Homo sapiens Gene: FRA10AC1
Summary
InnateDB Gene IDBG-82932.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FRA10AC1
Gene Name fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000148690
Encoded Proteins
fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a nuclear phosphoprotein of unknown function. The 5' UTR of this gene is part of a CpG island and contains a tandem CGG repeat region that normally consists of 8-14 repeats but can expand to over 200 repeats. The expanded allele becomes hypermethylated and is not transcribed; however, an expanded repeat region has not been associated with any disease phenotype. This gene is found within the rare FRA10A folate-sensitive fragile site. [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:93667883-93702572
Strand Reverse strand
Band q23.33
Transcripts
ENST00000359204 ENSP00000360488
ENST00000460752
ENST00000483229
ENST00000462771
ENST00000472153
ENST00000482719
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 39 experimentally validated interaction(s) in this database.
Experimentally validated
Total 39 [view]
Protein-Protein 39 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.586650 Hs.622576 Hs.641669
RefSeq NM_145246 XM_005269515 XM_005269516
HUGO
OMIM
CCDS CCDS7430
HPRD 12319
IMGT
EMBL
GenPept
RNA Seq Atlas