Clec1b Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Clec1b
C-type lectin domain family 1, member b
MGI:1913287

39 phenotypes from 7 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Clec1b^tm1.1Arte/Clec1b^tm1.1Arte Tg(Pf4-icre)Q3Rsko/0 involves: C57BL/6	abnormal blood coagulation	J:217963
	abnormal blood vessel morphology	J:181715
	abnormal lymphatic vessel endothelial cell morphology	J:181715
	abnormal lymphatic vessel morphology	J:181715
	abnormal platelet physiology	J:181715
	ascites	J:181715
	edema	J:181715
	intracranial hemorrhage	J:181715
	normal respiratory system phenotype	J:181715
Clec1b^tm1.1Ksi/Clec1b⁺ involves: C57BL/6	lethality throughout fetal growth and development, incomplete penetrance	J:165898
Clec1b^tm1.1Ksi/Clec1b^tm1.1Ksi involves: C57BL/6	abnormal blood vessel morphology	J:165898
	abnormal lymphatic system physiology	J:165898
	abnormal lymphatic vessel morphology	J:165898
	abnormal platelet activation	J:165898
	decreased platelet aggregation	J:165898
	hemorrhage	J:165898
	lethality throughout fetal growth and development, incomplete penetrance	J:165898
	neonatal lethality, complete penetrance	J:165898
	skin edema	J:165898
Clec1b^tm1.2Arte/Clec1b^tm1.2Arte involves: 129 * C57BL/6	abnormal platelet physiology	J:181754
	neonatal lethality, incomplete penetrance	J:181754
	perinatal lethality, incomplete penetrance	J:181754
	premature death	J:181754
Clec1b^tm1.2Arte/Clec1b^tm1.2Arte Not Specified	abnormal brain vasculature morphology	J:181715
	abnormal lung morphology	J:181715
	abnormal lymphatic vessel morphology	J:181715
	chylous ascites	J:181715
	decreased lymphatic vessel endothelial cell number	J:181715
	decreased platelet aggregation	J:181715
	edema	J:181715
	intracranial hemorrhage	J:181715
	neonatal lethality, incomplete penetrance	J:181715
	perinatal lethality, incomplete penetrance	J:181715
	premature death	J:181715
	primary atelectasis	J:181715
	respiratory distress	J:181715
	skin hemorrhage	J:181715
	spinal hemorrhage	J:181715
Clec1b^tm1Ksi/Clec1b^tm1Ksi Tg(Pf4-icre)Q3Rsko/0 involves: C57BL/6	abnormal lymphatic vessel morphology	J:187533
	abnormal small intestine morphology	J:187533
	intestinal edema	J:187533
Clec1b^tm1Lex/Clec1b^tm1Lex involves: 129S5/SvEvBrd * C57BL/6J	abnormal brain vasculature morphology	J:161922
	abnormal mononuclear cell morphology	J:161922
	anemia	J:161922
	brain vascular congestion	J:161922
	decreased hematocrit	J:161922
	decreased hemoglobin content	J:161922
	decreased systemic arterial blood pressure	J:161922
	internal hemorrhage	J:161922
	perinatal lethality, incomplete penetrance	J:161922
	preweaning lethality, incomplete penetrance	J:161922
	thrombocytopenia	J:161922
Clec1b^tm1Mlkn/Clec1b^tm1Mlkn involves: 129S4/SvJae * C57BL/6	abnormal lymphatic vessel morphology	J:162815
	abnormal platelet activation	J:162815
	intestinal edema	J:162815
Clec1b^tm2Mlkn/Clec1b^tm2Mlkn Tg(Pf4-icre)Q3Rsko/0 involves: C57BL/6 * SJL	lymph node hemorrhage	J:205423

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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