Symbol
Name
ID
|
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Synonyms
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1810065L06Rik, D9Bwg1455e
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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(34)
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Alleles
and
phenotypes
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All alleles(6) :
Gene trapped(5)
Spontaneous(1)
| Homozygous mutants have progressive retinal atrophy, limb paralysis, and seizures that lead to early death. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
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Polymorphisms
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SNPs within 2kb(21 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
|
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Expression
|
Literature Summary: (1 records)
Data Summary:
Assays (1)
Results (13)
Tissues (9)
Images (7)
Theiler Stages: 20,22,24,26,28
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Assay Type |
Assays |
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Results |
| |
RNA in situ |
1 |
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13 |
cDNA source data(6)
External Resources:
Allen Brain Atlas
GENSAT
GEO
|
Molecular
reagents
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All nucleic(8)
cDNA(7)
Primer pair(1)
Microarray probesets(2)
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Other database
links
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References
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(Earliest)
J:44483
Brady KP et al.,
"Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis."
Genome Res 1997 Nov;7(11):1085-93
(Latest)
J:153101
Kielar C et al.,
"Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease."
Hum Mol Genet 2009 Nov 1;18(21):4066-80
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All references(15)
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Other
accession IDs
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MGD-MRK-34102, MGI:106408, MGI:1202067, MGI:1923774, MGI:2143349
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