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 skeleton physiology
Accession: MP:0001533
browse the term
Definition: any functional anomaly of the bony framework of the body
Synonyms: exact_synonym: abnormal bone/ skeleton physiology; bone/ skeletal physiology abnormalities
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Prkg2
protein kinase cGMP-dependent 2
IAGP
DNA:deletion:cds (rat)
RGD
PMID:15466490
RGD:150429792
NCBI chr14:10,864,020...10,972,617
Ensembl chr14:10,864,186...10,972,614
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F8
coagulation factor VIII
treatment
IMP
RGD
PMID:27060449
RGD:150520059
NCBI chr18:155,237...187,186
Ensembl chr18:155,309...186,683
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F8em1Sage
coagulation factor VIII, procoagulant component; zinc finger nuclease induced mutant1, Sage
treatment
IMP
RGD
PMID:27060449
RGD:150520059
G
Prkg2
protein kinase cGMP-dependent 2
IAGP
DNA:deletion:cds (rat)
RGD
PMID:19149413
RGD:150429793
NCBI chr14:10,864,020...10,972,617
Ensembl chr14:10,864,186...10,972,614
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Zbtb16
zinc finger and BTB domain containing 16
IAGP
RGD
PMID:27727328
RGD:40924666
NCBI chr 8:57,885,886...58,073,507
Ensembl chr 8:57,891,081...58,073,507
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Golgb1
golgin B1
IAGP
RGD
PMID:21851869
RGD:40902994
NCBI chr11:77,348,573...77,406,165
Ensembl chr11:77,348,961...77,406,006
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Mkx
mohawk homeobox
IMP
compared to Wistar
RGD
PMID:27370800
RGD:40924660
NCBI chr17:59,772,113...59,851,160
Ensembl chr17:59,773,570...59,850,345
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Mkxem1Asah
mohawk homeobox; CRISPR/Cas9 system induced mutant 1, Asah
IMP
compared to Wistar
RGD
PMID:27370800
RGD:40924660
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F8
coagulation factor VIII
treatment
IMP
RGD
PMID:27060449 PMID:31899798
RGD:150520059 , RGD:150520060
NCBI chr18:155,237...187,186
Ensembl chr18:155,309...186,683
G
F8em1Sage
coagulation factor VIII, procoagulant component; zinc finger nuclease induced mutant1, Sage
treatment
IMP
RGD
PMID:31899798 PMID:27060449
RGD:150520060 , RGD:150520059
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F8em1Mcwi
coagulation factor VIII, procoagulant component; CRISPR/Cas9 induced mutant1, Mcwi
treatment
IMP
RGD
PMID:31899798
RGD:150520060
G
Mkx
mohawk homeobox
IMP
compared to Wistar
RGD
PMID:27370800
RGD:40924660
NCBI chr17:59,772,113...59,851,160
Ensembl chr17:59,773,570...59,850,345
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Mkxem1Asah
mohawk homeobox; CRISPR/Cas9 system induced mutant 1, Asah
IMP
compared to Wistar
RGD
PMID:27370800
RGD:40924660
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Ncf1
neutrophil cytosolic factor 1
IAGP
RGD
PMID:12461526
RGD:628543
NCBI chr12:28,121,816...28,131,080
Ensembl chr12:28,121,366...28,131,079
G
F8
coagulation factor VIII
treatment
IMP
RGD
PMID:27060449
RGD:150520059
NCBI chr18:155,237...187,186
Ensembl chr18:155,309...186,683
G
F8em1Sage
coagulation factor VIII, procoagulant component; zinc finger nuclease induced mutant1, Sage
treatment
IMP
RGD
PMID:27060449
RGD:150520059
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Cyp27b1
cytochrome P450, family 27, subfamily b, polypeptide 1
treatment
IMP
compared to Jcl:Wi and treated
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:64,756,626...64,761,570
Ensembl chr 7:64,756,626...64,761,570
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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 treated
RGD
PMID:32231239
RGD:32716373
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Vdr
vitamin D receptor
IMP
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:130,864,764...130,916,757
Ensembl chr 7:130,866,745...130,916,757
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Vdrem1Thka
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka
IMP
RGD
PMID:32231239
RGD:32716373
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