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| General information | Expression | Regulation | Mutation | Interaction |
|
Basic Information |
|
|---|---|
Gene ID | 5002 |
Name | SLC22A18 |
Synonymous | BWR1A|BWSCR1A|HET|IMPT1|ITM|ORCTL2|SLC22A1L|TSSC5|p45-BWR1A;solute carrier family 22, member 18;SLC22A18;solute carrier family 22, member 18 |
Definition | Beckwith-Wiedemann syndrome chromosome region 1, candidate A|ORCTL-2|beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein|efflux transporter-like protein|imprinted multi-membrane spanning polyspecific transporter-related protein 1|imp |
Position | 11p15.5 |
Gene Type | protein-coding |
Gene Mutation: | Substitution Insertion & Deletion Other Mutation |
Substitution | | Top | |
There is no record for SLC22A18 |
Indel | | Top | |
There is no record for SLC22A18 |
Other Mutation | | Top | |
There is no record for SLC22A18 |