Slc22a18 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a18
solute carrier family 22 (organic cation transporter), member 18
MGI:1336884

25 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Tg(BAC144D14)5A2Masu/0 B6J.Cg-Tg(BAC144D14)5A2Masu	abnormal interscapular fat pad morphology	J:232408
	abnormal retroperitoneal fat pad morphology	J:232408
	abnormal white adipose tissue morphology	J:232408
	decreased birth weight	J:232408
	decreased body weight	J:232408
	decreased fetal weight	J:232408
	decreased food intake	J:232408
	decreased inguinal fat pad weight	J:232408
	decreased mesenteric fat pad weight	J:232408
	decreased retroperitoneal fat pad weight	J:232408
	hypoglycemia	J:232408
	increased body temperature	J:232408
	increased brain weight	J:232408
	increased brown adipose tissue amount	J:232408
	increased brown fat cell number	J:232408
	increased interscapular fat pad weight	J:232408
Tg(BAC144D14)5D3Masu/0 B6.Cg-Tg(BAC144D14)5D3Masu	abnormal hypothalamus morphology	J:239325
	abnormal sucrose solution preference	J:239325
	decreased locomotor activity	J:239325
	decreased prepulse inhibition	J:239325
	impaired hearing	J:239325
	reduced sensorimotor gating	J:239325
Tg(BAC144D14)5D3Masu/0 B6J.Cg-Tg(BAC144D14)5D3Masu	abnormal beige fat cell morphology	J:232408
	abnormal interscapular fat pad morphology	J:232408
	abnormal retroperitoneal fat pad morphology	J:232408
	abnormal white adipose tissue morphology	J:232408
	decreased birth weight	J:232408
	decreased body weight	J:232408
	decreased fetal weight	J:232408
	decreased inguinal fat pad weight	J:232408
	decreased mesenteric fat pad weight	J:232408
	decreased retroperitoneal fat pad weight	J:232408
	hypoglycemia	J:232408
	increased body temperature	J:232408
	increased brown adipose tissue amount	J:232408
	increased brown fat cell number	J:232408
	increased interscapular fat pad weight	J:232408
Tg(YACW408A5)1952Ricc/0 involves: 129/Sv * SD7	abnormal imprinting	J:96366
Tg(YACW408A5)1952Ricc/0 involves: 129/Sv * SD7	fetal growth retardation	J:96366

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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