Symbol
Name
ID
|
|
|
Synonyms
|
D15Ertd221e, mKIAA1581
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian homology
|
|
|
Sequences
|
All sequences(22)
|
Alleles and phenotypes
|
All alleles(4) :
Targeted, knock-out(1)
Targeted, other(1)
Gene trapped(1)
Spontaneous(1)
| Homozygous mutant animals exhibit joint stiffness due to increased calcium deposits in calcified cartilages and die prematurely. |
Phenotype Images (1)
|
|
Polymorphisms
|
SNPs within 2kb(814 from dbSNP Build 128)
|
Gene Ontology (GO) classifications
|
|
|
Expression
|
Literature Summary: (2 records)
cDNA source data(132)
External Resources:
Allen Brain Atlas
GENSAT
GEO
|
Molecular reagents
|
All nucleic(135)
Genomic(1)
cDNA(133)
Primer pair(1)
Microarray probesets(2)
|
Other database links
|
|
Protein domains
|
| InterPro ID |
Description |
| IPR009887 |
Progressive ankylosis |
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:6580
Sweet HO et al.,
"Progressive ankylosis, a new skeletal mutation in the mouse."
J Hered 1981 Mar-Apr;72(2):87-93
(Latest)
J:133339
Silvestri C et al.,
"Genome-wide identification of Smad/Foxh1 targets reveals a role for Foxh1 in retinoic acid regulation and forebrain development."
Dev Cell 2008 Mar;14(3):411-23
|
All references(31)
|
Other accession IDs
|
MGD-MRK-1323, MGI:1098556, MGI:88023
|