Gene Expression Data
Assay Details
Assay
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Reference:
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J:273624
Bourgeois JR, et al., Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement. Dev Biol. 2019 Apr 1;448(1):36-47
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:7255022
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Gene symbol:
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Atp1a1
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Gene name:
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ATPase, Na+/K+ transporting, alpha 1 polypeptide
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Results
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Specimen
6C:
postnatal day 21
(more )
Specimen
6C:
(close )
Genetic Background:
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involves: C57BL/6J * FVB/NJ
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Age:
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postnatal day 21
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Sex:
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Male
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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 |
Cell Type |
Level |
Pattern |
Image |
Note |
TS28: rectus femoris |
skeletal muscle fiber |
Present |
Regionally restricted |
6C
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Expression in sarcolemma.
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Specimen
6D:
(close )
Genetic Background:
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involves: C57BL/6J * FVB/NJ
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Mutant Allele(s):
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Ahi1tm1Rujf/Ahi1tm1Rujf
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Age:
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postnatal day 21
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Sex:
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Male
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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 |
Cell Type |
Level |
Pattern |
Image |
Note |
TS28: rectus femoris |
skeletal muscle fiber |
Present |
Regionally restricted |
6D
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Reduction in cross sectional area (CSA) of muscle fibers
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