1. Gene
  2. SLC22A6 - solute carrier family 22 member 6 Gene

SLC22A6 - solute carrier family 22 member 6 Gene

Homo sapiens

Also known as OAT1; PAHT; HOAT1; ROAT1

Gene ID: 9356 | Gene type: protein coding

About SLC22A6

Cytogenetic location: 11q12.3 Genomic coordinates (GRCh38): 11:62,976,597-62,984,967 (from NCBI)

This gene has 6 transcripts (splice variants), 489 orthologues and 22 paralogues. Restricted expression toward kidney (RPKM 150.9).

Summary

The protein encoded by this gene is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SLC22A6 Products(4)

mRNA Protein Name
NM_004790.5 NP_004781.2 solute carrier family 22 member 6 isoform a
NM_153276.3 NP_695008.1 solute carrier family 22 member 6 isoform b
NM_153277.3 NP_695009.1 solute carrier family 22 member 6 isoform c
NM_153278.3 NP_695010.1 solute carrier family 22 member 6 isoform d
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables alpha-ketoglutarate transmembrane transporter activity IDA
IDA: Inferred from direct assay
9950961 GOA
enables antiporter activity IDA
IDA: Inferred from direct assay
9950961 GOA
enables organic anion transmembrane transporter activity IDA
IDA: Inferred from direct assay
9950961 GOA
enables organic anion transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
22169006 GOA
enables prostaglandin transmembrane transporter activity IDA
IDA: Inferred from direct assay
11907186 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables sodium-independent organic anion transmembrane transporter activity IDA
IDA: Inferred from direct assay
9887087 GOA
enables solute:inorganic anion antiporter activity IDA
IDA: Inferred from direct assay
15037815 GOA
enables transmembrane transporter activity IDA
IDA: Inferred from direct assay
26377792 GOA
enables xenobiotic transmembrane transporter activity IDA
IDA: Inferred from direct assay
14675047 GOA
Biological Process GO Annotation Evidence Reference Source
involved in alpha-ketoglutarate transport IDA
IDA: Inferred from direct assay
9950961 GOA
involved in organic anion transport IDA
IDA: Inferred from direct assay
9950961 GOA
involved in organic anion transport IMP
IMP: Inferred from mutant phenotype
22169006 GOA
involved in prostaglandin transport IDA
IDA: Inferred from direct assay
11907186 GOA
involved in renal tubular secretion IMP
IMP: Inferred from mutant phenotype
22169006 GOA
involved in sodium-independent organic anion transport IDA
IDA: Inferred from direct assay
9887087 GOA
Cellular Component GO Annotation Evidence Reference Source
located in basal plasma membrane IDA
IDA: Inferred from direct assay
35307651 GOA
located in basolateral plasma membrane IDA
IDA: Inferred from direct assay
9887087 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
14749323 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC22A6 Protein Structure

Sugar_tr

Sugar_tr: Sugar (and other) transporter (135 - 512)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 563 a.a.
Protein Preferred Names Protein Names

solute carrier family 22 member 6

PAH transporter

SLC22A6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SLC22A6 Q4U2R8 APPBP2 Homo sapiens Q92624
Y2H Pooling
16189514
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hyperuricemia

Blood Urate Raized

Uricacidemia

Fanconi-Like Syndrome

Fanconi Like Syndrome

Gout

Gouty Arthritis

Articular Gout

Gouty Arthropathy

Arthritis, Gouty

Arthritis Gouty

Idiopathic Gout

Idiopathic Gout, Unspecified Site

Gouty Bursitis

Uratic Arthritis

Gout Nos

Gouty

Gouty Diathesis

Acute Kidney Failure

Acute Renal Failure

Acute Kidney Injury

Renal Failure Acute

Kidney Failure, Acute

Pre-Renal Acute Kidney Injury

Nontraumatic Acute Kidney Injury

Aki - [Acute Kidney Injury]

Arf - [Acute Kidney Failure]

Acute Kidney Disease

Acute Kidney Impairment

Acute Ischaemic Renal Failure

Acute Hypoxic Kidney Failure

Acute Kidney Shutdown

Acute Renal Oedema

Acute Renal Impairment

Acute Kidney Collapse

Acute Necrotising Kidney

Acute Renal Suppression

Fanconi Syndrome

Infantile Nephropathic Cystinosis

Adult Fanconi Syndrome

Congenital Fanconi Syndrome

De Toni-Fanconi Syndrome

Fanconi-De Toni Syndrome

Lignac-Fanconi Syndrome

Fanconi Renotubular Syndrome

Primary Fanconi Renotubular Syndrome

De Toni-Debre-Fanconi Syndrome

Adult Fanconi Anemia

Detoni Fanconi Syndrome

Fanconi-De-Toni Syndrome

Primary Fanconi Syndrome

Detoni-Debre-Fanconi Syndrome

Primary Fanconi Renal Syndrome

Fanconi Anemia

Cystinosis, Infantile Nephropathic

Fanconi-Bickel Syndrome

Renal Fanconi Syndrome

Lowe-Bickel Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus SLC22A6 RGD RGD:69338
Felis catus SLC22A6 VGNC VGNC:104330
Macaca mulatta SLC22A6 VGNC VGNC:77421
Canis familiaris SLC22A6 VGNC VGNC:46280
Mus musculus SLC22A6 MGD MGI:892001
Others SLC22A6 NCBI