Gene Gene information from NCBI Gene database.
Entrez ID 114798
Gene name SLIT and NTRK like family member 1
Gene symbol SLITRK1
Synonyms (NCBI Gene)
LRRC12TTM
Chromosome 13
Chromosome location 13q31.1
Summary This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin re
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs191284403 C>A,T Pathogenic 3 prime UTR variant
rs193302861 G>- Pathogenic Coding sequence variant, frameshift variant
miRNA miRNA information provided by mirtarbase database.
67
miRTarBase ID miRNA Experiments Reference
MIRT005653 hsa-miR-24-1-5p GFP reporter assayIn situ hybridizationLuciferase reporter assay 16224024
MIRT018680 hsa-miR-335-5p Microarray 18185580
MIRT1369719 hsa-miR-15a CLIP-seq
MIRT1369720 hsa-miR-15b CLIP-seq
MIRT1369721 hsa-miR-16 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
34
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 19640509, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005886 Component Plasma membrane TAS
GO:0006897 Process Endocytosis IEA
GO:0007399 Process Nervous system development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609678 20297 ENSG00000178235
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96PX8
Protein name SLIT and NTRK-like protein 1 (Leucine-rich repeat-containing protein 12)
Protein function It is involved in synaptogenesis and promotes excitatory synapse differentiation (PubMed:27273464, PubMed:27812321). Enhances neuronal dendrite outgrowth (PubMed:16224024, PubMed:19640509). {ECO:0000269|PubMed:16224024, ECO:0000269|PubMed:196405
PDB 4RCA , 4RCW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 83 142 Leucine rich repeat Repeat
PF13855 LRR_8 138 189 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in the frontal lobe of the cerebral cortex of the brain. Also expressed in some astrocytic brain tumors such as astrocytomas, oligodendrogliomas, glioblastomas, gangliogliomas and primitive neuroectodermal tumor
Sequence
MLLWILLLETSLCFAAGNVTGDVCKEKICSCNEIEGDLHVDCEKKGFTSLQRFTAPTSQF
YHLFLHGNSLTRLFPNEFANFYNAVSLHMENNGLHEIVPGAFLGLQLVKRLHINNNKIKS
FRKQTFLGLDDLEYLQA
DFNLLRDIDPGAFQDLNKLEVLILNDNLISTLPANVFQYVPIT
HLDLRGNRL
KTLPYEEVLEQIPGIAEILLEDNPWDCTCDLLSLKEWLENIPKNALIGRVV
CEAPTRLQGKDLNETTEQDLCPLKNRVDSSLPAPPAQEETFAPGPLPTPFKTNGQEDHAT
PGSAPNGGTKIPGNWQIKIRPTAAIATGSSRNKPLANSLPCPGGCSCDHIPGSGLKMNCN
NRNVSSLADLKPKLSNVQELFLRDNKIHSIRKSHFVDYKNLILLDLGNNNIATVENNTFK
NLLDLRWLYMDSNYLDTLSREKFAGLQNLEYLNVEYNAIQLILPGTFNAMPKLRILILNN
NLLRSLPVDVFAGVSLSKLSLHNNYFMYLPVAGVLDQLTSIIQIDLHGNPWECSCTIVPF
KQWAERLGSEVLMSDLKCETPVNFFRKDFMLLSNDEICPQLYARISPTLTSHSKNSTGLA
ETGTHSNSYLDTSRVSISVLVPGLLLVFVTSAFTVVGMLVFILRNRKRSKRRDANSSASE
INSLQTVCDSSYWHNGPYNADGAHRVYDCGSHSLSD
Sequence length 696
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Cell adhesion molecules   Receptor-type tyrosine-protein phosphatases
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
109
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Tourette syndrome Pathogenic rs193302861, rs191284403 RCV000001644
RCV000001646
Trichotillomania Pathogenic rs193302861 RCV000001645
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
SLITRK1-related disorder Uncertain significance; Likely benign rs2501000717, rs761823041, rs150504822 RCV003394441
RCV003947124
RCV003919709
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 36085162
Breast Neoplasms Associate 19153192
Carcinoma Ductal Breast Associate 19153192
Cardiomyopathy Hypertrophic Associate 27600940
Multiple Organ Failure Associate 27600940
Obsessive Compulsive Disorder Associate 23154099, 36085162
Prader Willi Syndrome Associate 37491450
Schizophrenia Associate 30082721, 36085162
Tourette Syndrome Associate 35456478