Del(13)36H Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Del(13)36H
deletion, Chr 13, Harwell 36
MGI:104137

38 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Foxq1^sa/Foxq1⁺ Sox4^M91Ark/Del(13)36H involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal aortic arch morphology	J:101156
	abnormal cardiovascular development	J:101156
	abnormal heart development	J:101156
	abnormal heart morphology	J:101156
	abnormal kidney development	J:101156
	abnormal mitral valve morphology	J:101156
	double outlet right ventricle	J:101156
	holoprosencephaly	J:101156
	ostium primum atrial septal defect	J:101156
	prenatal lethality, complete penetrance	J:101156
	renal hypoplasia	J:101156
	ventricular septal defect	J:101156
Foxq1^sa/Foxq1⁺ M1073b/Del(13)36H involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal craniofacial morphology	J:101156
	abnormal ear morphology	J:101156
	abnormal eye morphology	J:101156
	abnormal forebrain morphology	J:101156
	abnormal palate morphology	J:101156
	abnormal tooth morphology	J:101156
	absent mandible	J:101156
	holoprosencephaly	J:101156
	microcephaly	J:101156
	micrognathia	J:101156
	prenatal lethality	J:101156
M54b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal craniofacial morphology	J:101156
	abnormal ear morphology	J:101156
	abnormal forebrain morphology	J:101156
	abnormal lateral ventricle morphology	J:101156
	abnormal palate morphology	J:101156
	abnormal tooth morphology	J:101156
	absent mandible	J:101156
	anophthalmia	J:101156
	holoprosencephaly	J:101156
	microcephaly	J:101156
	micrognathia	J:101156
	prenatal lethality	J:101156
M241b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal forebrain morphology	J:101156
	anophthalmia	J:101156
	embryonic lethality, incomplete penetrance	J:101156
	holoprosencephaly	J:101156
M369b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	exencephaly	J:101156
	prenatal lethality	J:101156
M412b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal craniofacial morphology	J:101156
	abnormal ear morphology	J:101156
	abnormal eye morphology	J:101156
	abnormal forebrain morphology	J:101156
	abnormal hindbrain morphology	J:101156
	abnormal lateral ventricle morphology	J:101156
	abnormal palate morphology	J:101156
	abnormal tooth morphology	J:101156
	absent mandible	J:101156
	holoprosencephaly	J:101156
	microcephaly	J:101156
	micrognathia	J:101156
	prenatal lethality	J:101156
M624b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal eye morphology	J:101156
	abnormal forebrain morphology	J:101156
	holoprosencephaly	J:101156
	prenatal lethality	J:101156
M876b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	prenatal lethality	J:101156
M1185b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal heart morphology	J:101156
	embryonic lethality, incomplete penetrance	J:101156
M1616b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	embryonic lethality, incomplete penetrance	J:101156
	failure of chorioallantoic fusion	J:101156
M1645b/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	embryonic lethality, incomplete penetrance	J:101156
sau/Del(13)36H Foxq1^sa/Foxq1⁺ involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR	abnormal eye development	J:101156
	cyclopia	J:101156
	holoprosencephaly	J:101156
	lethality throughout fetal growth and development, incomplete penetrance	J:101156
Sox4^Igt4/Del(13)36H involves: 101/H * C3H/HeH * C57BL/6	abnormal atrioventricular valve morphology	J:141688
	cleft palate	J:141688
	double outlet right ventricle	J:141688
	extremity edema	J:141688
	interrupted aortic arch	J:141688
	lethality throughout fetal growth and development, complete penetrance	J:141688
	renal hypoplasia	J:141688
	subarterial ventricular septal defect	J:141688
	thymus hypoplasia	J:141688

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/19/2024 MGI 6.24