AutismKB 2.0

Evidence Details for NUDT16L1


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Basic Information Top
Gene Symbol:NUDT16L1 ( MGC11275,SDOS )
Gene Full Name: nudix (nucleoside diphosphate linked moiety X)-type motif 16-like 1
Band: 16p13.3
Quick LinksEntrez ID:84309; OMIM: NA; Uniprot ID:SDOS_HUMAN; ENSEMBL ID: ENSG00000168101; HGNC ID: 28154
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>NUDT16L1|84309|nucleotide
ATGTCGACGGCGGCGGTTCCGGAGCTGAAGCAGATCAGCCGGGTGGAGGCGATGCGCCTAGGGCCGGGCTGGAGCCACTCGTGCCACGCCATGCTGTACGCCGCC
AACCCTGGGCAGCTCTTCGGCCGCATCCCCATGCGCTTCTCGGTGCTGATGCAGATGCGTTTCGACGGGCTGCTGGGCTTCCCCGGGGGCTTCGTGGACCGGCGC
TTCTGGTCGCTGGAGGACGGCCTGAACCGGGTGCTGGGCCTGGGCCTGGGCTGCCTGCGCCTCACCGAGGCCGACTACCTGAGCTCGCACCTGACCGAGGGCCCA
CACCGCGTCGTGGCGCACCTGTACGCGCGGCAGCTGACGCTGGAGCAGCTGCACGCCGTGGAGATCAGCGCGGTGCACTCGCGCGACCACGGCCTGGAGGTGGGG
CCGCCGCCCGGGCCCCGCCCCCCGCCCCGGGGTTTGGCTCTGGCCCCGTGGAAGGCACCGATGGGTGCTGGGCCTCGTGCGGGTCCCGCTGTACACCCAGAAGGA
CCGAGTCGGAGGCTTCCCCAACTTCCTGAGCAACGCCTTCGTGAGCACGGCTAA





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>NUDT16L1|84309|protein
MSTAAVPELKQISRVEAMRLGPGWSHSCHAMLYAANPGQLFGRIPMRFSVLMQMRFDGLLGFPGGFVDRRFWSLEDGLNRVLGLGLGCLRLTEADYLSSHLTEGP
HRVVAHLYARQLTLEQLHAVEISAVHSRDHGLEVGPPPGPRPPPRGLALAPWKAPMGAGPRAGPAVHPEGPSRRLPQLPEQRLREHG



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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) 1 (2) 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
Bremer, 2011 - aCGHASD - - - - 223 - 223
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Buxbaum, 2004 USA microsatellite-based genomic screenautism 115 - 115 - - - -
Lauritsen, 2006 Faroe Islands microsatellite-based genomic screenautism - - - - 12 44 56
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
Iossifov I, 2014 2508 - 1194 The contribution of de novo coding mutations to autism spectrum disorder.
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018