Gpr161 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Gpr161
G protein-coupled receptor 161
MGI:2685054

48 phenotypes from 3 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gpr161^tm1.2Smuk/Gpr161^tm1.2Smuk H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ involves: C57BL/6J * CBA/J	abnormal craniofacial bone morphology	J:316181
	abnormal craniofacial development	J:316181
	abnormal craniofacial morphology	J:316181
	abnormal intramembranous bone ossification	J:316181
	abnormal mandible morphology	J:316181
	abnormal maxilla morphology	J:316181
	abnormal midbrain development	J:316181
	abnormal midbrain morphology	J:316181
	abnormal spinal cord morphology	J:316181
	absent frontal bone	J:316181
	anophthalmia	J:316181
	anotia	J:316181
	cleft hard palate	J:316181
	encephalomeningocele	J:316181
	enlarged cerebral aqueduct	J:316181
	enlarged fourth ventricle	J:316181
	enlarged nasal bone	J:316181
	enlarged tectum	J:316181
	increased midbrain size	J:316181
	increased neuronal precursor proliferation	J:316181
	mandible hypoplasia	J:316181
	microphthalmia	J:316181
	nasal septum hypoplasia	J:316181
	palatal shelves fail to meet at midline	J:316181
	perinatal lethality, complete penetrance	J:316181
	short maxilla	J:316181
	small ears	J:316181
	small frontal bone	J:316181
	small mandible	J:316181
	small maxilla	J:316181
	small parietal bone	J:316181
	small premaxilla	J:316181
Gpr161^tm1.2Smuk/Gpr161^tm1.2Smuk Tg(Nes-cre)1Kln/0 involves: C57BL/6 * C57BL/6J * SJL	enlarged tectum	J:316181
	polydactyly	J:316181
Gpr161^tm1Lex/Gpr161^tm1Lex involves: 129S/SvEv * C57BL/6N	abnormal craniofacial morphology	J:193395
	abnormal dorsal-ventral axis patterning	J:193395
	abnormal limb development	J:193395
	abnormal neural tube morphology	J:193395
	absent apical ectodermal ridge	J:193395
	normal embryo phenotype	J:193395
	embryonic lethality during organogenesis, complete penetrance	J:193395
	enlarged floor plate	J:193395
	exencephaly	J:193395
	spina bifida	J:193395
Gpr161^vl/Gpr161^vl C3Fe;C3Sn-Gpr161^vl/J	abnormal neural fold formation	J:2004
	belly spot	J:13464
	cataract	J:13464
	normal hematopoietic system phenotype	J:29151
	lens vacuoles	J:13464
	spina bifida	J:13464
Gpr161^vl/Gpr161^vl involves: C3H/HeSnJ * C57BL/6J	hindlimb paralysis	J:131929
Gpr161^vl/Gpr161^vl involves: C3H/HeSnJ * C57BL/6J	spina bifida	J:131929
Gpr161^vl/Gpr161^vl involves: C3H/HeSnJ * CAST/Ei	hindlimb paralysis	J:131929
Gpr161^vl/Gpr161^vl involves: C3H/HeSnJ * CAST/Ei	spina bifida	J:131929

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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