Symbol
Name
ID
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Synonyms
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5033403E17Rik, 9030223K07Rik, D230012E17Rik, oto, PGAP1
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Genetic Map
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Chromosome 1
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Syntenic
|
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Mapping data(
2)
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(35)
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Alleles
and
phenotypes
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All alleles(12) :
Targeted, knock-out(1)
Gene trapped(10)
Radiation induced(1)
| Mice homozygous for a radiation-induced mutation exhibit a variety of forebrain, eye, jaw, craniofacial, ear, and vertebra defects that are background sensitive. |
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Polymorphisms
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SNPs within 2kb(376 from dbSNP Build 128)
SNPs within 2kb including multiple locations(382)
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Gene Ontology
(GO)
classifications
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Expression
|
Literature Summary: (1 records)
cDNA source data(53)
External Resources:
Allen Brain Atlas
GEO
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Molecular
reagents
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All nucleic(55)
Genomic(2)
cDNA(53)
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:7938
Juriloff DM et al.,
"Genetic and developmental studies of a new mouse mutation that produces otocephaly."
J Craniofac Genet Dev Biol 1985;5(2):121-45
(Latest)
J:151594
Zoltewicz JS et al.,
"Wnt signaling is regulated by endoplasmic reticulum retention."
PLoS One 2009;4(7):e6191
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All references(10)
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Other
accession IDs
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MGD-MRK-13085, MGI:1923226, MGI:2444805, MGI:97449
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