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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fam161a
family with sequence similarity 161, member A
MGI:1921123
32 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fam161aGt(462E7)Cmhd/Fam161aGt(462E7)Cmhd
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
abnormal electroretinogram waveform feature J:214319
abnormal photoreceptor connecting cilium morphology J:214319
abnormal photoreceptor outer segment morphology J:214319
abnormal retina photoreceptor morphology J:214319
abnormal vision J:214319
decreased a-wave amplitude J:214319
decreased b-wave amplitude J:214319
disorganized photoreceptor outer segment J:214319
increased a-wave implicit time J:214319
increased b-wave implicit time J:214319
increased retina apoptosis J:214319
increased susceptibility to age-related retinal degeneration J:214319
microgliosis J:214319
retina outer nuclear layer degeneration J:214319
retina photoreceptor degeneration J:214319
thin retina outer nuclear layer J:214319
Fam161atm1b(KOMP)Wtsi/Fam161atm1b(KOMP)Wtsi
C57BL/6N-Fam161atm1b(KOMP)Wtsi/J
abnormal lens morphology J:211773
abnormal optic disk morphology J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina morphology J:211773
abnormal retina vasculature morphology J:211773
decreased circulating cholesterol level J:211773
decreased circulating HDL cholesterol level J:211773
decreased coping response J:211773
decreased exploration in new environment J:211773
increased circulating sodium level J:211773
increased grip strength J:211773
increased heart rate J:211773
increased heart weight J:211773
increased lean body mass J:211773
increased startle reflex J:211773
shortened RR interval J:211773

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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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory