RGD Reference Report - Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism. - Rat Genome Database

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Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism.

Authors: Serajee, FJ  Nabi, R  Zhong, H  Mahbubul Huq, AH 
Citation: Serajee FJ, etal., J Med Genet. 2003 Nov;40(11):e119.
RGD ID: 6482702
Pubmed: PMID:14627686   (View Abstract at PubMed)
PMCID: PMC1735327   (View Article at PubMed Central)

Abstract for this paper unavailable

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
autistic disorder  IAGP 6482702DNA:SNP:exon:rs1129293 (human)RGD 
autistic disorder  ISOPIK3CG (Homo sapiens)6482702; 6482702DNA:SNP:exon:rs1129293 (human)RGD 

Objects Annotated

Genes (Rattus norvegicus)
Pik3cg  (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma)

Genes (Mus musculus)
Pik3cg  (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma)

Genes (Homo sapiens)
PIK3CG  (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma)


Additional Information