Entrez Summary: The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008].
UniProt Summary: Required for the uptake of creatine in muscles and brain.
Pfam DomainsGO Terms
Pfam Domains
SNF
GO Terms
creatine:sodium symporter activity
creatine transmembrane transporter activity
creatine transmembrane transport
choline transmembrane transporter activity
creatine metabolic process
choline transport
neurotransmitter:sodium symporter activity
modified amino acid transport
organic cation transport
ammonium transport
drug transmembrane transport
carboxylic acid transmembrane transport
organic acid transmembrane transport
monocarboxylic acid transport
drug transport
sodium ion transport
neurotransmitter transport
cellular modified amino acid metabolic process
muscle contraction
anion transmembrane transport
carboxylic acid transport
organic acid transport
muscle system process
monovalent inorganic cation transport
organic anion transport
drug metabolic process
monocarboxylic acid metabolic process
anion transport
metal ion transport
molecular function
cation transport
carboxylic acid metabolic process
ion transmembrane transport
oxoacid metabolic process
response to drug
organic acid metabolic process
transmembrane transport
ion transport
integral component of plasma membrane
small molecule metabolic process
nitrogen compound transport
system process
CRISPR Data
Compound HitMost Correlated Genes in ChemogenomicsTissues where Essential in the Avana Dataset (DepMap 20Q1)
Compound Hit
No hits were found.
Most Correlated Genes in Chemogenomics
No correlation found to any other genes in chemogenomics.
Tissues where Essential in the Avana Dataset (DepMap 20Q1)
Global Fraction of Cell Lines Where Essential: 0/694