Gene Expression Data
Assay Details
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Assay
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Reference:
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J:276459
Lahrouchi N, et al., Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly. Nat Commun. 2019 Mar 12;10(1):1180
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Assay type:
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RNA in situ
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MGI Accession ID:
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MGI:8261034
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Gene symbol:
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Fat2
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Gene name:
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FAT atypical cadherin 2
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Probe:
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Fat2 probe
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Probe preparation:
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Antisense RNA
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Results
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Specimen
not shown:
embryonic day 10.5
(more  )
Specimen
not shown:
(close  )
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Genetic Background:
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C57BL/6J
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Age:
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embryonic day 10.5
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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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4% Paraformaldehyde
|
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Embedding:
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Cryosection
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| Structure |
Level |
Pattern |
Image |
Note |
| TS17: eye |
Absent |
|
|
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Specimen
not shown:
embryonic day 11.5
(more )
Specimen
not shown:
(close )
|
Genetic Background:
|
C57BL/6J
|
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Age:
|
embryonic day 11.5
|
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Sex:
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Not Specified
|
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Type:
|
section
|
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Fixation:
|
4% Paraformaldehyde
|
|
Embedding:
|
Cryosection
|
| Structure |
Level |
Pattern |
Image |
Note |
| TS19: eye |
Absent |
|
|
|
Specimen
not shown:
embryonic day 12.5
(more )
Specimen
not shown:
(close )
|
Genetic Background:
|
C57BL/6J
|
|
Age:
|
embryonic day 12.5
|
|
Sex:
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Not Specified
|
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Type:
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section
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Fixation:
|
4% Paraformaldehyde
|
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Embedding:
|
Cryosection
|
| Structure |
Level |
Pattern |
Image |
Note |
| TS20: eye |
Absent |
|
|
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Analysis Tools
