: |
95 |
Issue: |
22 |
Pages: |
13097-102 |
|
•
•
•
•
•
|
Publication |
First Author: |
Leder A |
Year: |
2002 |
Journal: |
Oncogene |
Title: |
Genetic interaction between the unstable v-Ha-RAS transgene (Tg.AC) and the murine Werner syndrome gene: transgene instability and tumorigenesis. |
Volume: |
21 |
Issue: |
43 |
Pages: |
6657-68 |
|
•
•
•
•
•
|
Publication |
First Author: |
Deschênes F |
Year: |
2005 |
Journal: |
Hum Mol Genet |
Title: |
In vivo misregulation of genes involved in apoptosis, development and oxidative stress in mice lacking both functional Werner syndrome protein and poly(ADP-ribose) polymerase-1. |
Volume: |
14 |
Issue: |
21 |
Pages: |
3293-308 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lebel M |
Year: |
2003 |
Journal: |
Am J Pathol |
Title: |
Genetic cooperation between the Werner syndrome protein and poly(ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal rearrangements, and cancer in mice. |
Volume: |
162 |
Issue: |
5 |
Pages: |
1559-69 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pignolo RJ |
Year: |
2008 |
Journal: |
Aging Cell |
Title: |
Defects in telomere maintenance molecules impair osteoblast differentiation and promote osteoporosis. |
Volume: |
7 |
Issue: |
1 |
Pages: |
23-31 |
|
•
•
•
•
•
|
Publication |
First Author: |
Suzuki T |
Year: |
2001 |
Journal: |
Oncogene |
Title: |
Diverged nuclear localization of Werner helicase in human and mouse cells. |
Volume: |
20 |
Issue: |
20 |
Pages: |
2551-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Cheng WH |
Year: |
2003 |
Journal: |
Mol Cell Biol |
Title: |
Werner syndrome protein phosphorylation by abl tyrosine kinase regulates its activity and distribution. |
Volume: |
23 |
Issue: |
18 |
Pages: |
6385-95 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kawabe Y |
Year: |
2000 |
Journal: |
J Biol Chem |
Title: |
Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1. |
Volume: |
275 |
Issue: |
28 |
Pages: |
20963-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lebel M |
Year: |
2002 |
Journal: |
Carcinogenesis |
Title: |
Increased frequency of DNA deletions in pink-eyed unstable mice carrying a mutation in the Werner syndrome gene homologue. |
Volume: |
23 |
Issue: |
1 |
Pages: |
213-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lebel M |
Year: |
2001 |
Journal: |
Cancer Res |
Title: |
Tumorigenic effect of nonfunctional p53 or p21 in mice mutant in the Werner syndrome helicase. |
Volume: |
61 |
Issue: |
5 |
Pages: |
1816-9 |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus caroli |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus pahari |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus spretus |
|
•
•
•
•
•
|
Publication |
First Author: |
Imamura O |
Year: |
1997 |
Journal: |
Genomics |
Title: |
Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization. |
Volume: |
41 |
Issue: |
2 |
Pages: |
298-300 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rekik K |
Year: |
2017 |
Journal: |
Behav Brain Res |
Title: |
Cognitive deficit in hippocampal-dependent tasks in Werner syndrome mouse model. |
Volume: |
323 |
|
Pages: |
68-77 |
|
•
•
•
•
•
|
Publication |
First Author: |
Brennan TA |
Year: |
2014 |
Journal: |
Dis Model Mech |
Title: |
Mouse models of telomere dysfunction phenocopy skeletal changes found in human age-related osteoporosis. |
Volume: |
7 |
Issue: |
5 |
Pages: |
583-92 |
|
•
•
•
•
•
|
Publication |
First Author: |
Oshima J |
Year: |
2000 |
Journal: |
In Vivo |
Title: |
Comparative aspects of the Werner syndrome gene. |
Volume: |
14 |
Issue: |
1 |
Pages: |
165-72 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yu CE |
Year: |
1996 |
Journal: |
Science |
Title: |
Positional cloning of the Werner's syndrome gene. |
Volume: |
272 |
Issue: |
5259 |
Pages: |
258-62 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675700 |
Assay Type: |
RT-PCR |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1876728 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675713 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
+/+ |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675700 |
Assay Type: |
RT-PCR |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1876728 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675713 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
+/- |
Detected: |
true |
Specimen Num: |
2 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675700 |
Assay Type: |
RT-PCR |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1876728 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675713 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
-/- |
Detected: |
true |
Specimen Num: |
3 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675702 |
Assay Type: |
Northern blot |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1737328 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675709 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
+/+ |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675702 |
Assay Type: |
Northern blot |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1737328 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675709 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
+/- |
Detected: |
true |
Specimen Num: |
2 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:2675702 |
Assay Type: |
Northern blot |
Annotation Date: |
2003-10-06 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1737328 |
|
Stage: |
TS28 |
Assay Id: |
MGI:2675709 |
Age: |
postnatal |
Image: |
2 |
|
Specimen Label: |
-/- |
Detected: |
true |
Specimen Num: |
3 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3526321 |
Assay Type: |
RNA in situ |
Annotation Date: |
2005-02-14 |
Strength: |
Present |
Sex: |
Male |
Emaps: |
EMAPS:1797321 |
Pattern: |
Not Specified |
Stage: |
TS21 |
Assay Id: |
MGI:3526379 |
Age: |
embryonic day 12.5 |
|
Note: |
Authors report epithelial expression. |
Specimen Label: |
not shown |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3526321 |
Assay Type: |
RNA in situ |
Annotation Date: |
2005-02-14 |
Strength: |
Absent |
Sex: |
Female |
Emaps: |
EMAPS:1796221 |
|
Stage: |
TS21 |
Assay Id: |
MGI:3526379 |
Age: |
embryonic day 12.5 |
|
|
Specimen Label: |
not shown |
Detected: |
false |
Specimen Num: |
2 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chung L |
Year: |
2015 |
Journal: |
Oncogene |
Title: |
The FEN1 E359K germline mutation disrupts the FEN1-WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers. |
Volume: |
34 |
Issue: |
7 |
Pages: |
902-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang H |
Year: |
2013 |
Journal: |
J Mol Med (Berl) |
Title: |
R-Spondin 1 promotes vibration-induced bone formation in mouse models of osteoporosis. |
Volume: |
91 |
Issue: |
12 |
Pages: |
1421-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang H |
Year: |
2012 |
Journal: |
Aging Cell |
Title: |
Impairment of osteoblast differentiation due to proliferation-independent telomere dysfunction in mouse models of accelerated aging. |
Volume: |
11 |
Issue: |
4 |
Pages: |
704-13 |
|
•
•
•
•
•
|
Publication |
First Author: |
Drosopoulos WC |
Year: |
2015 |
Journal: |
J Cell Biol |
Title: |
BLM helicase facilitates telomere replication during leading strand synthesis of telomeres. |
Volume: |
210 |
Issue: |
2 |
Pages: |
191-208 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yu Q |
Year: |
2015 |
Journal: |
Cell Rep |
Title: |
DNA-damage-induced type I interferon promotes senescence and inhibits stem cell function. |
Volume: |
11 |
Issue: |
5 |
Pages: |
785-797 |
|
•
•
•
•
•
|
Publication |
First Author: |
Dron M |
Year: |
2000 |
Journal: |
Genomics |
Title: |
Mouse scrapie responsive gene 1 (Scrg1): genomic organization, physical linkage to sap30, genetic mapping on chromosome 8, and expression in neuronal primary cell cultures. |
Volume: |
70 |
Issue: |
1 |
Pages: |
140-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sebastiani G |
Year: |
2006 |
Journal: |
Hum Mol Genet |
Title: |
Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice. |
Volume: |
15 |
Issue: |
15 |
Pages: |
2313-23 |
|
•
•
•
•
•
|
Publication |
First Author: |
McClive PJ |
Year: |
2003 |
Journal: |
Genesis |
Title: |
Subtractive hybridisation screen identifies sexually dimorphic gene expression in the embryonic mouse gonad. |
Volume: |
37 |
Issue: |
2 |
Pages: |
84-90 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li Y |
Year: |
2015 |
Journal: |
Nature |
Title: |
Global genetic analysis in mice unveils central role for cilia in congenital heart disease. |
Volume: |
521 |
Issue: |
7553 |
Pages: |
520-4 |
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Publication |
First Author: |
Lo C |
Year: |
2011 |
Journal: |
MGI Direct Data Submission (B2B/CvDC) |
Title: |
Information submitted by the NHLBI Cardiovascular Development Consortium (CvDC), Bench to Bassinet Program (B2B/CvDC) |
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Publication |
First Author: |
Shanghai Model Organisms Center |
Year: |
2017 |
Journal: |
MGI Direct Data Submission |
Title: |
Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China |
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Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2001 |
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Title: |
Gene Ontology Annotation by the MGI Curatorial Staff |
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Publication |
First Author: |
GO Central curators, GOA curators, Rhea curators |
Year: |
2020 |
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Title: |
Automatic Gene Ontology annotation based on Rhea mapping |
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Publication |
First Author: |
MGI and IMPC |
Year: |
2018 |
Journal: |
Database Release |
Title: |
MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC) |
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Publication |
First Author: |
Cyagen Biosciences Inc. |
Year: |
2022 |
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Title: |
Cyagen Biosciences Website. |
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Publication |
First Author: |
Hansen GM |
Year: |
2008 |
Journal: |
Genome Res |
Title: |
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells. |
Volume: |
18 |
Issue: |
10 |
Pages: |
1670-9 |
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Publication |
First Author: |
DDB, FB, MGI, GOA, ZFIN curators |
Year: |
2001 |
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Title: |
Gene Ontology annotation through association of InterPro records with GO terms |
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Publication |
First Author: |
The Gene Ontology Consortium |
Year: |
2014 |
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Title: |
Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs |
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Publication |
First Author: |
Carninci P |
Year: |
2005 |
Journal: |
Science |
Title: |
The transcriptional landscape of the mammalian genome. |
Volume: |
309 |
Issue: |
5740 |
Pages: |
1559-63 |
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Publication |
First Author: |
Zambrowicz BP |
Year: |
2003 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. |
Volume: |
100 |
Issue: |
24 |
Pages: |
14109-14 |
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Publication |
First Author: |
Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI) |
Year: |
2008 |
Journal: |
Database Download |
Title: |
Mouse Gene Trap Data Load from dbGSS |
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Publication |
First Author: |
GemPharmatech |
Year: |
2020 |
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Title: |
GemPharmatech Website. |
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Publication |
First Author: |
AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators |
Year: |
2011 |
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Title: |
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity |
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Publication |
First Author: |
GOA curators |
Year: |
2016 |
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Title: |
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara |
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Publication |
First Author: |
UniProt-GOA |
Year: |
2012 |
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Title: |
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping |
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Publication |
First Author: |
The Jackson Laboratory Mouse Radiation Hybrid Database |
Year: |
2004 |
Journal: |
Database Release |
Title: |
Mouse T31 Radiation Hybrid Data Load |
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