|
Select
|
Genotype (Background)
|
Allele
[previous names]
|
Affected
Gene(s)
[previous names]
|
Construct
Name
|
Phenotype
|
Genotyping
|
Line
Type
|
ZIRC
Catalog ID
|
Availability
|
|
|
rnf2ibl31 (AB)
|
ibl31
|
rnf2 [fa19h05, ring1b, wu:fa19h05, wz4566]
|
|
atrioventricular canal, atrioventricular valve, atrium, brain, branchiomeric skeletal muscle development, cardiac chamber development, cardiac conduction system, cardiac muscle, cardiac muscle cell, cardiac ventricle, chondrocyte differentiation, cleithrum, cranium, direct ossification, embryonic neurocranium morphogenesis, embryonic viscerocranium morphogenesis, endochondral ossification, eye, gut, head, heart, heart looping, histone H2A ubiquitin ligase activity, melanocyte, neurocranial trabecula, opercle, parasphenoid, pectoral fin, pectoral fin morphogenesis, pericardium, pharyngeal arch, pharyngeal arch cartilage, pharyngeal pouch, post-vent region, retina, retina morphogenesis in camera-type eye, sinoatrial node, sternohyoid, trunk, whole organism, xanthophore
atrioventricular canal, atrioventricular valve
(all 41)
|
- |
Allele with one small deletion
|
ZL13866
|
frozen |
|
|
rnf2ibl31
|
ibl31
|
rnf2 [fa19h05, ring1b, wu:fa19h05, wz4566]
|
|
atrioventricular canal, atrioventricular valve, atrium, brain, branchiomeric skeletal muscle development, cardiac chamber development, cardiac conduction system, cardiac muscle, cardiac muscle cell, cardiac ventricle, chondrocyte differentiation, cleithrum, cranium, direct ossification, embryonic neurocranium morphogenesis, embryonic viscerocranium morphogenesis, endochondral ossification, eye, gut, head, heart, heart looping, histone H2A ubiquitin ligase activity, melanocyte, neurocranial trabecula, opercle, parasphenoid, pectoral fin, pectoral fin morphogenesis, pericardium, pharyngeal arch, pharyngeal arch cartilage, pharyngeal pouch, post-vent region, retina, retina morphogenesis in camera-type eye, sinoatrial node, sternohyoid, trunk, whole organism, xanthophore
atrioventricular canal, atrioventricular valve
(all 41)
|
- |
Allele with one small deletion
|
ZL13866
|
frozen |
|
|
|
|
