Gene Gene information from NCBI Gene database.
Entrez ID 55324
Gene name ATP binding cassette subfamily F member 3
Gene symbol ABCF3
Synonyms (NCBI Gene)
EST201864
Chromosome 3
Chromosome location 3q27.1
Summary This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ATP-binding cassette proteins transport various molecules across extra- and intracellular membranes. The protein encoded by this gene displays antiviral effect against f
miRNA miRNA information provided by mirtarbase database.
434
miRTarBase ID miRNA Experiments Reference
MIRT607603 hsa-miR-8485 HITS-CLIP 22927820
MIRT607603 hsa-miR-8485 HITS-CLIP 23313552
MIRT607602 hsa-miR-329-3p HITS-CLIP 23313552
MIRT607601 hsa-miR-362-3p HITS-CLIP 23313552
MIRT607600 hsa-miR-603 HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0005515 Function Protein binding IPI 21516116, 25416956, 26871637, 31515488
GO:0005524 Function ATP binding IBA
GO:0005524 Function ATP binding IEA
GO:0016020 Component Membrane HDA 19946888
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618967 72 ENSG00000161204
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NUQ8
Protein name ATP-binding cassette sub-family F member 3
Protein function Displays an antiviral effect against flaviviruses such as west Nile virus (WNV) in the presence of OAS1B.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00005 ABC_tran 193 356 ABC transporter Domain
PF12848 ABC_tran_Xtn 395 480 ABC transporter Domain
PF00005 ABC_tran 508 639 ABC transporter Domain
Sequence
MATCAEILRSEFPEIDGQVFDYVTGVLHSGSADFESVDDLVEAVGELLQEVSGDSKDDAG
IRAVCQRMYNTLRLAEPQSQGNSQVLLDAPIQLSKITENYDCGTKLPGLLKREQSSTVNA
KKLEKAEARLKAKQEKRSEKDTLKTSNPLVLEEASASQAGSRKESRLESSGKNKSYDVRI
ENFDVSFGDRVLLAGADVNLAWGRRYGLVGRNGLGKTTLLKMLATRSLRVPAHISLLHVE
QEVAGDDTPALQSVLESDSVREDLLRRERELTAQIAAGRAEGSEAAELAEIYAKLEEIEA
DKAPARASVILAGLGFTPKMQQQPTREFSGGWRMRLALARALFARPDLLLLDEPTN
MLDV
RAILWLENYLQTWPSTILVVSHDRNFLNAIATDIIHLHSQRLDGYRGDFETFIKSKQERL
LNQQREYEAQQQYRQHIQVFIDRFRYNANRASQVQSKLKMLEKLPELKPVDKESEVVMKF

PDGFEKFSPPILQLDEVDFYYDPKHVIFSRLSVSADLESRICVVGENGAGKSTMLKLLLG
DLAPVRGIRHAHRNLKIGYFSQHHVEQLDLNVSAVELLARKFPGRPEEEYRHQLGRYGIS
GELAMRPLASLSGGQKSRVAFAQMTMPCPNFYILDEPTN
HLDMETIEALGRALNNFRGGV
ILVSHDERFIRLVCRELWVCEGGGVTRVEGGFDQYRALLQEQFRREGFL
Sequence length 709
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Prostate cancer Uncertain significance rs143852274 RCV000149252
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Uterine Cervical Neoplasms Associate 17504382