NUFIP1

NUFIP1
Identifiers
Aliases	NUFIP1, NUFIP, bA540M5.1, FMR1 interacting protein 1, nuclear FMR1 interacting protein 1, Rsa1
External IDs	OMIM: 604354; MGI: 1351474; HomoloGene: 8216; GeneCards: NUFIP1; OMA:NUFIP1 - orthologs
Gene location (Human)
Chr.	Chromosome 13 (human)
End	44,989,471 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	76,374,819 bp
RNA expression pattern
	Top expressed in
	endothelial cell; ; gonad; ; secondary oocyte; ; ventricular zone; ; testicle; ; ganglionic eminence; ; Brodmann area 23; ; gastrocnemius muscle; ; Achilles tendon; ; islet of Langerhans;
	Top expressed in
	primitive streak; ; epiblast; ; renal corpuscle; ; medullary collecting duct; ; external carotid artery; ; Gonadal ridge; ; internal carotid artery; ; Paneth cell; ; abdominal wall; ; endothelial cell of lymphatic vessel;
	More reference expression data
	; ; ; ;
	More reference expression data
Gene ontology
Molecular function	protein binding; ATPase binding; identical protein binding; protein-macromolecule adaptor activity; snoRNA binding; RNA binding; metal ion binding; DNA binding; nucleic acid binding;
Cellular component	nuclear matrix; nucleus; pre-snoRNP complex; perichromatin fibrils; nucleolus; cytosolic ribosome; transcription elongation factor complex; fibrillar center; presynaptic active zone; protein-containing complex; synapse;
Biological process	box C/D snoRNP assembly; positive regulation of transcription by RNA polymerase II; RNA processing; protein complex oligomerization;
	Sources:Amigo / QuickGO
Orthologs
	26747
	27275
	ENSG00000083635
	ENSMUSG00000022009
	Q9UHK0
	Q9QXX8
	NM_012345
	NM_013745
	NP_036477
	NP_038773
	Wikidata
View/Edit Human	View/Edit Mouse

Nuclear fragile X mental retardation-interacting protein 1 is a protein that in humans is encoded by the NUFIP1 gene.