Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (480) GO Terms (15) Nucleotides (243) Proteins (42) Interactants (2179) Wiki
XB-GENEPAGE-1017497

myod1     myogenic differentiation 1

Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormally irregular spatial pattern of somite (4 sources), increased size of the hypaxial muscle (3 sources), abnormal myocyte morphology (2 sources), abnormal somite morphology (2 sources), absent pronephric tubule (2 sources), increased size of the myotome (2 sources), abnormal nucleus morphology (1 source), abnormal presomitic mesoderm morphology (1 source), abnormally anteriorly mislocalised somite (1 source), abnormally localised myocyte (1 source), abnormally localised nucleus (1 source), decreased size of the myocyte (1 source), decreased size of the presomitic mesoderm (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: myod1 manipulated (19 sources), myod1 assayed (16 sources)
Computed annotations: myod1 assayed (28 sources)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + myod1 MO (16 sources), Xla Wt + myod1 (6 sources), Xla Wt + Dre.lbx1 + myod1 (4 sources), Xla Wt + myod1 (4 sources)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (53 sources): Abnormality of abdomen morphology, Abnormality of pelvic girdle bone morphology, Absent palmar crease, Absent septum pellucidum, Akinesia, Arthrogryposis multiplex congenita, Blepharophimosis, Bradykinesia, Camptodactyly of finger, Cavum septum pellucidum, [+]
Mouse (6 sources): abnormal muscle development, abnormal myogenesis, abnormal skeletal muscle regeneration, decreased physiological sensitivity to xenobiotic, increased satellite cell number, no abnormal phenotype detected

View all ortholog results at Monarch