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XB-GENEPAGE-941216
zc4h2 zinc finger, C4H2 domain containing
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| abnormal eye (1 source), abnormal head (1 source), abnormal whole organism (1 source), abnormally decreased number of pigment cell (1 source), decreased length of anterior-posterior axis (1 source), decreased length of trunk (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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| Manual annotations: zc4h2 manipulated (4 sources) |
| Computed annotations: zc4h2 assayed (4 sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + zc4h2 MO (4 sources), Xla Wt + zc4h2 + zc4h2 MO (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (62 sources): Abnormal dermatoglyphics, Abnormality of eye movement, Abnormality of movement, Anteverted nares, Apnea, Apraxia, Areflexia, Arthrogryposis multiplex congenita, Broad alveolar ridges, Camptodactyly, [+] |
| Mouse (6 sources): abnormal spinal cord interneuron morphology, decreased motor neuron number, decreased survivor rate, neonatal lethality, complete penetrance, premature death, skeleton phenotype |
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View all ortholog results at Monarch |