Homo sapiens Gene: PKD1L1
Summary
InnateDB Gene IDBG-15982.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PKD1L1
Gene Name polycystic kidney disease 1 like 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000158683
Encoded Proteins
polycystic kidney disease 1 like 1
polycystic kidney disease 1 like 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:47774652-47948491
Strand Reverse strand
Band p12.3
Transcripts
ENST00000289672 ENSP00000289672
ENST00000433506 ENSP00000393466
ENST00000483616
ENST00000462350
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005262 calcium channel activity
GO:0005515 protein binding
Biological Process
GO:0003127 detection of nodal flow
GO:0016337 single organismal cell-cell adhesion
GO:0050982 detection of mechanical stimulus
GO:0070588 calcium ion transmembrane transport
GO:0070986 left/right axis specification
Cellular Component
GO:0005929 cilium
GO:0016020 membrane
GO:0031513 nonmotile primary cilium
GO:0034704 calcium channel complex
GO:0060170 ciliary membrane
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt Q8TDX9
TrEMBL
UniProt Splice Variant
Entrez Gene 168507
UniGene Hs.195979
RefSeq NM_138295
HUGO HGNC:18053
OMIM 609721
CCDS CCDS34633
HPRD 10154
IMGT
EMBL AB061683 AY358757
GenPept AAQ89117 BAB85807
RNA Seq Atlas 168507