Slc6a17 - solute carrier family 6 (neurotransmitter transporter), member 17 Gene

Also Known as Ntt4; D130012J15Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 229706

Summary

Predicted to enable symporter activity. Involved in brain development. Predicted to be located in several cellular components, including cell projection; cytoplasmic vesicle; and synapse. Predicted to be integral component of plasma membrane. Predicted to be active in synaptic vesicle. Predicted to be intrinsic component of membrane. Is expressed in several structures, including nervous system. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human SLC6A17 (solute carrier family 6 member 17). [provided by Alliance of Genome Resources, Apr 2022]

Slc6a17 Products (2)

mRNA Protein Name
NM_001293689.1 NP_001280618.1 sodium-dependent neutral amino acid transporter SLC6A17 isoform 1
NM_172271.2 NP_758475.1 sodium-dependent neutral amino acid transporter SLC6A17 isoform2

Gene Ontology

  • Biological Process
Biological Process GO Annotation Evidence References Source
involved in brain development IDA
IDA: Inferred from direct assay
25704603 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

sodium-dependent neutral amino acid transporter SLC6A17

  • orphan sodium- and chloride-dependent neurotransmitter transporter NTT4

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13303 SLC6A17 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc6a17 NCBI NCBI:388662