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XB-GENEPAGE-989233
acbd6 acyl-CoA binding domain containing 6
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| abnormal gastrulation (6 sources), abnormal eye morphology (4 sources), decreased size of the head (4 sources), abnormal chondrocranium (3 sources), abnormal craniofacial region (3 sources), abnormal pharyngeal region (3 sources), absent eye (3 sources), decreased length of anterior-posterior axis (3 sources), abnormal brain morphology (2 sources), abnormally delayed closure of blastopore (2 sources), wholly ventralized embryo (2 sources), abnormal anterior-posterior axis, curved lateral (1 source), abnormal axis elongation (1 source), abnormal bending of tail (1 source), abnormal jaw muscle (1 source), abnormal main body axis (1 source), abnormal midbrain morphology (1 source), abnormal oropharynx (1 source), abnormal swimming behavior (1 source), absent head (1 source), absent tail (1 source), decreased swimming behavior (1 source) |
| 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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| microcephaly (4AP sources), microphthalmia (3AP sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xtr Wt + acbd6 CRISPR (68) (8 sources), Xtr Wt + acbd6 MO (3 sources), Xtr Wt + acbd6 MO (2 sources), Xtr Wt + acbd6 CRISPR (71) (1 source) |