Type |
Details |
Score |
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chimpanzee |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
dog, domestic |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
cattle |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chicken |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
macaque, rhesus |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Publication |
First Author: |
Bressler J |
Year: |
2001 |
Journal: |
Nat Genet |
Title: |
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice. |
Volume: |
28 |
Issue: |
3 |
Pages: |
232-40 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Publication |
First Author: |
Blaydes SM |
Year: |
1999 |
Journal: |
Mamm Genome |
Title: |
Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice. |
Volume: |
10 |
Issue: |
6 |
Pages: |
549-55 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gray TA |
Year: |
1999 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
An imprinted, mammalian bicistronic transcript encodes two independent proteins. |
Volume: |
96 |
Issue: |
10 |
Pages: |
5616-21 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gabriel JM |
Year: |
1998 |
Journal: |
Mamm Genome |
Title: |
Structure and function correlations at the imprinted mouse Snrpn locus. |
Volume: |
9 |
Issue: |
10 |
Pages: |
788-93 |
|
•
•
•
•
•
|
Publication |
First Author: |
Barr JA |
Year: |
1995 |
Journal: |
Mamm Genome |
Title: |
Ubiquitous expression and imprinting of Snrpn in the mouse. |
Volume: |
6 |
Issue: |
6 |
Pages: |
405-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Peery EG |
Year: |
2007 |
Journal: |
Mamm Genome |
Title: |
A targeted deletion upstream of Snrpn does not result in an imprinting defect. |
Volume: |
18 |
Issue: |
4 |
Pages: |
255-62 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Publication |
First Author: |
Cattanach BM |
Year: |
1992 |
Journal: |
Nat Genet |
Title: |
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. |
Volume: |
2 |
Issue: |
4 |
Pages: |
270-4 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bielinska B |
Year: |
2000 |
Journal: |
Nat Genet |
Title: |
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. |
Volume: |
25 |
Issue: |
1 |
Pages: |
74-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gray TA |
Year: |
1999 |
Journal: |
Nucleic Acids Res |
Title: |
Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci. |
Volume: |
27 |
Issue: |
23 |
Pages: |
4577-84 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shemer R |
Year: |
1997 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. |
Volume: |
94 |
Issue: |
19 |
Pages: |
10267-72 |
|
•
•
•
•
•
|
Publication |
First Author: |
Leff SE |
Year: |
1992 |
Journal: |
Nat Genet |
Title: |
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. |
Volume: |
2 |
Issue: |
4 |
Pages: |
259-64 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gregory RI |
Year: |
2001 |
Journal: |
Mol Cell Biol |
Title: |
DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1. |
Volume: |
21 |
Issue: |
16 |
Pages: |
5426-36 |
|
•
•
•
•
•
|
Publication |
First Author: |
Toder R |
Year: |
1996 |
Journal: |
Chromosome Res |
Title: |
The human/mouse imprinted genes IGF2, H19, SNRPN and ZNF127 map to two conserved autosomal clusters in a marsupial. |
Volume: |
4 |
Issue: |
4 |
Pages: |
295-300 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tsai TF |
Year: |
1999 |
Journal: |
Hum Mol Genet |
Title: |
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. |
Volume: |
8 |
Issue: |
8 |
Pages: |
1357-64 |
|
•
•
•
•
•
|
Publication |
First Author: |
Huntriss JD |
Year: |
1994 |
Journal: |
Mol Biol Rep |
Title: |
Mice lacking Snrpn expression show normal regulation of neuronal alternative splicing events. |
Volume: |
20 |
Issue: |
1 |
Pages: |
19-25 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Publication |
First Author: |
Szabó PE |
Year: |
1996 |
Journal: |
EMBO J |
Title: |
Maternal and paternal genomes function independently in mouse ova in establishing expression of the imprinted genes Snrpn and Igf2r: no evidence for allelic trans-sensing and counting mechanisms. |
Volume: |
15 |
Issue: |
22 |
Pages: |
6018-25 |
|
•
•
•
•
•
|
Publication |
First Author: |
Miyazaki K |
Year: |
2009 |
Journal: |
Gene |
Title: |
Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene. |
Volume: |
432 |
Issue: |
1-2 |
Pages: |
97-101 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nicholls RD |
Year: |
1999 |
Journal: |
Acta Paediatr Suppl |
Title: |
Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models. |
Volume: |
88 |
Issue: |
433 |
Pages: |
99-104 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tsai TF |
Year: |
2002 |
Journal: |
Hum Mol Genet |
Title: |
Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice. |
Volume: |
11 |
Issue: |
14 |
Pages: |
1659-68 |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Publication |
First Author: |
Vitali P |
Year: |
2010 |
Journal: |
J Cell Sci |
Title: |
Long nuclear-retained non-coding RNAs and allele-specific higher-order chromatin organization at imprinted snoRNA gene arrays. |
Volume: |
123 |
Issue: |
Pt 1 |
Pages: |
70-83 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yang T |
Year: |
1998 |
Journal: |
Nat Genet |
Title: |
A mouse model for Prader-Willi syndrome imprinting-centre mutations. |
Volume: |
19 |
Issue: |
1 |
Pages: |
25-31 |
|
•
•
•
•
•
|
Publication |
First Author: |
Leung KN |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. |
Volume: |
18 |
Issue: |
22 |
Pages: |
4227-38 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu MY |
Year: |
2006 |
Journal: |
Genes Dev |
Title: |
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain. |
Volume: |
20 |
Issue: |
20 |
Pages: |
2859-70 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu MY |
Year: |
2006 |
Journal: |
Genesis |
Title: |
Mouse imprinting defect mutations that model Angelman syndrome. |
Volume: |
44 |
Issue: |
1 |
Pages: |
12-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Smith EY |
Year: |
2011 |
Journal: |
PLoS Genet |
Title: |
Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. |
Volume: |
7 |
Issue: |
12 |
Pages: |
e1002422 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rodriguez-Jato S |
Year: |
2013 |
Journal: |
PLoS One |
Title: |
Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain. |
Volume: |
8 |
Issue: |
2 |
Pages: |
e52390 |
|
•
•
•
•
•
|
Publication |
First Author: |
Golding DM |
Year: |
2017 |
Journal: |
J Endocrinol |
Title: |
Paradoxical leanness in the imprinting-centre deletion mouse model for Prader-Willi syndrome. |
Volume: |
232 |
Issue: |
1 |
Pages: |
123-135 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yazdi PG |
Year: |
2013 |
Journal: |
Clin Transl Sci |
Title: |
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome. |
Volume: |
6 |
Issue: |
5 |
Pages: |
347-55 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chamberlain SJ |
Year: |
2004 |
Journal: |
Hum Mol Genet |
Title: |
Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. |
Volume: |
13 |
Issue: |
23 |
Pages: |
2971-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Relkovic D |
Year: |
2010 |
Journal: |
Eur J Neurosci |
Title: |
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. |
Volume: |
31 |
Issue: |
1 |
Pages: |
156-64 |
|
•
•
•
•
•
|
Publication |
First Author: |
Davies JR |
Year: |
2015 |
Journal: |
Eur J Neurosci |
Title: |
Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome. |
Volume: |
42 |
Issue: |
4 |
Pages: |
2105-13 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ozçelik T |
Year: |
1992 |
Journal: |
Nat Genet |
Title: |
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. |
Volume: |
2 |
Issue: |
4 |
Pages: |
265-9 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
rabbit, European |
|
•
•
•
•
•
|
Publication |
First Author: |
Welden JR |
Year: |
2018 |
Journal: |
Neurosci Lett |
Title: |
The posterior pituitary expresses the serotonin receptor 2C. |
Volume: |
684 |
|
Pages: |
132-139 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chamberlain SJ |
Year: |
2001 |
Journal: |
Genomics |
Title: |
The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. |
Volume: |
73 |
Issue: |
3 |
Pages: |
316-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Doe CM |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour. |
Volume: |
18 |
Issue: |
12 |
Pages: |
2140-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
de los Santos T |
Year: |
2000 |
Journal: |
Am J Hum Genet |
Title: |
Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain. |
Volume: |
67 |
Issue: |
5 |
Pages: |
1067-82 |
|
•
•
•
•
•
|
Publication |
First Author: |
Johnstone KA |
Year: |
2006 |
Journal: |
Hum Mol Genet |
Title: |
A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. |
Volume: |
15 |
Issue: |
3 |
Pages: |
393-404 |
|
•
•
•
•
•
|
Publication |
First Author: |
DuBose AJ |
Year: |
2010 |
Journal: |
Neurogenetics |
Title: |
Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC. |
Volume: |
11 |
Issue: |
2 |
Pages: |
145-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Villar AJ |
Year: |
1994 |
Journal: |
Mol Reprod Dev |
Title: |
Spatially restricted imprinting of mouse chromosome 7. |
Volume: |
37 |
Issue: |
3 |
Pages: |
247-54 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shemer R |
Year: |
2000 |
Journal: |
Nat Genet |
Title: |
The imprinting box of the Prader-Willi/Angelman syndrome domain. |
Volume: |
26 |
Issue: |
4 |
Pages: |
440-3 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lopes FL |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Reproductive and epigenetic outcomes associated with aging mouse oocytes. |
Volume: |
18 |
Issue: |
11 |
Pages: |
2032-44 |
|
•
•
•
•
•
|
Publication |
First Author: |
Stefan M |
Year: |
2011 |
Journal: |
Am J Physiol Endocrinol Metab |
Title: |
Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome. |
Volume: |
300 |
Issue: |
5 |
Pages: |
E909-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bhalla K |
Year: |
2024 |
Journal: |
Biochim Biophys Acta Mol Basis Dis |
Title: |
Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome. |
Volume: |
1870 |
Issue: |
5 |
Pages: |
167175 |
|
•
•
•
•
•
|
Publication |
First Author: |
Dubose AJ |
Year: |
2011 |
Journal: |
Hum Mol Genet |
Title: |
A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center. |
Volume: |
20 |
Issue: |
17 |
Pages: |
3461-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Meng L |
Year: |
2012 |
Journal: |
Hum Mol Genet |
Title: |
Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a. |
Volume: |
21 |
Issue: |
13 |
Pages: |
3001-12 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu MY |
Year: |
2012 |
Journal: |
PLoS One |
Title: |
An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice. |
Volume: |
7 |
Issue: |
4 |
Pages: |
e34348 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gérard M |
Year: |
1999 |
Journal: |
Nat Genet |
Title: |
Disruption of the mouse necdin gene results in early post-natal lethality. |
Volume: |
23 |
Issue: |
2 |
Pages: |
199-202 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kitsberg D |
Year: |
1993 |
Journal: |
Nature |
Title: |
Allele-specific replication timing of imprinted gene regions. |
Volume: |
364 |
Issue: |
6436 |
Pages: |
459-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Szabó PE |
Year: |
1995 |
Journal: |
Genes Dev |
Title: |
Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms. |
Volume: |
9 |
Issue: |
24 |
Pages: |
3097-108 |
|
•
•
•
•
•
|
Publication |
First Author: |
Choi JD |
Year: |
2001 |
Journal: |
Mamm Genome |
Title: |
Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes. |
Volume: |
12 |
Issue: |
10 |
Pages: |
758-64 |
|
•
•
•
•
•
|
Publication |
First Author: |
Szabó P |
Year: |
1994 |
Journal: |
Development |
Title: |
Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines. |
Volume: |
120 |
Issue: |
6 |
Pages: |
1651-60 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ogawa H |
Year: |
2006 |
Journal: |
FEBS Lett |
Title: |
Disruption of parental-specific expression of imprinted genes in uniparental fetuses. |
Volume: |
580 |
Issue: |
22 |
Pages: |
5377-84 |
|
•
•
•
•
•
|
Publication |
First Author: |
Meng L |
Year: |
2013 |
Journal: |
PLoS Genet |
Title: |
Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model. |
Volume: |
9 |
Issue: |
12 |
Pages: |
e1004039 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mould AW |
Year: |
2013 |
Journal: |
Epigenetics Chromatin |
Title: |
Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation. |
Volume: |
6 |
Issue: |
1 |
Pages: |
19 |
|
•
•
•
•
•
|
Publication |
First Author: |
Marjonen H |
Year: |
2018 |
Journal: |
PLoS One |
Title: |
Early prenatal alcohol exposure alters imprinted gene expression in placenta and embryo in a mouse model. |
Volume: |
13 |
Issue: |
5 |
Pages: |
e0197461 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
71
 |
Fragment?: |
false |
|
•
•
•
•
•
|
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 |
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Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus pahari |
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Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus spretus |
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Publication |
First Author: |
DuBose AJ |
Year: |
2012 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Temporal and developmental requirements for the Prader-Willi imprinting center. |
Volume: |
109 |
Issue: |
9 |
Pages: |
3446-50 |
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Publication |
First Author: |
Mann MR |
Year: |
2003 |
Journal: |
Biol Reprod |
Title: |
Disruption of imprinted gene methylation and expression in cloned preimplantation stage mouse embryos. |
Volume: |
69 |
Issue: |
3 |
Pages: |
902-14 |
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GXD Expression |
Probe: |
MGI:1328255 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-01-29 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328263 |
Age: |
embryonic day 9.5 |
Image: |
1 |
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Specimen Label: |
1 |
Detected: |
true |
Specimen Num: |
1 |
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GXD Expression |
Probe: |
MGI:1328255 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-01-29 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328263 |
Age: |
embryonic day 9.5 |
Image: |
1 |
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Specimen Label: |
2 |
Detected: |
true |
Specimen Num: |
2 |
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GXD Expression |
Probe: |
MGI:1328255 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-01-29 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328263 |
Age: |
embryonic day 9.5 |
Image: |
1 |
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Specimen Label: |
3 |
Detected: |
true |
Specimen Num: |
3 |
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GXD Expression |
Probe: |
MGI:1328255 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-01-29 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603920 |
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Stage: |
TS20 |
Assay Id: |
MGI:1328263 |
Age: |
embryonic day 12.5 |
Image: |
1 |
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Specimen Label: |
8 |
Detected: |
true |
Specimen Num: |
8 |
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GXD Expression |
Probe: |
MGI:1328255 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-01-29 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603920 |
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Stage: |
TS20 |
Assay Id: |
MGI:1328263 |
Age: |
embryonic day 12.5 |
Image: |
1 |
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Specimen Label: |
9 |
Detected: |
true |
Specimen Num: |
9 |
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GXD Expression |
Probe: |
MGI:1328838 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-02-08 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328963 |
Age: |
embryonic day 9.5 |
Image: |
4 |
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Specimen Label: |
+/+ |
Detected: |
true |
Specimen Num: |
1 |
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GXD Expression |
Probe: |
MGI:1328838 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-02-08 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328963 |
Age: |
embryonic day 9.5 |
Image: |
4 |
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Specimen Label: |
+/- |
Detected: |
true |
Specimen Num: |
2 |
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GXD Expression |
Probe: |
MGI:1328838 |
Assay Type: |
RT-PCR |
Annotation Date: |
1999-02-08 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:1603915 |
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Stage: |
TS15 |
Assay Id: |
MGI:1328963 |
Age: |
embryonic day 9.5 |
Image: |
4 |
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Specimen Label: |
-/- |
Detected: |
true |
Specimen Num: |
3 |
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