Samd1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Samd1
sterile alpha motif domain containing 1
MGI:2142433

32 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Samd1^tm1Pfi/Samd1⁺ involves: C57BL/6J * C57BL/6N	abnormal adipose tissue amount	J:333561
	abnormal circulating insulin level	J:333561
	abnormal glucose tolerance	J:333561
	decreased body weight	J:333561
	decreased circulating HDL cholesterol level	J:333561
	decreased circulating VLDL cholesterol level	J:333561
	increased circulating aldosterone level	J:333561
	increased circulating angiotensin II level	J:333561
	increased circulating corticosterone level	J:333561
	postnatal lethality, incomplete penetrance	J:333561
Samd1^tm1Pfi/Samd1^tm1Pfi involves: C57BL/6J * C57BL/6N	abnormal bronchiole morphology	J:333561
	abnormal embryo development	J:333561
	abnormal heart development	J:333561
	abnormal liver development	J:333561
	abnormal lung development	J:333561
	abnormal neurocranium morphology	J:333561
	abnormal vascular development	J:333561
	absent umbilical cord blood vessels	J:333561
	absent visceral yolk sac	J:333561
	decreased erythrocyte cell number	J:333561
	decreased fetal size	J:333561
	edema	J:333561
	exencephaly	J:333561
	fetal growth retardation	J:333561
	hemorrhage	J:333561
	lethality during fetal growth through weaning, complete penetrance	J:333561
	pale placenta	J:333561
	pale yolk sac	J:333561
	pallor	J:333561
	poor circulation	J:333561
	premature bone ossification	J:333561
	skeletal muscle degeneration	J:333561

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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