Gas2l2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Gas2l2
growth arrest-specific 2 like 2
MGI:3652048

49 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gas2l2^{tm1a(KOMP)Wtsi}/Gas2l2^{tm1a(KOMP)Wtsi} C57BL/6N-Gas2l2^{tm1a(KOMP)Wtsi}/Wtsi	abnormal auditory brainstem response	J:211773
	abnormal auditory tube morphology	J:239583
	abnormal basisphenoid bone morphology	J:239583
	abnormal ductus venosus valve morphology	J:239583
	abnormal external carotid artery origin	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal forebrain morphology	J:239583
	abnormal left vena cava superior connection	J:239583
	abnormal Meckel's cartilage morphology	J:239583
	abnormal midbrain morphology	J:239583
	abnormal middle cerebral artery origin	J:239583
	abnormal Mullerian duct topology	J:239583
	abnormal ophthalmic artery origin	J:239583
	abnormal optic stalk morphology	J:239583
	abnormal snout morphology	J:239583
	abnormal thymus topology	J:239583
	abnormal vertebral artery topology	J:239583
	abnormal vertebral body morphology	J:239583
	absent optic cup	J:239583
	absent pinna reflex	J:211773
	absent salivary gland	J:239583
	absent segment of anterior cerebral artery	J:239583
	absent stapedial artery	J:239583
	absent tongue	J:239583
	absent vertebral arch	J:239583
	anophthalmia	J:239583
	aphakia	J:239583
	biliary cyst	J:239583
	decreased total body fat amount	J:211773
	dilated liver sinusoidal space	J:239583
	dilated ureter	J:239583
	embryo tumor	J:239583
	female infertility	J:211773
	fused dorsal root ganglion	J:239583
	fusion of vertebral arches	J:239583
	incomplete rostral neuropore closure	J:239583
	increased trigeminal neuroma incidence	J:239583
	male infertility	J:211773
	no abnormal phenotype detected	J:239583
	oral atresia	J:239583
	perimembraneous ventricular septal defect	J:239583
Gas2l2^{tm1a(KOMP)Wtsi}/Gas2l2^{tm1a(KOMP)Wtsi} involves: C57BL/6N	abnormal nasal cavity morphology	J:277289
	abnormal paranasal sinus morphology	J:277289
	abnormal tracheal ciliated epithelium morphology	J:277289
	dextrocardia	J:277289
	hydrocephaly	J:277289
	impaired mucociliary clearance	J:277289
	neonatal lethality, incomplete penetrance	J:277289
	situs ambiguus	J:277289
Gas2l2^{tm1c(KOMP)Wtsi}/Gas2l2^{tm1c(KOMP)Wtsi} Foxj1^{tm1.1(cre/ERT2/GFP)Htg}/Foxj1⁺ involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N	abnormal nasal cavity morphology	J:277289
	abnormal paranasal sinus morphology	J:277289
	hydrocephaly	J:277289
	impaired mucociliary clearance	J:277289
Gas2l2^{tm1c(KOMP)Wtsi}/Gas2l2^{tm1c(KOMP)Wtsi} Gt(ROSA)26Sor^{tm1(cre/ERT)Nat}/Gt(ROSA)26Sor⁺ involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	neonatal lethality, incomplete penetrance	J:277289

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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