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- Table of Contents
Facts about Solute carrier family 22 member 18.
.
Human | |
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Gene Name: | SLC22A18 |
Uniprot: | Q96BI1 |
Entrez: | 5002 |
Belongs to: |
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major facilitator (TC 2.A.1) superfamily |
BWR1AORCTL2; BWSCR1Asolute carrier family 22 (organic cation transporter), member 1-like; Efflux transporter-like protein; HET; imprinted multi-membrane spanning polyspecific transporter-related protein 1; Imprinted multi-membrane-spanning polyspecific transporter-related protein 1; IMPT1DKFZp667A184; ITMp45-BWR1A; ORCTL-2; organic cation transporter-like 2; Organic cation transporter-like protein 2; p45 Beckwith-Wiedemann region 1A; SLC22A1Lcandidate A; solute carrier family 22 member 18; Solute carrier family 22 member 1-like; solute carrier family 22, member 18; TSSC5p45-Beckwith-Wiedemann
Mass (kDA):
44.846 kDA
Human | |
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Location: | 11p15.4 |
Sequence: | 11; NC_000011.10 (2899691..2925246) |
Expressed at high levels in adult and fetal kidney and liver, and adult colon. Expressed in fetal renal proximal tubules (at protein level). Expressed at lower levels in heart, brain and lung.
Apical cell membrane; Multi-pass membrane protein. Localized at the apical membrane surface of renal proximal tubules.
PMID: 9751628 by Lee M.P., et al. Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.
PMID: 9802569 by Morisaki H., et al. A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice.