SLC22A17 (solute carrier family 22 member 17)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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51310 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Solute carrier family 22 member 17 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SLC22A17 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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24p3R, BOCT, BOIT, NGALR, NGALR2, NGALR3, hBOIT |
Chromosome
Chromosome number
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14 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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14q11.2 |
miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein | |||||||||||
UniProt ID | 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
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Tissue specificity | TISSUE SPECIFICITY: Expressed in brain. | ||||||||||
Sequence |
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Sequence length | 538 | ||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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