Symbol
Name
ID
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Genetic Map
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(29)
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Alleles
and
phenotypes
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All alleles(14) :
Targeted, other(5)
Gene trapped(5)
Transgenic(1)
Spontaneous(3)
| Mutant homozygotes die at embryonic day 8-10, exhibiting neuroectodermal defects and axial duplications. Heterozygotes exhibit skeletal, cardiac, and neurological defects including short, bent tails, and deafness with circling behavior. |
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Polymorphisms
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RFLP(1)
SNPs within 2kb(57 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (10 records)
Data Summary:
Assays (4)
Results (23)
Tissues (7)
Images (7)
Theiler Stages: 17,21,24,26,28
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Assay Type |
Assays |
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Results |
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Western blot |
3 |
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14 |
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RNA in situ |
1 |
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9 |
cDNA source data(105)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular
reagents
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All nucleic(106)
cDNA(106)
Antibodies(1)
Microarray probesets(3)
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Other database
links
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Protein
domains
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Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:12953
Reed SC,
"The Inheritance and Expression of Fused, a New Mutation in the House Mouse."
Genetics 1937 Jan;22(1):1-13
(Latest)
J:147293
Chia IV et al.,
"Both the RGS Domain and the Six C-Terminal Amino Acids of Mouse Axin Are Required for Normal Embryogenesis."
Genetics 2009 Apr;181(4):1359-68
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All references(66)
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Other
accession IDs
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MGD-MRK-11553, MGD-MRK-11586, MGD-MRK-9891, MGI:2146821, MGI:95592
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