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Heritable Phenotypic Marker : Krd kidney and retinal defects

Primary Identifier	MGI:99258	Organism	mouse, laboratory
Chromosome	19	Mgi Type	heritable phenotypic marker

description

PHENOTYPE: Heterozygotes for a large, transgene-associated deletion exhibit aplastic, hypoplastic and cystic kidneys, retinal defects, growth retardation and variable survival. Homozygotes die in utero. [provided by MGI curators]

synonyms:
Krd,
Del(19)TgN8052Mm,
kidney and retinal defects,
MGD-MRK-16017

earliestPublication:
Keller SA, et al. (1994) Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics 23(2):309-20

Features --> Cross References

Genome

Sequence Feature Displayer

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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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