Xla Wt + shh has 7 phenotype(s)

Images

Sources

Experiment + Assay

Phenotypes

Human Diseases

fig.S2.d

Peyrot SM et al. (2011)

Xla Wt + shh

NF15 (in situ hybridization)

Expression Phenotype
increased amount ptch1.S expression in neural plate mislocalised ptch1.S expression in neural plate

fig.3.c

Peyrot SM et al. (2011)

Xla Wt + shh

NF17 (in situ hybridization)

Expression Phenotype
increased amount ntn1.L expression in floor plate

fig.6.i

Peyrot SM et al. (2011)

Xla Wt + shh

NF20-22 (in situ hybridization)

Expression Phenotype
increased amount ntn1.L expression in neural tube

fig.5.i

Peyrot SM et al. (2011)

Xla Wt + shh

NF22 (in situ hybridization)

Expression Phenotype
increased amount nkx2-2.L expression in brain increased amount nkx2-2.L expression in spinal cord mislocalised nkx2-2.L expression in brain

fig.S3.e

Peyrot SM et al. (2011)

Xla Wt + shh

NF42 (morphology)

Anatomical Phenotype
abnormally increased number of melanophore

fig.S3.e^1

Peyrot SM et al. (2011)

Xla Wt + shh

NF42 (morphology)

Anatomical Phenotype
abnormally wholly ventralized eye

fig.S3.e'

Peyrot SM et al. (2011)

Xla Wt + shh

NF42 (morphology)

Anatomical Phenotype
abnormal development of alimentary system abnormal intestine morphology