B9d1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

B9d1
B9 protein domain 1
MGI:1351471

37 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
B9d1^{tm1a(EUCOMM)Wtsi}/B9d1⁺ C57BL/6N-B9d1^{tm1a(EUCOMM)Wtsi}/Ics	abnormal response to tactile stimuli	J:165965
	abnormal startle reflex	J:165965
	increased body weight	J:165965
B9d1^{tm1a(EUCOMM)Wtsi}/B9d1^{tm1a(EUCOMM)Wtsi} involves: C57BL/6N	cleft palate	J:178421
	decreased embryonic cilium length	J:178421
	decreased embryonic cilium number	J:178421
	exencephaly	J:178421
	holoprosencephaly	J:178421
	lethality throughout fetal growth and development, complete penetrance	J:178421
	preaxial polydactyly	J:178421
	telencephalon hypoplasia	J:178421
	thin myocardium	J:178421
	ventricular septal defect	J:178421
B9d1^{tm1a(EUCOMM)Wtsi}/B9d1^{tm1a(EUCOMM)Wtsi} involves: C57BL/6N * CD-1	abnormal bile duct development	J:178421
	abnormal facial morphology	J:178421
	abnormal kidney morphology	J:178421
	abnormal liver morphology	J:178421
	abnormal renal tubule epithelial cell primary cilium morphology	J:178421
	bile duct hyperplasia	J:178421
	dextrocardia	J:178421
	dilated nephron	J:178421
	enlarged kidney	J:178421
	lethality throughout fetal growth and development, incomplete penetrance	J:178421
	microphthalmia	J:178421
	perinatal lethality, complete penetrance	J:178421
	polycystic kidney	J:178421
	renal tubule hypertrophy	J:178421
B9d1^{tm1d(EUCOMM)Wtsi}/B9d1^{tm1d(EUCOMM)Wtsi} involves: C57BL/6 * FVB/N * SJL	abnormal cardiovascular system morphology	J:178421
	abnormal craniofacial morphology	J:178421
	abnormal embryo development	J:178421
	abnormal hepatobiliary system morphology	J:178421
	abnormal kidney morphology	J:178421
	abnormal limb morphology	J:178421
	preweaning lethality, complete penetrance	J:178421
B9d1^{tm1d(EUCOMM)Wtsi}/B9d1^{tm1d(EUCOMM)Wtsi} involves: C57BL/6N	abnormal blood vessel morphology	J:178978
	abnormal embryonic neuroepithelium morphology	J:178978
	abnormal nervous system development	J:178978
	lethality throughout fetal growth and development, complete penetrance	J:178978
	microphthalmia	J:178978
	polydactyly	J:178978

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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