Symbol
Name
ID
|
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian
homology
|
|
|
Sequences
|
All sequences(22)
|
Alleles
and
phenotypes
|
All alleles(22) :
Targeted, other(4)
Gene trapped(18)
| Mice homozygous for disruptions in this gene display a lethal phenotype. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
|
|
Polymorphisms
|
RFLP(1)
SNPs within 2kb(1401 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
Literature Summary: (9 records)
Data Summary:
Assays (3)
Results (38)
Tissues (38)
Images (9)
Theiler Stages: 9,11,13,17,19,21,24
| |
Assay Type |
Assays |
|
Results |
| |
RNA in situ |
3 |
|
38 |
cDNA source data(89)
External Resources:
Allen Brain Atlas
GEO
|
Molecular
reagents
|
All nucleic(90)
cDNA(89)
Primer pair(1)
Microarray probesets(2)
|
Other database
links
|
|
Protein
domains
|
| InterPro ID |
Description |
| IPR004263 |
Exostosin-like |
| IPR015338 |
EXTL2, alpha-1,4-N-acetylhexosaminyltransferase |
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:48118
Hennekam RC,
"Hereditary multiple exostoses."
J Med Genet 1991 Apr;28(4):262-6
(Latest)
J:152572
Iwao K et al.,
"Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-beta2 signaling."
J Clin Invest 2009 Jul;119(7):1997-2008
|
All references(31)
|
Other
accession IDs
|
MGI:2145899
|
