Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23360
Gene name Gene Name - the full gene name approved by the HGNC.
Formin binding protein 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FNBP4
Synonyms (NCBI Gene) Gene synonyms aliases
FBP30
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT719586 hsa-miR-211-3p HITS-CLIP 19536157
MIRT719585 hsa-miR-4270 HITS-CLIP 19536157
MIRT719584 hsa-miR-4441 HITS-CLIP 19536157
MIRT719583 hsa-miR-6754-5p HITS-CLIP 19536157
MIRT719582 hsa-miR-139-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 17500595
GO:0016607 Component Nuclear speck IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615265 19752 ENSG00000109920
Protein
UniProt ID Q8N3X1
Protein name Formin-binding protein 4 (Formin-binding protein 30)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00397 WW 218 246 WW domain Domain
PF00397 WW 597 627 WW domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the eye. {ECO:0000269|PubMed:23703728}.
Sequence
MGKKSRAVPGRRPILQLSPPGPRGSTPGRDPEPEPDTEPDSTAAVPSQPAPSAATTTTTA
VTAAAASDDSPSEDEQEAVQEVPRVVQNPPKPVMTTRPTAVKATGGLCLLGAYADSDDDD
NDVSEKLAQSKETNGNQSTDIDSTLANFLAEIDAITAPQPAAPVGASAPPPTPPRPEPKE
AATSTLSSSTSNGTDSTQTSGWQYDTQCSLAGVGIEMGDWQEVWDENTGCYYYWNTQTNE
VTWELP
QYLATQVQGLQHYQPSSVPGAETSFVVNTDIYSKEKTISVSSSKSGPVIAKREV
KKEVNEGIQALSNSEEEKKGVAASLLAPLLPEGIKEEEERWRRKVICKEEPVSEVKETST
TVEEATTIVKPQEIMLDNIEDPSQEDLCSVVQSGESEEEEEQDTLELELVLERKKAELRA
LEEGDGSVSGSSPRSDISQPASQDGMRRLMSKRGKWKMFVRATSPESTSRSSSKTGRDTP
ENGETAIGAENSEKIDENSDKEMEVEESPEKIKVQTTPKVEEEQDLKFQIGELANTLTSK
FEFLGINRQSISNFHVLLLQTETRIADWREGALNGNYLKRKLQDAAEQLKQYEINATPKG
WSCHWDRDHRRYFYVNEQSGESQWEFP
DGEEEEEESQAQENRDETLAKQTLKDKTGTDSN
STESSETSTGSLCKESFSGQVSSSSLMPLTPFWTLLQSNVPVLQPPLPLEMPPPPPPPPE
SPPPPPPPPPPAEDGEIQEVEMEDEGSEEPPAPGTEEDTPLKPSAQTTVVTSQSSVDSTI
SSSSSTKGIKRKATEISTAVVQRSATIGSSPVLYSQSAIATGHQAAGIGNQATGIGHQTI
PVSLPAAGMGHQARGMSLQSNYLGLAAAPAIMSYAECSVPIGVTAPSLQPVQARGAVPTA
TIIEPPPPPPPPPPPPPPAPKMPPPEKTKKGRKDKAKKSKTKMPSLVKKWQSIQRELDEE
DNSSSSEEDRESTAQKRIEEWKQQQLVSGMAERNANFEALPEDWRARLKRRKMAPNT
Sequence length 1017
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Microphthalmia with limb anomalies Waardenburg Anophthalmia Syndrome rs376672665, rs863223317, rs751356341, rs1114167455, rs1566709754, rs1566709825, rs1365818420, rs1326644602, rs370866589
Unknown
Disease term Disease name Evidence References Source
Neuroticism Neuroticism GWAS
Insomnia Insomnia GWAS
Myocardial Infarction Myocardial Infarction GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 25417742
Lymphoma Large B Cell Diffuse Associate 27835906
Myofibroma Associate 33830670