Publication	Data		Fish	Anatomy
Lencer et al., 2021	Figure 4		prdm1am805/m805	Rohon-Beard neuron cxcr4b expression absent, abnormal Rohon-Beard neuron fgf13a expression absent, abnormal Rohon-Beard neuron ab1-hnk-1 labeling absent, abnormal xanthoblast aox5 expression absent, abnormal xanthoblast gjb8 expression absent, abnormal
Iwanaga et al., 2020	Fig. 3		prdm1am805/m805	whole organism dct expression decreased amount, abnormal whole organism dct expression increased amount, abnormal whole organism mc1r expression decreased amount, abnormal whole organism mitfa expression decreased amount, abnormal whole organism sox10 expression decreased amount, abnormal whole organism sox10 expression increased amount, abnormal whole organism tyr expression decreased amount, abnormal
Kamei et al., 2018	Fig. 6		WT + MO2-prdm1a	developmental growth decreased rate, abnormal
Yin et al., 2018	Fig. 7		prdm1atp39/tp39; i106Tg	fast muscle cell cell morphogenesis delayed, abnormal slow muscle cell muscle cell migration arrested, abnormal
Jackson et al., 2015	Fig. 6		prdm1am805/m805	migratory slow muscle precursor cell smyhc1 expression decreased amount, abnormal slow muscle cell tnnc1b expression absent, abnormal
LaMonica et al., 2015	Fig. 1		prdm1am805/m805	pharyngeal arch decreased object quality, abnormal
	Fig. 2		prdm1am805/m805	embryonic viscerocranium morphogenesis decreased process quality, abnormal pharyngeal arch cartilage lacks all parts of type ceratobranchial 3 cartilage, abnormal pharyngeal arch cartilage lacks all parts of type ceratobranchial 4 cartilage, abnormal pharyngeal arch cartilage lacks all parts of type ceratobranchial 5 cartilage, abnormal
	Fig. 3		AB + MO2-prdm1a	pharyngeal arch 3 decreased object quality, abnormal pharyngeal arch 4 decreased object quality, abnormal pharyngeal arch cartilage has fewer parts of type ceratobranchial cartilage, abnormal
	Fig. 4		prdm1am805/m805	pharyngeal arch cell population proliferation decreased occurrence, abnormal
Ding et al., 2013	Fig. 4		WT + MO2-prdm1a	ceratobranchial 2 cartilage absent, abnormal ceratobranchial 3 cartilage absent, abnormal ceratobranchial 4 cartilage absent, abnormal ceratobranchial 5 cartilage absent, abnormal ceratohyal cartilage inverted, abnormal embryonic neurocranium morphogenesis disrupted, abnormal neurocranial trabecula shortened, abnormal neurocranium decreased width, abnormal
	Fig. 5		prdm1am805/m805	ceratobranchial 2 cartilage absent, abnormal ceratobranchial 3 cartilage absent, abnormal ceratobranchial 4 cartilage absent, abnormal ceratobranchial 5 cartilage absent, abnormal ethmoid cartilage decreased size, abnormal neurocranial trabecula shortened, abnormal neurocranium decreased width, abnormal
Culbertson et al., 2011	Fig. 2		prdm1anl3/nl3	cartilage morphogenesis decreased process quality, abnormal ceratobranchial cartilage absent, abnormal ceratobranchial cartilage malformed, abnormal ceratohyal cartilage malformed, abnormal vagal ganglion malformed, abnormal
Olesnicky et al., 2010	Fig. 1		prdm1am805/m805	post-vent region kinked, abnormal
	Fig. 2		prdm1am805/m805	post-vent region kinked, abnormal
	Fig. 3		prdm1am805/m805	post-vent region kinked, abnormal
	Fig. 4		prdm1am805/m805	post-vent region kinked, abnormal
	Fig. 5		prdm1am805/m805	pigment cell decreased amount, abnormal post-vent region kinked, abnormal somite U-shaped, abnormal
	text only		prdm1am805/m805	post-vent region kinked, abnormal somite U-shaped, abnormal
Birkholz et al., 2009	Fig. 3		prdm1am805/m805 ,   prdm1am805/m805; i106Tg	ceratohyal bone inverted, abnormal otolith decreased size, abnormal pharyngeal pouch disorganized, abnormal whole organism has fewer parts of type pharyngeal pouch, abnormal whole organism lacks all parts of type ceratobranchial 2 cartilage, abnormal whole organism lacks all parts of type ceratobranchial 3 cartilage, abnormal whole organism lacks all parts of type ceratobranchial 4 cartilage, abnormal whole organism lacks all parts of type ceratobranchial 5 cartilage, abnormal whole organism lacks all parts of type ceratobranchial 5 tooth, abnormal whole organism lacks parts or has fewer parts of type dermal bone, abnormal
	Fig. 4		prdm1am805/m805	cell population proliferation decreased occurrence, abnormal pharyngeal arch physical object quality, abnormal
Elworthy et al., 2008	Fig. 8		prdm1atp39/tp39	slow muscle cell multinucleate, abnormal
	Fig. S3		prdm1am805/m805 ,   prdm1atp39/tp39	cephalic musculature morphology, abnormal ceratobranchial cartilage aplastic, abnormal muscle attachment process quality, abnormal ventral transverse aplastic, abnormal
Menelaou et al., 2008	Fig. 4		prdm1am805/m805	secondary motor neuron defasciculated, abnormal
	Fig. 5		prdm1am805/m805	secondary motor neuron morphology, abnormal
Lee et al., 2006	Fig. 3		prdm1atp39 ,   WT + MO2-prdm1a	cleithrum decreased size, abnormal pectoral fin bud hypoplastic, abnormal pectoral fin skeleton aplastic, abnormal pectoral fin skeleton decreased size, abnormal pectoral fin truncated, abnormal
Phenotype Annotation (1994-2006)	Fig. for (m805)		prdm1am805/m805	melanocyte quality, abnormal nervous system quality, abnormal pharyngeal arch 3-7 skeleton quality, abnormal
	Fig. for (tp39)		prdm1atp39/tp39	fin malformed, abnormal melanocyte irregular spatial pattern, abnormal myoseptum quality, abnormal notochord quality, abnormal somite quality, abnormal surface structure quality, abnormal whole organism lethal (sensu genetics), abnormal
Wilm et al., 2005	Fig. 6		WT + MO1-prdm1a	dorsal/ventral pattern formation disrupted, abnormal
	Fig. 7		WT + MO1-prdm1a	axis increased length, abnormal somite increased width, abnormal
	text only		WT + MO1-prdm1a	whole organism wholly dorsalized, abnormal
Artinger et al., 1999	Fig. 2		prdm1am805/m805	dorsal longitudinal fasciculus hypoplastic, abnormal Rohon-Beard neuron absent, abnormal Rohon-Beard neuron aplastic, abnormal
	Fig. 3		prdm1am805/m805	caudal fin mesenchyme hypoplastic, abnormal pigment cell decreased amount, abnormal
	Fig. 4		prdm1am805/m805	dorsal root ganglion hypoplastic, abnormal dorsal root ganglion lacks parts or has fewer parts of type neuron, abnormal lateral line curved, abnormal
Granato et al., 1996	Table 4		prdm1atp39/tp39	larval locomotory behavior process quality, abnormal notochord morphology, abnormal somite morphology, abnormal whole organism decreased behavioural activity, abnormal whole organism viability, abnormal
Kelsh et al., 1996	Table 5		prdm1atp39/tp39	iridophore decreased amount, abnormal iridophore decreased pigmentation, abnormal iridophore low saturation, abnormal lateral larval melanophore stripe lacks all parts of type melanocyte, abnormal melanocyte decreased amount, abnormal melanocyte decreased pigmentation, abnormal melanocyte degenerate, abnormal melanocyte low saturation, abnormal ventral larval melanophore stripe has fewer parts of type melanocyte, abnormal xanthophore decreased amount, abnormal xanthophore decreased pigmentation, abnormal xanthophore desaturated yellow, abnormal
van Eeden et al., 1996	Table 1		prdm1atp39/tp39	fin degenerate, abnormal horizontal myoseptum absent, abnormal
	Table 2		prdm1atp39/tp39	median fin fold rough, abnormal pectoral fin rough, abnormal
	text only		prdm1atp39/tp39	median fin fold decreased length, abnormal median fin fold deformed, abnormal median fin fold increased thickness, abnormal
van Eeden et al., 1996	Table 3		prdm1atp39/tp39	fin edge shape, abnormal horizontal myoseptum aplastic, abnormal melanocyte decreased amount, abnormal whole organism movement behavioral quality, abnormal