Gene Gene information from NCBI Gene database.
Entrez ID 51310
Gene name Solute carrier family 22 member 17
Gene symbol SLC22A17
Synonyms (NCBI Gene)
24p3RBOCTBOITNGALRNGALR2NGALR3hBOIT
Chromosome 14
Chromosome location 14q11.2
miRNA miRNA information provided by mirtarbase database.
71
miRTarBase ID miRNA Experiments Reference
MIRT675003 hsa-miR-3529-3p HITS-CLIP 23824327
MIRT675002 hsa-miR-5195-5p HITS-CLIP 23824327
MIRT675003 hsa-miR-3529-3p HITS-CLIP 23824327
MIRT675002 hsa-miR-5195-5p HITS-CLIP 23824327
MIRT1354387 hsa-miR-1257 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0004888 Function Transmembrane signaling receptor activity ISS
GO:0005515 Function Protein binding IPI 32814053
GO:0005773 Component Vacuole IEA
GO:0005774 Component Vacuolar membrane IEA
GO:0005886 Component Plasma membrane IDA 17253959
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611461 23095 ENSG00000092096
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WUG5
Protein name Solute carrier family 22 member 17 (24p3 receptor) (24p3R) (Brain-type organic cation transporter) (Lipocalin-2 receptor) (Neutrophil gelatinase-associated lipocalin receptor) (NgalR)
Protein function Cell surface receptor for LCN2 (24p3) that plays a key role in iron homeostasis and transport. Able to bind iron-bound LCN2 (holo-24p3), followed by internalization of holo-24p3 and release of iron, thereby increasing intracellular iron concentr
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 89 507 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain.
Sequence
Sequence length 538
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Iron uptake and transport
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 Evidence Score
LARGE ARTERY STROKE 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
ANOPHTHALMIA AND PULMONARY HYPOPLASIA Syndromic microphthalmia BEFREE 28249896
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 19047093
★☆☆☆☆
Found in Text Mining only
Conventional (Clear Cell) Renal Cell Carcinoma Renal Carcinoma BEFREE 30138675
★☆☆☆☆
Found in Text Mining only
Esophageal carcinoma Esophageal Carcinoma BEFREE 17253959, 19047093
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 21184133
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 22728279
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of esophagus Esophagus Neoplasm GWASDB_DG 21642993
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 22728279
★☆☆☆☆
Found in Text Mining only
Melanoma Cutaneous Malignant Melanoma Pubtator 39358721 Inhibit
★☆☆☆☆
Found in Text Mining only
Myeloid Leukemia, Chronic Myeloid Leukemia BEFREE 19047093, 21950422
★☆☆☆☆
Found in Text Mining only