About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mertk
MER proto-oncogene tyrosine kinase
MGI:96965
40 phenotypes from 4 alleles in 8 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Mertknmf12/Mertknmf12
C57BL/6J-Mertknmf12/J
abnormal retina morphology J:82238
decreased total retina thickness J:82238
Mertknmf12/Mertknmf12
involves: C57BL/6J
abnormal eye electrophysiology J:175587
abnormal retina photoreceptor layer morphology J:175587
abnormal retina pigmentation J:175587
abnormal tumor necrosis factor level J:175587
decreased retina photoreceptor cell number J:175587
increased retina apoptosis J:175587
retina photoreceptor degeneration J:175587
thin retina outer nuclear layer J:175587
Mertknmf12/Mertktm1Gkm
involves: 129P2/OlaHsd * C57BL/6J
abnormal retina morphology J:175587
decreased retina photoreceptor cell number J:175587
thin retina outer nuclear layer J:175587
Mertktm1Gkm/Mertktm1Gkm
B6.129P2-Mertktm1Gkm
decreased autoantibody level J:136377
decreased susceptibility to graft versus host disease J:136377
Mertktm1Gkm/Mertktm1Gkm
involves: 129P2/OlaHsd
abnormal cone electrophysiology J:81618
abnormal photoreceptor outer segment morphology J:81618
abnormal retina morphology J:81618
abnormal retina outer nuclear layer morphology J:81618
abnormal retina pigment epithelium morphology J:81618
abnormal retina vasculature morphology J:81618
abnormal rod electrophysiology J:81618
disorganized photoreceptor outer segment J:81618
photoreceptor outer segment degeneration J:81618
retina degeneration J:81618
retina pigment epithelium atrophy J:81618
retina rod cell degeneration J:81618
thin retina outer nuclear layer J:81618
Mertktm1Gkm/Mertktm1Gkm
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
abnormal small intestine morphology J:53423
increased circulating tumor necrosis factor level J:53423
increased susceptibility to endotoxin shock J:53423
increased susceptibility to induced morbidity/mortality J:53423
increased tumor necrosis factor secretion J:53423
Mertktm1Gkm/Mertktm1Gkm
NOD.129P2-Mertktm1Gkm
abnormal mononuclear cell morphology J:147153
decreased susceptibility to autoimmune diabetes J:147153
decreased T cell number J:147153
increased T cell apoptosis J:147153
insulitis J:147153
Mertktm1Grl/Mertktm1Grl
involves: 129P2/OlaHsd
abnormal photoreceptor outer segment morphology J:116526
abnormal retina pigment epithelium morphology J:116526
blindness J:116526
normal cardiovascular system phenotype J:198769
decreased Sertoli cell phagocytosis J:133455
disorganized photoreceptor outer segment J:116526
enlarged spleen J:54681
retina photoreceptor degeneration J:116526
vagina atresia J:142166
Mertktm1Lex/Mertktm1Lex
involves: 129S5/SvEvBrd * C57BL/6
decreased platelet aggregation J:102333
decreased susceptibility to induced thrombosis J:102333

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
12/10/2024
MGI 6.24
The Jackson Laboratory