Nephrogenesis (Homo sapiens)

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Description

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Ontology Terms

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Bibliography

1. Cheng HT, Kim M, Valerius MT, Surendran K, Schuster-Gossler K, Gossler A, McMahon AP, Kopan R; ''Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephron.''; Development, 2007 PubMed Europe PMC Scholia
2. Vivante A, Mark-Danieli M, Davidovits M, Harari-Steinberg O, Omer D, Gnatek Y, Cleper R, Landau D, Kovalski Y, Weissman I, Eisenstein I, Soudack M, Wolf HR, Issler N, Lotan D, Anikster Y, Dekel B; ''Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling.''; J Am Soc Nephrol, 2013 PubMed Europe PMC Scholia

History

External references

DataNodes

Name	Type	Database reference	Comment
ALDH1A2	GeneProduct	ENSG00000128918 (Ensembl)
BMP7	GeneProduct	ENSG00000101144 (Ensembl)
FGF20	GeneProduct	ENSG00000078579 (Ensembl)
FGF8	GeneProduct	ENSG00000107831 (Ensembl)
FOXD1	GeneProduct	ENSG00000251493 (Ensembl)
GREB1L	GeneProduct	ENSG00000141449 (Ensembl)
JAG1	GeneProduct	ENSG00000101384 (Ensembl)
LHX1	GeneProduct	ENSG00000274577 (Ensembl)
MEIS1	GeneProduct	ENSG00000143995 (Ensembl)
NOTCH2	GeneProduct	ENSG00000134250 (Ensembl)
OSR1	GeneProduct	ENSG00000143867 (Ensembl)
PAX2	GeneProduct	ENSG00000075891 (Ensembl)
RSPO1	GeneProduct	ENSG00000169218 (Ensembl)
RSPO3	GeneProduct	ENSG00000146374 (Ensembl)
SIX2	GeneProduct	ENSG00000170577 (Ensembl)
TCF21	GeneProduct	ENSG00000118526 (Ensembl)
WNT3A	GeneProduct	ENSG00000154342 (Ensembl)
WNT4	GeneProduct	ENSG00000162552 (Ensembl)
WNT9B	GeneProduct	ENSG00000158955 (Ensembl)

Annotated Interactions

No annotated interactions