Gene Gene information from NCBI Gene database.
Entrez ID 200030
Gene name NBPF member 11
Gene symbol NBPF11
Synonyms (NCBI Gene)
NBPF24
Chromosome 1
Chromosome location 1q21.2
miRNA miRNA information provided by mirtarbase database.
824
miRTarBase ID miRNA Experiments Reference
MIRT569394 hsa-miR-3617-5p PAR-CLIP 20371350
MIRT569393 hsa-miR-641 PAR-CLIP 20371350
MIRT569392 hsa-miR-1324 PAR-CLIP 20371350
MIRT569391 hsa-miR-8060 PAR-CLIP 20371350
MIRT569390 hsa-miR-1250-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614001 31993 ENSG00000263956
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86T75
Protein name NBPF family member NBPF11 (Neuroblastoma breakpoint family member 11) (Neuroblastoma breakpoint family member 24)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06758 Olduvai 178 240 Olduvai domain Domain
PF06758 Olduvai 449 511 Olduvai domain Domain
PF06758 Olduvai 535 597 Olduvai domain Domain
PF06758 Olduvai 607 672 Olduvai domain Domain
PF06758 Olduvai 682 747 Olduvai domain Domain
PF06758 Olduvai 757 821 Olduvai domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in spinal cord. {ECO:0000269|PubMed:16079250}.
Sequence
MVVSAGPWSSEKAEMNILEINEKLRPQLAENKQQFRNLKERCFLTQLAGFLANRQKKYKY
EECKDLIKFMLRNERQFKEEKLAEQLKQAEELRQYKVLVHSQERELTQLREKLREGRDAS
RSLNEHLQALLTPDEPDKSQGQDLQEQLAEGCRLAQHLVQKLSPENDEDEDEDVQVEEDE
KVLESSAPREVQKAEESKVPEDSLEECAITCSNSHGPCDSIQPHKNIKITFEEDKVNSSL

VVDRESSHDGCQDALNILPVPGPTSSATNVSMVVSAGPLSSEKAEMNILEINEKLCPQLA
EKKQQFRSLKEKCFVTQVACFLAKQQNKYKYEECKDLIKSMLRNERQFKEEKLAEQLKQA
EELRQYKVLVHSQERELTQLREKLREGRDASRSLNEHLQALLTPDEPDKSQGQDLQEQLA
EGCRLAQHLVQKLSPENDNDDDEDVQVEVAEKVQKSSSPREMQKAEEKEVPEDSLEECAI
TCSNSHGPYDSNQPHRKTKITFEEDKVDSTL
IGSSSHVEWEDAVHIIPENESDDEEEEEK
GPVSPRNLQESEEEEVPQESWDEGYSTLSIPPERLASYQSYSSTFHSLEEQQVCMAV
DIG
RHRWDQVKKEDQEATGPRLSRELLDEKEPEVLQDSLDRCYSTPSVYLGLTDSCQPYRSAF
YVLEQQRIGLAV
DMDEIEKYQEVEEDQDPSCPRLSRELLAEKEPEVLQDSLDRCYSTPSG
YLELPDLGQPYRSAVYSLEEQYLGLAL
DVDRIKKDQEEEEDQGPPCPRLSRELLEVVEPE
VLQDSLDVIQLLPVVLNSLTPASPTEVPFMHWRKNMLAFLL
TWEKLKRRGRGRKEGEEDQ
RRKEEGEEKKGKKIKTHHAPGSAAC
Sequence length 865
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations