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 (532) GO Terms (16) Nucleotides (154) Proteins (48) Interactants (1744) Wiki
XB-GENEPAGE-493705

wnt8a     Wnt family member 8A

Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
obsolete duplicated anterior-posterior axis (10 sources), decreased length of anterior-posterior axis (6 sources), duplicated head (6 sources), duplicated main body axis (5 sources), partially dorsalized embryo (5 sources), abnormal anterior/posterior axis specification (3 sources), decreased size of the head (3 sources), obsolete duplicated dorsal-ventral axis (3 sources), abnormal alimentary system (2 sources), abnormal embryo morphology (2 sources), abnormal neural crest (2 sources), abnormal ventral trunk morphology (2 sources), abnormally dorsalized embryo (2 sources), absent cement gland (2 sources), obsolete duplicated anatomical axis (2 sources), abnormal alimentary system morphology (1 source), abnormal bending of tail (1 source), abnormal dorsal-ventral axis (1 source), abnormal fin morphology (1 source), abnormal tail morphology (1 source), abnormally anterioralized embryo (1 source), abnormally localised head (1 source), abnormally ventralized embryo (1 source), absent brain (1 source), absent dorsal pancreatic bud (1 source), absent eye (1 source), absent head (1 source), absent liver (1 source), absent ventral pancreatic bud (1 source), decreased size of the foregut (1 source), decreased size of the tail (1 source), decreased size of the trunk (1 source), edematous ventral trunk (1 source), increased size of the head (1 source), increased size of the ventral trunk (1 source), partially ventralized embryo (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.
Manual annotations: wnt8a manipulated (24 sources), wnt8a assayed (32 sources)
Computed annotations: wnt8a manipulated (6 sources), wnt8a assayed (31 sources)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + wnt8a (6 sources), Xtr WT + wnt8a (6 sources), Xla Wt + wnt8a MO (4 sources), Xla Wt + wnt8a (3 sources), Xtr Wt + wnt8a (3 sources), Xla Wt + tbx6-VP16-GR + wnt8a MO (2 sources), Xla Wt + wnt8a (2 sources), Xla.pigmented(Nasco) + wnt8a (2 sources), Xtr Wt + wnt8a MO (2 sources), Xla Wt + sox17b.2 + wnt8a (1 source), Xla Wt + wnt16 + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a (1 source), Xla Wt + wnt8a + animal cap explant (1 source), Xla Wt + wnt8a + animal cap explant (1 source), Xla Wt + wnt8a + animal cap explant (1 source), Xla Wt + wnt8a + animal cap explant (1 source), Xla Wt + wnt8a + animal cap explant (1 source), Xla Wt + wnt8a + nodal2 + animal cap explant (1 source), Xla Wt + wnt8a + Quercitrin (1 source), Xla Wt + wnt8a + sia1 MO (1 source), Xla Wt + wnt8a + sia2 MO (1 source), Xla Wt + wnt8a + yap1 MO (1 source), Xla Wt + dnbmpr1a + dnwnt8a (1 source), Xtr Wt + trabd2b + wnt8a (1 source), Xtr Wt + wnt8a (1 source), Xtr Wt + wnt8a MO (1 source), Xtr Wt + wnt8a MO (1 source), Xtr Wt + wnt8a MO + wnt8a (1 source)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (1 source): no abnormal phenotype detected