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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ap3b1
adaptor-related protein complex 3, beta 1 subunit
MGI:1333879
23 phenotypes from 14 alleles in 14 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ap3b1m1Btlr/Ap3b1m1Btlr
C57BL/6J-Ap3b1m1Btlr
abnormal foot pigmentation J:132673
decreased ear pigmentation J:132673
decreased tail pigmentation J:132673
diluted coat color J:132673
increased susceptibility to Herpesvirales infection J:132673
Ap3b1m2Btlr/Ap3b1m2Btlr
C57BL/6J-Ap3b1m2Btlr
diluted coat color J:264641
Ap3b1pe-5J/?
CBA/J-Ap3b1pe-5J
abnormal coat/hair pigmentation J:30778
Ap3b1pe-7J/Ap3b1pe-7J
involves: DBA/1LacJ
diluted coat color J:63693
Ap3b1pe-8J/Ap3b1pe-8J
DBA/2J-Ap3b1pe-8J/J
abnormal coat/hair pigmentation J:78381
abnormal eye pigmentation J:78381
diluted coat color J:78381
Ap3b1pe-10J/Ap3b1pe-10J
C57BL/6J-Ap3b1pe-10J
abnormal coat/hair pigmentation J:52521
decreased eye pigmentation J:52521
diluted coat color J:52521
Ap3b1pe-11J/Ap3b1pe-11J
B10.RIII H2r H2-T18b/(71NS)Sn-Ap3b1pe-11J/J
diluted coat color J:51188
Ap3b1pe-13J/Ap3b1pe-13J
STOCK Tg(CAG-EGFP)B5Nagy/J
diluted coat color J:95723
Ap3b1pe-14J/Ap3b1pe-14J
B6;129S2 Seletm1Hyn-Ap3b1pe-14J/GrsrJ
abnormal skin pigmentation J:99882
diluted coat color J:99882
Ap3b1pe-15J/Ap3b1pe-15J
C3(SW)-H2b Ap3b1pe-15J/GrsrJ
abnormal eye pigmentation J:105128
abnormal skin pigmentation J:105128
decreased ear pigmentation J:105128
decreased tail pigmentation J:105128
diluted coat color J:105128
Ap3b1pe-16J/Ap3b1pe-16J
C57BL/6J-Sobpjc Ap3b1pe-16J/GrsrJ
abnormal foot pigmentation J:105129
decreased ear pigmentation J:105129
decreased tail pigmentation J:105129
diluted coat color J:105129
Ap3b1pe-rim2/Ap3b1pe-rim2
involves: B10.A(R201) * C57BL/10Slc
abnormal platelet dense granule physiology J:42685
anophthalmia J:42685
cataract J:42685
decreased eye pigmentation J:42685
decreased platelet ADP level J:42685
decreased platelet aggregation J:42685
decreased platelet ATP level J:42685
hypopigmentation J:42685
Ap3b1tm1.1Sms/Ap3b1tm1.1Sms
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
normal behavior/neurological phenotype J:66256
diluted coat color J:66256
Ap3b1tm1Sms/Ap3b1tm1Sms
B6.129-Ap3b1tm1Sms
abnormal nervous system physiology J:94942
normal behavior/neurological phenotype J:94942
diluted coat color J:94942
hypopigmentation J:94942
Ap3b1tm1Sms/Ap3b1tm1Sms
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal eye pigmentation J:66256
abnormal lysosome morphology J:66256
abnormal melanosome morphology J:66256
abnormal mineral homeostasis J:66256
normal behavior/neurological phenotype J:66256
diluted coat color J:66256
normal hearing/vestibular/ear phenotype J:66256
increased bleeding time J:66256

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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
04/30/2024
MGI 6.23
The Jackson Laboratory