Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100132406
Gene name Gene Name - the full gene name approved by the HGNC.
NBPF member 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NBPF10
Synonyms (NCBI Gene) Gene synonyms aliases
AB6, AG1, NBPF9
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q21.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT541948 hsa-miR-8485 HITS-CLIP 21572407
MIRT707288 hsa-miR-329-3p HITS-CLIP 21572407
MIRT707287 hsa-miR-362-3p HITS-CLIP 21572407
MIRT541947 hsa-miR-603 HITS-CLIP 21572407
MIRT707286 hsa-miR-4789-3p HITS-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22681889
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614000 31992 ENSG00000271425
Protein
UniProt ID Q6P3W6
Protein name NBPF family member NBPF10 (Neuroblastoma breakpoint family member 10)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06758 Olduvai 178 240 Olduvai domain Domain
PF06758 Olduvai 450 511 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 757 822 Olduvai domain Domain
Sequence
MVVSAGPWSSEKAEMNILEINEKLRPQLAENKQQFGNLKERCFVTQLAGFLANQQKKYNY
EECKDLIKFMLRNERQFKEEKLAEQLKQAEELRQYKVLVHSQERELTQLREKLREGRDAS
RSLNEHLQALLTLDEPDKSQGQDLQEQLAEGCRLAQHLVQKLSPENDEDEDEDVQVEEAE
KVQKSSAPREVQKTEESKVPEDSLEECAITCSNSHGPCDSNQPHKNIKITFEEDEVNSTL

VVDRESSHDECQDALNILPVPGPTSSATNVSMVVSAGPLSSEKAEMNILEINEKLHPQLA
EKKQQFRNLKERCFVTQLAGFLANQQKKYKYEECKDLIKSMLRNERQFKEEKLAEQLKQA
EELRQYKVLVHAQERELTQLREKLREGRDASRSLNEHLQALLTPDEPDKSQGQDLQEQLA
EGCRLAQHLVQKLSPENDNDDDEDVQVELAEKVQKSSAPREMQKAEEKEVPEDSQEECAI
TYSNSHGPYDSNQPHRKTKITFEEDKVDSTL
IGSSSHVEWEDAVHIIPENESDDEEEEEK
GPVSPRNLQESEEEEVPQESWDEGYSTLSIPPEMLASYQSYSSTFHSLEEQQVCMAV
DIG
RHRWDQVKKEDQEATGPRLSRELLDEKGPEVLQDSLDRCYSTPSGCLELTDSCQPYRSAF
YVLEQQRVGLAV
DMDEIEKYQEVEEDQDPSCPRLSRELLDEKEPEVLQDSLDRCYSTPSG
YLELPDLGQPYSSAVYSLEEQYLGLAL
DVDRTKKDQEEEEDQGPPCPRLSRELLEVVEPE
VLQDSLDRCYSTPSSCLEQPDSCQPYGSSFYALEEKHVGFSL
DVGEIEKKGKGKKRRGRR
S
Sequence length 841
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Unknown
Disease term Disease name Evidence References Source
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Acute Coronary Syndrome Stimulate 30242056
Breast Neoplasms Associate 37454130
Neoplasms Associate 37454130