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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pde6b
phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide
MGI:97525
42 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Cacnb2tm1Rgg/Cacnb2tm1Rgg
Pde6brd1/Pde6brd1
Tg(Myh6-Cacnb2)1Rgg/0
involves: 129S7/SvEvBrd * C57BL/6J * FVB
abnormal cone electrophysiology J:80080
abnormal eye electrophysiology J:80080
abnormal eye physiology J:80080
decreased retina photoreceptor cell number J:79923
disorganized retina outer plexiform layer J:80080
retina photoreceptor degeneration J:79923
thin retina outer nuclear layer J:79923
thin retina outer plexiform layer J:80080
Casp3tm1Flv/Casp3tm1Flv
Pde6brd1/Pde6brd1
involves: 129S1/Sv * C3H/FeJ * C57BL/6J
abnormal apoptosis J:88367
abnormal eye development J:88367
decreased retina rod cell number J:88367
thick retina outer nuclear layer J:88367
Cry1tm1Asn/Cry1tm1Asn
Cry2tm1Asn/Cry2tm1Asn
Pde6brd1/Pde6brd1
involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6
abnormal circadian behavior phase J:66580
abnormal locomotor circadian rhythm J:66580
abnormal retina morphology J:66580
abnormal retina outer nuclear layer morphology J:66580
absent photoreceptor outer segment J:66580
absent retina rod cells J:66580
decreased locomotor activity J:66580
decreased retina cone cell number J:66580
impaired pupillary reflex J:81500
retina degeneration J:66580
Cry1tm1Asn/Cry1tm1Asn
Pde6brd1/Pde6brd1
involves: 129P2/OlaHsd
impaired pupillary reflex J:81500
Cry2tm1Asn/Cry2tm1Asn
Pde6brd1/Pde6brd1
involves: 129P2/OlaHsd
impaired pupillary reflex J:81500
Hps4le/Hps4le
Pde6brd1/Pde6brd1
B6.C3-Pde6brd1 Hps4le
abnormal retina inner nuclear layer morphology J:5812
decreased ear pigmentation J:5812
normal vision/eye phenotype J:5812
Hps4le/Hps4le
Pde6brd1/Pde6brd1
B6.C3-Pde6brd1 Hps4le/J
abnormal platelet activation J:221384
decreased platelet aggregation J:221384
Opn4tm1Skay/Opn4tm1Skay
Pde6brd1/Pde6brd1
B6.Cg-Pde6brd1 Opn4tm1Skay
abnormal eye physiology J:227078
Opn4tm1Skay/Opn4tm1Skay
Pde6brd1/Pde6brd1
involves: 129S1/SvImJ * C57BL/6
abnormal circardian behavior entrainment J:137151
impaired pupillary reflex J:137151
Pde6anmf282/Pde6a+
Pde6brd1-2J/Pde6b+
involves: A/J * C57BL/6J
normal vision/eye phenotype J:142108
Pde6anmf363/Pde6a+
Pde6brd1-2J/Pde6b+
C57BL/6J-Pde6brd1-2J Pde6anmf363
normal vision/eye phenotype J:142108
Pde6brd1/Pde6brd1
Pde6gtm1Goff/Pde6gtm1Goff
either: (involves: 129S/SvEv * C57BL/6 * MF1 * Swiss Webster) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * MF1 * Swiss Webster)
abnormal eye electrophysiology J:33048
abnormal retina photoreceptor layer morphology J:33048
Pde6brd1/Pde6brd1
Prkcqrpea1/Prkcqrpea1
ABJ/LeJ-Prkcqrpea1/Boc
abnormal ocular fundus morphology J:237977
buphthalmos J:237977
cataract J:237977
decreased retina ganglion cell number J:237977
decreased retina photoreceptor cell number J:237977
ocular hypertension J:237977
Pde6brd1/Pde6brd1
Prkcqrpea1/Prkcqrpea1
B6.ABJ-Prkcqrpea1 Pde6brd1/Boc
abnormal ocular fundus morphology J:237977
buphthalmos J:237977
cataract J:237977
decreased retina ganglion cell number J:237977
decreased retina photoreceptor cell number J:237977
ocular hypertension J:237977
retina detachment J:237977
serous retina detachment J:237977
Pde6brd1/Pde6brd1
Prph2Rd2/Prph2Rd2
either: C.Cg-Pde6brd1 Prph2Rd2 or C3.Cg-Pde6brd1 Prph2Rd2
abnormal Muller cell morphology J:27850
absent photoreceptor outer segment J:27850
retina photoreceptor degeneration J:27850
Pde6brd1/Pde6brd1
Prph2Rd2/Prph2Rd2
involves: C3Hf/HeA * C57BL/LiA * O20/A
retina outer nuclear layer degeneration J:12044
Pde6brd1/Pde6brd1
Rhotm2(RHO/GFP)Jhw/Rho+
either: (involves: 129S7/SvEvBrd * C57BL/6J * FVB) or (involves: 129S7/SvEvBrd * C57BL/6-Tyrc * FVB)
retina degeneration J:91038
Pde6brd1/Pde6brd1
Tg(OPN1LW-DT)1Mame/?
involves: C3H/He * C57BL/6 * C57BL/6J
abnormal retina morphology J:128149
abnormal retina outer nuclear layer morphology J:128478
abnormal retina photoreceptor morphology J:128478
normal behavior/neurological phenotype J:128149, J:128478
retina degeneration J:128149
thin retina inner nuclear layer J:128149
Pde6brd1/Pde6brd1
Tg(OPN1LW-DT)1Mame/?
Not Specified
abnormal visual contrast sensitivity J:199509

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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
04/09/2024
MGI 6.23
The Jackson Laboratory