Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (0) GO Terms (1) Nucleotides (106) Proteins (49) Interactants (10) Wiki
XB-GENEPAGE-973184

slc25a15.2     solute carrier family 25 member 15, gene 2

Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (49 sources): Abnormal circulating citrulline concentration, Abnormal pyramidal sign, Abnormality of the coagulation cascade, Acute encephalopathy, Acute hepatitis, Cerebral cortical atrophy, Chorioretinal atrophy, Chorioretinal hypopigmentation, Clonus, Cognitive impairment, [+]
Mouse (4 sources): abnormal kidney morphology, abnormal startle reflex, increased startle reflex, preweaning lethality, complete penetrance

View all ortholog results at Monarch