Gene Expression Data
Assay Details
Assay
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Reference:
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J:96395
Lee S, et al., Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum Mol Genet. 2005 Mar 1;14(5):627-37
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:6514715
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Gene symbol:
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L1cam
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Gene name:
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L1 cell adhesion molecule
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Results
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Specimen
5D:
embryonic day 16.5
(more )
Specimen
5D:
(close )
Genetic Background:
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Not Specified
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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Paraformaldehyde
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Embedding:
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Cryosection
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Structure |
Level |
Pattern |
Image |
Note |
TS24: forebrain |
Present |
Regionally restricted |
5D
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Expression was detected in thalamocortical tracts.
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Specimen
5D':
embryonic day 16.5; Ndntm2Stw/Ndn +
(more )
Note: Specimen carried a paternally inherited necdin deficiency and was functionally necdin null.
Specimen
5D':
(close )
Genetic Background:
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involves: 129S1/Sv * C57BL/6J
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Mutant Allele(s):
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Ndntm2Stw/Ndn+
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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Paraformaldehyde
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Embedding:
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Cryosection
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Note:
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Specimen carried a paternally inherited necdin deficiency and was functionally necdin null.
|
Structure |
Level |
Pattern |
Image |
Note |
TS24: forebrain |
Present |
Regionally restricted |
5D'
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Expression was detected in the reduced thalamocortical axons and in the mutant ectopic axon bundle in the anterior hypothalamic region dorsolateral to the optic chiasm and rostral to the zona incerta and lateral hypothalamus.
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TS24: corpus striatum |
Present |
Regionally restricted |
5D'
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Expression was detected in ectopic axonal whorls in the striatum of necdin null embryos.
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Specimen
6H:
embryonic day 13.5
(more )
Specimen
6H:
(close )
Genetic Background:
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Not Specified
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Age:
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embryonic day 13.5
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Sex:
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Not Specified
|
Type:
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section
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Fixation:
|
Paraformaldehyde
|
Embedding:
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Cryosection
|
Specimen
6H':
embryonic day 13.5; Ndntm2Stw/Ndn +
(more )
Note: Specimen carried a paternally inherited necdin deficiency and was functionally necdin null.
Specimen
6H':
(close )
Genetic Background:
|
involves: 129S1/Sv * C57BL/6J
|
Mutant Allele(s):
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Ndntm2Stw/Ndn+
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Age:
|
embryonic day 13.5
|
Sex:
|
Not Specified
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Type:
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section
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Fixation:
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Paraformaldehyde
|
Embedding:
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Cryosection
|
Note:
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Specimen carried a paternally inherited necdin deficiency and was functionally necdin null.
|
Structure |
Level |
Pattern |
Image |
Note |
TS22: dorsal thalamus |
Present |
Regionally restricted |
6H'
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Aberrant staining was noted in the ventral region of the necdin null dorsal thalamus.
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