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Insertion of a gene trap construct, pGT1.8TM, into the gene between the two exons encoding the N-terminal seqences of the agrin isoforms. The insertion abolished activity of the long N-terminal basal laminae isoform (LN-agrin) but had no detectable affects on the short N-terminal cell associated isoform (SN-agrin). (J:64996)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
