Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
158293
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 120 member A opposite strand
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM120AOS
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf10OS
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q22.31
Summary Summary of gene provided in NCBI Entrez Gene.
Differences in the expression level of this gene are associated with the survival rate of those with glioma. [provided by RefSeq, May 2017]
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs140119177 G>A Likely-pathogenic Coding sequence variant, non coding transcript variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT026475 hsa-miR-192-5p Microarray 19074876
MIRT674231 hsa-miR-130a-3p HITS-CLIP 23824327
MIRT674230 hsa-miR-130b-3p HITS-CLIP 23824327
MIRT674229 hsa-miR-301a-3p HITS-CLIP 23824327
MIRT674228 hsa-miR-301b-3p 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 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 Q5T036
Protein name Uncharacterized protein FAM120AOS (FAM120A opposite strand protein)
Family and domains
Sequence
MGKTKDIGDDDTVASEFWSGALSQPSSVPTRPRTPNRDSWRRAWAARGLHPRPSILQPGP
ARLSRARAGGTRCPQRRHGRATFCALGRGIGVRRGPGPRPARIPGLTLTWKRMSARRMQW
AMQTGGRNQTFGGGVPLFWTWLTICCAVWRSLPCRLTHSCSRAFSSAPLKKTKSSMLPPK
QALASAARNLCRGAGCNRQAVAGQLLPSTWSLHAHGLAKEAPILPVKKISRSCSVNNKVS
KKTTKPPTLRSFLSPI
Sequence length 256
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cutis laxa Cutis Laxa rs80356758, rs80356750, rs119489101, rs119489102, rs193302865, rs121918374, rs121918375, rs1598354372, rs1371235353, rs1598358449, rs121918376, rs121918377, rs121918378, rs137854453, rs1797225811
View all (31 more)
Scoliosis Scoliosis, unspecified rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085
Unknown
Disease term Disease name Evidence References Source
Neuroticism Neuroticism GWAS
Insomnia Insomnia GWAS