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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		a
nonagouti
MGI:87853
141 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
a/a
Bloc1s6pa/Bloc1s6pa
involves: C57BL/6J 		abnormal retina melanin granule morphology J:5346
a/a
Ces1ce/Ces1ce
B6;D2-a Ces1ce/EiJ 		abnormal enzyme/coenzyme activity J:345412
abnormal xenobiotic metabolism J:345412
a/a
Corintm1Bamo/Corintm1Bamo
involves: 129X1/SvJ * C57BL/6 * FVB/N 		normal integument phenotype J:130426
a/a
DctSlt-lt/Dct+
involves: C3H/HeJ 		diluted coat color J:27515
a/a
DctSlt-lt/DctSlt-lt
involves: C3H/HeJ 		diluted coat color J:27515
A/A
Dkd/Dkd
LPT;C3-Dkd/GrsrJ 		abnormal dorsoventral coat patterning J:137334
normal hearing/vestibular/ear phenotype J:137334
normal vision/eye phenotype J:137334
a/a
Hps6ru-5J/Hps6ru-5J
Lystbg/Lystbg
involves: C3H/Rl * C57BL/6J 		abnormal coat/hair pigmentation J:26546
abnormal eye pigmentation J:26546
decreased eye pigmentation J:26546
diluted coat color J:26546
a/a
Hps6ru/Hps6ru
B6.Cg-Hps6ru 		abnormal coat/hair pigmentation J:6064
abnormal kidney physiology J:6422
abnormal lateral geniculate nucleus morphology J:6064
abnormal retina ganglion cell morphology J:6064
decreased platelet ADP level J:7327
decreased platelet ATP level J:7327
decreased platelet dense granule number J:7327
decreased platelet serotonin level J:7327, J:29748
decreased susceptibility to atherosclerosis J:29748
increased bleeding time J:7327
a/a
Hps6ru/Hps6ru
involves: C57BL/6J 		abnormal eye pigmentation J:5346
abnormal melanogenesis J:5346
abnormal melanosome morphology J:5346
a/a
Hps6ru/Hps6ru
Not Specified 		abnormal choroid pigmentation J:81444
abnormal eye pigmentation J:13122, J:81444
abnormal iris pigmentation J:13122
decreased eye pigmentation J:13122
diluted coat color J:13122
hypopigmentation J:12970
A/A
Hps6ru/Hps6ru
Not Specified 		diluted coat color J:13122
a/a
Hps6ru/Hps6ru
Lystbg/Lystbg
involves: C3H/Rl * C57BL/6J 		abnormal melanogenesis J:5346
abnormal melanosome morphology J:5346
abnormal retina melanin granule morphology J:5346
A/a
In(11Trp53;11Wnt3)8Brd/+
either: (involves: 129S7/SvEvBrd * C57BL/6Brd) or (involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6Brd) or (involves: 129S5/SvEvBrd * C57BL/6Brd * C57BL/6J) 		abnormal tail pigmentation J:56548
decreased ear pigmentation J:56548
a/a
In(11Trp53;11Wnt3)8Brd/+
involves: 129S7/SvEvBrd * C57BL/6Brd * C57BL/6J 		abnormal tail pigmentation J:56548
a/a
KitW-2J/Kit+
involves: C57BL/6J 		white spotting J:192797
a/a
Lystbg/Lystbg
involves: C3H/Rl * C57BL/6J 		abnormal choroid melanin granule morphology J:5346
abnormal retina melanin granule morphology J:5346
a/a
Lystbg/Lystbg
Oca2p-J/Oca2p-J
involves: C3H/HeJ * C3H/Rl * C57BL/6J 		abnormal choroid melanin granule morphology J:5346
abnormal melanosome morphology J:5346
a/a
Lystbg/Lystbg
Tyrc/Tyrc
involves: C3H/Rl * C57BL/6J 		abnormal choroid melanin granule morphology J:5346
abnormal melanogenesis J:5346
abnormal melanosome morphology J:5346
abnormal retina melanin granule morphology J:5346
a/a
Lystbg/Lystbg
Tyrp1b/Tyrp1b
involves: C3H/Rl * C57BL/6J 		abnormal choroid melanin granule morphology J:5346
abnormal retina melanin granule morphology J:5346
A/A
Mc1rE-tob/Mc1r+
M. m. domesticus poschiavinus 		abnormal coat/hair pigmentation J:22593
darkened coat color J:22593
A/A
Mc1rE-tob/Mc1rE-tob
M. m. domesticus poschiavinus 		abnormal coat/hair pigmentation J:22593
darkened coat color J:22593
a/A
Mc1re/Mc1re
Pomctm1Sora/Pomctm1Sora
Tg(MC1R)1Jkn/?
involves: 129S6/SvEvTac * C57BL/6Ha 		abnormal hair follicle pheomelanosome pheomelanin content J:129904
yellow coat color J:129904
a/a
Mc1re/Mc1re
Pomctm1Sora/Pomctm1Sora
Tg(MC1R)1Jkn/?
involves: 129S6/SvEvTac * C57BL/6Ha 		abnormal hair follicle pheomelanosome pheomelanin content J:129904
yellow coat color J:129904
a/a
Mlphln/Mlphln
involves: C57BL/J * C57BR 		abnormal choroid melanin granule morphology J:5346
abnormal hair follicle melanin granule distribution J:5346
a/a
Mlphln/Mlphln
Not Specified 		abnormal coat/hair pigmentation J:12970
abnormal hair follicle melanocyte morphology J:12970
abnormal hair shaft melanin granule distribution J:12970
diluted coat color J:12970
a/a
Mlphln/Mlphln
Tyrp1b/Tyrp1b
C57L/J 		abnormal coat/hair pigmentation J:5095
abnormal melanocyte morphology J:5095
diluted coat color J:5095
a/a
Mregdsu/Mregdsu
Hps6ru/Hps6ru
involves: C57BL/6J 		diluted coat color J:29467
phenotypic reversion J:29467
a/a
Mssq1KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq3KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq4KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq5C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq6C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq6KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq7KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq8C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq9C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq10KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq11KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq12KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq13C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq13KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq14KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq15C57BL/6JJcl/Mssq15KK/TaJcl
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Mssq16KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
a/a
Myo5ad/Myo5a+
Oca2p/Oca2+
Tyrp1B-lt/Tyrp1+
involves: C58 * CT/Ch 		diluted coat color J:13094
a/a
Myo5ad/Myo5ad
involves: DBA/2J 		abnormal choroid melanin granule morphology J:5346
abnormal hair follicle melanin granule distribution J:5346
a/a
Myo5ad/Myo5ad
Not Specified 		abnormal coat/hair pigmentation J:12958
abnormal eye pigmentation J:12958
abnormal hair shaft melanin granule distribution J:12958
abnormal hair shaft morphology J:12958
abnormal melanocyte morphology J:12970
diluted coat color J:12958
a/a
Oca2p-J/Oca2p-J
involves: C3H/HeJ 		abnormal choroid melanin granule morphology J:5346
abnormal melanogenesis J:5346
abnormal melanosome morphology J:5346
a/a
Oca2p/Oca2p
Not Specified 		abnormal coat/hair pigmentation J:12958, J:78801
abnormal hair follicle melanin granule distribution J:12958
abnormal hair follicle melanin granule morphology J:12958
abnormal hair follicle melanin granule shape J:12958
abnormal hair follicle melanocyte morphology J:78801
decreased ear pigmentation J:36414, J:78801
decreased eye pigmentation J:78801
decreased skin pigmentation J:36414
decreased tail pigmentation J:78801
a/a
Pax3Sp-1H/Pax3Sp-1H
involves: 101/H * C3H/HeH * C57BL/6 		abnormal cerebral cortex morphology J:19818
abnormal lateral ventricle morphology J:19818
absent choroid plexus J:19818
absent olfactory bulb J:19818
exencephaly J:19818
incomplete rostral neuropore closure J:19818
a/A
Pomctm1Sora/Pomctm1Sora
involves: 129S6/SvEvTac 		abnormal hair follicle pheomelanosome pheomelanin content J:129904
yellow coat color J:129904
a/a
Rab27aash/Rab27aash
involves: C3H/HeSnJ * C57BL/6J 		decreased platelet serotonin level J:77395
normal hematopoietic system phenotype J:77395
increased bleeding time J:77395
a/a
Rmi1Gt(pUHachi)0283Imeg/Rmi1+
involves: C57BL/6 * KK 		normal behavior/neurological phenotype J:168271
decreased body weight J:168271
decreased circulating glucose level J:168271
decreased gonadal fat pad weight J:168271
decreased liver weight J:168271
improved glucose tolerance J:168271
A/A
Tyrc-ch/Tyrc-ch
Not Specified 		abnormal coat appearance J:36414
abnormal coat/hair pigmentation J:36414
abnormal hair follicle pheomelanosome pheomelanin content J:36414
a/a
Tyrc-i/Tyrc-i
involves: STOCK Tyrc-r 		abnormal coat/hair pigmentation J:83666
diluted coat color J:83666
a/a
Tyrc/Tyrc
involves: C57BL/6J 		abnormal melanogenesis J:5346
a/a
Tyrc/Tyrem2Ove
involves: C57BL/6 * FVB 		decreased eye pigmentation J:94077
diluted coat color J:94077
a/a
Tyrc/Tyrem4Ove
involves: C57BL/6 * FVB 		abnormal eye pigmentation J:94077
diluted coat color J:94077
a/a
Tyrc/Tyrem9Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
a/a
Tyrc/Tyrem14Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
a/a
Tyrem2Ove/Tyrem2Ove
involves: C57BL/6 * FVB 		abnormal eye pigmentation J:94077
abnormal tail pigmentation J:94077
diluted coat color J:94077
a/a
Tyrem4Ove/Tyrem4Ove
involves: C57BL/6 * FVB 		abnormal eye pigmentation J:94077
decreased tail pigmentation J:94077
diluted coat color J:94077
a/a
Tyrem14Ove/Tyrem14Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
A/a
Tyrem15Ove/Tyrem15Ove
involves: C57BL/6 * FVB 		decreased tail pigmentation J:94077
diluted coat color J:94077
a/a
Tyrp1B-lt/Tyrp1+
Not Specified 		abnormal dorsoventral coat patterning J:13094
abnormal hair shaft melanin granule distribution J:13094
abnormal hair shaft melanin granule morphology J:13094
reduced hair shaft melanin granule number J:13094
a/a
Tyrp1B-lt/Tyrp1B-lt
Not Specified 		abnormal dorsoventral coat patterning J:13094
abnormal hair follicle melanin granule morphology J:13094
abnormal hair shaft melanin granule distribution J:13094
abnormal hair shaft melanin granule morphology J:13094
enlarged hair follicle melanin granules J:13094
reduced hair shaft melanin granule number J:13094
A/a
Tyrp1B-lt/Tyrp1B-lt
Not Specified 		diluted coat color J:13094
a/a
Tyrp1b/Tyrp1b
involves: C57BL/6J 		abnormal melanosome morphology J:5346
a/a
Tyrp1b/Tyrp1b
Not Specified 		abnormal coat/hair pigmentation J:12970
abnormal eye pigmentation J:12970
abnormal melanocyte morphology J:12970
a/a
Tyrp1b/Tyrp1b
wad/wad+
Not Specified 		diluted coat color J:162146
a/a
Tyrp1b/Tyrp1b
wad/wad
Not Specified 		diluted coat color J:162146
a/a
U/U
Not Specified 		abnormal coat/hair pigmentation J:78801
darkened coat color J:78801
A/A
U/U
Not Specified 		abnormal coat/hair pigmentation J:78801
darkened coat color J:280, J:78801
a/a
Zc3h4KK/Zc3h4KK
involves: C57BL/6J * KK-Ay 		increased body weight J:48704
a/Ay
Bwq2KK/Bwq2KK
involves: C57BL/6J * KK-Ay 		increased body weight J:93199, J:131439
increased susceptibility to weight gain J:93199
a/Ay
Bwq10C57BL/6J/Bwq10C57BL/6J
involves: C57BL/6J * KK-Ay 		increased body weight J:131439
a/Ay
Guq1KK/Guq1KK
involves: C57BL/6J * KK-Ay 		increased urine glucose level J:131439
a/Ay
Guq2C57BL/6J/Guq2C57BL/6J
involves: C57BL/6J * KK-Ay 		increased urine glucose level J:131439
a/Ay
Zc3h4C57BL/6J/Zc3h4KK
involves: C57BL/6J * KK-Ay 		increased body weight J:48704
a/Ay
Zc3h4KK/Zc3h4KK
involves: C57BL/6J * KK-Ay 		increased body weight J:48704, J:131439
A/?
DctSlt-lt/Dct+
involves: C3H/HeJ 		diluted coat color J:27515
A/?
DctSlt-lt/DctSlt-lt
involves: C3H/HeJ 		diluted coat color J:27515
A/?
Lystbg/Lystbg
Tyrp1+/?
Not Specified 		abnormal eye pigmentation J:29744
decreased ear pigmentation J:29744
decreased tail pigmentation J:29744
diluted coat color J:29744
irregular coat pigmentation J:29744
A/?
Lystbg/Lystbg
Tyrp1b/Tyrp1b
Not Specified 		decreased eye pigmentation J:29744
diluted coat color J:29744
A/?
Tyrc/Tyrem1Ove
involves: C57BL/6 * FVB 		decreased eye pigmentation J:94077
diluted coat color J:94077
A/?
Tyrc/Tyrem6Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
variegated eye pigmentation pattern J:94077
A/?
Tyrc/Tyrem7Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
A/?
Tyrc/Tyrem12Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
A/?
Tyrc/Tyrem13Ove
involves: C57BL/6 * FVB 		normal pigmentation phenotype J:94077
A/?
Tyrem1Ove/Tyrem1Ove
involves: C57BL/6 * FVB 		diluted coat color J:94077
A/?
Tyrem7Ove/Tyrem7Ove
involves: C57BL/6 * FVB 		abnormal eye pigmentation J:94077
diluted coat color J:94077
A/?
Tyrem8Ove/Tyrem8Ove
involves: C57BL/6 * FVB 		decreased ear pigmentation J:94077
decreased tail pigmentation J:94077
diluted coat color J:94077
variegated eye pigmentation pattern J:94077
A/?
Tyrem9Ove/Tyrem9Ove
involves: C57BL/6 * FVB 		decreased eye pigmentation J:94077
diluted coat color J:94077
A/?
Tyrem12Ove/Tyrem12Ove
involves: C57BL/6 * FVB 		decreased eye pigmentation J:94077
diluted coat color J:94077
A/?
Tyrem13Ove/Tyrem13Ove
involves: C57BL/6 * FVB 		normal pigmentation phenotype J:94077
ae/ae
Tbx15de-H/Tbx15de-H
involves: BTBR * C3H/HeJ * C57BL/6 * P * S 		abnormal skeleton morphology J:87455
abnormal skin pigmentation J:87455
decreased body size J:87455
normal integument phenotype J:87455
short hair J:87455
ajIs(17;In2)1Gso/ajIs(17;In2)1Gso
Fmn1ld-Is(17;In2)1Gso/Fmn1ld-Is(17;In2)1Gso
involves: 101/Rl * C3H/Rl * C57BL/E * SEC/Rl 		abnormal autopod morphology J:10399
abnormal autopod rotation J:10399
abnormal carpal bone morphology J:10399
abnormal forelimb morphology J:10399
abnormal hindlimb morphology J:10399
abnormal patella morphology J:10399
abnormal radius morphology J:10399
abnormal tarsal bone morphology J:10399
abnormal ulna morphology J:10399
absent fibula J:10399
brachydactyly J:10399
darkened coat color J:10399
dilated ureter J:10399
fused carpal bones J:10399
fused tarsal bones J:10399
hydronephrosis J:10399
hydroureter J:10399
oligodactyly J:10399
radius hypoplasia J:10399
renal hypoplasia J:10399
single kidney J:10399
syndactyly J:10399
synostosis J:10399
at/A
As/As+
Not Specified 		abnormal coat/hair pigmentation J:5027
at/at
As/As
Not Specified 		abnormal coat/hair pigmentation J:5027
darkened coat color J:5027
at/at
Tbx15de-H/Tbx15de-H
involves: BTBR * C3H/HeJ * C57BL/6 		abnormal dorsoventral coat patterning J:87455
abnormal ventral coat pigmentation J:87455
broad nasal bridge J:87455
decreased body size J:87455
irregular coat pigmentation J:87455
lowered ear position J:87455
narrow eye opening J:87455
ocular hypertelorism J:87455
shortened head J:87455
Atm1.1Arte/Atm1.1Arte
Tyrtm1Arte/Tyrtm1Arte
C57BL/6NTac-Atm1.1Arte Tyrtm1Arte 		absent coat pigmentation J:213411
absent eye pigmentation J:213411
Atm1Brd/Atm1Brd
Ypel4tm1a(EUCOMM)Wtsi/Ypel4tm1a(EUCOMM)Wtsi
C57BL/6N-Atm1Brd Ypel4tm1a(EUCOMM)Wtsi/WtsiIeg 		abnormal red blood cell deformability J:313842
anisocytosis J:313842
elliptocytosis J:313842
normal embryo phenotype J:313842
normal hematopoietic system phenotype J:313842
normal immune system phenotype J:313842
increased circulating erythropoietin level J:313842
increased hematocrit J:313842
increased mean corpuscular volume J:313842
macrocytosis J:313842
normal mortality/aging J:313842
polycythemia J:313842
reticulocytosis J:313842
Avy/a
Axin1Fu/Axin1+
involves: 129P4/RrRk * C67BL/6J 		genetic imprinting J:82396
Avy/A
Dnmt1MommeD2/Dnmt1+
involves: C57BL/6J * FVB/NJ 		yellow coat color J:99816
Avy/A
Smarca5MommeD4/Smarca5+
involves: C57BL/6J * FVB/NJ 		mottled coat J:99816
Avy/A
Smchd1MommeD1/Smchd1+
involves: C57BL/6J * FVB/NJ 		yellow coat color J:99816
Aw/a
Corintm1Bamo/Corintm1Bamo
involves: 129X1/SvJ * C57BL/6 * FVB/N 		diluted coat color J:130426
Aw/at
As/As+
Not Specified 		abnormal coat/hair pigmentation J:5027
Aw/Aw
As/As
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:5027
darkened coat color J:5027
Aw/Aw
Corintm1Bamo/Corintm1Bamo
involves: 129X1/SvJ * C57BL/6 * FVB/N 		diluted coat color J:130426
Ay-Jkn/A
Mc1re/Mc1re
involves: C57BL/6Ha * C57BL/6N 		yellow coat color J:129904
Ay-Jkn/A
Mc1re/Mc1re
Tg(MC1R)1Jkn/0
involves: C57BL/6Ha * C57BL/6N 		yellow coat color J:129904
Ay/a
Agrptm2(HBEGF)Rpa/Agrp+
involves: 129S4/SvJaeSor * KK/Upj 		abnormal eating behavior J:132184
decreased body weight J:132184
Ay/a
Apoetm1Unc/Apoetm1Unc
involves: 129P2/OlaHsd * C57BL/6J * KK/TaJcl 		abnormal glomerular mesangium morphology J:177084
abnormal inflammatory response J:177084
abnormal kidney morphology J:177084
atherosclerotic lesions J:177084
decreased circulating adiponectin level J:177084
glomerulosclerosis J:177084
hyperglycemia J:177084
increased circulating cholesterol level J:177084
increased circulating insulin level J:177084
increased circulating leptin level J:177084
increased circulating triglyceride level J:177084
increased monocyte cell number J:177084
insulin resistance J:177084
obese J:177084
Ay/a
Apoetm1Unc/Apoetm1Unc
Ccr2tm1Mae/Ccr2tm1Mae
involves: 129P2/OlaHsd * C57BL/6J * KK/TaJcl 		decreased circulating adiponectin level J:177084
normal homeostasis/metabolism phenotype J:177084
increased circulating cholesterol level J:177084
increased circulating leptin level J:177084
Ay/a
Dmbx1tm1Sse/Dmbx1tm1Sse
involves: ICR 		decreased body weight J:125193
Ay/a
Ednrbs/Ednrbs
Not Specified 		variable body spotting J:12954
Ay/a
Mssq1KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq2C57BL/6JJcl/Mssq2KK/TaJcl
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq3KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq4KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq5C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq6C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq6KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq7KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq9C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq10KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq11KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq12KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq13C57BL/6JJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq13KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq14KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Mssq16KK/TaJcl/?
involves: C57BL/6JJcl * KK/TaJcl 		large mandible J:143893
Ay/a
Npbwr1tm1Rck/Npbwr1tm1Rck
involves: 129P/Ola * C57BL/6J 		obese J:94820
Ay/A
Pepddal/Pepddal
involves: C3H/HeJ * CBA/J 		darkened coat color J:143333
obese J:143333
Ay/A
Prkar2btm2Gsm/Prkar2b+
involves: C57BL/6 		increased percent body fat/body weight J:131039
increased susceptibility to weight gain J:131039
polyphagia J:131039
Ay/A
Prkar2btm2Gsm/Prkar2btm2Gsm
involves: C57BL/6 		normal behavior/neurological phenotype J:131039
normal growth/size/body region phenotype J:131039
increased brown adipose tissue amount J:131039
increased gonadal fat pad weight J:131039
increased inguinal fat pad weight J:131039
increased locomotor activity J:131039
increased percent body fat/body weight J:131039
increased retroperitoneal fat pad weight J:131039
increased susceptibility to weight gain J:131039
yellow coat color J:131039
Ay/a
Rmi1Gt(pUHachi)0283Imeg/Rmi1+
involves: C57BL/6 * KK 		abnormal eating behavior J:168271
normal adipose tissue phenotype J:168271
decreased body weight J:168271
decreased circulating glucose level J:168271
decreased liver weight J:168271
improved glucose tolerance J:168271
Ay/a
Sik2tm1Htake/Sik2+
C57BL/6-Sik2tm1Htake 		darkened coat color J:215877
Ay/a
Tg(tetO-Ppargc1a)1Dpk/0
Tg(Tyr-rtTA)37Lc/0
involves: FVB 		abnormal hair follicle melanogenesis J:194191
darkened coat color J:194191
Ay/a
Tyrp1B-lt/?
Not Specified 		yellow coat color J:13094
As/As
A/A
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:5027
darkened coat color J:5027
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
04/23/2024
MGI 6.23 		The Jackson Laboratory