Wnt9a Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt9a
wingless-type MMTV integration site family, member 9A
MGI:2446084

16 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wnt9a^tm1.1Chha/Wnt9a^tm1.1Chha involves: 129X1/SvJ * C57BL/6J * SJL/J	abnormal basioccipital bone morphology	J:119030
	abnormal cervical atlas morphology	J:119030
	abnormal chondrocyte physiology	J:119030
	abnormal cranium morphology	J:119030
	abnormal frontal bone morphology	J:119030
	abnormal interfrontal bone morphology	J:119030
	abnormal joint morphology	J:119030
	abnormal sagittal suture morphology	J:119030
	abnormal skeleton development	J:119030
	abnormal supraoccipital bone morphology	J:119030
	decreased length of long bones	J:119030
	ectopic cartilage	J:119030
	fused joints	J:119030
	hyoid bone hypoplasia	J:119030
	neonatal lethality, complete penetrance	J:119030
	small basioccipital bone	J:119030
Wnt9a^tm2Chha/Wnt9a^tm2Chha involves: 129X1/SvJ	abnormal basioccipital bone morphology	J:119030
	abnormal cervical atlas morphology	J:119030
	abnormal chondrocyte physiology	J:119030
	abnormal cranium morphology	J:119030
	abnormal frontal bone morphology	J:119030
	abnormal interfrontal bone morphology	J:119030
	abnormal joint morphology	J:119030
	abnormal sagittal suture morphology	J:119030
	abnormal skeleton development	J:119030
	abnormal supraoccipital bone morphology	J:119030
	decreased length of long bones	J:119030
	ectopic cartilage	J:119030
	fused joints	J:119030
	hyoid bone hypoplasia	J:119030
	neonatal lethality, complete penetrance	J:119030
	small basioccipital bone	J:119030

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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