NUFIP2 (nuclear FMR1 interacting protein 2)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57532
Gene name Gene Name - the full gene name approved by the HGNC.
Nuclear FMR1 interacting protein 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NUFIP2
Synonyms (NCBI Gene) Gene synonyms aliases
182-FIP, 82-FIP, FIP-82, NUFP2, PIG1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q11.2
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(3245)
miRTarBase ID miRNA Experiments Reference
MIRT005142 hsa-miR-30a-5p pSILAC 18668040
MIRT016195 hsa-miR-590-3p Sequencing 20371350
MIRT019613 hsa-miR-340-5p Sequencing 20371350
MIRT021149 hsa-miR-186-5p Sequencing 20371350
MIRT021672 hsa-miR-140-3p Sequencing 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(15)
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0003723 Function RNA binding IBA 21873635
GO:0003723 Function RNA binding IDA 12837692
GO:0005515 Function Protein binding IPI 12837692, 16407062, 25416956, 26184334, 28514442, 32296183, 32814053
GO:0005634 Component Nucleus IDA 12837692, 26184334
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
609356 17634 ENSG00000108256
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q7Z417
Protein name FMR1-interacting protein NUFIP2 (82 kDa FMRP-interacting protein) (82-FIP) (Cell proliferation-inducing gene 1 protein) (FMRP-interacting protein 2) (Nuclear FMR1-interacting protein 2)
Protein function Binds RNA.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15293 NUFIP2 89 → 688 Nuclear fragile X mental retardation-interacting protein 2 Family
Sequence
Sequence length 695
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Causal Diseases (1)
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)		 23333116
Show/Hide Unknown Diseases (2)
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Gout Gout GWAS
Show/Hide Text Mining Associations (19)
Associations from Text Mining
Disease Name Relationship Type References
Abnormalities Drug Induced Associate 20439717
Alzheimer Disease Associate 37440991
Arthritis Rheumatoid Associate 33482886
Attention Deficit Disorder with Hyperactivity Associate 32460900
Autism Spectrum Disorder Associate 24267887, 27260404, 28344757, 32243819
Autistic Disorder Associate 27260404, 30664714, 36070702
Down Syndrome Associate 36070702
Fragile X Syndrome Inhibit 15649335
Fragile X Syndrome Associate 16407062, 23912948, 32460900, 32525608, 34312401, 36070702
Intellectual Disability Associate 33149277