Gene Gene information from NCBI Gene database.
Entrez ID 162387
Gene name Major facilitator superfamily domain containing 6 like
Gene symbol MFSD6L
Synonyms (NCBI Gene)
SLC73A2
Chromosome 17
Chromosome location 17p13.1
miRNA miRNA information provided by mirtarbase database.
31
miRTarBase ID miRNA Experiments Reference
MIRT017180 hsa-miR-335-5p Microarray 18185580
MIRT1146566 hsa-miR-3682-5p CLIP-seq
MIRT1551291 hsa-miR-214 CLIP-seq
MIRT1551292 hsa-miR-3619-5p CLIP-seq
MIRT1551293 hsa-miR-3909 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
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.
Q8IWD5
Protein name Major facilitator superfamily domain-containing protein 6-like
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12832 MFS_1_like 17 526 MFS_1 like family Family
Sequence
Sequence length 586
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CATARACT Disgenet
Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SQUAMOUS CELL LUNG CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Cataract Associate 22935719
★★☆☆☆
Found in Text Mining + Unknown/Other Associations