AutismKB 2.0

Evidence Details for CECR1


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Basic Information Top
Gene Symbol:CECR1 ( ADA2,ADGF,IDGFL )
Gene Full Name: cat eye syndrome chromosome region, candidate 1
Band: 22q11.2
Quick LinksEntrez ID:51816; OMIM: 607575; Uniprot ID:CECR1_HUMAN; ENSEMBL ID: ENSG00000093072; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>CECR1|51816|nucleotide
ATGTTGGTGGATGGCCCATCTGAGCGGCCAGCCCTGTGCTTCTTGCTGTTGGCTGTGGCAATGTCTTTCTTCGGCTCAGCTCTATCCATAGATGAAACACGGGCG
CATCTGTTGTTGAAAGAAAAGATGATGCGGCTGGGGGGGCGGCTGGTGCTGAATACCAAGGAGGAGCTGGCCAATGAGAGGCTCATGACGCTCAAAATCGCTGAG
ATGAAGGAGGCCATGAGGACCCTGATATTCCCACCCAGCATGCACTTTTTCCAGGCCAAGCATCTCATTGAGAGAAGTCAAGTGTTTAATATTCTAAGGATGATG
CCAAAAGGGGCTGCCTTGCACCTCCATGACATTGGCATCGTGACTATGGACTGGCTGGTGAGGAATGTCACCTACAGGCCTCACTGCCACATCTGTTTCACCCCA
AGGGGGATCATGCAGTTCAGATTTGCTCACCCAACTCCCCGTCCATCAGAAAAATGTTCCAAGTGGATTCTGCTGGAGGATTATCGGAAGCGGGTGCAGAACGTC
ACTGAGTTTGATGACAGCTTGCTGAGGAATTTCACTCTGGTGACCCAGCACCCGGAGGTGATTTACACAAACCAAAATGTTGTCTGGTCGAAATTTGAAACCATC
TTCTTCACCATCTCTGGTCTCATCCATTACGCACCAGTGTTCAGAGACTATGTCTTCCGGAGCATGCAGGAGTTCTACGAGGACAACGTGCTCTACATGGAGATC
AGAGCCAGGCTGCTGCCGGTGTATGAGCTCAGTGGAGAGCACCATGACGAAGAGTGGTCAGTGAAGACTTACCAGGAAGTAGCTCAGAAGTTTGTGGAAACTCAC
CCTGAGTTTATTGGAATCAAAATCATTTATTCGGATCACAGATCCAAAGATGTGGCTGTCATCGCAGAATCCATCCGAATGGCCATGGGGCTCCGAATCAAGTTC
CCCACGGTGGTGGCAGGGTTTGACCTGGTGGGGCATGAGGACACTGGCCACTCCTTGCATGACTACAAGGAAGCTCTGATGATCCCCGCCAAGGATGGCGTTAAG
CTGCCTTACTTCTTCCACGCCGGAGAAACAGACTGGCAGGGTACTTCCATAGACAGGAACATTCTGGATGCTCTGATGCTGAACACTACCAGAATCGGCCATGGA
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>CECR1|51816|protein
MLVDGPSERPALCFLLLAVAMSFFGSALSIDETRAHLLLKEKMMRLGGRLVLNTKEELANERLMTLKIAEMKEAMRTLIFPPSMHFFQAKHLIERSQVFNILRMM
PKGAALHLHDIGIVTMDWLVRNVTYRPHCHICFTPRGIMQFRFAHPTPRPSEKCSKWILLEDYRKRVQNVTEFDDSLLRNFTLVTQHPEVIYTNQNVVWSKFETI
FFTISGLIHYAPVFRDYVFRSMQEFYEDNVLYMEIRARLLPVYELSGEHHDEEWSVKTYQEVAQKFVETHPEFIGIKIIYSDHRSKDVAVIAESIRMAMGLRIKF
PTVVAGFDLVGHEDTGHSLHDYKEALMIPAKDGVKLPYFFHAGETDWQGTSIDRNILDALMLNTTRIGHGFALSKHPAVRTYSWKKDIPIEVCPISNQVLKLVSD
LRNHPVATLMATGHPMVISSDDPAMFGAKGLSYDFYEVFMGIGGMKADLRTLKQLAMNSIKYSTLLESEKNTFMEIWKKRWDKFIADVATK
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Evidence summary Top

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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 (0) 1 (3) 0 (0) 0 (0) 0 (0) 0 (2) 0 (0) 0 (0) 0 (0) 2 (5)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Roubertie, 2001 - FISHautism - - - - 1 - 1
Niklasson, 2002 Sweden FISHautism - - - - 1 - 1
Gai, 2011 AGRE SNP microarray--autism - - - - 1224 3801 5025
Linkage Studies Top