Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55007
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 118 member A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM118A
Synonyms (NCBI Gene) Gene synonyms aliases
C22orf8
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023325 hsa-miR-122-5p Microarray 17612493
MIRT029381 hsa-miR-26b-5p Microarray 19088304
MIRT043956 hsa-miR-378a-3p CLASH 23622248
MIRT707705 hsa-miR-548c-3p HITS-CLIP 21572407
MIRT707704 hsa-miR-6732-3p 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:0005515 Function Protein binding IPI 25416956, 29892012, 31515488, 32296183
GO:0016020 Component Membrane IEA
GO:0042802 Function Identical protein binding IPI 25416956, 32296183
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 Q9NWS6
Protein name Protein FAM118A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13289 SIR2_2 142 284 SIR2-like domain Family
Sequence
MDSVEKTTNRSEQKSRKFLKSLIRKQPQELLLVIGTGVSAAVAPGIPALCSWRSCIEAVI
EAAEQLEVLHPGDVAEFRRKVTKDRDLLVVAHDLIRKMSPRTGDAKPSFFQDCLMEVFDD
LEQHIRSPVVLQSILSLMDRGAMVLTTNYDNLLEAFGRRQNKPMESLDLKDKTKVLEWAR
GHMKYGVLHIHGLYTDPCGVVLDPSGYKDVTQDAEVMEVLQNLYRTKSFLFVGCGETLRD
QIFQALFLYSVPNKVDLEHYMLVLKENEDHFFKHQADMLLHGIK
VVSYGDCFDHFPGYVQ
DLATQICKQQSPDADRVDSTTLLGNACQDCAKRKLEENGIEVSKKRTQSDTDDAGGS
Sequence length 357
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
Colorectal Cancer Distal colorectal cancer N/A N/A GWAS
Dental caries Dental caries N/A N/A GWAS
Prostate cancer Prostate cancer N/A N/A GWAS