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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Adgrg6
adhesion G protein-coupled receptor G6
MGI:1916151
60 phenotypes from 7 alleles in 11 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Adgrg6em1Jlp/Adgrg6em1Jlp
C57BL/6-Adgrg6em1Jlp
abnormal forelimb morphology J:315981
abnormal hindlimb morphology J:315981
abnormal locomotor behavior J:315981
abnormal motor coordination/balance J:315981
abnormal myelination J:315981
abnormal nervous system development J:315981
normal cardiovascular system phenotype J:315981
decreased body size J:315981
joint contracture J:315981
normal mortality/aging J:315981
Adgrg6em2Jlp/Adgrg6em2Jlp
C57BL/6-Adgrg6em2Jlp
abnormal heart development J:315981
abnormal interventricular septum morphology J:315981
abnormal myocardial trabeculae morphology J:315981
abnormal placenta physiology J:315981
abnormal trophoblast glycogen cell morphology J:315981
abnormal trophoblast layer morphology J:315981
abnormal uterine spiral artery morphology J:315981
abnormal uterine spiral artery remodeling J:315981
dilated heart ventricle J:315981
disorganized placental labyrinth J:315981
embryonic lethality during organogenesis, complete penetrance J:315981
increased placenta intervillous maternal lacunae size J:315981
placenta hemorrhage J:315981
thin myocardium compact layer J:315981
thin ventricular wall J:315981
Adgrg6em2Jlp/Adgrg6em3Jlp
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj
no abnormal phenotype detected J:315981
Adgrg6em2Jlp/Adgrg6em3Jlp
Tg(Tek-cre)1Ywa/0
involves: C57BL/6 * SJL
no abnormal phenotype detected J:315981
Adgrg6em3Jlp/Adgrg6em3Jlp
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA
decreased body size J:315981
embryonic lethality during organogenesis, complete penetrance J:315981
joint contracture J:315981
lethality throughout fetal growth and development, incomplete penetrance J:315981
small heart J:315981
Adgrg6em3Jlp/Adgrg6em3Jlp
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj
no abnormal phenotype detected J:315981
Adgrg6em3Jlp/Adgrg6em3Jlp
Nfatc1tm1.1(cre)Bz/Nfatc1+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
no abnormal phenotype detected J:315981
Adgrg6em3Jlp/Adgrg6em3Jlp
Tg(Tek-cre)1Ywa/0
involves: C57BL/6 * SJL
no abnormal phenotype detected J:315981
Adgrg6tm1Apr/Adgrg6tm1Apr
either: 129S/SvEv-Gpr126tm1Apr or B6.129S-Gpr126tm1Apr or (involves: 129S/SvEv * MF1)
abnormal blood circulation J:167309
dilated heart ventricle J:167309
edema J:167309
embryonic lethality during organogenesis, complete penetrance J:167309
internal hemorrhage J:167309
thin myocardium J:167309
Adgrg6tm1Arte/Adgrg6tm1Arte
Tg(Col2a1-cre)#Amc/0
involves: 129S5/SvEvBrd
abnormal intervertebral disk morphology J:224002, J:313834
abnormal nucleus pulposus morphology J:313834
abnormal sternum morphology J:224002
increased chondrocyte apoptosis J:224002
scoliosis J:224002, J:313834
normal skeleton phenotype J:224002, J:313834
Adgrg6tm1Arte/Adgrg6tm1Arte
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
involves: 129S5/SvEvBrd
abnormal intervertebral disk morphology J:313834
scoliosis J:313834
Adgrg6tm1Arte/Adgrg6tm1Arte
Tg(Scx-GFP/cre)1Stzr/0
involves: 129S5/SvEvBrd
abnormal intervertebral disk morphology J:313834
abnormal nucleus pulposus morphology J:313834
abnormal tendon physiology J:313834
scoliosis J:313834
Adgrg6tm1Lex/Adgrg6tm1Lex
involves: 129S/SvEvBrd
myocardial trabeculae hypoplasia J:202002
Adgrg6tm1Lex/Adgrg6tm1Lex
involves: 129S/SvEvBrd * C57BL/6
abnormal axon fasciculation J:173574
abnormal axon morphology J:173574
abnormal axon radial sorting J:173574
abnormal cochlear nerve morphology J:173574
abnormal myelination J:173574
abnormal Schwann cell morphology J:173574
abnormal sciatic nerve morphology J:173574
abnormal somatic nervous system morphology J:173574
akinesia J:173574
decreased body size J:173574
impaired limb coordination J:173574
joint contracture J:173574
postnatal growth retardation J:173574
prenatal lethality, incomplete penetrance J:173574
preweaning lethality, complete penetrance J:173574
Adgrg6tm1Taki/Adgrg6tm1Taki
involves: C57BL/6
abnormal endocardium morphology J:202002
abnormal fetal cardiomyocyte mitochondrial morphology J:202002
abnormal fetal cardiomyocyte morphology J:202002
abnormal mitochondrial crista morphology J:202002
abnormal mitochondrial morphology J:202002
abnormal mitochondrial shape J:202002
abnormal myocardial trabeculae morphology J:202002
normal cardiovascular system phenotype J:202002
embryonic lethality during organogenesis, complete penetrance J:202002
increased cardiac muscle triglyceride level J:202002
pericardial edema J:202002
thin ventricular wall J:202002

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
11/12/2024
MGI 6.24
The Jackson Laboratory