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.

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 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
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