Gene Gene information from NCBI Gene database.
Entrez ID 222553
Gene name Solute carrier family 35 member F1
Gene symbol SLC35F1
Synonyms (NCBI Gene)
C6orf169dJ230I3.1
Chromosome 6
Chromosome location 6q22.2-q22.31
miRNA miRNA information provided by mirtarbase database.
276
miRTarBase ID miRNA Experiments Reference
MIRT052251 hsa-let-7b-5p CLASH 23622248
MIRT467760 hsa-miR-6808-5p PAR-CLIP 23446348
MIRT467759 hsa-miR-6893-5p PAR-CLIP 23446348
MIRT467758 hsa-miR-940 PAR-CLIP 23446348
MIRT505607 hsa-miR-3929 PAR-CLIP 23446348
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28514442, 32296183, 33961781
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IEA
GO:0030672 Component Synaptic vesicle membrane IDA 34269178
GO:0030672 Component Synaptic vesicle membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620349 21483 ENSG00000196376
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T1Q4
Protein name Solute carrier family 35 member F1
Protein function Putative solute transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06027 SLC35F 56 355 Solute carrier family 35 Family
Sequence
Sequence length 408
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
18
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
AORTIC VALVE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
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
Atrial Fibrillation Atrial Fibrillation GWASCAT_DG 28416818, 29892015, 30061737
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atrial Fibrillation Atrial Fibrillation CTD_human_DG 29892015
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Epilepsy Epilepsy BEFREE 24824130
★☆☆☆☆
Found in Text Mining only
Epilepsy Epilepsy Pubtator 24824130 Associate
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 30868340
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 30868340
★☆☆☆☆
Found in Text Mining only
Glomerulonephritis Membranous Membranous glomerulonephritis Pubtator 40018947 Associate
★☆☆☆☆
Found in Text Mining only
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation CTD_human_DG 29892015
★☆☆☆☆
Found in Text Mining only
Seizures Seizures Pubtator 24824130 Associate
★☆☆☆☆
Found in Text Mining only
Tremor Tremor Pubtator 24824130 Associate
★☆☆☆☆
Found in Text Mining only