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XB-GENEPAGE-855582
cyp26a1 cytochrome P450 family 26 subfamily A member 1
Anatomical Phenotypes
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decreased size of the head (7 sources), decreased size of the cement gland (5 sources), absent eye (4 sources), abnormal development of eye (2 sources) |
Expression Phenotypes
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Manual annotations: cyp26a1 manipulated (3 sources), cyp26a1 assayed (7 sources) |
Computed annotations: cyp26a1 manipulated (3 sources), cyp26a1 assayed (15 sources) |
Diseases
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microcephaly (5AP sources, 2 EP sources) |
Experiments (Reagents)
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Xla Wt + cyp26a1 + aldh1a3 MO (2 sources), Xla Wt + cyp26a1 (1 source), Xla Wt + cyp26a1 (1 source), Xla Wt + cyp26a1 (1 source), Xla Wt + cyp26a1 + aldh1a2 MO (1 source), Xla Wt + cyp26a1 + DEAB (1 source), Xla Wt + cyp26a1 + DEAB (1 source), Xla Wt + nog + vegt + cyp26a1 + Retinoic acid + animal cap explant (1 source), Xla Wt + nog + vegt + cyp26a1 + Retinoic acid + CHX + animal cap explant (1 source), Xla Wt + vegt + nog + cyp26a1 + CHX + animal cap explant (1 source) |
Monarch Ortholog Phenotypes
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Mouse (33 sources): abnormal digestive system development, abnormal heart development, abnormal heart looping, abnormal hindbrain development, abnormal hindgut morphology, abnormal hindlimb morphology, abnormal kidney morphology, abnormal maxillary nerve morphology, abnormal mesonephros morphology, abnormal ophthalmic nerve morphology, [+] |