slc45a2 solute carrier family 45 member 2
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
|decreased pigmentation in the retinal pigmented epithelium (1 source)|
Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
|Computed annotations: slc45a2 assayed (5 sources)|
These are short form descriptions of experiments using reagents targeting the gene of interest.
|Xtr Wt + slc45a2 CRISPR (1 source)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (17 sources):
Abnormality of the optic nerve,
Basal cell carcinoma,
Hypopigmentation of hair,
Hypopigmentation of the fundus,
Hypopigmentation of the skin,
Hypoplasia of the fovea,
Melanoma, Nystagmus, Photophobia, Squamous cell carcinoma of the skin, Strabismus, Thickened skin, Visual impairment[+]
|Mouse (8 sources): abnormal eye pigmentation, abnormal pinna hair pigmentation, absent eye pigmentation, decreased body size, decreased eye pigmentation, diluted coat color, homeostasis/metabolism phenotype, irregular coat pigmentation|
View all ortholog results at Monarch