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English
Hh mutants abrogate ligand secretion
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5387390)
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Statements
instance of
biological pathway
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
part of
Diseases of signal transduction by growth factor receptors and second messengers
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
exact match
https://identifiers.org/reactome:R-HSA-5387390
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
has part(s)
Hh mutants are degraded by ERAD
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
HHAT G278V doesn't palmitoylate Hh-Np
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
cites work
A review of hedgehog signaling in cranial bone development
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding Hedgehog protein palmitoylation and signaling
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
The molecular genetics of holoprosencephaly
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
Identifiers
Reactome ID
R-HSA-5387390
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5387390
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