Nephrocystin 3 (Q21117131)

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mammalian protein found in Homo sapiens
  • cilia and flagella associated protein 31
  • NPHP3
  • Meckel syndrome, type 7
  • nephrocystin-3
  • nephronophthisis 3 (adolescent)
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Language Label Description Also known as
English
Nephrocystin 3
mammalian protein found in Homo sapiens
  • cilia and flagella associated protein 31
  • NPHP3
  • Meckel syndrome, type 7
  • nephrocystin-3
  • nephronophthisis 3 (adolescent)

Statements

molecular function
protein binding
determination method
IPI
8 references
retrieved
9 May 2019
stated in
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
GOA
curator
UniProt
UniProt protein ID
Q7Z494
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia
GOA
curator
UniProt
UniProt protein ID
Q7Z494
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary cilium
GOA
curator
UniProt
UniProt protein ID
Q7Z494
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression
GOA
curator
UniProt
UniProt protein ID
Q7Z494
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
Structural basis for Arl3-specific release of myristoylated ciliary cargo from UNC119.
GOA
curator
IntAct protein interaction database
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
GOA
curator
IntAct protein interaction database
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
GOA
curator
IntAct protein interaction database
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
retrieved
9 May 2019
stated in
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
GOA
curator
HUGO Gene Nomenclature Committee
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494
determination method
IPI
cell component
biological process

Identifiers

 
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                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q21117131&oldid=2022969209"