AutismKB 2.0

Evidence Details for TBX22


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Basic Information Top
Gene Symbol:TBX22 ( CLPA,TBXX,dJ795G23.1 )
Gene Full Name: T-box 22
Band: Xq21.1
Quick LinksEntrez ID:50945; OMIM: 300307; Uniprot ID:TBX22_HUMAN; ENSEMBL ID: ENSG00000122145; HGNC ID: 11600
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>TBX22|50945|nucleotide
ATGGCTCTGAGCTCTCGGGCGCGTGCCTTCTCCGTGGAAGCCTTGGTGGGGAGACCCAGCAAAAGAAAACTCCAAGACCCAATACAGGCGGAGCAGCCTGAGCTG
CGGGAGAAAAAGGGCGGAGAGGAAGAGGAGGAGAGAAGGAGCAGCGCTGCAGGGAAGAGCGAGCCGCTTGAAAAACAACCTAAGACAGAGCCCTCAACATCTGCT
TCCTCTGGCTGCGGCAGCGACAGCGGCTACGGCAACAGCTCTGAAAGTCTGGAAGAGAAAGATATTCAAATGGAGCTTCAAGGATCTGAACTGTGGAAAAGATTC
CATGACATCGGGACTGAGATGATCATTACTAAAGCGGGCAGGCGGATGTTCCCCTCTGTTCGGGTCAAGGTGAAAGGGTTGGATCCAGGGAAGCAGTACCATGTG
GCCATCGATGTGGTGCCGGTGGATTCCAAACGCTATAGGTACGTCTATCACAGCTCACAGTGGATGGTAGCTGGGAATACAGACCATTTGTGCATCATTCCTAGA
TTCTATGTTCACCCGGACTCACCCTGCTCGGGAGAGACCTGGATGCGGCAGATCATCAGCTTTGATCGCATGAAACTCACCAACAATGAGATGGATGACAAAGGC
CACATCATTCTGCAATCCATGCATAAGTACAAACCCCGAGTGCACGTGATAGAGCAAGGCAGCAGTGTTGACCTGTCCCAGATTCAGTCCTTGCCCACTGAAGGT
GTTAAAACATTCTCCTTTAAAGAAACTGAGTTCACCACAGTAACGGCTTACCAAAACCAACAGATTACGAAACTAAAAATAGAAAGAAATCCTTTTGCTAAAGGA
TTTAGAGATACTGGAAGAAACAGGGGTGTATTGGATGGGCTTTTAGAGACCTACCCATGGAGGCCTTCTTTCACTCTCGATTTTAAAACCTTTGGCGCAGACACA
CAAAGTGGAAGCAGTGGCTCATCTCCAGTGACCTCTAGTGGAGGGGCCCCCTCTCCTTTGAACTCCTTACTTTCTCCACTTTGCTTTTCACCTATGTTTCATTTA
CCTACAAGCTCCCTTGGAATGCCCTGTCCAGAGGCATACCTGCCCAATGTCAACCTGCCTCTATGCTACAAGATTTGTCCAACTAATTTTTGGCAACAGCAACCT
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>TBX22|50945|protein
MALSSRARAFSVEALVGRPSKRKLQDPIQAEQPELREKKGGEEEEERRSSAAGKSEPLEKQPKTEPSTSASSGCGSDSGYGNSSESLEEKDIQMELQGSELWKRF
HDIGTEMIITKAGRRMFPSVRVKVKGLDPGKQYHVAIDVVPVDSKRYRYVYHSSQWMVAGNTDHLCIIPRFYVHPDSPCSGETWMRQIISFDRMKLTNNEMDDKG
HIILQSMHKYKPRVHVIEQGSSVDLSQIQSLPTEGVKTFSFKETEFTTVTAYQNQQITKLKIERNPFAKGFRDTGRNRGVLDGLLETYPWRPSFTLDFKTFGADT
QSGSSGSSPVTSSGGAPSPLNSLLSPLCFSPMFHLPTSSLGMPCPEAYLPNVNLPLCYKICPTNFWQQQPLVLPAPERLASSNSSQSLAPLMMEVPMLSSLGVTN
SKSGSSEDSSDQYLQAPNSTNQMLYGLQSPGNIFLPNSITPEALSCSFHPSYDFYRYNFSMPSRLISGSNHLKVNDDSQVSFGEGKCNHVHWYPAINHYL
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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) 0 (0) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 0 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top