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 intestine morphology
Accession: MP:0000477
browse the term
Definition: any structural anomaly of the digestive tube passing from the stomach to the anus, consisting of the small and large intestine divisions
Synonyms: exact_synonym: Volvulus; abnormal bowel morphology; intestinal abnormalities
narrow_synonym: abnormal bowel wall morphology; bowel wall abnormalities; intestinal dysplasia; intestine dysplasia
alt_id: MP:0000475
xref: HP:0002580
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
G
Men1
menin 1
severity
IMP
RGD
PMID:15054094
RGD:1304318
NCBI chr 1:203,638,905...203,644,871
Ensembl chr 1:203,639,000...203,644,871
G
Cplx1
complexin 1
IMP
RGD
PMID:31875236
RGD:127285808
NCBI chr14:1,184,677...1,216,392
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
G
Cftr
CF transmembrane conductance regulator
IMP
RGD
PMID:24608905
RGD:11566051
NCBI chr 4:46,561,269...46,728,759
Ensembl chr 4:46,560,885...46,728,756
G
Cftrem1Sage
cystic fibrosis transmembrane conductance regulator; ZFN induced mutant 1 Sage
IMP
RGD
PMID:24608905
RGD:11566051
G
Ednrb
endothelin receptor type B
IAGP
RGD
PMID:21915282 PMID:22132166
RGD:6480217 , RGD:6480215
NCBI chr15:80,640,839...80,672,115
Ensembl chr15:80,643,043...80,672,115
G
Ednrbsl
endothelin receptor type B, spotting lethal
IAGP
RGD
PMID:21915282 PMID:22132166
RGD:6480217 , RGD:6480215
G
Apc
APC regulator of WNT signaling pathway
IMP
RGD
PMID:17360473
RGD:1601201
NCBI chr18:25,828,558...25,925,511
Ensembl chr18:25,864,222...25,922,696
G
ApcPirc
APC, WNT signaling pathway regulator; polyposis in the rat colon
IMP
RGD
PMID:17360473
RGD:1601201
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
G
Cplx1
complexin 1
IMP
RGD
PMID:31875236
RGD:127285808
NCBI chr14:1,184,677...1,216,392
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
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