| cyp26c1 | Stage | Hours | ZFIN expression range | deep blastomere | blastoderm | neural plate | presumptive rhombomere 2 | presumptive rhombomere 3 | presumptive rhombomere 4 | presumptive rhombomere 5 | presumptive rhombomere 6 | midbrain hindbrain boundary neural keel | eye | rhombomere 2 | rhombomere 4 | rhombomere 5 | rhombomere 6 | diencephalon | hindbrain | midbrain | splanchnocranium | telencephalon | otic vesicle | retina | pectoral fin | mandibular arch | whole organism | unspecified |
| Zygote | 1-cell | 0 | ||||||||||||||||||||||||||
| Cleavage | 2-cell | 0.75 | ||||||||||||||||||||||||||
| 4-cell | 1.0 | |||||||||||||||||||||||||||
| 8-cell | 1.25 | |||||||||||||||||||||||||||
| 16-cell | 1.5 | |||||||||||||||||||||||||||
| 32-cell | 1.75 | |||||||||||||||||||||||||||
| 64-cell | 2.0 | |||||||||||||||||||||||||||
| Blastula | 124-cell | 2.25 | ||||||||||||||||||||||||||
| 256-cell | 2.5 | |||||||||||||||||||||||||||
| 512-cell | 2.75 | |||||||||||||||||||||||||||
| 1k-cell | 3.0 | X | ||||||||||||||||||||||||||
| High | 3.33 | |||||||||||||||||||||||||||
| Oblong | 3.66 | |||||||||||||||||||||||||||
| Sphere | 4.0 | |||||||||||||||||||||||||||
| Dome | 4.33 | ! | ||||||||||||||||||||||||||
| 30% epiboly | 4.66 | |||||||||||||||||||||||||||
| Gastrula | 50%-epiboly | 5.25 | X | X | ||||||||||||||||||||||||
| Germ-ring | 5.66 | |||||||||||||||||||||||||||
| Shield | 6.0 | |||||||||||||||||||||||||||
| 75% epiboly stage | 8.0 | |||||||||||||||||||||||||||
| 90% epiboly | 9.0 | |||||||||||||||||||||||||||
| bud stage | 10.0 | |||||||||||||||||||||||||||
| Segmentation | 1-4 somites | 10.33 | ||||||||||||||||||||||||||
| 5-9 somites | 11.66 | |||||||||||||||||||||||||||
| 10-13 somites | 14.0 | |||||||||||||||||||||||||||
| 14-19 somites | 16.0 | |||||||||||||||||||||||||||
| 20-25 somites | 19.0 | |||||||||||||||||||||||||||
| 26+ somites | 22.0 | I | I | I | ||||||||||||||||||||||||
| Pharyngula | Prim-5 | 24.0 | ||||||||||||||||||||||||||
| Prim-15 | 30.0 | |||||||||||||||||||||||||||
| Prim-25 | 36.0 | I | I | I | I | I | ||||||||||||||||||||||
| High-pec | 42.0 | |||||||||||||||||||||||||||
| Hatching | Long-pec | 48.0 | I | I | I | |||||||||||||||||||||||
| Pec-fin | 60.0 | I | I | I |
| Evidence for Interaction | Inactivation of Spry2 causes an expansion of the expression domain of a marker of dorsal ectoderm (anterior neurectoderm) cyp26a and the concomitant reduction of ventral ectoderm (epidermis) revealed by foxi1 expression . |
| Target Gene | cyp26c1 |
| Upstream Gene | spry2 |
| Interaction Type | repress |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Inactivation of Spry2 causes an expansion of the expression domain of a marker of dorsal ectoderm (anterior neurectoderm) cyp26a and the concomitant reduction of ventral ectoderm (epidermis) revealed by foxi1 expression . |
| Target Gene | cyp26c1 |
| Upstream Gene | spry2 |
| Interaction Type | repress |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Inactivation of Spry2 causes an expansion of the expression domain of a marker of dorsal ectoderm (anterior neurectoderm) cyp26a and the concomitant reduction of ventral ectoderm (epidermis) revealed by foxi1 expression . |
| Target Gene | cyp26c1 |
| Upstream Gene | spry2 |
| Interaction Type | repress |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Cyp26 enzymes generate the retinoic acid response pattern necessary for hindbrain development. Hnf1b is expressed in the posterior hindbrain up to the r5-r6 boundary (arrowheads) and is shifted anteriorly in Cyp26-depleted embryos. |
| Target Gene | hnf1b |
| Upstream Gene | cyp26c1 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | hindbrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Moens, C.B. |
| Journal | Development |
| Year | 2007 |
| Vol | 134(1) |
| Start Page | 177 |
| Evidence for Interaction | cyp26a1 expression domain is reduced in rbpja MO-injected embryos |
| Target Gene | cyp26c1 |
| Upstream Gene | rbpja |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | tailbud and posterior PSM |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Oates, A.C. |
| Journal | Dev. Biol. |
| Year | 2007 |
| Vol | 301 |
| Start Page | 388 |
| Evidence for Interaction | cyp26a1 expression domain is reduced in rbpja MO-injected embryos |
| Target Gene | cyp26c1 |
| Upstream Gene | rbpja |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | tailbud and posterior PSM |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Oates, A.C. |
| Journal | Dev. Biol. |
| Year | 2007 |
| Vol | 301 |
| Start Page | 388 |