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GENE - TERM ANNOTATION REPORT

RGD ID: 1312280
Species: Homo sapiens
RGD Object: Gene
Symbol: TUBGCP5
Name: tubulin gamma complex component 5
Acc ID: DOID:0060041
Term: autism spectrum disorder
Definition: A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Autism_spectrum_disorder "DO" "DO", http://www.neurodevnet.ca "DO" "DO", https://www.genome.gov/Genetic-Disorders/Autism "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
TUBGCP5 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autism spectrum disorderPMID:21187176 PMID:25255310
TUBGCP5 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autism spectrum disorderPMID:25741868 PMID:27569545
TUBGCP5 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autism spectrum disorderPMID:21844811 PMID:23044707 PMID:23495136 PMID:25741868 PMID:27569545
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