Slc39a13 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc39a13
solute carrier family 39 (metal ion transporter), member 13
MGI:1915677

29 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc39a13^tm1Thir/Slc39a13^tm1Thir involves: 129S1/Sv * 129X1/SvJ	abnormal alveolar process morphology	J:143911
	abnormal bone structure	J:143911
	abnormal dermal layer morphology	J:143911
	abnormal epiphyseal plate morphology	J:143911
	abnormal eyelid aperture	J:143911
	abnormal incisor morphology	J:143911
	abnormal jaw morphology	J:143911
	abnormal long bone epiphyseal plate proliferative zone	J:143911
	abnormal long bone epiphysis morphology	J:143911
	abnormal long bone hypertrophic chondrocyte zone	J:143911
	abnormal long bone metaphysis morphology	J:143911
	abnormal long bone morphology	J:143911
	abnormal molar root morphology	J:143911
	abnormal osteoblast physiology	J:143911
	abnormal tooth morphology	J:143911
	brittle teeth	J:143911
	decreased bone mineral density	J:143911
	decreased bone mineral density of femur	J:143911
	decreased bone trabecula number	J:143911
	decreased compact bone thickness	J:143911
	decreased cornea thickness	J:143911
	decreased length of long bones	J:143911
	enophthalmos	J:143911
	kyphosis	J:143911
	malocclusion	J:143911
	postnatal growth retardation	J:143911
	small mandible	J:143911
	small maxilla	J:143911
	thickened long bone epiphysis	J:143911

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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