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XB-GENEPAGE-1013929
prdm15 PR domain 15
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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| Manual annotations: prdm15 manipulated (2 sources) |
| Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes
from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
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| Galloway-Mowat syndrome 1 (2 EP sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + prdm15 MO + GFP (2 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Mouse (13 sources): abnormal anterior head development, abnormal embryonic neuroepithelium morphology, abnormal forebrain development, abnormal lateral ganglionic eminence morphology, abnormal medial ganglionic eminence morphology, abnormal rostral-caudal axis patterning, abnormal visceral yolk sac endoderm morphology, decreased embryo size, embryonic growth retardation, excessive folding of visceral yolk sac, [+] |