Symbol
Name
ID
|
|
|
Synonyms
|
A730019I05Rik, Cycn, Cyn, Dz, Edy, Flo, GENA 47, Gena 52, GENA 60, Lda, Mt, Obt, Todo, WBE1, Whi
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian
homology
|
|
|
Sequences
|
All sequences(31)
|
Alleles
and
phenotypes
|
All alleles(27) :
Gene trapped(18)
Chemically induced(9)
| Heterozygotes for mutations of this gene exhibit a variety of combinations of hyperactivity, circling, head-bobbing, semicircular canal defects, hearing loss, reduced size, and tail-kink. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (2)
Phenotype Images (2)
|
|
Polymorphisms
|
SNPs within 2kb(947 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
Literature Summary: (6 records)
Data Summary:
Assays (3)
Results (5)
Tissues (5)
Images (1)
Theiler Stages: 11,13,17,22
| |
Assay Type |
Assays |
|
Results |
| |
RT-PCR |
1 |
|
2 |
| |
RNA in situ |
2 |
|
3 |
cDNA source data(64)
External Resources:
GENSAT
GEO
|
Molecular
reagents
|
All nucleic(67)
Genomic(2)
cDNA(64)
Primer pair(1)
Microarray probesets(30)
|
Other database
links
|
|
Protein
domains
|
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:63816
Nolan PM et al.,
"A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse."
Nat Genet 2000 Aug;25(4):440-3
(Latest)
J:148116
Layman WS et al.,
"Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome."
Hum Mol Genet 2009 Jun 1;18(11):1909-23
|
All references(15)
|
Other
accession IDs
|
MGI:1861982, MGI:1861985, MGI:1861987, MGI:1861988, MGI:1862038, MGI:1890591, MGI:1890592, MGI:2662565, MGI:2662566
|
|
