Symbol
Name
ID
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Synonyms
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1110035E02Rik, 1700007L07Rik, fsn, hea
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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(34)
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Alleles and phenotypes
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All alleles(5) :
Targeted, other(2)
Spontaneous(3)
| Homozygotes for a spontaneous mutation exhibit reduced growth, sparse hair, thickened, scaly skin, increased numbers of splenic B cells, macrophages, and erythroid cells, elevated IgE, glomerulonephritis, and forestomach papillomas. |
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Polymorphisms
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SNPs within 2kb(352 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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cDNA source data(71)
External Resources:
Allen Brain Atlas
GEO
ArrayExpress
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Molecular reagents
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All nucleic(72)
cDNA(72)
Microarray probesets(1)
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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:7515
Shimizu K et al.,
"Hereditary erythroblastic anaemia in the laboratory mouse."
Lab Anim 1983 Jul;17(3):198-202
(Latest)
J:147542
Takabayashi S et al.,
"The novel tetratricopeptide repeat domain 7 mutation, Ttc7fsn-Jic, with deletion of the TPR-2B repeat causes severe flaky skin phenotype."
Exp Biol Med (Maywood) 2007 May;232(5):695-9
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All references(32)
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Other accession IDs
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MGD-MRK-10690, MGD-MRK-9877, MGI:1922718, MGI:95584, MGI:96068
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