Gene Gene information from NCBI Gene database.
Entrez ID 118611
Gene name Chromosome 10 open reading frame 90
Gene symbol C10orf90
Synonyms (NCBI Gene)
FATSbA422P15.2
Chromosome 10
Chromosome location 10q26.2
miRNA miRNA information provided by mirtarbase database.
14
miRTarBase ID miRNA Experiments Reference
MIRT829322 hsa-miR-1280 CLIP-seq
MIRT829323 hsa-miR-1825 CLIP-seq
MIRT829324 hsa-miR-199a-5p CLIP-seq
MIRT829325 hsa-miR-199b-5p CLIP-seq
MIRT829326 hsa-miR-2355-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0000209 Process Protein polyubiquitination ISS
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IDA 20844083
GO:0005737 Component Cytoplasm IEA
GO:0005813 Component Centrosome IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617735 26563 ENSG00000154493
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96M02
Protein name (E2-independent) E3 ubiquitin-conjugating enzyme FATS (EC 2.3.2.-) (Centrosomal protein C10orf90) (E2/E3 hybrid ubiquitin-protein ligase FATS) (Fragile-site associated tumor suppressor homolog) (FATS)
Protein function Tumor suppressor that is required to sustain G2/M checkpoint after DNA damage. Acts as a p53/TP53 activator by inhibiting MDM2 binding to p53/TP53 and stimulating non-proteolytic polyubiquitination of p53/TP53. Exhibits ubiquitin ligase (E3) act
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17730 Centro_C10orf90 52 563 Centrosomal C10orf90 Family
PF15309 ALMS_motif 567 697 ALMS motif Family
Sequence
Sequence length 699
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Benign rs74814928 RCV005908782
Nonpapillary renal cell carcinoma Benign rs74814928 RCV005908783
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alcohol Related Disorders Associate 26223354
Breast Neoplasms Associate 26223354, 28402275
Carcinogenesis Associate 26223354, 28402275
Carcinoma Non Small Cell Lung Inhibit 33037185
Colorectal Neoplasms Inhibit 39408824
Melanoma Associate 30672666
Neoplasm Metastasis Associate 30672666
Neoplasms Associate 28402275
Neoplasms Inhibit 30672666, 33037185, 34769520, 39408824
Pinguecula Inhibit 34769520