About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Scarb2
scavenger receptor class B, member 2
MGI:1196458
64 phenotypes from 2 alleles in 3 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Scarb2em2(IMPC)Tcp/Scarb2em2(IMPC)Tcp
C57BL/6NCrl-Scarb2em2(IMPC)Tcp/Tcp 		abnormal QT variability J:211773
abnormal sinus arrhythmia J:211773
cardiovascular system phenotype J:211773
decreased mean corpuscular volume J:211773
decreased monocyte cell number J:211773
decreased total body fat amount J:211773
enlarged kidney J:211773
enlarged lymph nodes J:211773
increased blood urea nitrogen level J:211773
increased bone mineral content J:211773
increased heart rate variability J:211773
increased lean body mass J:211773
increased leukocyte cell number J:211773
increased lymphocyte cell number J:211773
increased neutrophil cell number J:211773
preweaning lethality, incomplete penetrance J:211773
prolonged RR interval J:211773
thrombocytosis J:211773
Scarb2tm1Psa/Scarb2tm1Psa
involves: 129P2/OlaHsd * C57BL/6J 		abnormal auditory brainstem response J:82474, J:121998
abnormal distortion product otoacoustic emission J:121998
abnormal nervous system morphology J:82474
abnormal otolithic membrane morphology J:82474
abnormal phrenic nerve morphology J:82474
abnormal Schwann cell morphology J:82474
abnormal stria vascularis morphology J:82474, J:121998
abnormal stria vascularis vasculature morphology J:121998
abnormal strial marginal cell morphology J:82474, J:121998
abnormal ureter morphology J:82474
abnormal ureter smooth muscle morphology J:82474
abnormal ureteropelvic junction morphology J:82474
abnormal urothelium morphology J:82474
abnormal vestibular hair cell physiology J:121998
absent endocochlear potential J:82474
absent otoliths J:82474
absent startle reflex J:82474
albuminuria J:82474
cochlear ganglion degeneration J:82474, J:121998
cochlear inner hair cell degeneration J:82474
cochlear outer hair cell degeneration J:82474
deafness J:82474
decreased endocochlear potential J:82474
decreased urine glucose level J:82474
decreased urine osmolality J:82474
demyelination J:82474
dilated kidney calyx J:82474
distended abdomen J:82474
hydronephrosis J:82474
leukocyturia J:82474
polydipsia J:82474
polyuria J:82474
premature death J:82474
sensorineural hearing loss J:121998
stria vascularis degeneration J:82474, J:121998
ureteropelvic junction obstruction J:82474
Scarb2tm1Psa/Scarb2tm1Psa
involves: 129P2/OlaHsd * C57BL/6N 		abnormal behavior J:216676
abnormal enzyme/coenzyme activity J:216676
abnormal nervous system morphology J:216676
abnormal neuron morphology J:216676
astrocytosis J:216676
decreased body weight J:216676
limb grasping J:216676
microgliosis J:216676
neurodegeneration J:216676
paralysis J:216676
premature death J:216676
tremors J:216676
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 		The Jackson Laboratory