Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
222553
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 35 member F1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC35F1
Synonyms (NCBI Gene) Gene synonyms aliases
C6orf169, dJ230I3.1
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q22.2-q22.31
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620349 21483 ENSG00000196376
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Hypertension Hypertension (confirmatory factor analysis Factor 12) N/A N/A GWAS
Hypertrophic cardiomyopathy Hypertrophic cardiomyopathy N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Epilepsy Associate 24824130
Glomerulonephritis Membranous Associate 40018947
HIV Infections Associate 21897333
Seizures Associate 24824130
Tremor Associate 24824130