AutismKB 2.0

Evidence Details for MEIS3


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Basic Information Top
Gene Symbol:MEIS3 ( DKFZp547H236,MRG2 )
Gene Full Name: Meis homeobox 3
Band: 19q13.32
Quick LinksEntrez ID:56917; OMIM: NA; Uniprot ID:MEIS3_HUMAN; ENSEMBL ID: ENSG00000105419; HGNC ID: 29537
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>MEIS3|56917|nucleotide
ATGGCCCGGAGGTATGATGAGCTGCCGCACTACCCAGGCATCGTGGATGGCCCCGCAGCCCTGGCTAGCTTCCCAGAGACAGTGCCCGCAGTACCAGGGCCCTAT
GGCCCGCACCGGCCTCCCCAGCCCCTGCCCCCAGGCTTGGACAGCGACGGCCTGAAGAGGGAGAAGGATGAGATCTATGGACACCCGCTCTTCCCCCTCTTGGCC
CTGGTCTTTGAGAAATGTGAACTGGCTACATGCTCTCCCCGTGACGGGGCCGGAGCTGGGCTGGGGACACCCCCTGGAGGTGACGTCTGCTCCTCTGATTCCTTC
AACGAGGACATCGCTGCCTTTGCCAAGCAGGTTCGCTCTGAGAGGCCCCTCTTCTCCTCCAACCCAGAACTGGACAATCTGATGATCCAGGCCATCCAGGTGCTG
CGGTTCCACCTGCTGGAGCTGGAGAAGGGAAAGATGCCCATCGACCTGGTCATCGAGGATCGGGACGGCGGCTGCAGGGAGGACTTCGAGGACTACCCAGCCTCC
TGCCCCAGCCTCCCAGACCAGAATAATATGTGGATTCGAGACCATGAGGATAGTGGGTCTGTACATTTGGGGACCCCAGGTCCATCCAGTGGGGGCCTGGCCTCC
CAGAGTGGGGACAACTCCAGTGACCAAGGAGACGGGCTGGACACCAGCGTGGCCTCTCCCAGTTCTGGTGGAGAAGATGAGGACTTGGACCAGGAGCGACGGCGA
AACAAGAAGAGGGGGATCTTCCCCAAGGTGGCCACCAACATCATGCGAGCCTGGTTGTTCCAGCACCTCTCGCACCCGTACCCCTCGGAGGAGCAGAAGAAACAG
CTGGCGCAGGACACGGGGCTCACCATCCTGCAAGTCAACAACTGGTTCATTAACGCCCGGAGACGCATCGTGCAACCTATGATCGATCAATCCAACCGCACAGGG
CAGGGTGCAGCCTTCAGCCCAGAGGGCCAGCCCATCGGGGGCTATACCGAGACGCAGCCACACGTGGCCGTCCGGCCTCCGGGATCAGTGGGGATGAGTTTGAAC
TTGGAAGGAGAATGGCATTATCTATAG
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>MEIS3|56917|protein
MARRYDELPHYPGIVDGPAALASFPETVPAVPGPYGPHRPPQPLPPGLDSDGLKREKDEIYGHPLFPLLALVFEKCELATCSPRDGAGAGLGTPPGGDVCSSDSF
NEDIAAFAKQVRSERPLFSSNPELDNLMIQAIQVLRFHLLELEKGKMPIDLVIEDRDGGCREDFEDYPASCPSLPDQNNMWIRDHEDSGSVHLGTPGPSSGGLAS
QSGDNSSDQGDGLDTSVASPSSGGEDEDLDQERRRNKKRGIFPKVATNIMRAWLFQHLSHPYPSEEQKKQLAQDTGLTILQVNNWFINARRRIVQPMIDQSNRTG
QGAAFSPEGQPIGGYTETQPHVAVRPPGSVGMSLNLEGEWHYL

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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 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 0 (2)
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
Linkage Studies Top