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(33)
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Phenotypes
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All phenotypic
alleles(5) :
Targeted, knock-out(1)
Targeted, other(4)
| Homozygous null mutants display multiple defects in craniofacial structures, including ears, nose, mandible and calvaria, and die shortly after birth, with some exhibiting exencephaly. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (2)
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Polymorphisms
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SNPs within 2kb(55 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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All GO classifications(17)
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Expression
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Literature Summary: (131 records)
Data Summary:
Assays (27)
Results (308)
Tissues (239)
Images (76)
Theiler Stages: 8,9,10,11,12,13,14,15,17,18,19,20,21,22,23,24,25,26,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
4 |
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28 |
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In situ reporter (knock in) |
1 |
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1 |
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RNA in situ |
19 |
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256 |
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Immunohistochemistry |
2 |
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21 |
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Northern blot |
1 |
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2 |
cDNA source data(22)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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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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Molecular reagents
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All nucleic(40)
Genomic(2)
cDNA(24)
Primer pair(6)
Other(8)
Antibodies(1)
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References
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(Earliest)
J:17176
Simeone A et al.,
"Cloning and characterization of two members of the vertebrate Dlx gene family."
Proc Natl Acad Sci U S A 1994 Mar 15;91(6):2250-4
(Latest)
J:142510
Abraira VE et al.,
"Cross-repressive interactions between Lrig3 and netrin 1 shape the architecture of the inner ear."
Development 2008 Dec;135(24):4091-9
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All references(144)
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Other accession IDs
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MGD-MRK-18757, MGI:2141401
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