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Gene Expression Image Detail
Reference
Figure
ID
J:333283 Guan N, et al., Disruption of mitochondrial complex III in cap mesenchyme but not in ureteric progenitors results in defective nephrogenesis associated with amino acid deficiency. Kidney Int. 2022 Jul;102(1):108-120
S4
MGI:7718695
Image
Caption Abb.: CM, cap mesenchyme; CSB, comma-shaped body; gl, glomerulus; Lhx1, LIM homeobox 1; Pax2; paired box gene 2, Rel, relative; Ret; ret proto-oncogene; RV, renal vesicle; SSB; S-shaped body; Wnt9b, wingless-type MMTV integration site family, member 9b.
This image is from Guan N, Kidney Int 2022 Jul;102(1):108-120, and is displayed under the terms of the Creative Commons Attribution 4.0 International License.
Associated
Assays
Label Assay & Result Details (Gene Symbol) Spatial Mapping
C Megalin left MGI:7718701 (Lrp2)
C Megalin right MGI:7718701 (Lrp2)
C SIX2 left MGI:7718728 (Six2)
C SIX2 right MGI:7718728 (Six2)
D Six2 MGI:7718786 (Six2)
D Pax2 MGI:7718787 (Pax2)
D Lhx1 MGI:7718788 (Lhx1)
D Ret MGI:7718789 (Ret)
D Wnt9b MGI:7718791 (Wnt9b)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
09/08/2026
MGI 6.24
The Jackson Laboratory