FMR1

Gene Information
 
Gene Symbol
FMR1
 
Aliases
FMRP, FRAXA, POF, POF1
 
Entrez Gene ID
 
Gene Name
FMRP translational regulator 1
 
Chromosomal Location
Xq27.3
 
HGNC ID
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

SNPs

SNP
SNP ID
Associated disease
References
750 repeats of CGG
Precocious puberty

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0000381 Biological process Regulation of alternative mRNA splicing, via spliceosome IBA 21873635
GO:0000381 Biological process Regulation of alternative mRNA splicing, via spliceosome IDA 18653529
GO:0001934 Biological process Positive regulation of protein phosphorylation IBA 21873635
GO:0002092 Biological process Positive regulation of receptor internalization IDA 25561520
GO:0006974 Biological process Cellular response to DNA damage stimulus IDA 24813610
Protein Information
 
Protein Name
Synaptic functional regulator FMR1, fragile X mental retardation 1, fragile X mental retardation protein 1, truncated FMRP
 
Function
 
Refseq Proteins
 
UniProt
 
PDB
Pathways
 
KEGG
 
 

RNA transport

 

     
References
 
 
PubMed ID Disease SNP/Mutation Study population Ethnicity Age of study population Type of sample
Precocious puberty 
The mutation responsible for fragile X syndrome involves expansion of (CGG) segment.  
Girls:1 
 
7 years, 7 months 

| © 2020, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400 012
Tel: 91-22-24192104, Fax No: 91-22-24139412