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FAM120AOS (family with sequence similarity 120 member A opposite strand)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
158293
Gene nameGene Name - the full gene name approved by the HGNC.
Family with sequence similarity 120 member A opposite strand
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
FAM120AOS
SynonymsGene synonyms aliases
C9orf10OS
ChromosomeChromosome number
9
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q22.31
SummarySummary 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]
SNPsSNP 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
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Causal
Disease name Disease term dbSNP ID References
Cutis laxa Cutis Laxa rs80356758, rs80356750, rs119489101, rs119489102, rs193302865, rs121918374, rs121918375, rs1598354372, rs1371235353, rs1598358449, rs121918376, rs121918377, rs121918378, rs137854453, rs1797225811, rs80356756, rs367543007, rs80356751, rs80356753, rs193302868, rs193302867, rs193302869, rs193302870, rs193302864, rs193302866, rs1566294545, rs397514683, rs794729201, rs752669339, rs863225044, rs863225045, rs886039351, rs745590426, rs144346996, rs1060505031, rs1028534806, rs1060505037, rs139751598, rs762218403, rs755867227, rs1555042727, rs888015688, rs1591064775, rs1598358440, rs752297179, rs1180294322
Scoliosis Scoliosis, unspecified rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085
Unknown
Disease name Disease term dbSNP ID References
Congenital pectus excavatum Congenital pectus excavatum
Lung diseases Chronic lung disease

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