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Cancer Genome Characterization Initiative

Visit the database of genomic characterization data for multiple tumor types.


Gene Info

Gene Information For:Hs. FMR1, fragile X mental retardation 1
Sequence ID:NM_001185075
NM_001185076
NM_001185081
NM_001185082
NM_002024
NR_033699
NR_033700
RefSeqGene ID:NG_007529
Entrez Gene ID:2332
Ensembl ID:ENSG00000102081

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaDTPSNPSNP: GeneViewSNP: VarViewAssembliesRNAi

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
FRAGILE X SYNDROME 
FRAGILE X TREMOR/ATAXIA SYNDROME 
PREMATURE OVARIAN FAILURE 1 

Cytogenetic Location (from UniGene)

Cytogenetic Location:Xq27.3Mitelman Breakpoint Data

Chromosomal Position (from UCSC)

Chromosomal Position:X: 147009187 - 147032639

 Exon Info From UCSC:
NM_001185075
NM_001185076
NM_001185081
NM_001185082
NM_002024

Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
30347992Full LengthBC086957fragile X mental retardation 1

Protein Similarities Based on Shared Motif Content

Find gene products sharing protein motifs with:  NP_002015  

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_001185075 NP_001172004    
NM_001185076 NP_001172005    
NM_001185081 NP_001172010    
NM_001185082 NP_001172011    
NM_002024 NP_002015 Q06787 KH_1
Agenet

Related Sequences

 
mRNAGenPeptSwissProt
M67468 AAA52458 Q06787
S65791 AAB28395 Q06787
BC038998 AAH38998 Q8IXW7
BC086957 AAH86957 Q06787
AB209188 BAD92425 Q59GC1
AK294104 BAG57439 B4DFH8
AK302707 BAG63929 B4DZ17
X69962 CAA49586 Q06787

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens FMR1 NP_001172005 M.musculus Fmr1 14265 Gene Info NP_032057 98
R.norvegicus Fmr1 24948   NP_434691 97

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)