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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Carm1
coactivator-associated arginine methyltransferase 1
MGI:1913208
40 phenotypes from 5 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Carm1m9Bei/Carm1m9Bei
involves: A/J * C57BL/6
abnormal corpus callosum morphology J:199782
abnormal craniofacial morphology J:199782
abnormal limb morphology J:199782
cleft palate J:199782
decreased embryo size J:199782
omphalocele J:199782
Carm1m9Bei/Carm1m9Bei
involves: A/J * C57BL/6J
abnormal craniofacial morphology J:327081
abnormal heart left atrium morphology J:327081
abnormal limb morphology J:327081
cleft palate J:327081
decreased embryo size J:327081
double outlet right ventricle J:327081
heart hemorrhage J:327081
heart left atrium hypoplasia J:327081
hemothorax J:327081
increased atrioventricular cushion size J:327081
increased heart right atrium size J:327081
omphalocele J:327081
persistent truncus arteriosus J:327081
preweaning lethality, complete penetrance J:327081
ventricular septal defect J:327081
Carm1tm1.1Mtb/Carm1tm1.1Mtb
Tg(Stra8-icre)1Reb/0
involves: 129 * C57BL/6J * FVB/NJ
abnormal cauda epididymis morphology J:265753
abnormal sperm head morphology J:265753
abnormal sperm midpiece morphology J:265753
abnormal spermatid morphology J:265753
abnormal spermiogenesis J:265753
absent sperm head J:265753
asthenozoospermia J:265753
decreased litter size J:265753
decreased male germ cell number J:265753
decreased testis weight J:265753
male infertility J:265753
oligozoospermia J:265753
reduced male fertility J:265753
Carm1tm1b(EUCOMM)Hmgu/Carm1+
C57BL/6N-Carm1tm1b(EUCOMM)Hmgu/Nju
decreased lymphocyte cell number J:211773
Carm1tm1b(EUCOMM)Hmgu/Carm1tm1b(EUCOMM)Hmgu
C57BL/6N-Carm1tm1b(EUCOMM)Hmgu/Nju
preweaning lethality, complete penetrance J:211773
Carm1tm1Mtb/Carm1+
involves: 129S6/SvEvTac * Black Swiss
postnatal lethality, incomplete penetrance J:83623
Carm1tm1Mtb/Carm1tm1Mtb
involves: 129S6/SvEvTac
abnormal adipose tissue development J:159958
arrested T cell differentiation J:159958
double outlet right ventricle J:327081
hemothorax J:327081
neonatal lethality, complete penetrance J:159958
persistent truncus arteriosus J:327081
preweaning lethality, complete penetrance J:327081
ventricular septal defect J:327081
Carm1tm1Mtb/Carm1tm1Mtb
involves: 129S6/SvEvTac * Black Swiss
abnormal lung morphology J:83623
decreased fetal size J:83623
lethality throughout fetal growth and development, incomplete penetrance J:83623
perinatal lethality, incomplete penetrance J:83623
respiratory failure J:83623
Carm1tm2.1Mtb/Carm1tm2.1Mtb
involves: 129S4/SvJaeSor * 129S6/SvEvTac * Black Swiss
abnormal adipose tissue development J:159958
arrested T cell differentiation J:159958
decreased fetal size J:159958
neonatal lethality, complete penetrance J:159958
thymus hypoplasia J:159958

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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
11/19/2024
MGI 6.24
The Jackson Laboratory