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bn:00193010n
Noun Named Entity
Categories: Amphetamine, Solute carrier family, Genes on human chromosome 5
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

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