PEDIGREE

Border Collie Collie Eye Anomaly pedigree — autosomal recessive

This Border Collie pedigree chart illustrates Collie Eye Anomaly as an autosomal recessive condition. Two carrier parents produce an affected female proband. The proband later mates with a carrier male, which makes both an affected and a carrier puppy possible in generation III. Each affected dog in the example has two parents capable of passing on the disease allele.

UPDATED 2026-09-23
EXAMPLEBorder Collie Collie Eye Anomaly pedigree — autosomal recessive
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CASE ANALYSIS

Scenario

A Border Collie breeder is reviewing a family affected by Collie Eye Anomaly, an autosomal recessive developmental eye condition.

Key decisions

  • The two generation-I parents are carriers, allowing an affected daughter.
  • The female proband is affected and therefore has two disease alleles.
  • Her carrier mate provides the second disease allele needed for the affected puppy.
  • The unaffected generation-II sibling remains genetically unclassified.

When to reuse this

Use this case to explain a recessive dog-breeding pedigree alongside DNA testing and veterinary ophthalmic assessment. It is not a substitute for clinical or breeding advice.

FAQ

Frequently asked questions

Is Collie Eye Anomaly recessive?01
Yes. Collie Eye Anomaly is commonly inherited as an autosomal recessive condition.
Why can the affected proband have an affected puppy?02
The affected proband contributes a disease allele to every offspring, and the carrier mate can contribute the second allele.
Does an unaffected dog have clear status?03
No. An unaffected dog may be genetically clear or a carrier; DNA testing can distinguish those outcomes.
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