This ENU-induced T to A transversion in intron 3 disrupts a 5-prime splice donor sequence and has been shown to cause two novel splicing events in retinal pigment epithelium, one of which includes a portion of the intron downstream of exon 3 and is predicted to encode a short N-terminal polypeptide with 11 non-native amino acids and premature stop codon, and the other of which exon 3 is skipped leading to premature termination. (J:321062)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Single point
Recessive
1
--
2

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:
Show/Hide columns
Phenotypes

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top