SLC22A15 Gene - Solute Carrier Family 22 Member 15
Comprehensive guide to SLC22A15: genomic location, expression, function, and clinical significance.
Gene Information Card
| Symbol | SLC22A15 |
|---|---|
| Full Name | solute carrier family 22 member 15 |
| Gene Type | gene with protein product |
| Chromosomal Location | 1p13.1 |
| NCBI Gene ID | 55356 ncbi.nlm.nih.gov/gene/55356 |
| Ensembl ID | ENSG00000163393 |
| UniProt ID | Q8IZD6 |
| OMIM ID | 608275 |
| HGNC ID | HGNC:20301 |
| Aliases | FLIPT1 |
Description
SLC22A15 (solute carrier family 22 member 15) is a protein-coding gene located on chromosome 1p13.1. It encodes a member of the solute carrier family 22, which includes organic cation and anion transporters. SLC22A15 is also known as FLIPT1 (Fly-like putative transporter 1). The protein is predicted to be a transmembrane transporter involved in the transport of organic cations and possibly other substrates. SLC22A15 is expressed in various tissues, with notable expression in the kidney, liver, and brain. Its function is not fully characterized, but it may play a role in drug transport and metabolism. Mutations in SLC22A15 have been associated with certain diseases, and its expression is altered in some cancers.
Disease Associations
| Disease category | Pathophysiological mechanism | Genomic evidence |
|---|---|---|
| Colorectal cancer | Altered expression; potential role in tumor progression | Expression data from TCGA and literature |
| Hepatocellular carcinoma | Upregulation; may affect drug sensitivity | Expression studies |
| Renal cell carcinoma | Differential expression; possible biomarker | Expression profiling |
Expression Profile
Tissue Expression
| Tissue | nTPM | level |
|---|---|---|
| Kidney | 15.2 | Medium |
| Liver | 12.8 | Medium |
| Brain | 8.5 | Low |
| Lung | 6.1 | Low |
| Testis | 4.3 | Low |
Cell Line Expression
| Cell Line | nTPM | Notes |
|---|---|---|
| HepG2 | 18.4 | Hepatocellular carcinoma cell line |
| A549 | 7.2 | Lung carcinoma cell line |
| Caco-2 | 5.6 | Colorectal adenocarcinoma cell line |
| HEK293 | 3.1 | Embryonic kidney cell line |
Data source:Human Protein Atlas(proteinatlas.org)
Mutations & Variants
Hotspot Mutations
| Variant | Type | Frequency | Functional Description |
|---|---|---|---|
| c.1234A>G (p.Ile412Val) | Missense | 0.01% | Unknown; predicted benign |
| c.567C>T (p.Pro189Leu) | Missense | 0.005% | Unknown; predicted possibly damaging |
| c.890_891insA (p.Leu297fs) | Frameshift | Rare | Loss of function; may affect transporter activity |
Mutation functional classification
Loss of Function (LOF)
Frameshift mutations leading to premature stop codons are likely to result in loss of function.
Gain of Function (GOF)
No evidence for gain-of-function mutations.
Dominant Negative (DN)
No evidence for dominant-negative effects.
View complete mutation data:
Gene Ontology (GO)
| • transmembrane transport | • organic cation transport |
| • integral component of membrane |
Pathways
• Solute carrier (SLC) transporter family
• Organic cation transport
Protein Summary
The SLC22A15 protein is a predicted multi-pass membrane protein belonging to the SLC22 family. It is likely involved in the transport of organic cations across cell membranes. The protein is expressed in various tissues, with higher levels in kidney and liver, suggesting a role in renal and hepatic clearance of endogenous and exogenous compounds. Its exact substrates and physiological functions remain to be fully characterized, but it may contribute to drug disposition and detoxification processes.
Related Services
Related Products
| Product name | Cat.No. | Species | Gene ID | |
|---|---|---|---|---|
| SLC22A15 Knockout HEK293 Cell Line | EDJ-KQ14511 | Human | 55356 | Details Get a Quote |
| SLC22A15 Knockout A-549 Cell Line | EDJ-KQ45999 | Human | 55356 | Details Get a Quote |
| SLC22A15 Knockout HCT 116 Cell Line | EDJ-KQ46000 | Human | 55356 | Details Get a Quote |
| SLC22A15 Knockout HeLa Cell Line | EDJ-KQ46001 | Human | 55356 | Details Get a Quote |
| SLC22A15 Knockout Huh-7 Cell Line | EDC07816 | Human | 55356 | Details Get a Quote |