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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + AFF2  RefSeq IDs +
Approved Name + AF4/FMR2 family, member 2 NM_002025 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:3776 Accession Numbers +
Status + Approved U48436 GenBank  EMBL DDBJ UCSC
Chromosome + Xq28 Mouse Genome Database ID (mapped data supplied by MGI) +
Previous Symbols + FMR2 MGI:1202294 MGD ID 
Previous Names + "fragile X mental retardation 2" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + FRAXE RGD:1565592 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 2334 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS14684.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
VEGA IDs +
OTTHUMG00000022613 VEGA GeneView 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000155966 Ensembl GeneView  UCSC 
Specialist Database Links OMIM ID (mapped data supplied by NCBI) +
COSMIC Orphanet:15469
 
300806 OMIM 
UCSC ID (mapped data supplied by UCSC) +
Locus Specific Database Links uc004fcp.2 UCSC Index 
Mental Retardation database  UniProt ID (mapped data supplied by UniProt) +
Q7Z2F7 UniProt  UCSC 
 

See Column definitions for descriptions of the various data fields. Also see our custom downloads page for bulk access to our data

 


The work of the HGNC is supported by NHGRI grant P41 HG003345, the UK Medical Research Council and the Wellcome Trust.