AutismKB 2.0

Evidence Details for CXorf23


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Basic Information Top
Gene Symbol:CXorf23 ( - )
Gene Full Name: chromosome X open reading frame 23
Band: Xp22.12
Quick LinksEntrez ID:256643; OMIM: NA; Uniprot ID:CX023_HUMAN; ENSEMBL ID: ENSG00000173681; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>CXorf23|256643|nucleotide
ATGGCACGGTCACGATCTAGATCCCCCAGGTGGAAACACAGGTCTTTATCACCAGTACCTAGAAATGCTGAACACTACAAGCAAAGACATTCACACGGGCATTAT
GGCTGTGAATATAGGAAGGATCCAAAAAGACCCGTCGCGTGGAGAATGGACAGTGAGAAACATGGACAGAGTAAACCAAGGATTCCCTCTCGTGGAAATATATAT
TACCAGTCTTATGAACATAGATCACCTTCCCCTAACATAAGAAACTCTTTAGAAAATGTTTATATGTATAAGCCTCACAGAGGATATTCGCCTGGAAGAGGGGAC
AGTAACAGGAGAGCTCAGTATATGCCCAAATACTCAGAGGGTATACCCTACAAAGAGCATGAAAGGAATTCTTATCCCCAGAAAGTGCAAGGAGGGCATAGTCCT
GATGACCACAGAGTTAGAGGAAGTGGAAAAGGAGGGAAACCACCTCAGAGGTCAATAGCAGATTCTTTTAGATTTGAAGGAAAGTGGCATGAAGATGAGTTGAGG
CACCAGAGGATACAAGAAGAAAAATACTCCCAGTCAACTAGAAGAGGCTCTGAAGACTTTGAGACAAGGAGCTCATTTCAGAAGAGGTATCCTGAGGATCGTGAT
TTCAGAAAATATGGACACACATCAAAAAGACCTAAAGACGTGGAGAGGTATGAAAGCAGAGAGCCTGCCAGGAACCCAAAGTGGAAGCCTGAGCATTCCCTCCCA
CCTTACCAAGAGGACACAGACCAGTGGAACCTTGGGCCCCAAACTTATCGACATGCTGAGAGGGAACACCCAGAGACCAGTTCAGCAACCAAAGTATCCTATGAC
TATCGTCACAAACGTCCTAAGCTCTTGGATGGGGACCAGGACTTTTCTGATGGGAGAACTCAGAAGTACTGTAAGGAAGAAGATAGAAAATATAGTTTTCAAAAA
GGCCCTCTAAATAGAGAGTTAGATTGTTTTAATACTGGAAGAGGGAGAGAGACTCAAGATGGACAAGTCAAAGAACCTTTTAAACCGTCTAAGAAAGACAGCATT
GCCTGTACTTATTCAAATAAAAATGATGTTGATTTGCGATCTAGTAATGACAAATGGAAGGAAAAAATAAAGAAAGAAGGGGATTGTAGAAAAGAGAGCAATTCT
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>CXorf23|256643|protein
MARSRSRSPRWKHRSLSPVPRNAEHYKQRHSHGHYGCEYRKDPKRPVAWRMDSEKHGQSKPRIPSRGNIYYQSYEHRSPSPNIRNSLENVYMYKPHRGYSPGRGD
SNRRAQYMPKYSEGIPYKEHERNSYPQKVQGGHSPDDHRVRGSGKGGKPPQRSIADSFRFEGKWHEDELRHQRIQEEKYSQSTRRGSEDFETRSSFQKRYPEDRD
FRKYGHTSKRPKDVERYESREPARNPKWKPEHSLPPYQEDTDQWNLGPQTYRHAEREHPETSSATKVSYDYRHKRPKLLDGDQDFSDGRTQKYCKEEDRKYSFQK
GPLNRELDCFNTGRGRETQDGQVKEPFKPSKKDSIACTYSNKNDVDLRSSNDKWKEKIKKEGDCRKESNSSSNQLDKSQKLPDVKPSPINLRKKSLTVKVDVKKT
VDTFRVASSYSTERQMSHDLVAVGRKSENFHPVFEHLDSTQNTENKPTGEFAQEIITIIHQVKANYFPSPGITLHERFSTMQDIHKADVNEIPLNSDPEIHRRID
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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 (1) 0 (0) 0 (0) 0 (0) 2 (4)
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
Pinto, 2010 - SNP microarray, qPCRASD - - - - 996 1287 2283
Vazna, 2010 Czech aCGHASD - - - - 1 - 1
Edens, 2011 Honduras aCGHautism - - - - 1 - 1
Edens, 2011 Austria FISH, aCGHautism - - - - 1 - 1
Linkage Studies Top