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Search references for PDZK1. Phrases containing PDZK1
See searches and references containing PDZK1!PDZK1
Protein-coding gene in humans
regulatory cofactor NHE-RF3 is a protein that in humans is encoded by the PDZK1 gene. PDZK1 has been shown to interact with: AKAP10, CLCN3, Cystic fibrosis transmembrane
PDZK1
Protein-coding gene in the species Homo sapiens
PDZK1-interacting protein 1 is a protein that in humans is encoded by the PDZK1IP1 gene. PDZK1IP1 has been shown to interact with PDZK1. GRCh38: Ensembl
PDZK1IP1
Mammalian protein found in Homo sapiens
hypouricemia. SLC22A12 has been shown to have a protein-protein interaction with PDZK1. Lesinurad, ruzinurad, darbinurad, verinurad, epaminurad, lingdolinurad
SLC22A12
Protein-coding gene in humans
("ergothioneine transporter"). SLC22A4 has been shown to interact with PDZK1. Solute carrier family GRCh38: Ensembl release 89: ENSG00000197208 – Ensembl
SLC22A4
Protein-coding gene in the species Homo sapiens
humans is encoded by the FARP2 gene. FARP2 has been shown to interact with PDZK1. FARP1 FERM domain RhoGEF domain Pleckstrin homology domain GRCh38: Ensembl
FARP2
Protein-coding gene in the species Homo sapiens
phosphate concentration at the kidney. SLC34A3 has been shown to interact with PDZK1. A mutation in the SLC34A3 gene has been known to cause the autosomal recessive
Sodium-dependent phosphate transport protein 2C
Sodium-dependent_phosphate_transport_protein_2C
Protein-coding gene in the species Homo sapiens
and G protein signal transduction. AKAP10 has been shown to interact with PDZK1 and PRKAR1A. GRCm38: Ensembl release 89: ENSMUSG00000047804 – Ensembl, May
AKAP10
Organic compound
SLC2A9; ABCG2; SLC17A1; SLC22A11; SLC22A12; SLC16A9; GCKR; LRRC16A; and PDZK1. GLUT9, encoded by the SLC2A9 gene, is known to transport both uric acid
Uric_acid
Mammalian protein found in humans
transmembrane conductance regulator has been shown to interact with: DNAJC5, GOPC, PDZK1, PRKCE, SLC4A8, SNAP23, SLC9A3R1, SLC9A3R2, and STX1A, Congenital bilateral
Cystic fibrosis transmembrane conductance regulator
Cystic_fibrosis_transmembrane_conductance_regulator
Protein and gene in humans
dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 3 NINJ2 Ninjurin-2 PDZK1IP1 PDZK1-interacting protein 1 PKMYT1 Membrane-associated tyrosine- and threonine-specific
TMEM101
Protein found in humans
N, Gilchrist A, Pal R, Tognazzi K, Brown LF, et al. (September 1999). "PDZK1, a novel PDZ domain-containing protein up-regulated in carcinomas and mapped
ATP-binding cassette sub-family C member 2
ATP-binding_cassette_sub-family_C_member_2
Protein-coding gene in the species Homo sapiens
1001/archderm.144.9.1129. PMID 18794456. Ghosh MG, Thompson DA, Weigel RJ (2000). "PDZK1 and GREB1 are estrogen-regulated genes expressed in hormone-responsive breast
GREB1
Protein-coding gene in the species Homo sapiens
(breakpoint cluster region) protein binds to PDZ-domains of scaffold protein PDZK1 and vesicle coat protein Mint3". J. Cell Sci. 117 (Pt 23): 5535–41. doi:10
APBA3
Protein-coding gene in the species Homo sapiens
C-terminus of the transmembrane mucin MUC17 binds to the scaffold protein PDZK1 that stably localizes it to the enterocyte apical membrane in the small
Mucin_17
Protein-coding gene in the species Homo sapiens
PMC 139241. PMID 12477932. Gisler SM, Pribanic S, Bacic D, et al. (2004). "PDZK1: I. a major scaffolder in brush borders of proximal tubular cells". Kidney
Sodium-dependent phosphate transport protein 1
Sodium-dependent_phosphate_transport_protein_1
Protein family
PDLIM3 PDLIM4 PDLIM5 PDLIM7 PDZD11 PDZD2 PDZD3 PDZD4 PDZD5A PDZD7 PDZD8 PDZK1 PDZRN3 PDZRN4 PICK1 PPP1R9A PPP1R9B PREX1 PRX PSCDBP PTPN13 PTPN3 PTPN4
PDZ_domain
Protein-coding gene in the species Homo sapiens
carnitine deficiency in newborns is about 1 in 40,000. SLC22A5 interacts with PDZK1. Solute carrier family GRCh38: Ensembl release 89: ENSG00000197375 – Ensembl
SLC22A5
Protein-coding gene in the species Homo sapiens
interact with: ADRB2, Beta-catenin, CFTR, GNAQ, OPRK1, PAG1, PDGFRA, PDGFRB, PDZK1, PTH1R, SLC4A8, YAP1, and EZR Cystic fibrosis transmembrane conductance
Sodium-hydrogen antiporter 3 regulator 1
Sodium-hydrogen_antiporter_3_regulator_1
Genetic mutation
RBM8A, PEX11B, ITGA10, ANKRD35, PIAS3, NUDT17, POLR3C, RNF115, CD160, PDZK1, and GPR89A.[citation needed] Genes related to the distal area are PDE4DIP
1q21.1_copy_number_variations
Protein-coding gene in the species Homo sapiens
is encoded by the SLK gene. SLK (gene) has been shown to interact with PDZK1. SLK is a mammalian gene located on chromosome 10, it has also been cloned
SLK_(gene)
Protein-coding gene in the species Homo sapiens
PMID 15489334. Wang P, Wang JJ, Xiao Y, et al. (2005). "Interaction with PDZK1 is required for expression of organic anion transporting protein 1A1 on
Solute carrier organic anion transporter family member 4A1
Solute_carrier_organic_anion_transporter_family_member_4A1
Protein-coding gene in humans
humans is encoded by the CLCN3 gene. CLCN3 has been shown to interact with PDZK1 and TMEM9. Chloride channel GRCh38: Ensembl release 89: ENSG00000109572
CLCN3
Q8NEN9 11929 PDZD9 HGNC:28740; Q8IXQ8 11930 PDZD11 HGNC:28034; Q5EBL8 11931 PDZK1 HGNC:8821; Q5T2W1 11932 PDZK1IP1 HGNC:16887; Q13113 11933 PDZRN3 HGNC:17704;
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
Protein-coding gene in the species Homo sapiens
PMID 15981923. Noshiro R, Anzai N, Sakata T, et al. (2006). "The PDZ domain protein PDZK1 interacts with human peptide transporter PEPT2 and enhances its transport
SLC15A2
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