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 digestive system physiology
Accession: MP:0001663
browse the term
Definition: any functional anomaly of the organ system that converts ingested food to nutrients and energy
Synonyms: exact_synonym: digestive system physiology abnormalities; digestive system: functional anomalies
alt_id: MP:0002142
xref: MGI:2173602
G
Ghsr
growth hormone secretagogue receptor
IMP
compared to wild type rats in response to ghrelin (CHEBI:75431)
RGD
PMID:21258824
RGD:150520012
NCBI chr 2:110,268,489...110,271,865
Ensembl chr 2:110,268,489...110,271,865
G
Ghsrm1Mcwi
growth hormone secretagogue receptor; mutation 1, Medical College of Wisconsin
IMP
compared to wild type rats in response to ghrelin (CHEBI:75431)
RGD
PMID:21258824
RGD:150520012
G
Abcb1a
ATP binding cassette subfamily B member 1A
IMP
RGD
PMID:22049154
RGD:8657330
NCBI chr 4:25,357,467...25,529,941
Ensembl chr 4:25,158,362...25,442,709
G
Abcb1aem2Sage
ATP binding cassette subfamily B member 1A; ZFN induced mutant 2, Sage
IMP
RGD
PMID:22049154
RGD:8657330
G
Pmch
pro-melanin-concentrating hormone
IMP
RGD
PMID:19934402
RGD:150429945
NCBI chr 7:22,511,934...22,513,250
Ensembl chr 7:22,511,934...22,513,250
G
Pmchm1Hubr
pro-melanin-concentrating hormone; ENU induced mutant1, Hubr
IMP
RGD
PMID:19934402
RGD:150429945
G
Gad1
glutamate decarboxylase 1
IMP
RGD
PMID:33293518
RGD:158012686
NCBI chr 3:55,369,704...55,410,335
Ensembl chr 3:55,369,704...55,410,333
G
Gad1em15Yyan
glutamate decarboxylase 1; CRISPR/Cas9 induced mutant 15, Yyan
IMP
RGD
PMID:33293518
RGD:158012686
G
Mc4r
melanocortin 4 receptor
IMP
RGD
PMID:21527895
RGD:6478803
NCBI chr18:60,419,832...60,421,719
Ensembl chr18:60,419,832...60,421,719
G
Mc4rm1Hubr
melanocortin 4 receptor; ENU induced mutation 1, Hubr
IMP
RGD
PMID:21527895
RGD:6478803
G
Kcnq1
potassium voltage-gated channel subfamily Q member 1
IAGP
DNA:deletion:exon (rat)
RGD
PMID:16368876
RGD:1581602
NCBI chr 1:198,291,711...198,624,683
Ensembl chr 1:198,291,766...198,624,669
G
Kcnq1dfk
potassium voltage-gated channel subfamily Q member 1;deafness Kyoto
IAGP
RGD
PMID:16368876
RGD:1581602
G
Kit
KIT proto-oncogene receptor tyrosine kinase
IMP
RGD
PMID:7542218
RGD:12910748
NCBI chr14:32,547,459...32,624,694
Ensembl chr14:32,548,877...32,624,652
G
Apc
APC regulator of WNT signaling pathway
sexual_dimorphism
IMP
compared to females
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
sexual_dimorphism
IMP
compared to females
RGD
PMID:17360473
RGD:1601201
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