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XB-GENEPAGE-947684
slc45a2 solute carrier family 45 member 2
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| decreased pigmentation in the retinal pigmented epithelium (1 source) |
| Expression Phenotypes
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.
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| Computed annotations: slc45a2 assayed (2 sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xtr Wt + slc45a2 CRISPR (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (17 sources): Abnormality of the optic nerve, Albinism, Basal cell carcinoma, Blue irides, Hypopigmentation of hair, Hypopigmentation of the fundus, Hypopigmentation of the skin, Hypoplasia of the fovea, Iris hypopigmentation, Macular hypoplasia, [+] |
| 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 |
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View all ortholog results at Monarch |