Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
150864
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 117 member B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM117B
Synonyms (NCBI Gene) Gene synonyms aliases
ALS2CR13
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q33.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003728 hsa-miR-122-5p Luciferase reporter assay, qRT-PCR 19296470
MIRT045030 hsa-miR-186-5p CLASH 23622248
MIRT045030 hsa-miR-186-5p HITS-CLIP 23824327
MIRT628235 hsa-miR-3133 HITS-CLIP 23824327
MIRT606966 hsa-miR-6867-5p HITS-CLIP 23824327
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, 26496610, 27173435, 28514442, 31515488, 32296183, 32814053
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 Q6P1L5
Protein name Protein FAM117B (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 13 protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15388 FAM117 215 529 Protein Family FAM117 Family
Sequence
MSQRVRRNGSPTPAGSLGGGAVATAGGPGSRLQPMRATVPFQLKQQQQQQHGSPTRSGGG
GGGNNNGGCCGGASGPAGGGGGGGPRTASRSTSPTRGGGNAAARTSPTVATQTGASATST
RGTSPTRSAAPGARGSPPRPPPPPPLLGTVSSPSSSPTHLWTGEVSAAPPPARVRHRRRS
PEQSRSSPEKRSPSAPVCKAGDKTRQPSSSPSSIIRRTSSLDTLAAPYLAGHWPRDSHGQ
AAPCMRDKATQTESAWAEEYSEKKKGSHKRSASWGSTDQLKEIAKLRQQLQRSKHSSRHH
RDKERQSPFHGNHAAINQCQAPVPKSALIPVIPITKSTGSRFRNSVEGLNQEIEIIIKET
GEKEEQLIPQDIPDGHRAPPPLVQRSSSTRSIDTQTPGGADRGSNNSSRSQSVSPTSFLT
ISNEGSEESPCSADDLLVDPRDKENGNNSPLPKYATSPKPNNSYMFKREPPEGCERVKVF
EECSPKQLHEIPAFYCPDKNKVNFIPKSGSAFCLVSILKPLLPTPDLTL
KGSGHSLTVTT
GMTTTLLQPIAVASLSTNTEQDRVSRGTSTVMPSASLLPPPEPIEEAEG
Sequence length 589
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Sarcoidosis Sarcoidosis 26051272 ClinVar, GWAS
Myocardial Infarction Myocardial Infarction GWAS
Associations from Text Mining
Disease Name Relationship Type References
Cerebral Small Vessel Diseases Associate 31430377
Sarcoidosis Associate 26051272