Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2314
Gene name Gene Name - the full gene name approved by the HGNC.
FLII actin remodeling protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FLII
Synonyms (NCBI Gene) Gene synonyms aliases
CMD2J, FLI, FLIL, Fli1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CMD2J
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein with a gelsolin-like actin binding domain and an N-terminal leucine-rich repeat-protein protein interaction domain. The protein is similar to a Drosophila protein involved in early embryogenesis and the structural organization
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022789 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT052017 hsa-let-7b-5p CLASH 23622248
MIRT048726 hsa-miR-96-5p CLASH 23622248
MIRT043515 hsa-miR-331-3p CLASH 23622248
MIRT042489 hsa-miR-423-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IDA 9525888
GO:0005515 Function Protein binding IPI 9671805, 10366446
GO:0005546 Function Phosphatidylinositol-4,5-bisphosphate binding IBA 21873635
GO:0005634 Component Nucleus IBA 21873635
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600362 3750 ENSG00000177731
Protein
UniProt ID Q13045
Protein name Protein flightless-1 homolog
Protein function Is a regulator of actin polymerization, required for proper myofibril organization and regulation of the length of sarcomeric thin filaments (By similarity). It also plays a role in the assembly of cardiomyocyte cell adhesion complexes (By simil
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 33 91 Leucine rich repeat Repeat
PF13855 LRR_8 127 186 Leucine rich repeat Repeat
PF00626 Gelsolin 508 591 Gelsolin repeat Domain
PF00626 Gelsolin 628 703 Gelsolin repeat Domain
PF00626 Gelsolin 756 832 Gelsolin repeat Domain
PF00626 Gelsolin 1177 1255 Gelsolin repeat Domain
Tissue specificity TISSUE SPECIFICITY: Strongest expression in skeletal muscle with high expression also in the heart and lung. {ECO:0000269|PubMed:9525888}.
Sequence
MEATGVLPFVRGVDLSGNDFKGGYFPENVKAMTSLRWLKLNRTGLCYLPEELAALQKLEH
LSVSHNNLTTLHGELSSLPSLRAIVARANSL
KNSGVPDDIFKLDDLSVLDLSHNQLTECP
RELENAKNMLVLNLSHNSIDTIPNQLFINLTDLLYLDLSENRLESLPPQMRRLVHLQTLV
LNGNPL
LHAQLRQLPAMTALQTLHLRSTQRTQSNLPTSLEGLSNLADVDLSCNDLTRVPE
CLYTLPSLRRLNLSSNQITELSLCIDQWVHVETLNLSRNQLTSLPSAICKLSKLKKLYLN
SNKLDFDGLPSGIGKLTNLEEFMAANNNLELVPESLCRCPKLRKLVLNKNHLVTLPEAIH
FLTEIEVLDVRENPNLVMPPKPADRAAEWYNIDFSLQNQLRLAGASPATVAAAAAAGSGP
KDPMARKMRLRRRKDSAQDDQAKQVLKGMSDVAQEKNKKQEESADARAPSGKVRRWDQGL
EKPRLDYSEFFTEDVGQLPGLTIWQIENFVPVLVEEAFHGKFYEADCYIVLKTFLDDSGS
LNWEIYYWIGGEATLDKKACSAIHAVNLRNYLGAECRTVREEMGDESEEFL
QVFDNDISY
IEGGTASGFYTVEDTHYVTRMYRVYGKKNIKLEPVPLKGTSLDPRFVFLLDRGLDIYVWR
GAQATLSSTTKARLFAEKINKNERKGKAEITLLVQGQELPEFW
EALGGEPSEIKKHVPED
FWPPQPKLYKVGLGLGYLELPQINYKLSVEHKQRPKVELMPRMRLLQSLLDTRCVYILDC
WSDVFIWLGRKSPRLVRAAALKLGQELCGMLHRPRHATVSRSLEGTEAQVFK
AKFKNWDD
VLTVDYTRNAEAVLQSPGLSGKVKRDAEKKDQMKADLTALFLPRQPPMSLAEAEQLMEEW
NEDLDGMEGFVLEGKKFARLPEEEFGHFYTQDCYVFLCRYWVPVEYEEEEKKEDKEEKAE
GKEGEEATAEAEEKQPEEDFQCIVYFWQGREASNMGWLTFTFSLQKKFESLFPGKLEVVR
MTQQQENPKFLSHFKRKFIIHRGKRKAVQGAQQPSLYQIRTNGSALCTRCIQINTDSSLL
NSEFCFILKVPFESEDNQGIVYAWVGRASDPDEAKLAEDILNTMFDTSYSKQVINEGEEP
ENFFWVGIGAQKPYDDDAEYMKHTRLFRCSNEKGYFAVTEKCSDFCQDDLADDDIMLLDN
GQEVYMWVGTQTSQVEIKLSLKACQVYIQHMRSKEHERPRRLRLVRKGNEQHAFT
RCFHA
WSAFCKALA
Sequence length 1269
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019
Brachydactyly Brachydactyly rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Hearing loss Conductive hearing loss rs267607135, rs267606855, rs779841884, rs267606854, rs28942097, rs121908073, rs121908076, rs74315289, rs121908144, rs111033313, rs74315437, rs121908348, rs121908349, rs121908350, rs397515359
View all (184 more)
Unknown
Disease term Disease name Evidence References Source
Otitis media Chronic otitis media ClinVar
Cardiomyopathy cardiomyopathy, dilated, 2j GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenomatous Polyposis Coli Associate 23106643
Breast Neoplasms Inhibit 17172821
Carcinogenesis Associate 12086853, 23527175
Disease Inhibit 37033921
Melanoma Associate 29048432
Menkes Kinky Hair Syndrome Associate 7703487
Neoplasms Associate 35298000, 36615603
Sarcoma Associate 35238118
Sarcoma Ewing Associate 12086853, 18626011, 19920188, 22749036, 23527175, 24812032, 25025207, 27792997, 28720588, 28847958, 29091716, 29358035, 32658189, 32842875, 34145397
View all (3 more)
Thrombocytopenia Associate 7703487