Symbol
Name
ID
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Synonyms
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Lmx1.1, shaker short-tail, sst
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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(15)
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Alleles
and
phenotypes
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All alleles(13) :
Spontaneous(13)
| Mutations in the dreher locus produce neurological and skeletal abnormalities, inner ear defects, and belly spotting. Deafness and hypoplasia of Mullerian duct derivatives are also reported for some alleles. |
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Polymorphisms
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SNPs within 2kb(890 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (44 records)
Data Summary:
Assays (7)
Results (66)
Tissues (55)
Images (12)
Theiler Stages: 2,3,4,5,16,17,19,20,21,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
1 |
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15 |
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RNA in situ |
5 |
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47 |
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Immunohistochemistry |
1 |
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4 |
cDNA source data(8)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular
reagents
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All nucleic(15)
Genomic(3)
cDNA(8)
Primer pair(1)
Other(3)
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:15346
FALCONER DS et al.,
"[Dreher, a new gene of the waltzer-shaker group in the house mouse.]"
Z Indukt Abstamm Vererbungsl 1951;84(2):71-3
(Latest)
J:152851
Huang X et al.,
"Sonic hedgehog signaling regulates a novel epithelial progenitor domain of the hindbrain choroid plexus."
Development 2009 Aug;136(15):2535-43
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All references(70)
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Other
accession IDs
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MGD-MRK-14613, MGD-MRK-8891, MGI:94923
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