AutismKB 2.0

Evidence Details for C22orf15


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Basic Information Top
Gene Symbol:C22orf15 ( FLJ36561,N27C7-3 )
Gene Full Name: chromosome 22 open reading frame 15
Band: 22q11.23
Quick LinksEntrez ID:150248; OMIM: NA; Uniprot ID:CV015_HUMAN; ENSEMBL ID: ENSG00000169314; HGNC ID: 15558
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C22orf15|150248|nucleotide
ATGTTTATCAAGGTGATGTTTGGGGCTGGCTGCTCGGTGCTGGTGAACACCTCTTGCAGGCTGGTGAACCTCACCGCCCACCTGAGGCAGAAAGCAGGGTTGCCC
CCAGATGCGACCATTGCTCTCCTGGCTGAGGATGGCAACCTAGTGAGCCTGGAGGAGGACCTGAAGGAAGGGGCTTCCCGGGCCCAGACCATGGGCAACTCCCTA
CTGAAGGAGCGAGCCATATATGTCCTCGTTCGGATCATCAAGGGAGAGGACATGGCCTCCACCCGCTATGAGTCCCTATTGGAGAACCTGGATGACCATTACCCA
GAGCTGGCAGAGGAACTGCGCAGGCTGTCAGGCCTCTCCTCTGTGGGCCACAACTGGAGGAAGCGTATGGGCACTCGGCGAGGCCGCCATGAGCAAAGCCCCACT
TCAAGGCCCAGAAAGGGCCCTGATTAA






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>C22orf15|150248|protein
MFIKVMFGAGCSVLVNTSCRLVNLTAHLRQKAGLPPDATIALLAEDGNLVSLEEDLKEGASRAQTMGNSLLKERAIYVLVRIIKGEDMASTRYESLLENLDDHYP
ELAEELRRLSGLSSVGHNWRKRMGTRRGRHEQSPTSRPRKGPD



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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 (0) 1 (6) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 2 (6)
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
Ramelli, 2008 - FISHASD - - - - 1 - 1
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Linkage Studies Top