Gene Gene information from NCBI Gene database.
Entrez ID 54733
Gene name Solute carrier family 35 member F2
Gene symbol SLC35F2
Synonyms (NCBI Gene)
HSNOV1
Chromosome 11
Chromosome location 11q22.3
miRNA miRNA information provided by mirtarbase database.
484
miRTarBase ID miRNA Experiments Reference
MIRT020783 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT027677 hsa-miR-98-5p Microarray 19088304
MIRT712765 hsa-miR-6771-3p HITS-CLIP 19536157
MIRT712764 hsa-miR-1283 HITS-CLIP 19536157
MIRT712763 hsa-miR-7110-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005575 Component Cellular_component ND
GO:0008150 Process Biological_process ND
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620350 23615 ENSG00000110660
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IXU6
Protein name Solute carrier family 35 member F2
Protein function Putative solute transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06027 SLC35F 35 334 Solute carrier family 35 Family
Sequence
Sequence length 374
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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 Evidence Score
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Cell Transformation Neoplastic Stimulate 29274137
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Stimulate 29274137
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 29274137, 33418944, 34815782
★☆☆☆☆
Found in Text Mining only
Non Muscle Invasive Bladder Neoplasms Stimulate 33418944
★☆☆☆☆
Found in Text Mining only
Thyroid Cancer Papillary Associate 29274137
★☆☆☆☆
Found in Text Mining only
Thyroid Neoplasms Associate 29274137
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Associate 33418944
★☆☆☆☆
Found in Text Mining only