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: food allergy
Accession: DOID:3044
browse the term
Definition: A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system. (DO)
Synonyms: exact_synonym: food allergies; food hypersensitivity
primary_id: MESH:D005512
xref: NCI:C172304
For additional species annotation, visit the
Alliance of Genome Resources .
G
Ifnl3
interferon, lambda 3
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:22295096
NCBI chr 1:83,814,456...83,816,096
Ensembl chr 1:83,814,564...83,816,096
G
Il13
interleukin 13
ISO
mRNA:increased expression:small intestine
RGD
PMID:22038918
RGD:5684372
NCBI chr10:37,790,130...37,792,687
Ensembl chr10:37,790,130...37,792,737
G
Il5
interleukin 5
ISO
RGD
PMID:22077487
RGD:5687145
NCBI chr10:37,874,342...37,877,213
Ensembl chr10:37,874,342...37,877,213
G
Madcam1
mucosal vascular addressin cell adhesion molecule 1
IMP
RGD
PMID:14670821
RGD:2311549
NCBI chr 7:10,036,301...10,039,703
Ensembl chr 7:10,036,301...10,039,703
G
Nlrp3
NLR family, pyrin domain containing 3
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:19767079
NCBI chr10:44,326,770...44,353,814
Ensembl chr10:44,328,566...44,352,811
G
Slc11a1
solute carrier family 11 member 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:16597321
NCBI chr 9:75,957,193...75,968,115
Ensembl chr 9:75,957,316...75,968,101
G
Grin2b
glutamate ionotropic receptor NMDA type subunit 2B
IEP
protein:increased expression:brain, cingulate cortex (rat)
RGD
PMID:19208366
RGD:2326032
NCBI chr 4:168,580,824...169,044,110
Ensembl chr 4:168,599,546...169,042,279
G
Il13
interleukin 13
ISO
associated with Dermatitis, Atopic; DNA:SNPs:promoter, cds:-1112C>T, p.R130Q (c.389G>A) (rs1800925, rs20541) (human)
RGD
PMID:19220774
RGD:8549541
NCBI chr10:37,790,130...37,792,687
Ensembl chr10:37,790,130...37,792,737
G
Il13
interleukin 13
ISO
associated with Dermatitis, Atopic; DNA:missense mutation:cds:p.R130Q (c.389G>A) (rs20541) (human)
RGD
PMID:19220774
RGD:8549541
NCBI chr10:37,790,130...37,792,687
Ensembl chr10:37,790,130...37,792,737
G
Ahr
aryl hydrocarbon receptor
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:21804081
NCBI chr 6:52,234,089...52,271,568
Ensembl chr 6:52,234,089...52,271,568
G
Il13
interleukin 13
ISO
associated with Dermatitis, Atopic; DNA:SNPs:promoter, cds:-1112C>T, p.R130Q (c.389G>A) (rs1800925, rs20541) (human)
RGD
PMID:19220774
RGD:8549541
NCBI chr10:37,790,130...37,792,687
Ensembl chr10:37,790,130...37,792,737
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