| Entrez Gene ID | 9389 |
|---|---|
| Official Gene Symbol | SLC22A14 (GeneCards) |
| Full name | solute carrier family 22 member 14 |
| Location | 3p22.2 |
| Other ids | Vega : OTTHUMG00000131082 MIM : 604048 HGNC : HGNC:8495 Ensembl : ENSG00000144671 |
| Other names | OCTL2, OCTL4, ORCTL4 |
| Summary | This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
Found 3 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 852 | 9389 | SLC22A14 | 3 | 38347790 | 38347790 | Human Skin Fibroblasts | HiSeq 2500 |
| 1536 | 9389 | SLC22A14 | 3 | 38349069 | 38349069 | Autism Spectrum Disorders | HiSeq 2500 NextSeq500 v2 |
| 29742 | 9389 | SLC22A14 | 3 | 38349069 | 38349069 | Autism Spectrum Disorders | HiSeq 2500 NextSeq500 v2 NextSeq500 |