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 (4) GO Terms (3) Nucleotides (146) Proteins (45) Interactants (198) Wiki
XB-GENEPAGE-988836

nelfa     negative elongation factor complex member A

Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormal chondrocranium morphology (2 sources), decreased size of the head (2 sources), abnormal craniofacial region morphology (1 source), decreased size of the ceratohyal (1 source), decreased size of the forebrain (1 source), decreased size of the midbrain (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.
Wolf-Hirschhorn syndrome (4AP sources)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + nelfa MO (4 sources)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (4 sources): abnormal embryo size, embryonic lethality prior to organogenesis, prenatal lethality prior to heart atrial septation, preweaning lethality, complete penetrance