Xla Wt + fbrsl1 MO has 6 phenotype(s)

Images

Sources

Experiment + Assay

Phenotypes

Human Diseases

Fig 5. C r3

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF 40

Anatomical Phenotype
abnormal chondrocranium decreased size of the eye

syndromic intellectual disability

Fig. 7 A r3, B, C, D, E

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF 40

Anatomical Phenotype
abnormal chondrocranium abnormal head morphology decreased size of the eye

syndromic intellectual disability

Fig. 5 F G H

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF 40

Anatomical Phenotype
abnormal brain morphology abnormal cartilage tissue abnormal chondrocranium abnormal craniofacial region

syndromic intellectual disability

Fig. 5 D r3

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF 40 IHC Col2a

Anatomical Phenotype
abnormal branchial basket abnormal chondrocranium abnormal Meckel's cartilage abnormal palatoquadrate

syndromic intellectual disability

Fig. 5. E r3

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF 44IHC Ncam

Anatomical Phenotype
abnormal brain morphology

syndromic intellectual disability

Fig. 6. A r3, B

Ufartes R et al. (2020)

Xla Wt + fbrsl1 MO

NF40 IHC Ncam

Anatomical Phenotype
abnormal brain morphology abnormal cranial nerve morphology abnormal motor neuron abnormally localised cranial nerve

syndromic intellectual disability