Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
283777
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 169 member B, pseudogene
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM169BP
Synonyms (NCBI Gene) Gene synonyms aliases
FAM169B
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q26.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT640286 hsa-miR-8485 HITS-CLIP 23824327
MIRT640285 hsa-miR-3607-5p HITS-CLIP 23824327
MIRT640284 hsa-miR-5681a HITS-CLIP 23824327
MIRT640283 hsa-miR-6730-5p HITS-CLIP 23824327
MIRT640282 hsa-miR-488-3p HITS-CLIP 23824327
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 Q8N8A8
Protein name Protein FAM169BP (FAM169BP pseudogene)
Family and domains
Sequence
MKVQSFGERVVLFILNAIIFGRLERNLDDDDMFFLPHSVKEQAKILWRRGAAVGFYTTKM
KGRLCGDGTGACYLLPVFDTVFIRRKHWHRGLGTAMLRDFCETFPEDEALGVSCSMSPAM
YQAHPGNSEDVSRHARTSQNDRPRQPAPGDGSKERMCGEELEDTKDDPECGVEEEDAGLA
GQPPGKLTRSSP
Sequence length 192
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
Dementia Dementia N/A N/A GWAS