Enc Gene Detail

Summary

• Symbol
  Enc
• Name
  embryonic nucleus cataract

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:95391
  NCBI Gene: 104374
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Human Diseases

• Diseases
  1 with Enc mouse models

Human Disease

Mouse Models

cataract

IDs

cataract      

DOID:83
ICD10CM:H26
ICD9CM:366.8
OMIM:601371
OMIM:PS116200
UMLS_CUI:C0029531

View 1 model

Mouse Models

Human Disease Modeled: cataract

Allelic Composition	Genetic Background	Reference	Phenotypes
Enc/Enc+	involves: 101 * C3H	J:9528	View

Click on a disease name to see all genes associated with that disease.

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotypes from 1 allele in 1 genetic background
  2 phenotype references
  

• All Mutations and Alleles
  1
• Radiation induced
  1
• Find Mice (IMSR)
  0 strains or lines available

Mice homozygous for a radiation-induced mutation die prior to birth. Heterozygous mutants are fully viable and fertile but exhibit a small bilateral opacity limited to the central part of the lens, with incomplete penetrance; opacities of the embryonic nucleus and the posterior suture are observed.

Sequences &
Gene Models

• NCBI Gene
  104374

Other
Accession IDs

MGD-MRK-9501

References

• Summaries
  All 3

  Diseases 1

  Phenotypes 2
• Earliest
  J:9528 Kratochvilova J, et al., Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice. Genet Res. 1988 Oct;52(2):125-34