Memo1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Memo1
mediator of cell motility 1
MGI:1924140

57 phenotypes from 5 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ Memo1^{tm1c(EUCOMM)Wtsi}/Memo1^{tm1c(EUCOMM)Wtsi} involves: C57BL/6 * CBA/J * SJL	abnormal craniofacial bone morphology	J:233609
	abnormal endochondral bone ossification	J:233609
	abnormal nasal bridge morphology	J:233609
	absent gastric milk in neonates	J:233609
	cleft palate	J:233609
	domed cranium	J:233609
	maxillary shelf hypoplasia	J:233609
	palatine bone horizontal plate hypoplasia	J:233609
	premaxilla hypoplasia	J:233609
	presphenoid bone hypoplasia	J:233609
	preweaning lethality, complete penetrance	J:233609
	small basisphenoid bone	J:233609
	wide coronal suture	J:233609
	wide metopic suture	J:233609
Memo1^m1Will/Memo1^m1Will involves: 129S1/SvImJ * C57BL/6J	abnormal bone ossification	J:233609
	abnormal cranial cartilage development	J:233609
	abnormal craniofacial bone morphology	J:233609
	abnormal cranium morphology	J:233609
	abnormal endochondral bone ossification	J:233609
	abnormal nasal bridge morphology	J:233609
	abnormal neurocranium morphology	J:233609
	abnormal otic capsule morphology	J:233609
	abnormal vasculogenesis	J:233609
	absent gastric milk in neonates	J:233609
	absent maxillary shelf	J:233609
	absent palatine bone horizontal plate	J:233609
	basioccipital bone hypoplasia	J:233609
	basisphenoid bone hypoplasia	J:233609
	cleft palate	J:233609
	decreased angiogenesis	J:233609
	domed cranium	J:233609
	embryonic lethality during organogenesis	J:233609
	failure of endochondral bone ossification	J:233609
	failure of palatal shelf elevation	J:233609
	generalized edema	J:233609
	hemorrhage	J:233609
	maxilla hypoplasia	J:233609
	palate bone hypoplasia	J:233609
	premaxilla hypoplasia	J:233609
	presphenoid bone hypoplasia	J:233609
	preweaning lethality, complete penetrance	J:233609
Memo1^tm1.1Neh/Memo1^tm1.1Neh Tg(CAG-cre/Esr1)1Lbe/0 involves: 129P2/OlaHsd 129S1/Sv * 129X1/SvJ	abnormal coat/hair pigmentation	J:206626
	abnormal reflex	J:206626
	abnormal sex gland morphology	J:206626
	alopecia	J:206626
	azoospermia	J:206626
	decreased body size	J:206626
	decreased body weight	J:206626
	decreased subcutaneous adipose tissue amount	J:206626
	decreased white adipose tissue amount	J:206626
	normal homeostasis/metabolism phenotype	J:206626
	improved glucose tolerance	J:206626
	increased circulating calcium level	J:206626
	increased circulating parathyroid hormone level	J:206626
	increased insulin sensitivity	J:206626
	increased vitamin D level	J:206626
	kyphosis	J:206626
	premature death	J:206626
	weight loss	J:206626
Memo1^{tm1a(EUCOMM)Wtsi}/Memo1⁺ C57BL/6N-Memo1^{tm1a(EUCOMM)Wtsi}/Bay	trunk curl	J:211773
Memo1^{tm1a(EUCOMM)Wtsi}/Memo1^{tm1a(EUCOMM)Wtsi} C57BL/6N-Memo1^{tm1a(EUCOMM)Wtsi}/Bay	preweaning lethality, complete penetrance	J:211773
Memo1^{tm1b(EUCOMM)Wtsi}/Memo1⁺ C57BL/6N-Memo1^{tm1b(EUCOMM)Wtsi}/Bay	thick ventricular wall	J:211773
	unresponsive to tactile stimuli	J:211773
Memo1^{tm1b(EUCOMM)Wtsi}/Memo1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Memo1^{tm1b(EUCOMM)Wtsi}/Bay	abnormal embryo size	J:211773
	abnormal pericardium morphology	J:211773
	edema	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773
Memo1^{tm1b(EUCOMM)Wtsi}/Memo1^{tm1b(EUCOMM)Wtsi} involves: Black Swiss * C57BL/6 * FVB/N	abnormal nasal bridge morphology	J:233609
	cleft secondary palate	J:233609
	domed cranium	J:233609
	preweaning lethality, complete penetrance	J:233609

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