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This phenotypic mutation has been localized to chromosome 9 distal to D9Mit279. Nucleotide 118,855,090 is joined to 119,089,970 (Build 37) indicating that this is a 234 kb deletion. The deletion region contains Vill, Plcd1, Dlec1, Acaa1b, and parts of Ctdspl and Slc22a14. (J:142517)
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：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
