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Gene Gene information from NCBI Gene database.
Entrez ID 84804
Gene name Solute carrier family 67 member 2
Gene symbol SLC67A2
Synonyms (NCBI Gene)
MFSD9
Chromosome 2
Chromosome location 2q12.1
miRNA miRNA information provided by mirtarbase database.
344 Show/Hide all (344)
miRTarBase ID miRNA Experiments Reference
MIRT029603 hsa-miR-26b-5p Microarray 19088304
MIRT561950 hsa-miR-4311 PAR-CLIP 20371350
MIRT561949 hsa-miR-1276 PAR-CLIP 20371350
MIRT561948 hsa-miR-583 PAR-CLIP 20371350
MIRT561947 hsa-miR-548a-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IEA
GO:0055085 Process Transmembrane transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620301 28158 ENSG00000135953
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NBP5
Protein name Major facilitator superfamily domain-containing protein 9
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 49 → 427 Major Facilitator Superfamily Family
Sequence
Sequence length 474
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
Uterine corpus endometrial carcinoma Uncertain significance 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
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 17846126
★★★★★
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer UNIPROT_DG
★★★★★
★☆☆☆☆
Found in Text Mining only