Mia3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mia3
MIA SH3 domain ER export factor 3
MGI:2443183

21 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Mia3^tm1Lex/Mia3^tm1Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal cartilage development	J:172737
	abnormal cell morphology	J:172737
	abnormal cell physiology	J:172737
	abnormal chondrocyte morphology	J:172737
	abnormal chondrocyte physiology	J:172737
	abnormal cutaneous collagen fibril morphology	J:172737
	abnormal dermal layer morphology	J:172737
	abnormal skeleton development	J:172737
	absent bone trabeculae	J:172737
	decreased fetal size	J:172737
	decreased osteoblast cell number	J:172737
	decreased skin tensile strength	J:172737
	delayed bone mineralization	J:172737
	delayed bone ossification	J:172737
	disproportionate dwarf	J:172737
	edema	J:172737
	internal hemorrhage	J:172737
	perinatal lethality, complete penetrance	J:172737
	respiratory failure	J:172737
	short limbs	J:172737
	short snout	J:172737

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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