Symbol
Name
ID
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Synonyms
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Ltbp2
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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(18)
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Alleles and phenotypes
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All alleles(5) :
Targeted, knock-out(1)
Gene trapped(3)
Chemically induced(1)
| Homozygotes for a targeted null mutation exhibit craniofacial malformations including an overshot mandible and ossification of synchondroses. Mutants develop osteosclerosis of long bones and osteoarthritis, and, in some cases, high corticosterone levels. |
Phenotype Images (4)
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Polymorphisms
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SNPs within 2kb(55 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (6 records)
Data Summary:
Assays (1)
Results (61)
Tissues (61)
Images (13)
Theiler Stages: 14,21,24,28
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Assay Type |
Assays |
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Results |
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RNA in situ |
1 |
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61 |
cDNA source data(122)
External Resources:
Allen Brain Atlas
GEO
ArrayExpress
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Molecular reagents
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All nucleic(132)
Genomic(2)
cDNA(125)
Primer pair(3)
Other(2)
Microarray probesets(2)
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Other database links
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Protein domains
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Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:22443
Li X et al.,
"Mapping of human and murine genes for latent TGF-beta binding protein-2 (LTBP2)."
Mamm Genome 1995 Jan;6(1):42-5
(Latest)
J:128012
Todorovic V et al.,
"Long form of latent TGF-beta binding protein 1 (Ltbp1L) is essential for cardiac outflow tract septation and remodeling."
Development 2007 Oct;134(20):3723-32
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All references(22)
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