MAMMALIAN PHENOTYPE - ANNOTATIONS
The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term: abnormal heart ventricle size
Accession: MP:0031543
browse the term
Definition: anomaly in the average size of either one or both of the heart ventricles compared to the average for a particular population
Synonyms: exact_synonym: abnormal cardiac ventricle size; abnormal heart ventricular size
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Camk2n1
calcium/calmodulin-dependent protein kinase II inhibitor 1
IMP
RGD
PMID:31327268
RGD:18899561
NCBI chr 5:150,674,819...150,676,600
Ensembl chr 5:150,673,507...150,676,600
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Camk2n1em1Tja
calcium/calmodulin-dependent protein kinase II inhibitor 1; ZFN induced mutant 1, Tja
IMP
RGD
PMID:31327268
RGD:18899561
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Cyp11b2
cytochrome P450, family 11, subfamily b, polypeptide 2
IAGP
RGD
PMID:11832364
RGD:727991
NCBI chr 7:106,838,590...106,845,004
Ensembl chr 7:106,838,590...106,845,004
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Ednra
endothelin receptor type A
IDA
RGD
PMID:16157796
RGD:1581830
NCBI chr19:30,233,540...30,303,727
Ensembl chr19:30,233,571...30,297,049
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Egfr
epidermal growth factor receptor
IDA
RGD
PMID:12624003
RGD:1580955
NCBI chr14:91,176,979...91,349,722
Ensembl chr14:91,177,067...91,344,382
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Lepr
leptin receptor
treatment
IAGP
RGD
PMID:33568522
RGD:401965412
NCBI chr 5:116,294,409...116,477,904
Ensembl chr 5:116,289,823...116,475,908
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Myh7b
myosin heavy chain 7B
IMP
RGD
PMID:32207065
RGD:126925946
NCBI chr 3:144,076,911...144,122,714
Ensembl chr 3:144,098,190...144,122,084
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Myh7bem1Blar
myosin heavy chain 7B; CRISPR/Cas9 induced mutant 1, Blar
IMP
RGD
PMID:32207065
RGD:126925946
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Sod3
superoxide dismutase 3
IMP
compared to SS/JrHsdMcwi
RGD
PMID:31972339
RGD:150573712
NCBI chr14:58,610,104...58,615,845
Ensembl chr14:58,609,958...58,615,990
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Sod3m1Mcwi
superoxide dismutase 3; mutation 1, Medical College of Wisconsin
IMP
compared to SS/JrHsdMcwi
RGD
PMID:31972339
RGD:150573712
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Lepr
leptin receptor
IAGP
DNA:mutations:cds: : (rat)
RGD
PMID:32710530
RGD:401960103
NCBI chr 5:116,294,409...116,477,904
Ensembl chr 5:116,289,823...116,475,908
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Ddah1
dimethylarginine dimethylaminohydrolase 1
exacerbates
IMP
RGD
PMID:31402164
RGD:151347602
NCBI chr 2:234,667,499...234,800,322
Ensembl chr 2:234,667,491...234,799,339
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Ddah1em1Ywxu
dimethylarginine dimethylaminohydrolase 1; CRISPR/Cas9 induced mutant 1, Ywxu
exacerbates
IMP
RGD
PMID:31402164
RGD:151347602
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