Sema5a Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Sema5a
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
MGI:107556

11 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Sema5a^tm1.2Alk/Sema5a^tm1.2Alk Sema5b^tm1.2Alk/Sema5b^tm1.2Alk involves: 129 * BALB/cJ * C57BL/6	abnormal amacrine cell morphology	J:174679
	abnormal dendrite morphology	J:174679
	abnormal eye physiology	J:174679
	abnormal neurite morphology	J:174679
	abnormal retina bipolar cell morphology	J:174679
	abnormal retina development	J:174679
	abnormal retina ganglion cell morphology	J:174679
	abnormal retina inner nuclear layer morphology	J:174679
	abnormal retina inner plexiform layer morphology	J:174679
	abnormal retina neuronal layer morphology	J:174679
	abnormal rod electrophysiology	J:174679
Sema5a^tm1.2Alk/Sema5a^tm1.2Alk Sema5b^tm1.2Alk/Sema5b^tm1.2Alk Tg(Thy1-EGFP)MJrs/0 involves: 129 * BALB/cJ * C57BL/6 * CBA	abnormal dendrite morphology	J:174679
	abnormal retina ganglion cell morphology	J:174679

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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