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XB-GENEPAGE-493705
wnt8a Wnt family member 8A
Anatomical Phenotypes
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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), abnormally dorsalized embryo (2 sources), abnormal neural crest (2 sources), abnormal ventral trunk morphology (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), abnormally anterioralized embryo (1 source), abnormally localised head (1 source), abnormally ventralized embryo (1 source), abnormal tail morphology (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
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Manual annotations: wnt8a manipulated (24 sources), wnt8a assayed (32 sources) |
Computed annotations: wnt8a manipulated (6 sources), wnt8a assayed (31 sources) |
Experiments (Reagents)
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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.pigmented(Nasco) + wnt8a (2 sources), Xla Wt + tbx6-VP16-GR + wnt8a MO (2 sources), Xla Wt + wnt8a (2 sources), Xtr Wt + wnt8a MO (2 sources), Xla Wt + dnbmpr1a + dnwnt8a (1 source), 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), 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
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Mouse (1 source): no abnormal phenotype detected |