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XB-GENEPAGE-6464684
fbrsl1 fibrosin-like 1
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| abnormal chondrocranium (4 sources), abnormal brain morphology (3 sources), decreased size of the eye (2 sources), abnormal Meckel's cartilage (1 source), abnormal branchial basket (1 source), abnormal cartilage tissue (1 source), abnormal cranial nerve morphology (1 source), abnormal craniofacial region (1 source), abnormal head morphology (1 source), abnormal motor neuron (1 source), abnormal palatoquadrate (1 source), abnormally localised cranial nerve (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.
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| Computed annotations: fbrsl1 assayed (5 sources) |
| Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes
from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
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| syndromic intellectual disability (6AP sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + fbrsl1 MO (6 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Mouse (4 sources): abnormal retina blood vessel morphology, abnormal retina vasculature morphology, abnormal tail morphology, preweaning lethality, incomplete penetrance |