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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 food intake
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Accession:MP:0005449 term browser browse the term
Definition:any anomaly in the total number of calories/food amount taken in over time when compared to the normal state
Synonyms:exact_synonym: abnormal calorie consumption;   abnormal energy intake;   abnormal food consumption;   abnormal ingestion


show annotations for term's descendants           Sort by:
decreased food intake term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bmal1 basic helix-loop-helix ARNT like 1 IMP compared to wild type RGD PMID:32306766 RGD:155598602 NCBI chr 1:167,331,756...167,430,235
Ensembl chr 1:167,331,633...167,430,231 		JBrowse link
G Bmal1em1Mcwi basic helix-loop-helix ARNT like 1;CRISPR/Cas9 induced mutant 1,Mcwi IMP compared to wild type RGD PMID:32306766 RGD:155598602
G Fmr1 fragile X messenger ribonucleoprotein 1 IMP compared to wild type RGD PMID:35328827 RGD:405100966 NCBI chr  X:147,240,239...147,278,057
Ensembl chr  X:147,240,301...147,278,050 		JBrowse link
G Fmr1em1Sage FMRP translational regulator 1; zinc finger nuclease induced mutant 1, Sigma Advanced Genetic Engineering Labs IMP compared to wild type RGD PMID:35328827 RGD:405100966
G Ghsr growth hormone secretagogue receptor IMP compared to wild type rats in response to ghrelin (CHEBI:75431)
DNA:missense mutation:cds:nucleotide 1027		 RGD PMID:12045256 PMID:21258824 PMID:27129673 PMID:29453460 RGD:625699, RGD:150520012, RGD:150520013, RGD:13825258 NCBI chr 2:110,268,489...110,271,865
Ensembl chr 2:110,268,489...110,271,865 		JBrowse link
G Ghsrm1Mcwi growth hormone secretagogue receptor; mutation 1, Medical College of Wisconsin IMP compared to wild type rats
compared to wild type rats in response to ghrelin (CHEBI:75431)		 RGD PMID:27129673 PMID:21258824 RGD:150520013, RGD:150520012
G Ghsrem1Ottc growth hormone secretagogue receptor;CRISPR induced mutant 1, Ottc IMP RGD PMID:29453460 RGD:13825258
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 		JBrowse link
G Pmchm1Hubr pro-melanin-concentrating hormone; ENU induced mutant1, Hubr IMP RGD PMID:19934402 RGD:150429945
increased food intake term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Lepr leptin receptor IAGP compared to age-matched lean heterozygous +/fa rats RGD PMID:9843879 RGD:628910 NCBI chr 5:116,294,409...116,477,904
Ensembl chr 5:116,289,823...116,475,908 		JBrowse link
G Leprfa leptin receptor; fa mutant IAGP compared to age-matched lean heterozygous +/fa rats RGD PMID:9843879 RGD:628910
G Sod3 superoxide dismutase 3 IMP compared to SS/JrHsdMcwi RGD PMID:31972339 RGD:150573712 NCBI chr14:58,610,104...58,615,845
Ensembl chr14:58,609,958...58,615,990 		JBrowse link
G Sod3m1Mcwi superoxide dismutase 3; mutation 1, Medical College of Wisconsin IMP compared to SS/JrHsdMcwi RGD PMID:31972339 RGD:150573712
polyphagia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cckar cholecystokinin A receptor IAGP RGD PMID:9530226 RGD:7257724 NCBI chr14:57,292,397...57,300,747
Ensembl chr14:57,292,397...57,300,747 		JBrowse link
G Lepr leptin receptor IAGP RGD PMID:23154293 RGD:13432147 NCBI chr 5:116,294,409...116,477,904
Ensembl chr 5:116,289,823...116,475,908 		JBrowse link
G Leprfa leptin receptor; fa mutant IAGP RGD PMID:23154293 RGD:13432147
G Mc4r melanocortin 4 receptor IMP RGD PMID:21527895 PMID:24400148 RGD:6478803, RGD:13825242 NCBI chr18:60,419,832...60,421,719
Ensembl chr18:60,419,832...60,421,719 		JBrowse link
G Mc4rm1Hubr melanocortin 4 receptor; ENU induced mutation 1, Hubr IMP RGD PMID:21527895 PMID:24400148 RGD:6478803, RGD:13825242
G Prlhr prolactin releasing hormone receptor IAGP RGD PMID:15854142 RGD:1641829 NCBI chr 1:259,606,704...259,608,391
Ensembl chr 1:259,606,704...259,608,391 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5420
    behavior/neurological phenotype 612
      abnormal behavior 611
        abnormal consumption behavior 197
          abnormal eating behavior 86
            abnormal food intake 75
              abnormal saccharin consumption 1
              aphagia + 0
              decreased food intake + 19
              dysphagia 0
              increased food intake + 54
paths to the root