Nephrogenesis (Homo sapiens)
From WikiPathways
Description
This pathway describes the gene signaling pathways active in early nephrogenesis in human development. Mutations in essential genes can lead to development of CAKUT (congenital anomalies of the kidney and urinary tract).
Quality Tags
Ontology Terms
Bibliography
- 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
- 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
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External references
DataNodes
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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