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 calcium level
Accession: MP:0020879
browse the term
Definition: any anomaly in the concentration of calcium in the body or bodily fluids
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Csf1r
colony stimulating factor 1 receptor
IMP
RGD
PMID:30249809
RGD:41404725
NCBI chr18:56,834,152...56,860,804
Ensembl chr18:54,546,659...54,590,415
G
Csf1rtm(EGFP)Tset
colony stimulating factor 1 receptor; target mutant, Tset
IMP
RGD
PMID:30249809
RGD:41404725
G
Cyp27b1
cytochrome P450, family 27, subfamily b, polypeptide 1
treatment
IMP
compared to Jcl:Wi and untreated
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:64,756,626...64,761,570
Ensembl chr 7:62,871,297...62,876,241
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Cyp27b1em1Thka
cytochrome P450, family 27, subfamily b, polypeptide 1; CRISPR/Cas9 induced mutant 1, Thka
treatment
IMP
compared to Jcl:Wi and untreated
RGD
PMID:32231239
RGD:32716373
G
Vdr
vitamin D receptor
treatment
IMP
compared to Jcl:Wi and untreated
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:130,864,764...130,916,757
Ensembl chr 7:128,987,981...129,037,677
G
Vdrem1Thka
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka
treatment
IMP
compared to Jcl:Wi and untreated
RGD
PMID:32231239
RGD:32716373
G
Myh7b
myosin heavy chain 7B
IMP
RGD
PMID:32207065
RGD:126925946
NCBI chr 3:164,537,211...164,582,441
Ensembl chr 3:144,098,190...144,122,084
G
Myh7bem1Blar
myosin heavy chain 7B; CRISPR/Cas9 induced mutant 1, Blar
IMP
RGD
PMID:32207065
RGD:126925946
G
Ctns
cystinosin, lysosomal cystine transporter
IMP
RGD
PMID:35695380
RGD:155630629
NCBI chr10:58,300,069...58,315,725
Ensembl chr10:57,801,456...57,817,120
G
Gla
galactosidase, alpha
onset
IMP
compared to Wild type
RGD
PMID:29979634
RGD:401976416
NCBI chr X:102,062,497...102,073,915
Ensembl chr X:97,768,996...97,780,664
G
Glaem2Mcwi
galactosidase, alpha; CRISPR/Cas9 system induced mutant 2, Medical College of Wisconsin
onset
IMP
compared to Wild type
RGD
PMID:29979634
RGD:401976416
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