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| Nomenclature |
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Symbol:
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Fsttm1Zuk
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Name:
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follistatin;
targeted mutation 1, Martin M Matzuk
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MGI ID: |
MGI:1857467 |
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Synonyms: |
fsm1, Fst-, Fsttm1 |
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Gene:
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Fst
Location:
Chr13:114452262-114458730 bp, - strand
Genetic Position: Chr13,
64.15 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:23925
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Parent Cell Line:
| AB2.1 (ES Cell) |
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Strain of Origin:
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129S7/SvEvBrd-Hprtb-m2
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
| |
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An Hprt expression cassette replaced the entire gene, including all 6 exons. (J:23925)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:23925
Matzuk MM et al.,
"Multiple defects and perinatal death in mice deficient in follistatin [see comments]"
Nature 1995 Mar 23;374(6520):360-3
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All: |
19 reference(s)
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Analysis Tools
