Human Disease and Mouse Model Detail

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Human Disease

Term: Chromosome 22q11.2 Deletion Syndrome, Distal
OMIM ID: 611867

Synonyms

Distal Chromosome 22q11.2 Deletion Syndrome

Transgenes and
other mutation types

Characteristics of this human disease are associated with transgenes and other mutation types in mouse.

Mouse Models

Genotype			Ref(s)
Allelic Composition	Note	Genetic Background
Models involving transgenes or other mutation types.¹
Del(16Es2el-Ufd1l)217Bld/+		B6.129S7-Del(16Es2el-Ufd1l)217Bld	J:190908
Del(16Es2el-Ufd1l)217Bld/+		involves: 129S7/SvEvBrd * C57BL/6	J:57757

¹Models involving transgenes or other mutation types may also appear in other sections of the table.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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