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Home › Dataset Library › Microarray analysis of iris gene expression in mice with mutations relevant to glaucoma

Dataset: Microarray analysis of iris gene expression in mice with mutations relevant to glaucoma

Several ocular diseases involve the iris, notably including oculocutaneous albinism, pigment dispersion syndrome, and exfoliation...

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Several ocular diseases involve the iris, notably including oculocutaneous albinism, pigment dispersion syndrome, and exfoliation syndrome. To screen for candidate genes that may be active in these diseases, genome-wide iris gene expression patterns were comparatively analyzed from mouse models of these conditions. Irides were obtained from healthy C57Bl/6J, B6-Lystbg-J/J which carry a mutation in the Lyst gene, B6(Cg)-TyrC-2J/J which carry a mutation in the tyr gene, and B6.D2-Tryp1bGpnmbR150X/Sj with mutations in both Tryp1 and Gpnmb. Four eyes from two mice were pooled for one sample. Three samples were prepared for each strain.

Species:
mouse

Samples:
12

Source:
E-GEOD-16994

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample STRAIN
GSM425397 C57BL/6J
GSM425397 C57BL/6J
GSM425397 C57BL/6J
GSM425400 B6-Lystbg-J
GSM425400 B6-Lystbg-J
GSM425400 B6-Lystbg-J
GSM520614 B6-(Cg)TyrC-2J
GSM520614 B6-(Cg)TyrC-2J
GSM520614 B6-(Cg)TyrC-2J
GSM520617 B6.D2(Tryp1-Gpnmb-)/SJ
GSM520617 B6.D2(Tryp1-Gpnmb-)/SJ
GSM520617 B6.D2(Tryp1-Gpnmb-)/SJ

Tags

  • exfoliation syndrome
  • genome
  • iris
  • oculocutaneous albinism
  • syndrome

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