Log In|Sign Up
EN
A member of the t<9> complementation group that resulted from a rare recombination event between a complete haplotype and a wild-type chromosome. The tw18 deletion extends over 4.3Mbp of Chromosome 17. The 3 end of the deletion is found approximately at position Chr 17:23600000 whereas the 5 end was roughly positioned between between Chromosome position 19.19 and 19.33Mb. (J:8922, J:10105, J:14421, J:34878, J:244157)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
