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tfap2am819/+ (AB)
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m819
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tfap2a [ap2, ap2a, cb93, fb83f04, fc31a07, lockjaw, low, mob, mont blanc, wu:fb83f04, wu:fc31a07]
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anterior catecholaminergic tract, autonomic nervous system development, basihyal cartilage, brain, caudal fin, ceratobranchial cartilage, ceratohyal cartilage, closure of optic fissure, dorsal root ganglion, embryonic viscerocranium morphogenesis, enteric nervous system, ethmoid cartilage, eye, gill, head, heart, hematopoietic multipotent progenitor cell, hematopoietic progenitor cell differentiation, hindbrain, hyosymplectic cartilage, locus coeruleus, mandibular arch skeleton, Meckel''s cartilage, medulla oblongata, melanocyte, melanocyte differentiation, mouth, nervous system, neurocranium, notochord, optic cup, optic cup morphogenesis involved in camera-type eye development, optic fissure, otic vesicle, palatoquadrate cartilage, peripheral nervous system, peripheral nervous system development, pharyngeal arch, pharyngeal arch 2, pharyngeal arch 2 skeleton, pharyngeal arch 3-7, pharyngeal arch 3-7 skeleton, pharyngeal arch 3 skeleton, pharyngeal arch 4 skeleton, pharyngeal arch 5 skeleton, pharyngeal arch 6 skeleton, pharyngeal arch 7 skeleton, pharyngeal arch cartilage, pigmentation, pigment cell, pronephric distal early tubule, pronephric distal late tubule, pronephric proximal straight tubule, quadrate, retinal pigmented epithelium, statoacoustic (VIII) ganglion, T cell, trabecula communis, trabecula cranii, trunk, trunk neural crest cell migration, whole organism
anterior catecholaminergic tract, autonomic nervous system development
(all 62)
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Allele with one point mutation
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ZL429
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frozen |
