ID FBX47_HUMAN Reviewed; 452 AA. AC Q5MNV8; B2RTZ4; DT 15-FEB-2005, integrated into UniProtKB/Swiss-Prot. DT 18-MAY-2010, sequence version 2. DT 10-JUN-2026, entry version 128. DE RecName: Full=F-box only protein 47; GN Name=FBXO47 {ECO:0000303|PubMed:28397838, GN ECO:0000312|HGNC:HGNC:31969}; OS Homo sapiens (Human). OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. OX NCBI_TaxID=9606; RN [1] RP NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, AND VARIANT ARG-209. RC TISSUE=Testis; RX PubMed=15723337; DOI=10.1002/gcc.20170; RA Simon-Kayser B., Scoul C., Renaudin K., Jezequel P., Bouchot O., Rigaud J., RA Bezieau S.; RT "Molecular cloning and characterization of FBXO47, a novel gene containing RT an F-box domain, located in the 17q12 band deleted in papillary renal cell RT carcinoma."; RL Genes Chromosomes Cancer 43:83-94(2005). RN [2] RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RX PubMed=16625196; DOI=10.1038/nature04689; RA Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., RA Nicholson C., Searle S.M., Wilming L., Young S.K., Abouelleil A., RA Allen N.R., Bi W., Bloom T., Borowsky M.L., Bugalter B.E., Butler J., RA Chang J.L., Chen C.-K., Cook A., Corum B., Cuomo C.A., de Jong P.J., RA DeCaprio D., Dewar K., FitzGerald M., Gilbert J., Gibson R., Gnerre S., RA Goldstein S., Grafham D.V., Grocock R., Hafez N., Hagopian D.S., Hart E., RA Norman C.H., Humphray S., Jaffe D.B., Jones M., Kamal M., Khodiyar V.K., RA LaButti K., Laird G., Lehoczky J., Liu X., Lokyitsang T., Loveland J., RA Lui A., Macdonald P., Major J.E., Matthews L., Mauceli E., McCarroll S.A., RA Mihalev A.H., Mudge J., Nguyen C., Nicol R., O'Leary S.B., Osoegawa K., RA Schwartz D.C., Shaw-Smith C., Stankiewicz P., Steward C., Swarbreck D., RA Venkataraman V., Whittaker C.A., Yang X., Zimmer A.R., Bradley A., RA Hubbard T., Birren B.W., Rogers J., Lander E.S., Nusbaum C.; RT "DNA sequence of human chromosome 17 and analysis of rearrangement in the RT human lineage."; RL Nature 440:1045-1049(2006). RN [3] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANT ARG-209. RX PubMed=15489334; DOI=10.1101/gr.2596504; RG The MGC Project Team; RT "The status, quality, and expansion of the NIH full-length cDNA project: RT the Mammalian Gene Collection (MGC)."; RL Genome Res. 14:2121-2127(2004). RN [4] RP VARIANT GLY-182. RX PubMed=28397838; DOI=10.1038/mp.2017.60; RA Harripaul R., Vasli N., Mikhailov A., Rafiq M.A., Mittal K., RA Windpassinger C., Sheikh T.I., Noor A., Mahmood H., Downey S., Johnson M., RA Vleuten K., Bell L., Ilyas M., Khan F.S., Khan V., Moradi M., Ayaz M., RA Naeem F., Heidari A., Ahmed I., Ghadami S., Agha Z., Zeinali S., Qamar R., RA Mozhdehipanah H., John P., Mir A., Ansar M., French L., Ayub M., RA Vincent J.B.; RT "Mapping autosomal recessive intellectual disability: combined microarray RT and exome sequencing identifies 26 novel candidate genes in 192 RT consanguineous families."; RL Mol. Psychiatry 23:973-984(2018). CC -!- FUNCTION: Probably recognizes and binds to some phosphorylated proteins CC and promotes their ubiquitination and degradation. {ECO:0000250}. CC -!- SUBUNIT: Part of a SCF (SKP1-cullin-F-box) protein ligase complex. CC {ECO:0000250}. CC -!- TISSUE SPECIFICITY: Widely expressed, with highest levels in kidney, CC liver and pancreas. Down-regulated in tumors. CC {ECO:0000269|PubMed:15723337}. CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AY700575; AAV91324.1; -; mRNA. DR EMBL; AC006441; -; NOT_ANNOTATED_CDS; Genomic_DNA. DR EMBL; BC140879; AAI40880.1; -; mRNA. DR EMBL; BC140880; AAI40881.1; -; mRNA. DR CCDS; CCDS32639.1; -. DR RefSeq; NP_001008777.2; NM_001008777.3. DR AlphaFoldDB; Q5MNV8; -. DR BioGRID; 138947; 2. DR ComplexPortal; CPX-8006; SCF E3 ubiquitin ligase complex, FBXO47 variant. DR FunCoup; Q5MNV8; 67. DR NDEx; IQUERY-CP-FBXO47; 1 NDEx IQuery Curated Pathway. DR STRING; 9606.ENSP00000367319; -. DR GlyGen; Q5MNV8; 1 site, 1 O-linked glycan (1 site). DR iPTMnet; Q5MNV8; -. DR PhosphoSitePlus; Q5MNV8; -. DR BioMuta; FBXO47; -. DR DMDM; 296434512; -. DR jPOST; Q5MNV8; -. DR PaxDb; 9606-ENSP00000367319; -. DR ProteomicsDB; 63588; -. DR Antibodypedia; 65659; 62 antibodies from 14 providers. DR DNASU; 494188; -. DR Ensembl; ENST00000378079.3; ENSP00000367319.2; ENSG00000204952.3. DR GeneID; 494188; -. DR KEGG; hsa:494188; -. DR MANE-Select; ENST00000378079.3; ENSP00000367319.2; NM_001008777.3; NP_001008777.2. DR UCSC; uc002hrc.2; human. DR AGR; HGNC:31969; -. DR ClinPGx; PA162388157; -. DR CTD; 494188; -. DR DisGeNET; 494188; -. DR GeneCards; FBXO47; -. DR HGNC; HGNC:31969; FBXO47. DR HPA; ENSG00000204952; Tissue enriched (testis). DR MIM; 609498; gene. DR OpenTargets; ENSG00000204952; -. DR VEuPathDB; HostDB:ENSG00000204952; -. DR eggNOG; ENOG502QV8T; Eukaryota. DR GeneTree; ENSGT00390000014175; -. DR HOGENOM; CLU_048746_0_0_1; -. DR InParanoid; Q5MNV8; -. DR OMA; AFACVTM; -. DR OrthoDB; 6346810at2759; -. DR PAN-GO; Q5MNV8; 0 GO annotations based on evolutionary models. DR PhylomeDB; Q5MNV8; -. DR PathwayCommons; Q5MNV8; -. DR Agora; ENSG00000204952; -. DR BioGRID-ORCS; 494188; 32 hits in 1182 CRISPR screens. DR ChiTaRS; FBXO47; human. DR GenomeRNAi; 494188; -. DR Pharos; Q5MNV8; Tbio. DR PRO; PR:Q5MNV8; -. DR Proteomes; UP000005640; Chromosome 17. DR RNAct; Q5MNV8; protein. DR Bgee; ENSG00000204952; Expressed in male germ line stem cell (sensu Vertebrata) in testis and 3 other cell types or tissues. DR GO; GO:0031146; P:SCF-dependent proteasomal ubiquitin-dependent protein catabolic process; NAS:ComplexPortal. DR CDD; cd22112; F-box_FBXO47; 1. DR InterPro; IPR056622; ARM_FBXO47. DR InterPro; IPR036047; F-box-like_dom_sf. DR InterPro; IPR001810; F-box_dom. DR InterPro; IPR038946; FBXO47. DR PANTHER; PTHR34098; F-BOX ONLY PROTEIN 47; 1. DR PANTHER; PTHR34098:SF1; F-BOX ONLY PROTEIN 47; 1. DR Pfam; PF24467; ARM_FBXO47; 1. DR Pfam; PF00646; F-box; 1. DR SUPFAM; SSF81383; F-box domain; 1. DR PROSITE; PS50181; FBOX; 1. PE 2: Evidence at transcript level; KW Reference proteome; Ubl conjugation pathway. FT CHAIN 1..452 FT /note="F-box only protein 47" FT /id="PRO_0000119952" FT DOMAIN 41..91 FT /note="F-box" FT /evidence="ECO:0000255|PROSITE-ProRule:PRU00080" FT VARIANT 182 FT /note="R -> G (found in a consanguineous family with FT intellectual disability; uncertain significance; FT dbSNP:rs759147995)" FT /evidence="ECO:0000269|PubMed:28397838" FT /id="VAR_080770" FT VARIANT 209 FT /note="Q -> R (in dbSNP:rs9906595)" FT /evidence="ECO:0000269|PubMed:15489334, FT ECO:0000269|PubMed:15723337" FT /id="VAR_049052" SQ SEQUENCE 452 AA; 51968 MW; 703CBF21CAF67FB9 CRC64; MASRINTNFT LIPNQKLRRS NRQTSCYSKT LGSGFQPIST FGNFKALPLE IFQIILKYLS VKDISMLSMV SKTVSQHIIN YISTSSGSKR LLLQDFHNLE LPDRRQDSAI LEHYRSLGLL FKRCTLLLPT KERLKYIHKI LTEVSCFKFN GCAAPMQCLG LTCYGMFLQT LTAGWDELEC HRVYNFLCEL TNLCRKIQMA VCSKPGSAQK LELRIRLFCR NVLLDHWTHR SDSAFWLTRI LKPWPMVNQA RLLYIIFGPI SPQDGQVVWQ EMIEEPTDEF SLKGLADAIK LLYDASTKEW TADDVISLVD ELSVVPREWL LENNARLLML SGNNICFSFM ASKAVNGRTI ELARLVVFLA LVCEKELYCM DWTVKMMQKV CKVFSTPVER KNFLQNVANA FACVIMEMLQ SIMSGDRDED DRSFLNLFHL VHAQANFHKE VLYLTMNTPL ST //