Amt Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Amt
aminomethyltransferase
MGI:3646700

21 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Amt^em1(IMPC)Tcp/Amt⁺ C57BL/6N-Amt^em1(IMPC)Tcp/Cmmr	abnormal retina blood vessel morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	increased erythrocyte cell number	J:211773
	short tibia	J:211773
Amt^em1(IMPC)Tcp/Amt^em1(IMPC)Tcp C57BL/6N-Amt^em1(IMPC)Tcp/Cmmr	abnormal abdominal wall morphology	J:211773
	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal head shape	J:211773
	abnormal head size	J:211773
	abnormal placenta size	J:211773
	anophthalmia	J:211773
	cleft palate	J:211773
	exencephaly	J:211773
	facial cleft	J:211773
	microphthalmia	J:211773
	preweaning lethality, complete penetrance	J:211773
	spina bifida	J:211773
Amt^{Gt(OST181110)Lex}/Amt^{Gt(OST181110)Lex} B6.129S5-Amt^{Gt(OST181110)Lex}	abnormal neural tube morphology	J:181568
	craniorachischisis	J:181568
	exencephaly	J:181568
	incomplete rostral neuropore closure	J:181568
	prenatal lethality	J:181568

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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