cldn1 claudin 1
Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
|Computed annotations: cldn1 assayed (17 sources)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (24 sources):
Abnormal dental enamel morphology,
Abnormality of blood and blood-forming tissues,
Ichthyosis, Jaundice, Oligodontia, Orthokeratosis, Parakeratosis, Portal hypertension, Scarring alopecia of scalp, Sparse and thin eyebrow, Sparse body hair, Sparse eyelashes, Splenomegaly, Thick hair, obsolete Hypotrichosis, obsolete Hypotrichosis of the scalp[+]
|Mouse (6 sources): abnormal embryo size, abnormal startle reflex, impaired skin barrier function, increased startle reflex, neonatal lethality, complete penetrance, preweaning lethality, complete penetrance|
View all ortholog results at Monarch