Symbol
Name
ID
|
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian homology
|
|
|
Sequences
|
All sequences(16)
|
|
Phenotypes
|
All phenotypic
alleles(4) :
Targeted, knock-out(2)
Targeted, other(2)
| Homozygotes for targeted null mutations exhibit rib defects, muscle hypoplasia, absence of kidneys and thymus, craniofacial defects, and ear and nose defects. Heterozygotes show partial hearing loss. |
|
|
Polymorphisms
|
RFLP(1)
SNPs within 2kb(14 from dbSNP Build 128)
|
Gene Ontology (GO) classifications
|
All GO classifications(27)
|
|
Expression
|
Literature Summary: (29 records)
Data Summary:
Assays (11)
Results (142)
Tissues (103)
Images (62)
Theiler Stages: 13,14,15,17,18,19,20,21,22,23,25,26,28
| |
Assay Type |
Assays |
|
Results |
| |
RT-PCR |
1 |
|
2 |
| |
In situ reporter (knock in) |
3 |
|
20 |
| |
RNA in situ |
6 |
|
119 |
| |
Northern blot |
1 |
|
1 |
cDNA source data(6)
External Resources:
Allen Brain Atlas
GENSAT
GEO
|
Other database links
|
|
Protein domains
|
Graphical View
of Protein Domain Structure
|
Molecular reagents
|
All nucleic(10)
cDNA(7)
Primer pair(1)
Other(2)
|
|
References
|
(Earliest)
J:23775
Oliver G et al.,
"Homeobox genes and connective tissue patterning."
Development 1995 Mar;121(3):693-705
(Latest)
J:131873
Depreux FF et al.,
"Eya4-deficient mice are a model for heritable otitis media."
J Clin Invest 2008 Feb;118(2):651-8
|
All references(42)
|
Other accession IDs
|
MGD-MRK-19688, MGI:2145072
|