SLC66A1LP solute carrier family 66 member 1 like, pseudogene
Gene ID: 152078, updated on 10-Dec-2024Gene type: pseudo
Also known as: PQLC2L; C3orf55; SLC66A1L; SLC66A2L
- See all available tests in GTR for this gene
- Go to complete Gene record for SLC66A1LP
- Go to Variation Viewer for SLC66A1LP variants
Summary
Predicted to enable L-lysine transmembrane transporter activity. Predicted to be involved in L-lysine transmembrane transport. Predicted to be active in lysosomal membrane. [provided by Alliance of Genome Resources, Dec 2024]
Genomic context
- Location:
- 3q25.32
- Sequence:
- Chromosome: 3; NC_000003.12 (157543312..157601094)
- Total number of exons:
- 7
Variation
Resource | Links for this gene |
---|---|
dbVar | Studies and variants |
SNP | Variation Viewer for SLC66A1LP variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.