Symbol
Name
ID
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Synonyms
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Wnt-3a
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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(12)
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Alleles and phenotypes
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All alleles(9) :
Targeted, knock-out(2)
Targeted, other(1)
Gene trapped(5)
Spontaneous(1)
| Homozygous null mutants die at embryonic day 10.5-12.5 with failed development of caudal somites, notochord and structures rostral to hindlimbs. Homozygotes for a hypomorphic allele have vertebral defects and a short tail due to loss of caudal vertebrae. |
Phenotype Images (1)
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Polymorphisms
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RFLP(1)
SNPs within 2kb(178 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (151 records)
Data Summary:
Assays (39)
Results (396)
Tissues (229)
Images (73)
Theiler Stages: 1,2,3,4,5,8,9,11,12,13,14,15,16,17,18,19,20,21,22,23,24,26,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
11 |
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83 |
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RNA in situ |
26 |
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300 |
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Northern blot |
1 |
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11 |
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RNase protection |
1 |
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2 |
cDNA source data(14)
External Resources:
Allen Brain Atlas
GENSAT
GEO
ArrayExpress
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Molecular reagents
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All nucleic(40)
Genomic(3)
cDNA(15)
Primer pair(13)
Other(9)
Antibodies(1)
Microarray probesets(2)
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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:13062
HESTON WE,
"The 'vestigial tail' mouse; a new recessive mutation."
J Hered 1951 Mar-Apr;42(2):71-4
(Latest)
J:155332
Fotaki V et al.,
"Loss of Wnt8b has no overt effect on hippocampus development but leads to altered Wnt gene expression levels in dorsomedial telencephalon."
Dev Dyn 2010 Jan;239(1):284-96
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All references(242)
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Other accession IDs
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MGD-MRK-15417, MGD-MRK-15441, MGD-MRK-15451
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