SLC22A15 - solute carrier family 22 member 15 Gene

Homo sapiens

Also known as FLIPT1; PRO34686

Gene ID: 55356 | Gene type: protein coding

About SLC22A15

Cytogenetic location: 1p13.1 Genomic coordinates (GRCh38): 1:115,976,513-116,070,054 (from NCBI)

This gene has 3 transcripts (splice variants), 188 orthologues and 22 paralogues. Broad expression in bone marrow (RPKM 6.8), skin (RPKM 3.1) and 19 other tissues.

Summary

Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, Hormones, neurotransmitters, and cellular metabolites. These transporters are also referred to as amphiphilic solute facilitators (ASFs).[supplied by OMIM, Apr 2004]

SLC22A15 Products(1)

mRNA	Protein	Name
NM_018420.3	NP_060890.2	solute carrier family 22 member 15

SLC22A15 Protein Structure

Sugar_tr

0
100
200
300
400
500
547 a.a.

Protein Preferred Names

Protein Names

solute carrier family 22 member 15

flipt 1

Related Diseases

Diseases

Alias

Carnitine Deficiency, Systemic Primary

Carnitine Uptake Defect	Renal Carnitine Transport Defect
Systemic Primary Carnitine Deficiency	CDSP
Systemic Carnitine Deficiency	Carnitine Transporter Deficiency
Cud	Primary Carnitine Deficiency
Carnitine Uptake Deficiency	Carnitine Deficiency, Systemic, Due To Defect In Renal Reabsorption Of Carnitine
Carnitine Deficiency, Primary	Systemic Primary Carnitine Deficiency Disease
Deficiency Of Plasma-Membrane Carnitine Transporter	Scd
Carnitine Transporter, Plasma-Membrane, Deficiency Of	Carnitine Transport Defect
Carnitine Plasma-Membrane Transporter Deficiency	Carnitine Transporter Defect
Spcd

Adams-Oliver Syndrome

Adams Oliver Syndrome	Aos
Congenital Scalp Defects With Distal Limb Reduction Anomalies	Aplasia Cutis Congenita With Terminal Transverse Limb Defects
Congenital Scalp Defects With Distal Limb Anomalies	Limb, Scalp And Skull Defects
Limb Scalp And Skull Defects	Absence Defect Of Limbs, Scalp, And Skull

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13068	SLC22A15 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLC22A15	RGD	RGD:1311184
Macaca mulatta	SLC22A15	VGNC	VGNC:77526
Mus musculus	SLC22A15	MGD	MGI:3607704
Canis familiaris	SLC22A15	VGNC	VGNC:46276
Felis catus	SLC22A15	VGNC	VGNC:65240
Bos taurus	SLC22A15	VGNC	VGNC:34723

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