|
XB-GENEPAGE-491497
ror2 receptor tyrosine kinase like orphan receptor 2
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
|
---|
abnormal incomplete closing of the neural tube (1 source), wholly ventralized embryo (1 source) |
Expression Phenotypes
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.
|
---|
Manual annotations: ror2 manipulated (2 sources) |
Computed annotations: ror2 assayed (21 sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
|
---|
Xla Wt + ror2 MO (2 sources), Xla Wt + ror2 MO (1 source) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|
---|
Human (131 sources): 2nd-5th toe middle phalangeal hypoplasia, Abnormal aortic morphology, Abnormal hip bone morphology, Abnormal palate morphology, Abnormal pulmonary valve morphology, Abnormal tricuspid valve morphology, Abnormality of the dentition, Absent fingernail, Absent uvula, Ankyloglossia, [+] |
Mouse (85 sources): abnormal Meckel's cartilage morphology, abnormal blood homeostasis, abnormal bone mineralization, abnormal cartilage development, abnormal caudal vertebrae morphology, abnormal cochlear hair cell morphology, abnormal cochlear outer hair cell morphology, abnormal craniofacial development, abnormal cranium morphology, abnormal digit development, [+] |
View all ortholog results at Monarch |