Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:00193010n
Noun Named Entity
Categories: Genes on human chromosome 5, Solute carrier family, Amphetamine
EN
SLC22A5  CDSP  OCTN2  solute carrier family 22 member 5
EN
SLC22A5 is a membrane transport protein associated with primary carnitine deficiency. Wikipedia
English:
gene
Definitions
Relations
Sources
EN
SLC22A5 is a membrane transport protein associated with primary carnitine deficiency. Wikipedia
Protein-coding gene in the species Homo sapiens Wikidata
IS A
gene
CHROMOSOME
chromosome 5
FOUND IN TAXON
early modern human
GENETIC ASSOCIATION
asthma
systemic primary carnitine deficiency
Wikipedia
EN
SLC22A5
Wikidata
EN
SLC22A5
Wikipedia Redirections
EN
OCTN2, SLC22A5 (gene)
Wikidata Alias
EN
CDSP, OCTN2, solute carrier family 22 member 5

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License