2. Gene
  3. SLC22A23 - solute carrier family 22 member 23 Gene

SLC22A23 - solute carrier family 22 member 23 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as C6orf85

Gene ID: 63027 | Gene type: protein coding

About SLC22A23

Cytogenetic location: 6p25.2 Genomic coordinates (GRCh38): 6:3,268,973-3,457,050 (from NCBI)

This gene has 12 transcripts (splice variants), 327 orthologues and 22 paralogues. Ubiquitous expression in stomach (RPKM 8.9), colon (RPKM 8.8) and 25 other tissues.

Summary

SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]

SLC22A23 Products(9)

mRNA Protein Name
NM_001286455.1 NP_001273384.1 solute carrier family 22 member 23 isoform b
NM_001286456.2 NP_001273385.1 solute carrier family 22 member 23 isoform c
NM_001382317.1 NP_001369246.1 solute carrier family 22 member 23 isoform d
NM_001382318.1 NP_001369247.1 solute carrier family 22 member 23 isoform e
NM_001382319.1 NP_001369248.1 solute carrier family 22 member 23 isoform f
NM_001382320.1 NP_001369249.1 solute carrier family 22 member 23 isoform g
NM_001382321.1 NP_001369250.1 solute carrier family 22 member 23 isoform h
NM_015482.2 NP_056297.1 solute carrier family 22 member 23 isoform a
NM_021945.6 NP_068764.3 solute carrier family 22 member 23 isoform b

SLC22A23 Protein Structure

Sugar_tr

Sugar_tr: Sugar (and other) transporter (235 - 623)

  • 0
  • 200
  • 400
  • 600
  • 686 a.a.
Protein Preferred Names Protein Names

solute carrier family 22 member 23

ion transporter protein

Related Diseases

Diseases Alias
Wolf-Hirschhorn Syndrome

Pitt-Rogers-Danks Syndrome

WHS

Chromosome 4p16.3 Deletion Syndrome

Wittwer Syndrome

4p- Syndrome

Pitt Syndrome

4p Deletion Syndrome

Distal Deletion 4p

Distal Monosomy 4p

Telomeric Deletion 4p

Prds

4p Syndrome

Chromosome 4p Syndrome

Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation

Wolf Syndrome

Chromosome 4p Deletion Syndrome

Chromosome 4p Monosomy

Del Syndrome

Monosomy 4p

Partial Monosomy 4p

Chromosome 4 Short Arm Deletion
Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS13073 SLC22A23 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta SLC22A23 VGNC VGNC:83466
Mus musculus SLC22A23 MGD MGI:1920352
Rattus norvegicus SLC22A23 RGD RGD:620302
Canis familiaris SLC22A23 VGNC VGNC:59141
Bos taurus SLC22A23 VGNC VGNC:54236
Felis catus SLC22A23 VGNC VGNC:65244