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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Marveld2
MARVEL (membrane-associating) domain containing 2
MGI:2446166
34 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Marveld2tm1.1Sria/Marveld2+
involves: 129X1/SvJ * C57BL/6J 		abnormal myocardial fiber morphology J:201580
abnormal olfactory epithelium morphology J:201580
increased body weight J:201580
Marveld2tm1.1Sria/Marveld2tm1.1Sria
involves: 129X1/SvJ * C57BL/6J 		abnormal distortion product otoacoustic emission J:201580
abnormal myocardial fiber morphology J:201580
abnormal olfactory epithelium morphology J:201580
abnormal organ of Corti morphology J:201580
abnormal salivary gland duct morphology J:201580
abnormal stria vascularis morphology J:201580
abnormal thyroid follicle morphology J:201580
abnormal utricular macula morphology J:201580
cochlear ganglion degeneration J:201580
cochlear hair cell degeneration J:201580
cochlear inner hair cell degeneration J:201580
cochlear outer hair cell degeneration J:201580
deafness J:201580
normal hearing/vestibular/ear phenotype J:201580
increased body weight J:201580
increased heart weight J:201580
increased kidney weight J:201580
increased liver weight J:201580
increased or absent threshold for auditory brainstem response J:201580
increased spleen weight J:201580
syndromic hearing loss J:201580
thin stria vascularis J:201580
Marveld2tm1b(EUCOMM)Wtsi/Marveld2tm1b(EUCOMM)Wtsi
C57BL/6N-Marveld2tm1b(EUCOMM)Wtsi/H 		abnormal auditory brainstem response J:211773
abnormal ear morphology J:211773
abnormal startle reflex J:211773
decreased prepulse inhibition J:211773
decreased startle reflex J:211773
enlarged heart J:211773
Marveld2tm1Sats/Marveld2tm1Sats
B6.Cg-Marveld2tm1Sats 		abnormal distortion product otoacoustic emission J:261357
absent pinna reflex J:261357
normal cardiovascular system phenotype J:261357
cochlear hair cell degeneration J:261357
cochlear inner hair cell degeneration J:261357
cochlear outer hair cell degeneration J:261357
deafness J:261357
normal digestive/alimentary phenotype J:261357
normal endocrine/exocrine gland phenotype J:261357
increased or absent threshold for auditory brainstem response J:261357
normal liver/biliary system phenotype J:261357
normal renal/urinary system phenotype J:261357
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory