RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: Hyperphagia
Accession: DOID:9002916
browse the term
Definition: Ingestion of a greater than optimal quantity of food.
Synonyms: exact_synonym: Overeating; Polyphagia; Polyphagias
primary_id: MESH:D006963
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Agrp
agouti related neuropeptide
ISO
associated with Diabetes Mellitus, Experimental;mRNA:increased expression:hypothalamus
RGD
PMID:11179781
RGD:2314004
NCBI chr 8:106,293,327...106,306,477
Ensembl chr 8:106,293,330...106,364,025
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Brs3
bombesin-like receptor 3
IMP
RGD
PMID:9367152
RGD:734661
NCBI chr X:56,088,434...56,094,118
Ensembl chr X:56,088,434...56,094,118
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Hcrt
hypocretin
ISO
CTD Direct Evidence: marker/mechanism
CTD RGD
PMID:27071101 PMID:12535169
RGD:1358429
NCBI chr11:100,652,519...100,653,757
Ensembl chr11:100,651,895...100,653,757
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Htr2a
5-hydroxytryptamine (serotonin) receptor 2A
ISO
RGD
PMID:12392096
RGD:1624374
NCBI chr14:74,878,314...74,944,299
Ensembl chr14:74,878,280...74,946,934
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Igf1
insulin-like growth factor 1
ISO
RGD
PMID:17567960
RGD:10046043
NCBI chr10:87,694,127...87,772,909
Ensembl chr10:87,694,127...87,772,904
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Igf1r
insulin-like growth factor I receptor
ISO
RGD
PMID:17567960
RGD:10046043
NCBI chr 7:67,601,486...67,883,416
Ensembl chr 7:67,602,575...67,883,416
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Il18
interleukin 18
IMP
RGD
PMID:16732281
RGD:14695532
NCBI chr 9:50,466,000...50,493,141
Ensembl chr 9:50,466,127...50,493,140
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Lep
leptin
ISO
CTD Direct Evidence: marker/mechanism|therapeutic
CTD
PMID:12177191 PMID:25086370 PMID:26186301 PMID:27071101
NCBI chr 6:29,060,220...29,073,875
Ensembl chr 6:29,060,219...29,073,876
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Lepr
leptin receptor
ISO
CTD Direct Evidence: marker/mechanism compared to age-matched lean +/fa rats
CTD RGD
PMID:3519326 PMID:15093691 PMID:17229951 PMID:9843879 PMID:26537785
RGD:628910 , RGD:12911216
NCBI chr 4:101,574,393...101,676,375
Ensembl chr 4:101,574,601...101,672,549
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Mc4r
melanocortin 4 receptor
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:23251400
NCBI chr18:66,990,776...66,993,558
Ensembl chr18:66,990,775...66,993,577
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Ntrk2
neurotrophic tyrosine kinase, receptor, type 2
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:15494731
NCBI chr13:58,954,363...59,281,782
Ensembl chr13:58,954,383...59,281,784
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Oprd1
opioid receptor, delta 1
ISO
RGD
PMID:9808678
RGD:9831410
NCBI chr 4:131,834,980...131,872,042
Ensembl chr 4:131,838,037...131,871,797
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Oprk1
opioid receptor, kappa 1
ISO
RGD
PMID:9808678
RGD:9831410
NCBI chr 1:5,658,673...5,676,357
Ensembl chr 1:5,658,689...5,676,354
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Oprl1
opioid receptor-like 1
ISO
RGD
PMID:9808678 PMID:9669488
RGD:9831410 , RGD:9835033
NCBI chr 2:181,356,585...181,362,778
Ensembl chr 2:181,356,809...181,362,778
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Oprm1
opioid receptor, mu 1
ISO
RGD
PMID:9808678 PMID:21368037
RGD:9831410 , RGD:401901088
NCBI chr10:6,708,593...6,988,209
Ensembl chr10:6,708,506...6,988,198
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Penk
preproenkephalin
ISO
RGD
PMID:20603139
RGD:10003144
NCBI chr 4:4,133,536...4,138,815
Ensembl chr 4:4,133,531...4,138,819
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Pomc
pro-opiomelanocortin-alpha
ISO
DNA:mutations:multiple (human)
RGD
PMID:15189116
RGD:1357925
NCBI chr12:4,004,945...4,010,643
Ensembl chr12:4,004,951...4,010,642
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Ucp3
uncoupling protein 3 (mitochondrial, proton carrier)
ISO
RGD
PMID:10935638
RGD:737762
NCBI chr 7:100,122,198...100,135,639
Ensembl chr 7:100,122,197...100,135,639
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Vgf
VGF nerve growth factor inducible
ISO
CTD Direct Evidence: therapeutic
CTD
PMID:12177191
NCBI chr 5:137,054,156...137,062,205
Ensembl chr 5:137,055,246...137,062,205
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Cck
cholecystokinin
ISO
RGD
PMID:8988922
RGD:1625799
NCBI chr 9:121,318,890...121,324,728
Ensembl chr 9:121,318,890...121,324,760
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Ghrl
ghrelin
ISO
RGD
PMID:15788704
RGD:1642818
NCBI chr 6:113,693,080...113,696,872
Ensembl chr 6:113,693,080...113,696,841
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Comt
catechol-O-methyltransferase
susceptibility
ISO
DNA:SNPs,haplotype:
RGD
PMID:21300128
RGD:13451125
NCBI chr16:18,225,632...18,247,006
Ensembl chr16:18,225,636...18,245,602
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Ntrk2
neurotrophic tyrosine kinase, receptor, type 2
ISO
CTD Direct Evidence: marker/mechanism ClinVar Annotator: match by term: NTRK2-related condition | ClinVar Annotator: match by term: Obesity, hyperphagia, and developmental delay
OMIM CTD ClinVar
PMID:9536098 PMID:15494731 PMID:17576681 PMID:25741868 PMID:27884935 PMID:28492532 PMID:29100083 PMID:35061034 More...
NCBI chr13:58,954,363...59,281,782
Ensembl chr13:58,954,383...59,281,784
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