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XB-GENEPAGE-5791256
tbc1d32 TBC1 domain family member 32
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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| increased pigmentation in the eye (3 sources), increased size of the cilium (3 sources), abnormal actin filament (2 sources), abnormal actin filament morphology (2 sources), abnormal ciliated cell (2 sources), decreased pigmentation in the eye (2 sources), decreased size of the photoreceptor layer (2 sources) |
| 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: tbc1d32 manipulated (16 sources) |
| Computed annotations: tbc1d32 assayed (3 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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| retinitis pigmentosa (11AP sources, 16 EP sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| tbc1d32 MO2 + NF St 3 (15 sources), tbc1d32 MO3 + NF St 3 (12 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Mouse (14 sources): abnormal embryonic neuroepithelium morphology, abnormal eye development, abnormal frontonasal prominence morphology, abnormal kidney morphology, abnormal retina pigment epithelium morphology, abnormal semilunar valve morphology, atrioventricular septal defect, dilated esophagus, dual inferior vena cava, duplex kidney, [+] |