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Descriptor English: Solute Carrier Family 22 Member 5
Descriptor Spanish: Miembro 5 de la Familia 22 de Transportadores de Solutos
Descriptor miembro 5 de la familia 22 de transportadores de solutos
Entry term(s) cotransportador de carnitina dependiente de sodio
proteína OCTN2
proteína SLC22A5
transportador 2 de cationes orgánicos de carnitina
transportador de carnitina de alta afinidad
Scope note: Cotransportador de alta afinidad de CARNITINA, que se une a ATP y se expresa ampliamente en los tejidos del riñón, músculo esquelético, corazón y placenta. Transporta un ión sodio junto a una molécula de carnitina. Tiene menor afinidad por otros cationes orgánicos y los transporta independientemente del sodio. Las mutaciones del gen SLC22A5 se asocian a la deficiencia sistémica de carnitina.
Descriptor Portuguese: Membro 5 da Família 22 de Carreadores de Soluto
Descriptor French: Membre-5 de la famille-22 de transporteurs de solutés
Entry term(s): Carnitine Cotransporter, Sodium-Dependent
Carnitine Transporter, High-Affinity
High Affinity Carnitine Transporter
High-Affinity Carnitine Transporter
OCTN2 Protein
Organic Cation Carnitine Transporter 2
Organic Cation-Carnitine Transporter 2
SLC22A5 Protein
Sodium Dependent Carnitine Cotransporter
Sodium-Dependent Carnitine Cotransporter
Transporter, High-Affinity Carnitine
Tree number(s): D12.776.157.530.450.250.812.750
D12.776.157.530.937.612.750
D12.776.543.585.450.250.812.750
D12.776.543.585.937.701.750
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000074058
Scope note: A high-affinity, ATP-binding, co-transporter for CARNITINE that is highly expressed in kidney, skeletal muscle, heart, and placental tissues. It transports one sodium ion with one carnitine molecule. It has a lower affinity for other organic cations and transports them independently of sodium. Mutations in the SLC22A5 gene are associated with systemic carnitine deficiency.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Previous Indexing: Carrier Proteins (1998-2017)
Organic Cation Transport Proteins (2004-2017)
Public MeSH Note: 2018
History Note: 2018
DeCS ID: 57087
Unique ID: D000074058
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2018/01/01
Date of Entry: 2017/07/11
Revision Date: 2017/03/31
Solute Carrier Family 22 Member 5 - Preferred
Concept UI M000625386
Scope note A high-affinity, ATP-binding, co-transporter for CARNITINE that is highly expressed in kidney, skeletal muscle, heart, and placental tissues. It transports one sodium ion with one carnitine molecule. It has a lower affinity for other organic cations and transports them independently of sodium. Mutations in the SLC22A5 gene are associated with systemic carnitine deficiency.
Preferred term Solute Carrier Family 22 Member 5
Entry term(s) Carnitine Cotransporter, Sodium-Dependent
Carnitine Transporter, High-Affinity
High Affinity Carnitine Transporter
High-Affinity Carnitine Transporter
OCTN2 Protein
Organic Cation Carnitine Transporter 2
Organic Cation-Carnitine Transporter 2
SLC22A5 Protein
Sodium Dependent Carnitine Cotransporter
Sodium-Dependent Carnitine Cotransporter
Transporter, High-Affinity Carnitine



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