AutismKB 2.0

Evidence Details for MAGT1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:MAGT1 ( DKFZp564K142,FLJ14726,IAP,MGC64926,MRX95,OST3B,PRO0756,bA217H1.1 )
Gene Full Name: magnesium transporter 1
Band: Xq21.1
Quick LinksEntrez ID:84061; OMIM: 300715; Uniprot ID:MAGT1_HUMAN; ENSEMBL ID: ENSG00000102158; HGNC ID: 28880
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>MAGT1|84061|nucleotide
ATGAGGAAAGGCAAGGGGCCGATTTGCCTGTTCTCACGCCCCACCCTCAGACCTAGCCGGAGCAAAGTTTCACTTATAGAAGGGAGAGGAGCGAACATGGCAGCG
CGTTGGCGGTTTTGGTGTGTCTCTGTGACCATGGTGGTGGCGCTGCTCATCGTTTGCGACGTTCCCTCAGCCTCTGCCCAAAGAAAGAAGGAGATGGTGTTATCT
GAAAAGGTTAGTCAGCTGATGGAATGGACTAACAAAAGACCTGTAATAAGAATGAATGGAGACAAGTTCCGTCGCCTTGTGAAAGCCCCACCGAGAAATTACTCC
GTTATCGTCATGTTCACTGCTCTCCAACTGCATAGACAGTGTGTCGTTTGCAAGCAAGCTGATGAAGAATTCCAGATCCTGGCAAACTCCTGGCGATACTCCAGT
GCATTCACCAACAGGATATTTTTTGCCATGGTGGATTTTGATGAAGGCTCTGATGTATTTCAGATGCTAAACATGAATTCAGCTCCAACTTTCATCAACTTTCCT
GCAAAAGGGAAACCCAAACGGGGTGATACATATGAGTTACAGGTGCGGGGTTTTTCAGCTGAGCAGATTGCCCGGTGGATCGCCGACAGAACTGATGTCAATATT
AGAGTGATTAGACCCCCAAATTATGCTGGTCCCCTTATGTTGGGATTGCTTTTGGCTGTTATTGGTGGACTTGTGTATCTTCGAAGAAGTAATATGGAATTTCTC
TTTAATAAAACTGGATGGGCTTTTGCAGCTTTGTGTTTTGTGCTTGCTATGACATCTGGTCAAATGTGGAACCATATAAGAGGACCACCATATGCCCATAAGAAT
CCCCACACGGGACATGTGAATTATATCCATGGAAGCAGTCAAGCCCAGTTTGTAGCTGAAACACACATTGTTCTTCTGTTTAATGGTGGAGTTACCTTAGGAATG
GTGCTTTTATGTGAAGCTGCTACCTCTGACATGGATATTGGAAAGCGAAAGATAATGTGTGTGGCTGGTATTGGACTTGTTGTATTATTCTTCAGTTGGATGCTC
TCTATTTTTAGATCTAAATATCATGGCTACCCATACAGCTTTCTGATGAGTTAA
Show »

>MAGT1|84061|protein
MRKGKGPICLFSRPTLRPSRSKVSLIEGRGANMAARWRFWCVSVTMVVALLIVCDVPSASAQRKKEMVLSEKVSQLMEWTNKRPVIRMNGDKFRRLVKAPPRNYS
VIVMFTALQLHRQCVVCKQADEEFQILANSWRYSSAFTNRIFFAMVDFDEGSDVFQMLNMNSAPTFINFPAKGKPKRGDTYELQVRGFSAEQIARWIADRTDVNI
RVIRPPNYAGPLMLGLLLAVIGGLVYLRRSNMEFLFNKTGWAFAALCFVLAMTSGQMWNHIRGPPYAHKNPHTGHVNYIHGSSQAQFVAETHIVLLFNGGVTLGM
VLLCEAATSDMDIGKRKIMCVAGIGLVVLFFSWMLSIFRSKYHGYPYSFLMS

Show »

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) 0 (1) 0 (0) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 1 (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