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 trabecular bone morphology
Accession: MP:0000130
browse the term
Definition: any structural anomaly of bone that has a lattice-like or spongy structure; it is highly vascular and contains intercommunicating spaces filled with bone marrow
Synonyms: exact_synonym: abnormal cancellous bone morphology; abnormal spongy bone morphology; abnormal spongy spongiosa morphology; abnormal spongy substance morphology; abnormal substantia trabecularis morphology
xref: HP:0100671
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Arsb
arylsulfatase B
IAGP
RGD
PMID:21887218
RGD:39131283
NCBI chr 2:26,736,395...26,895,682
Ensembl chr 2:26,736,957...26,897,611
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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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Vdrem2Thka
vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka
IMP
RGD
PMID:32231239
RGD:32716373
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Arsb
arylsulfatase B
IAGP
RGD
PMID:21887218
RGD:39131283
NCBI chr 2:26,736,395...26,895,682
Ensembl chr 2:26,736,957...26,897,611
G
Lrp5
LDL receptor related protein 5
IMP
RGD
PMID:32833527
RGD:40902996
NCBI chr 1:210,243,499...210,346,886
Ensembl chr 1:210,243,502...210,346,822
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Lrp5em1Vari
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari
IMP
RGD
PMID:32833527
RGD:40902996
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Lrp5em3Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5
LDL receptor related protein 5
IMP
RGD
PMID:32833527
RGD:40902996
NCBI chr 1:210,243,499...210,346,886
Ensembl chr 1:210,243,502...210,346,822
G
Lrp5em1Vari
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em2Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em3Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5
LDL receptor related protein 5
IMP
RGD
PMID:32833527
RGD:40902996
NCBI chr 1:210,243,499...210,346,886
Ensembl chr 1:210,243,502...210,346,822
G
Lrp5em1Vari
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em2Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em3Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari
IMP
RGD
PMID:32833527
RGD:40902996
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Cftr
CF transmembrane conductance regulator
IMP
RGD
PMID:29190650
RGD:151347176
NCBI chr 4:47,422,084...47,694,646
Ensembl chr 4:47,526,735...47,694,643
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Cftrem1Sage
cystic fibrosis transmembrane conductance regulator; ZFN induced mutant 1 Sage
IMP
RGD
PMID:29190650
RGD:151347176
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Lepr
leptin receptor
IMP
RGD
PMID:26537785
RGD:12911216
NCBI chr 5:121,409,735...121,593,201
Ensembl chr 5:121,474,099...121,591,215
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Leprem4Lizh
leptin receptor; CRISPR/Cas9 induced mutant 4, Lizh
IMP
RGD
PMID:26537785
RGD:12911216
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Lepr
leptin receptor
IMP
RGD
PMID:26537785
RGD:12911216
NCBI chr 5:121,409,735...121,593,201
Ensembl chr 5:121,474,099...121,591,215
G
Leprem4Lizh
leptin receptor; CRISPR/Cas9 induced mutant 4, Lizh
IMP
RGD
PMID:26537785
RGD:12911216
G
Lrp5
LDL receptor related protein 5
sexual_dimorphism
IMP
RGD
PMID:32833527 PMID:32833527
RGD:40902996 , RGD:40902996
NCBI chr 1:210,243,499...210,346,886
Ensembl chr 1:210,243,502...210,346,822
G
Lrp5em1Vari
LDL receptor related protein 5;CRISPR/Cas9 induced mutant 1, Vari
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em2Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, Vari
sexual_dimorphism
IMP
RGD
PMID:32833527
RGD:40902996
G
Lrp5em3Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 3, Vari
sexual_dimorphism
IMP
RGD
PMID:32833527
RGD:40902996
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Ctns
cystinosin, lysosomal cystine transporter
IMP
RGD
PMID:35695380
RGD:155630629
NCBI chr10:58,300,069...58,315,725
Ensembl chr10:58,299,967...58,321,661
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