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Heritable Phenotypic Marker : pal palloncino

Primary Identifier	MGI:5004958	Organism	mouse, laboratory
Chromosome	2	Mgi Type	heritable phenotypic marker

description

PHENOTYPE: Mutant embryos die during organogenesis, are smaller than controls and exhibit pharyngeal arch defects, otic defects, cranial ganglia defects, near agenesis of the nervous system, and vascular defects. [provided by MGI curators]

synonyms:
pal,
palloncino

earliestPublication:
Sandell LL, et al. (2011) A phenotype-driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development. Genesis 49(4):342-59

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

Other

0 Driver For

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