Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
113828
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 83 member F
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM83F
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT720265 hsa-miR-483-3p HITS-CLIP 19536157
MIRT720265 hsa-miR-483-3p HITS-CLIP 19536157
MIRT720264 hsa-miR-6887-3p HITS-CLIP 19536157
MIRT720263 hsa-miR-6795-3p HITS-CLIP 19536157
MIRT720262 hsa-miR-4667-3p 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 29789297
GO:0005886 Component Plasma membrane IEA
GO:0007165 Process Signal transduction IBA
GO:0016020 Component Membrane IEA
GO:0019901 Function Protein kinase binding IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q8NEG4
Protein name Protein FAM83F
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07894 FAM83 15 297 FAM83 A-H Family
Sequence
MAESQLNCLDEAHVNEKVTEAQAAFYYCERRRAALEALLGGGEQAYRERLKEEQLRDFLS
SPERQALRAAWSPYEDAVPAANARGKSKAKAKAPAPAPAESGESLAYWPDRSDTEVPPLD
LGWTDTGFYRGVSRVTLFTHPPKDEKAPHLKQVVRQMIQQAQKVIAVVMDLFTDGDIFQD
IVDAACKRRVPVYIILDEAGVKYFLEMCQDLQLTDFRIRNIRVRSVTGVGFYMPMGRIKG
TLSSRFLMVDGDKVATGSYRFTWSSSHVDRNLLLLLTGQNVEPFDTEFRELYAISEE
VDL
YRQLSLAGRVGLHYSSTVARKLINPKYALVSGCRHPPGEMMRWAARQQREAGGNPEGQEE
GASGGESAWRLESFLKDLVTVEQVLPPVEPIPLGELSQKDGRMVSHMHRDLKPKSREAPS
RNGMGEAARGEAAPARRFSSRLFSRRAKRPAAPNGMASSVSTETSEVEFLTGKRPNENSS
ADISGKTSPSSAKPSNCVIS
Sequence length 500
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Prostate cancer Prostate cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 35650627
Carcinoma Non Small Cell Lung Associate 30280778
Esophageal Squamous Cell Carcinoma Associate 26758433, 28770965
Glioma Associate 30556880
Neoplasms Associate 26758433, 35650627
Sarcoma Associate 28088687