Type |
Details |
Score |
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
frog, western clawed |
|
•
•
•
•
•
|
Gene |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
cattle |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chimpanzee |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
dog, domestic |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chicken |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
macaque, rhesus |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Calpain-3 (CAPN3) belongs to the calpain family, which consists of a group of Ca2+ dependent cysteine proteases that regulate functions of substrates by proteolysis [, ]. Calpain-3 is a calcium-dependent cysteine protease mainly expressed in skeletal muscle. It is involved in sarcomere maintenance and remodelling []. It interacts with myospryn, which is a muscle-specific protein that functions in vesicular trafficking and protein kinase A signalling []. Mutations of the calpain-3 gene cause limb-girdle muscular dystrophy 2A (LGMD2A), an autosomal recessive degenerative myopathy characterised by progressive symmetrical atrophy and weakness of the proximal limb muscles and elevated serum creatine kinase [, ]. |
|
•
•
•
•
•
|
Publication |
First Author: |
Lasa-Elgarresta J |
Year: |
2022 |
Journal: |
Front Cell Dev Biol |
Title: |
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 Mutations. |
Volume: |
10 |
|
Pages: |
822563 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sarparanta J |
Year: |
2010 |
Journal: |
J Biol Chem |
Title: |
Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies. |
Volume: |
285 |
Issue: |
39 |
Pages: |
30304-15 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
821
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
709
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
815
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
785
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
80
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
136
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
178
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
653
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
44
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
737
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
156
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
709
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
821
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
421
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
139
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
757
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
156
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
191
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Goll DE |
Year: |
2003 |
Journal: |
Physiol Rev |
Title: |
The calpain system. |
Volume: |
83 |
Issue: |
3 |
Pages: |
731-801 |
|
•
•
•
•
•
|
Publication |
First Author: |
Richard I |
Year: |
1995 |
Journal: |
Cell |
Title: |
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. |
Volume: |
81 |
Issue: |
1 |
Pages: |
27-40 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kawai H |
Year: |
1998 |
Journal: |
Muscle Nerve |
Title: |
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families. |
Volume: |
21 |
Issue: |
11 |
Pages: |
1493-501 |
|
•
•
•
•
•
|
Publication |
First Author: |
Duguez S |
Year: |
2006 |
Journal: |
FEBS J |
Title: |
Calpain 3: a key regulator of the sarcomere? |
Volume: |
273 |
Issue: |
15 |
Pages: |
3427-36 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jeong SY |
Year: |
2013 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Calpain-dependent cytoskeletal rearrangement exploited for anthrax toxin endocytosis. |
Volume: |
110 |
Issue: |
42 |
Pages: |
E4007-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
Huebsch KA |
Year: |
2005 |
Journal: |
Hum Mol Genet |
Title: |
Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain. |
Volume: |
14 |
Issue: |
19 |
Pages: |
2801-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Witt CC |
Year: |
2004 |
Journal: |
J Mol Biol |
Title: |
Induction and myofibrillar targeting of CARP, and suppression of the Nkx2.5 pathway in the MDM mouse with impaired titin-based signaling. |
Volume: |
336 |
Issue: |
1 |
Pages: |
145-54 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ojima K |
Year: |
2020 |
Journal: |
Biol Open |
Title: |
Developing fluorescence sensor probe to capture activated muscle-specific calpain-3 (CAPN3) in living muscle cells. |
Volume: |
9 |
Issue: |
9 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2018 |
Journal: |
Hum Mol Genet |
Title: |
Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy. |
Volume: |
27 |
Issue: |
9 |
Pages: |
1642-1653 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2006 |
Journal: |
Mol Cell Biol |
Title: |
Regulation of the M-cadherin-beta-catenin complex by calpain 3 during terminal stages of myogenic differentiation. |
Volume: |
26 |
Issue: |
22 |
Pages: |
8437-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Benayoun B |
Year: |
2008 |
Journal: |
FASEB J |
Title: |
NF-kappaB-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2A. |
Volume: |
22 |
Issue: |
5 |
Pages: |
1521-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ermolova N |
Year: |
2011 |
Journal: |
Hum Mol Genet |
Title: |
Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3. |
Volume: |
20 |
Issue: |
17 |
Pages: |
3331-45 |
|
•
•
•
•
•
|
Publication |
First Author: |
Liu J |
Year: |
2020 |
Journal: |
Cell Rep Med |
Title: |
A Small-Molecule Approach to Restore a Slow-Oxidative Phenotype and Defective CaMKIIβ Signaling in Limb Girdle Muscular Dystrophy. |
Volume: |
1 |
Issue: |
7 |
Pages: |
100122 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jaka O |
Year: |
2012 |
Journal: |
Neurogenetics |
Title: |
C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle aging. |
Volume: |
13 |
Issue: |
4 |
Pages: |
347-57 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tang Y |
Year: |
2007 |
Journal: |
Invest Ophthalmol Vis Sci |
Title: |
Age-related cataracts in alpha3Cx46-knockout mice are dependent on a calpain 3 isoform. |
Volume: |
48 |
Issue: |
6 |
Pages: |
2685-94 |
|
•
•
•
•
•
|
Publication |
First Author: |
Charton K |
Year: |
2015 |
Journal: |
Hum Mol Genet |
Title: |
CAPN3-mediated processing of C-terminal titin replaced by pathological cleavage in titinopathy. |
Volume: |
24 |
Issue: |
13 |
Pages: |
3718-31 |
|
•
•
•
•
•
|
Publication |
First Author: |
Stuelsatz P |
Year: |
2010 |
Journal: |
J Biol Chem |
Title: |
Down-regulation of MyoD by calpain 3 promotes generation of reserve cells in C2C12 myoblasts. |
Volume: |
285 |
Issue: |
17 |
Pages: |
12670-83 |
|
•
•
•
•
•
|
Publication |
First Author: |
van Haagen HH |
Year: |
2009 |
Journal: |
PLoS One |
Title: |
Novel protein-protein interactions inferred from literature context. |
Volume: |
4 |
Issue: |
11 |
Pages: |
e7894 |
|
•
•
•
•
•
|
Publication |
First Author: |
Taveau M |
Year: |
2003 |
Journal: |
Mol Cell Biol |
Title: |
Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components. |
Volume: |
23 |
Issue: |
24 |
Pages: |
9127-35 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2012 |
Journal: |
Hum Mol Genet |
Title: |
Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3. |
Volume: |
21 |
Issue: |
14 |
Pages: |
3193-204 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ermolova N |
Year: |
2015 |
Journal: |
J Biol Chem |
Title: |
Autolytic activation of calpain 3 proteinase is facilitated by calmodulin protein. |
Volume: |
290 |
Issue: |
2 |
Pages: |
996-1004 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2008 |
Journal: |
Hum Mol Genet |
Title: |
Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle. |
Volume: |
17 |
Issue: |
21 |
Pages: |
3271-80 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pistoni M |
Year: |
2013 |
Journal: |
PLoS Genet |
Title: |
Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD). |
Volume: |
9 |
Issue: |
1 |
Pages: |
e1003186 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2016 |
Journal: |
Hum Mol Genet |
Title: |
Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy). |
Volume: |
25 |
Issue: |
11 |
Pages: |
2194-2207 |
|
•
•
•
•
•
|
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: |
Richard I |
Year: |
1996 |
Journal: |
Mamm Genome |
Title: |
Molecular cloning of mouse canp3, the gene associated with limb-girdle muscular dystrophy 2A in human. |
Volume: |
7 |
Issue: |
5 |
Pages: |
377-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ojima K |
Year: |
2010 |
Journal: |
J Clin Invest |
Title: |
Dynamic distribution of muscle-specific calpain in mice has a key role in physical-stress adaptation and is impaired in muscular dystrophy. |
Volume: |
120 |
Issue: |
8 |
Pages: |
2672-83 |
|
•
•
•
•
•
|
Publication |
First Author: |
Richard I |
Year: |
2000 |
Journal: |
J Cell Biol |
Title: |
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice. |
Volume: |
151 |
Issue: |
7 |
Pages: |
1583-90 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fougerousse F |
Year: |
2003 |
Journal: |
Muscle Nerve |
Title: |
Force impairment in calpain 3-deficient mice is not correlated with mechanical disruption. |
Volume: |
27 |
Issue: |
5 |
Pages: |
616-23 |
|
•
•
•
•
•
|
Publication |
First Author: |
Combaret L |
Year: |
2003 |
Journal: |
Int J Biochem Cell Biol |
Title: |
Down-regulation of genes in the lysosomal and ubiquitin-proteasome proteolytic pathways in calpain-3-deficient muscle. |
Volume: |
35 |
Issue: |
5 |
Pages: |
676-84 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2005 |
Journal: |
Hum Mol Genet |
Title: |
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway. |
Volume: |
14 |
Issue: |
15 |
Pages: |
2125-34 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kramerova I |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle. |
Volume: |
18 |
Issue: |
17 |
Pages: |
3194-205 |
|
•
•
•
•
•
|
Publication |
First Author: |
Spencer MJ |
Year: |
2002 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Stable expression of calpain 3 from a muscle transgene in vivo: immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturation. |
Volume: |
99 |
Issue: |
13 |
Pages: |
8874-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ono Y |
Year: |
2010 |
Journal: |
J Biol Chem |
Title: |
Skeletal muscle-specific calpain is an intracellular Na+-dependent protease. |
Volume: |
285 |
Issue: |
30 |
Pages: |
22986-98 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tagawa K |
Year: |
2000 |
Journal: |
Hum Mol Genet |
Title: |
Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A. |
Volume: |
9 |
Issue: |
9 |
Pages: |
1393-402 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ono Y |
Year: |
2006 |
Journal: |
J Biol Chem |
Title: |
Suppressed disassembly of autolyzing p94/CAPN3 by N2A connectin/titin in a genetic reporter system. |
Volume: |
281 |
Issue: |
27 |
Pages: |
18519-31 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ojima K |
Year: |
2007 |
Journal: |
J Biol Chem |
Title: |
Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain. |
Volume: |
282 |
Issue: |
19 |
Pages: |
14493-504 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Absent |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603919 |
|
Stage: |
TS19 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 11.5 |
|
|
Specimen Label: |
E11.5 |
Detected: |
false |
Specimen Num: |
1 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603920 |
|
Stage: |
TS20 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 12.5 |
|
|
Specimen Label: |
E12.5 |
Detected: |
true |
Specimen Num: |
2 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603921 |
|
Stage: |
TS21 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 13.5 |
|
|
Specimen Label: |
E13.5 |
Detected: |
true |
Specimen Num: |
3 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603922 |
|
Stage: |
TS22 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 14.5 |
|
|
Specimen Label: |
E14.5 |
Detected: |
true |
Specimen Num: |
4 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603923 |
|
Stage: |
TS23 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 15.5 |
|
|
Specimen Label: |
E15.5 |
Detected: |
true |
Specimen Num: |
5 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603924 |
|
Stage: |
TS24 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 16.5 |
|
|
Specimen Label: |
E16.5 |
Detected: |
true |
Specimen Num: |
6 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603925 |
|
Stage: |
TS25 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 17.5 |
|
|
Specimen Label: |
E17.5 |
Detected: |
true |
Specimen Num: |
7 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603926 |
|
Stage: |
TS26 |
Assay Id: |
MGI:3767308 |
Age: |
embryonic day 18.5 |
|
|
Specimen Label: |
E18.5 |
Detected: |
true |
Specimen Num: |
8 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1783823 |
|
Stage: |
TS23 |
Assay Id: |
MGI:3767309 |
Age: |
embryonic day 15.5 |
|
|
Specimen Label: |
embryonic lens |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1783828 |
|
Stage: |
TS28 |
Assay Id: |
MGI:3767309 |
Age: |
postnatal month 6 |
|
|
Specimen Label: |
adult lens |
Detected: |
true |
Specimen Num: |
2 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:3598828 |
|
Stage: |
TS28 |
Assay Id: |
MGI:3767309 |
Age: |
postnatal week 9-11 |
|
|
Specimen Label: |
skeletal muscle |
Detected: |
true |
Specimen Num: |
3 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:3271728 |
|
Stage: |
TS28 |
Assay Id: |
MGI:3767309 |
Age: |
postnatal week 9-11 |
|
|
Specimen Label: |
smooth muscle |
Detected: |
true |
Specimen Num: |
4 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1610528 |
|
Stage: |
TS28 |
Assay Id: |
MGI:3767309 |
Age: |
postnatal week 9-11 |
|
|
Specimen Label: |
heart |
Detected: |
true |
Specimen Num: |
5 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767294 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1689428 |
|
Stage: |
TS28 |
Assay Id: |
MGI:3767309 |
Age: |
postnatal week 9-11 |
|
|
Specimen Label: |
brain |
Detected: |
true |
Specimen Num: |
6 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:3767295 |
Assay Type: |
RT-PCR |
Annotation Date: |
2008-01-13 |
Strength: |
Absent |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603919 |
|
Stage: |
TS19 |
Assay Id: |
MGI:3767310 |
Age: |
embryonic day 11.5 |
|
|
Specimen Label: |
E11.5 |
Detected: |
false |
Specimen Num: |
1 |
|
•
•
•
•
•
|