AutismKB 2.0

Evidence Details for CDYL2


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:CDYL2 ( FLJ38866 )
Gene Full Name: chromodomain protein, Y-like 2
Band: 16q23.2
Quick LinksEntrez ID:124359; OMIM: NA; Uniprot ID:CDYL2_HUMAN; ENSEMBL ID: ENSG00000166446; HGNC ID: 23030
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>CDYL2|124359|nucleotide
ATGGCTTCTGGGGACCTTTACGAGGTTGAAAGGATTGTAGACAAGAGGAAGAACAAGAAAGGAAAATGGGAGTATCTTATCCGATGGAAAGGCTACGGGAGCACC
GAGGACACGTGGGAGCCGGAGCACCACCTCTTGCACTGTGAGGAGTTTATTGATGAATTCAATGGGTTGCACATGTCCAAGGACAAGAGGATCAAGTCAGGGAAG
CAGTCCAGTACCTCCAAGCTGCTGCGTGACAGTCGAGGCCCGTCGGTTGAGAAACTGTCCCACAGACCTTCAGATCCTGGAAAGAGCAAGGGGACCTCCCATAAA
CGGAAGCGAATTAACCCTCCCCTGGCCAAGCCAAAAAAAGGGTATTCAGGCAAGCCCTCTTCAGGAGGTGACAGGGCCACCAAGACGGTGTCTTACAGGACTACC
CCCAGTGGTTTGCAAATAATGCCCCTGAAAAAGTCTCAGAACGGGATGGAAAATGGGGACGCCGGCTCTGAGAAGGATGAGAGGCACTTTGGAAATGGGTCCCAT
CAGCCTGGCTTGGATTTGAATGATCATGTTGGAGAGCAAGATATGGGTGAATGTGACGTGAATCACGCTACACTGGCGGAGAACGGGCTCGGCTCTGCTCTGACC
AACGGGGGATTGAACCTGCACAGTCCAGTGAAGAGGAAGCTGGAAGCGGAGAAGGACTACGTCTTTGACAAAAGGCTCAGATACAGTGTCCGCCAGAATGAAAGC
AACTGTCGGTTTCGAGACATCGTTGTGCGGAAGGAAGAAGGGTTCACGCACATCCTGCTGTCCAGTCAGACCTCGGATAACAATGCCCTGACACCTGAGATCATG
AAAGAAGTCCGGCGAGCGCTCTGCAACGCAGCCACAGACGACAGCAAACTGCTGCTCCTCAGCGCAGTGGGGAGCGTGTTCTGCAGCGGCCTGGATTATTCCTAC
CTAATTGGCCGGTTGTCCAGCGACCGGCGAAAGGAGAGCACTCGGATTGCAGAAGCCATCAGGGACTTTGTGAAGGCCTTTATCCAGTTTAAGAAGCCTATCGTG
GTGGCCATCAATGGGCCGGCCCTGGGCCTGGGTGCCTCCATCCTGCCCCTCTGTGACATCGTGTGGGCCAGTGAGAAGGCCTGGTTCCAGACGCCCTACGCCACC
Show »

>CDYL2|124359|protein
MASGDLYEVERIVDKRKNKKGKWEYLIRWKGYGSTEDTWEPEHHLLHCEEFIDEFNGLHMSKDKRIKSGKQSSTSKLLRDSRGPSVEKLSHRPSDPGKSKGTSHK
RKRINPPLAKPKKGYSGKPSSGGDRATKTVSYRTTPSGLQIMPLKKSQNGMENGDAGSEKDERHFGNGSHQPGLDLNDHVGEQDMGECDVNHATLAENGLGSALT
NGGLNLHSPVKRKLEAEKDYVFDKRLRYSVRQNESNCRFRDIVVRKEEGFTHILLSSQTSDNNALTPEIMKEVRRALCNAATDDSKLLLLSAVGSVFCSGLDYSY
LIGRLSSDRRKESTRIAEAIRDFVKAFIQFKKPIVVAINGPALGLGASILPLCDIVWASEKAWFQTPYATIRLTPAGCSSYTFPQILGVALANEMLFCGRKLTAQ
EACSRGLVSQVFWPTTFSQEVMLRVKEMASCSAVVLEESKCLVRSFLKSVLEDVNEKECLMLKQLWSSSKGLDSLFSYLQDKIYEV
Show »

Evidence summary Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
Evidences Syndromic Gene GWAS CNV Linkage Association Expression NGS de novo NGS Mosaic NGS Other Low-Scale Gene Studies Total
Score (No. of Studies) No 0 (1) 1 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (3)
Syndromic Autism Gene Top
Genome-Wide Association Studies (By Ethnic Group) Top
Family Based Association Studies: 1
Reference Stage Platform #Families Affecteds Result
#Subjects
(% Women)
ADI-R ADOS Diagnosis Age
(range)
IQ
(range)
CAUCASIAN
Hussman, 2011_1 Discovery Illumina Infinium Human 1 M beadship 597 -
(-)
ASD -
-
-
-
Case Control Based Association Studies: 0
Reference Stage Platform ASD Cases Normal Controls Result
#Subjects
(% Women)
ADI-R ADOS Diagnosis Age
(range)
IQ #Subjects
(% Women)
Age
(range)
No Evidence.
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Zwaag, 2009 - SNP microarrayautism - - - - 105 267 372
Linkage Studies Top