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Gene Gene information from NCBI Gene database.
Entrez ID 139231
Gene name Family with sequence similarity 199, X-linked
Gene symbol FAM199X
Synonyms (NCBI Gene)
CXorf39
Chromosome X
Chromosome location Xq22.2
miRNA miRNA information provided by mirtarbase database.
712 Show/Hide all (712)
miRTarBase ID miRNA Experiments Reference
MIRT020714 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT021764 hsa-miR-132-3p Microarray 17612493
MIRT022514 hsa-miR-124-3p Microarray 18668037
MIRT026364 hsa-miR-192-5p Microarray 19074876
MIRT046073 hsa-miR-125b-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27705803, 32296183, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6PEV8
Protein name Protein FAM199X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15814 FAM199X 66 → 388 Protein family FAM199X Family
Sequence
Sequence length 388
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Connective Tissue Diseases Connective tissue disease Pubtator 22208759 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only