NUFIP2

Nuclear fragile X mental retardation-interacting protein 2 is a protein that in humans is encoded by the NUFIP2 gene.^[5][6][7]

NUFIP2
Identifiers
Aliases	NUFIP2, 182-FIP, 82-FIP, FIP-82, PIG1, FMR1 interacting protein 2, nuclear FMR1 interacting protein 2, NUFP2
External IDs	OMIM: 609356; MGI: 1915814; HomoloGene: 10808; GeneCards: NUFIP2; OMA:NUFIP2 - orthologs
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17q11.2 Start 29,255,839 bp[1] End 29,294,148 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11|11 B5 Start 77,576,981 bp[2] End 77,632,747 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in caput epididymis corpus epididymis tail of epididymis cardiac muscle tissue of right atrium secondary oocyte tibialis anterior muscle trabecular bone pancreatic epithelial cell mucosa of ileum deltoid muscle Top expressed in hand zygote body of femur pineal gland tail of embryo umbilical cord human fetus secondary oocyte foot epithelium of small intestine More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 57532 68564 Ensembl ENSG00000108256 ENSMUSG00000037857 UniProt Q7Z417 Q5F2E7 RefSeq (mRNA) NM_020772 NM_001024205 RefSeq (protein) NP_065823 NP_065823.1 NP_001019376 Location (UCSC) Chr 17: 29.26 – 29.29 Mb Chr 11: 77.58 – 77.63 Mb PubMed search [3] [4]
Wikidata
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Interactions

NUFIP2 has been shown to interact with FMR1 and Roquin-1.^[8][5]