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PKD2L1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Polycystic kidney disease 2-like 1 protein also known as transient receptor potential polycystic 2 (TRPP2; formerly TRPP3) is a protein that in humans is encoded by the PKD2L1 gene.[5]

AliasesPKD2L1, PCL, PKD2L, PKDL, TRPP3, polycystin 2 like 1, transient receptor potential cation channel
PDBOrtholog search: PDBe RCSB
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PKD2L1
Identifiers
AliasesPKD2L1, PCL, PKD2L, PKDL, TRPP3, polycystin 2 like 1, transient receptor potential cation channel
External IDsOMIM: 604532; MGI: 1352448; GeneCards: PKD2L1
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001253837
NM_016112

NM_181422

RefSeq (protein)

NP_001240766
NP_057196

NP_852087

Location (UCSC)Chr 10: 100.29 – 100.33 MbChr 19: 44.14 – 44.18 Mb
PubMed search[3][4]
Wikidata
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Function

TRPP2 is a member of the polycystin protein family. TRPP2 contains multiple transmembrane domains, and cytoplasmic N- and C-termini. TRPP2 may be an integral membrane protein involved in cell-cell/matrix interactions. TRPP2 functions as a calcium-regulated nonselective cation channel. Alternative splice variants have been described but their full length sequences have not been determined.[5]

Interactions

PKD2L1 has been shown to interact with TNNI3.[6]

See also

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