Evidence Details for HMGXB3


Gene Symbol: | HMGXB3 ( HMGX3,KIAA0194,SMF ) |
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Gene Full Name: | HMG box domain containing 3 |
Band: | 5q32 |
Quick Links | Entrez ID:22993; OMIM: NA; Uniprot ID:HMGX3_HUMAN; ENSEMBL ID: ENSG00000113716; HGNC ID: 28982 |
Relate to Another Database: | SFARIGene; denovo-db |


>HMGXB3|22993|nucleotide
ATGGACGCATCATATGATGGTACTGAGGTAACTGTCGTGATGGAGGAAATTGAGGAAGCCTATTGTTACACCTCTCCTGGGCCACCCAAGAAGAAGAAAAAGTAT
AAAATACATGGAGAAAAGACAAAGAAACCCAGGTCTGCTTACCTTCTGTACTATTACGACATCTACCTGAAAGTGCAGCAGGAGCTCCCCCACCTCCCTCAGTCT
GAGATCAATAAGAAGATTAGTGAGAGTTGGAGGCTTCTCAGCGTGGCCGAGAGGAGTTACTACTTGGAGAAAGCCAAACTAGAGAAGGAAGGTTTGGATCCTAAC
TCTAAGCTCTCTGCACTGACTGCTGTGGTTCCGGACATCCCAGGTTTCCGCAAGATCCTCCCACGCTCAGATTATATCATCATCCCCAAGAGCAGCCTGCAGGAG
GACCGGAGCTGCCCTCAGCTAGAGCTATGTGTGGCTCAGAACCAGATGTCCCCGAAAGGACCTCCTCTTGTGTCCAACACTGCCCCGGAGACAGTGCCCAGCCAT
GCAGGCATGGCAGAGCAGTGCCTGGCTGTGGAGGCCCTGGCTGAGGAGGTGGGAGCCCTTACCCAGTCAGGTGCTGTACAGGAGATTGCCACCTCAGAGATCCTC
AGCCAGGATGTGCTCCTAGAGGACGCTTCCCTAGAAGTAGGGGAGAGCCACCAACCTTACCAGACAAGCCTGGTAATTGAAGAGACCTTGGTGAATGGCTCACCA
GACCTCCCCACTGGAAGCCTGGCTGTGCCCCACCCCCAGGTTGGGGAGAGTGTATCAGTGGTAACAGTCATGAGGGATTCCAGTGAGAGTAGCTCCTCTGCACCA
GCCACACAGTTCATCATGTTGCCTCTGCCTGCCTACTCGGTTGTGGAGAACCCCACCTCCATCAAACTGACCACTACATATACCCGCCGGGGCCATGGGACATGC
ACCAGCCCAGGGTGCTCCTTTACATATGTCACCAGGCACAAGCCACCTAAGTGCCCTACCTGTGGTAACTTCCTAGGAGGGAAGTGGATCCCAAAGGAAAAGCCA
GCCAAAGTAAAAGTGGAATTGGCTTCTGGCGTCTCTTCCAAAGGCTCTGTGGTGAAAAGAAATCAGCAACCTGTCACCACTGAGCAAAATTCCTCTAAGGAAAAT
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ATGGACGCATCATATGATGGTACTGAGGTAACTGTCGTGATGGAGGAAATTGAGGAAGCCTATTGTTACACCTCTCCTGGGCCACCCAAGAAGAAGAAAAAGTAT
AAAATACATGGAGAAAAGACAAAGAAACCCAGGTCTGCTTACCTTCTGTACTATTACGACATCTACCTGAAAGTGCAGCAGGAGCTCCCCCACCTCCCTCAGTCT
GAGATCAATAAGAAGATTAGTGAGAGTTGGAGGCTTCTCAGCGTGGCCGAGAGGAGTTACTACTTGGAGAAAGCCAAACTAGAGAAGGAAGGTTTGGATCCTAAC
TCTAAGCTCTCTGCACTGACTGCTGTGGTTCCGGACATCCCAGGTTTCCGCAAGATCCTCCCACGCTCAGATTATATCATCATCCCCAAGAGCAGCCTGCAGGAG
GACCGGAGCTGCCCTCAGCTAGAGCTATGTGTGGCTCAGAACCAGATGTCCCCGAAAGGACCTCCTCTTGTGTCCAACACTGCCCCGGAGACAGTGCCCAGCCAT
GCAGGCATGGCAGAGCAGTGCCTGGCTGTGGAGGCCCTGGCTGAGGAGGTGGGAGCCCTTACCCAGTCAGGTGCTGTACAGGAGATTGCCACCTCAGAGATCCTC
AGCCAGGATGTGCTCCTAGAGGACGCTTCCCTAGAAGTAGGGGAGAGCCACCAACCTTACCAGACAAGCCTGGTAATTGAAGAGACCTTGGTGAATGGCTCACCA
GACCTCCCCACTGGAAGCCTGGCTGTGCCCCACCCCCAGGTTGGGGAGAGTGTATCAGTGGTAACAGTCATGAGGGATTCCAGTGAGAGTAGCTCCTCTGCACCA
GCCACACAGTTCATCATGTTGCCTCTGCCTGCCTACTCGGTTGTGGAGAACCCCACCTCCATCAAACTGACCACTACATATACCCGCCGGGGCCATGGGACATGC
ACCAGCCCAGGGTGCTCCTTTACATATGTCACCAGGCACAAGCCACCTAAGTGCCCTACCTGTGGTAACTTCCTAGGAGGGAAGTGGATCCCAAAGGAAAAGCCA
GCCAAAGTAAAAGTGGAATTGGCTTCTGGCGTCTCTTCCAAAGGCTCTGTGGTGAAAAGAAATCAGCAACCTGTCACCACTGAGCAAAATTCCTCTAAGGAAAAT
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>HMGXB3|22993|protein
MDASYDGTEVTVVMEEIEEAYCYTSPGPPKKKKKYKIHGEKTKKPRSAYLLYYYDIYLKVQQELPHLPQSEINKKISESWRLLSVAERSYYLEKAKLEKEGLDPN
SKLSALTAVVPDIPGFRKILPRSDYIIIPKSSLQEDRSCPQLELCVAQNQMSPKGPPLVSNTAPETVPSHAGMAEQCLAVEALAEEVGALTQSGAVQEIATSEIL
SQDVLLEDASLEVGESHQPYQTSLVIEETLVNGSPDLPTGSLAVPHPQVGESVSVVTVMRDSSESSSSAPATQFIMLPLPAYSVVENPTSIKLTTTYTRRGHGTC
TSPGCSFTYVTRHKPPKCPTCGNFLGGKWIPKEKPAKVKVELASGVSSKGSVVKRNQQPVTTEQNSSKENASKLTLENSEAVSQLLNVAPPREVGEESEWEEVII
SDAHVLVKEAPGNCGTAVTKTPVVKSGVQPEVTLGTTDNDSPGADVPTPSEGTSTSSPLPAPKKPTGVDLLTPGSRAPELKGRARGKPSLLAAARPMRAILPAPV
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MDASYDGTEVTVVMEEIEEAYCYTSPGPPKKKKKYKIHGEKTKKPRSAYLLYYYDIYLKVQQELPHLPQSEINKKISESWRLLSVAERSYYLEKAKLEKEGLDPN
SKLSALTAVVPDIPGFRKILPRSDYIIIPKSSLQEDRSCPQLELCVAQNQMSPKGPPLVSNTAPETVPSHAGMAEQCLAVEALAEEVGALTQSGAVQEIATSEIL
SQDVLLEDASLEVGESHQPYQTSLVIEETLVNGSPDLPTGSLAVPHPQVGESVSVVTVMRDSSESSSSAPATQFIMLPLPAYSVVENPTSIKLTTTYTRRGHGTC
TSPGCSFTYVTRHKPPKCPTCGNFLGGKWIPKEKPAKVKVELASGVSSKGSVVKRNQQPVTTEQNSSKENASKLTLENSEAVSQLLNVAPPREVGEESEWEEVII
SDAHVLVKEAPGNCGTAVTKTPVVKSGVQPEVTLGTTDNDSPGADVPTPSEGTSTSSPLPAPKKPTGVDLLTPGSRAPELKGRARGKPSLLAAARPMRAILPAPV
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |














Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2012 | - | 343 | 50 | De novo gene disruptions in children on the autistic spectrum. |






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