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 hindlimb morphology
Accession: MP:0000556
browse the term
Definition: any structural anomaly of the projecting caudal-most paired appendages of an animal trunk, used in particular for movement and grasping; usually denotes the legs or back limbs in mammalian species
Synonyms: exact_synonym: Abnormality of the lower limb; abnormal hind limb morphology; hindlimb abnormalities
narrow_synonym: abnormal leg morphology; hind limb dysplasia; hindlimb dysplasia
broad_synonym: hind limb abnormalities
xref: HP:0002814
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Bckdk
branched chain ketoacid dehydrogenase kinase
IAGP
DNA:missense mutation:cds:G369E (rat)
RGD
PMID:27472223
RGD:39131293
NCBI chr 1:182,515,335...182,520,007
Ensembl chr 1:182,515,327...182,536,633
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Cyp27b1
cytochrome P450, family 27, subfamily b, polypeptide 1
treatment
IMP
compared to Jcl:Wi and untreated
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:62,869,340...62,876,242
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
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Lrp5
LDL receptor related protein 5
IMP
RGD
PMID:32833527
RGD:40902996
NCBI chr 1:200,814,247...200,917,581
Ensembl chr 1:200,814,250...200,917,581
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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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Lrp5em2Vari
LDL receptor related protein 5; CRISPR/Cas9 induced mutant 2, 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
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Vdr
vitamin D receptor
IMP
RGD
PMID:32231239
RGD:32716373
NCBI chr 7:128,987,981...129,037,677
Ensembl chr 7:128,987,981...129,037,677
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Vdrem1Thka
vitamin D receptor; CRISPR/Cas9 induced mutant 1, Thka
IMP
RGD
PMID:32231239
RGD:32716373
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Arsb
arylsulfatase B
IAGP
RGD
PMID:21887218
RGD:39131283
NCBI chr 2:25,002,210...25,162,675
Ensembl chr 2:25,002,346...25,162,671
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Bckdk
branched chain ketoacid dehydrogenase kinase
IAGP
DNA:missense mutation:cds:G369E (rat)
RGD
PMID:27472223
RGD:39131293
NCBI chr 1:182,515,335...182,520,007
Ensembl chr 1:182,515,327...182,536,633
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Cftr
CF transmembrane conductance regulator
IMP
RGD
PMID:29190650
RGD:151347176
NCBI chr 4:46,561,269...46,728,759
Ensembl chr 4:46,560,885...46,728,756
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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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Nppc
natriuretic peptide C
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
NCBI chr 9:87,320,051...87,324,251
Ensembl chr 9:87,320,051...87,324,251
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Nppcem3Kyo
natriuretic peptide C; ZFN induced mutant 3, Kyo
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
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Nppcem4Kyo
natriuretic peptide C; ZFN induced mutant 4, Kyo
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
G
Nppc
natriuretic peptide C
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
NCBI chr 9:87,320,051...87,324,251
Ensembl chr 9:87,320,051...87,324,251
G
Nppcem3Kyo
natriuretic peptide C; ZFN induced mutant 3, Kyo
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
G
Nppcem4Kyo
natriuretic peptide C; ZFN induced mutant 4, Kyo
IMP
compared to wild type
RGD
PMID:29566041
RGD:127284867
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