AutismKB 2.0

Annotation Detail for SNX29


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Basic Information Top
Gene Symbol:SNX29 ( A-388D4.1,FLJ00143 )
Gene Full Name: sorting nexin 29
Band: 16p13.13-p13.12
Quick LinksEntrez ID:92017; OMIM: NA; Uniprot ID:SNX29_HUMAN; ENSEMBL ID: ENSG00000048471; HGNC ID: 30542
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
254Phosphoserine.
256Phosphothreonine.
257Phosphoserine.
261Phosphoserine.
263Phosphoserine.
425Phosphoserine.
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
9635 mRNA LOC92017 chr16 12080191 12574366 3557 mRNA chr16 12088103 12091660 Non-exonic Bidirectional (NOB) pairs

Simple Query:


  (e.g. CHD8)

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