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: angiomyolipoma
Accession: DOID:3314
browse the term
Definition: A cell type benign neoplasm that is primarily located in the kidneys but may be found in the lungs, liver or other organs and is derived from perivascular epithelioid cells. (DO)
Synonyms: exact_synonym: angiomyolipomas
primary_id: MESH:D018207
xref: ICDO:8860/0; NCI:C3734
For additional species annotation, visit the
Alliance of Genome Resources .
Symbol
Object Name
Qualifiers
Evidence
Notes
Source
PubMed Reference(s)
RGD Reference(s)
Position
G
Ogg1
8-oxoguanine DNA glycosylase
no_association
ISO
associated with Tuberous Sclerosis;mRNA, protein:decreased expression:kidney associated with Tuberous Sclerosis;DNA:missense mutations: :p.R45Q, p.A85S, p.R229Q (human) associated with Tuberous Sclerosis;DNA:SNP: :p.S326C (rs1052133)(human)
RGD
PMID:19265534 PMID:17932460 PMID:17932460
RGD:8657154 , RGD:8657155 , RGD:8657155
NCBI chr 4:148,030,237...148,037,599
Ensembl chr 4:146,474,750...146,484,766
G
Pten
phosphatase and tensin homolog
ISO
protein:increased expression:kidney (human)
RGD
PMID:22737271
RGD:12802360
NCBI chr 1:240,043,707...240,110,330
Ensembl chr 1:230,630,338...230,696,838
G
Stat1
signal transducer and activator of transcription 1
ISO
protein:increased serine phosphorylation:kidney
RGD
PMID:15994429
RGD:2298537
NCBI chr 9:56,911,522...56,951,926
Ensembl chr 9:49,419,340...49,588,540
G
Stat3
signal transducer and activator of transcription 3
ISO
protein:increased tyrosine phosphorylation:kidney
RGD
PMID:15994429
RGD:2298537
NCBI chr10:86,311,528...86,363,513
Ensembl chr10:85,811,218...85,863,057
G
Tsc2
TSC complex subunit 2
ISO
associated with Tuberous Sclerosis;protein:decreased expression, increased threonine phosphorylation:kidney
RGD
PMID:19265534
RGD:8657154
NCBI chr10:14,125,679...14,160,317
Ensembl chr10:13,621,136...13,655,951
Symbol
Object Name
Qualifiers
Evidence
Notes
Source
PubMed Reference(s)
RGD Reference(s)
Position
G
Traf7
TNF receptor associated factor 7
ISO
DNA:missense mutations:multiple
RGD
PMID:29148537
RGD:151356962
NCBI chr10:14,038,117...14,056,832
Ensembl chr10:13,533,570...13,552,203
Symbol
Object Name
Qualifiers
Evidence
Notes
Source
PubMed Reference(s)
RGD Reference(s)
Position
G
Tsc2
TSC complex subunit 2
IAGP
DNA:mutations:multiple associated with tuberous sclerosis;DNA:mutations:multiple
RGD
PMID:29512829 PMID:22251200
RGD:21079730 , RGD:21079732
NCBI chr10:14,125,679...14,160,317
Ensembl chr10:13,621,136...13,655,951
Symbol
Object Name
Qualifiers
Evidence
Notes
Source
PubMed Reference(s)
RGD Reference(s)
Position
G
Mtor
mechanistic target of rapamycin kinase
treatment
ISO
associated with Tuberous Sclerosis
RGD
PMID:23054313
RGD:7245506
NCBI chr 5:164,167,985...164,277,438
Ensembl chr 5:158,884,804...158,994,311
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