SLITRK2 SLIT and NTRK like family member 2
Gene ID: 84631, updated on 4-Jan-2025Gene type: protein coding
Also known as: CXorf1; CXorf2; SLITL1; TMEM257; XLID111
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- Go to complete Gene record for SLITRK2
- Go to Variation Viewer for SLITRK2 variants
Summary
This gene encodes an integral membrane protein that contains two N-terminal leucine-rich repeats domains and contains C-terminal regions similar to neurotrophin receptors. The encoded protein may play a role in modulating neurite activity. Alternatively spliced transcript variants encoding the same protein have been described.[provided by RefSeq, Feb 2010]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Intellectual developmental disorder, X-linked 111 | not available |
Genomic context
- Location:
- Xq27.3
- Sequence:
- Chromosome: X; NC_000023.11 (145817829..145829856)
- Total number of exons:
- 5
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SLITRK2 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- SLITRK2 @ LOVD
- Variation ViewerRelated Variants
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