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GENE - TERM ANNOTATION REPORT

RGD ID: 1310227
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Dcdc2
Name: doublecortin domain containing 2
Acc ID: DOID:4428
Term: dyslexia
Definition: A reading disorder resulting from a developmental reading disability involving the inability to process graphic symbols resulting in impairment of reading ability. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Dyslexia "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)
Dcdc2 ISODcdc2a (Mus musculus)12910976RGD  
Dcdc2susceptibilityISODCDC2 (Homo sapiens)11532935RGDDNA:snp:intron:c.760-430G>A (human) (rs807724) 
Dcdc2susceptibilityISODCDC2 (Homo sapiens)12910971RGDDNA:snps:multiple (human) 
Dcdc2susceptibilityISODCDC2 (Homo sapiens)12910973RGDDNA:snps:introns:c.558-3950G>C, c.1326+252C>T (human) (rs1091047, rs1419228) 
Dcdc2susceptibilityISODCDC2 (Homo sapiens)12910975RGDDNA:deletion, snps:introns:multiple (human) 
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