AutismKB 2.0

Annotation Details for SLC22A14


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:SLC22A14 ( MGC163415,OCTL2,OCTL4,ORCTL4 )
Gene Full Name: solute carrier family 22, member 14
Band: 3p22.2
Quick LinksEntrez ID:9389; OMIM: 604048; Uniprot ID:S22AE_HUMAN; ENSEMBL ID: ENSG00000144671; HGNC ID: 8495
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005887IBA-integral component of plasma membrane-
GO:0005887NAS-integral component of plasma membrane10072596
GO ID Evidence Qualifier GO_term References
GO:0005452IBA-inorganic anion exchanger activity-
GO:0015101NAS-organic cation transmembrane transporter activity10072596
GO:0015347IBA-sodium-independent organic anion transmembrane transporter activity-
GO ID Evidence Qualifier GO_term References
GO:0015695NAS-organic cation transport10072596
GO:0015698IEA-inorganic anion transport-
GO:0043252IBA-sodium-independent organic anion transport-
GO:0055085IEA-transmembrane transport-
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:2685974
  • Data Attributes: HomoloGene calculated
No data
No data

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


Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved