1. Gene
  2. SLITRK1 - SLIT and NTRK like family member 1 Gene

SLITRK1 - SLIT and NTRK like family member 1 Gene

Homo sapiens

Also known as TTM; LRRC12

Gene ID: 114798 | Gene type: protein coding

About SLITRK1

Cytogenetic location: 13q31.1 Genomic coordinates (GRCh38): 13:83,877,205-83,882,474 (from NCBI)

This gene has 2 transcripts (splice variants), 187 orthologues, 25 paralogues and is associated with 3 phenotypes. Restricted expression toward brain (RPKM 10.6).

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 receptors. However, the protein encoded by this gene lacks the region of homology to neurotrophin receptors. This protein is thought to be involved in neurite outgrowth. Mutations in this gene may be associated with Tourette syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

SLITRK1 Products(2)

mRNA Protein Name
NM_001281503.2 NP_001268432.1 SLIT and NTRK-like protein 1 precursor
NM_052910.2 NP_443142.1 SLIT and NTRK-like protein 1 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
19640509 GOA
Biological Process GO Annotation Evidence Reference Source
involved in positive regulation of axonogenesis IMP
IMP: Inferred from mutant phenotype
23990902 GOA
involved in regulation of presynapse assembly IDA
IDA: Inferred from direct assay
23345436 GOA
involved in regulation of presynapse assembly IMP
IMP: Inferred from mutant phenotype
23345436 GOA
involved in synapse assembly IMP
IMP: Inferred from mutant phenotype
27273464 GOA
involved in synaptic membrane adhesion IDA
IDA: Inferred from direct assay
23345436 GOA
involved in synaptic membrane adhesion IMP
IMP: Inferred from mutant phenotype
23345436 GOA
Cellular Component GO Annotation Evidence Reference Source
is active in GABA-ergic synapse IDA
IDA: Inferred from direct assay
23345436 GOA
is active in GABA-ergic synapse IMP
IMP: Inferred from mutant phenotype
23345436 GOA
is active in glutamatergic synapse IDA
IDA: Inferred from direct assay
23345436 GOA
is active in glutamatergic synapse IMP
IMP: Inferred from mutant phenotype
23345436 GOA
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

SLITRK1 Protein Structure

LRR_8

LRR_8: Leucine rich repeat (132 - 189)

LRR_1

LRR_1: Leucine Rich Repeat (400 - 422)

LRR_8

LRR_8: Leucine rich repeat (425 - 483)

  • 0
  • 200
  • 400
  • 600
  • 696 a.a.
Protein Preferred Names Protein Names

SLIT and NTRK-like protein 1

leucine-rich repeat-containing protein 12

SLITRK1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SLITRK1 Q96PX8 UBQLN2 Homo sapiens Q9UHD9
Y2H Array
32296183
Intra
SLITRK1 Q96PX8 UBQLN2 Homo sapiens Q9UHD9
Validated Y2H
32296183
Intra
SLITRK1 Q96PX8 UBQLN2 Homo sapiens Q9UHD9
Y2H Prey Pooling
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SLITRK1 Proteins

Cat. No. Product Name Accession Purity
HY-P76077 SLITRK1 Protein, Human (HEK293, His-Fc) Q96PX8 (N18-S616) ≥95%
HY-P76078 SLITRK1 Protein, Human (HEK293, His) Q96PX8 (N18-S616) ≥95%

Related Diseases

Diseases Alias
Trichotillomania

TTM

Hair-Pulling Syndrome

Compulsive Hair Plucking

Hair Pulling Disorder

Gilles De La Tourette Syndrome

Tourette Syndrome

Tourette Disorder

GTS

Ts

Gilles De La Tourette'S Syndrome

Motor-Verbal Tic Disorder

Guinon'S Disease

Psychogenic Tics

Tourette'S Syndrome

Chronic Motor And Vocal Tic Disorder

Td

Tourette'S Disease

Combined Vocal And Multiple Motor Tic Disorder [De La Tourette]

Combined Vocal And Multiple Motor Tic Disorder

Tic De La Tourette

Obsessive-Compulsive Disorder

OCD

Obsessive-Compulsive Disorder, Susceptibility To

Anancastic Neurosis

Obsessive Compulsive Disorder

Anankastic Neurosis

Obsessive-Compulsive Neurosis

Obsessive Compulsive Behavior

Chronic Tic Disorder

Chronic Motor Or Vocal Tic Disorder

Tic Disorders

Tic Disorder

Tic Disorder Nos

Tic Nos

Tic Spasm Nos

Transient Tic Disorder
Tic Disorder

Tics

Behavioral Tic

Color Agnosia
Deafness, Autosomal Dominant 33

DFNA33

Autosomal Dominant Nonsyndromic Deafness 33

Autosomal Dominant Deafness 33

Trichothiodystrophy 5, Nonphotosensitive

TTD5

Nonphotosensitive Trichothiodystrophy 5

Trichothiodystrophy 5, Non-Photosensitive

Impulse Control Disorder

Disruptive, Impulse Control, And Conduct Disorders

Abcd Syndrome

ABCDS

Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut, And Deafness

Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut And Deafness

Echolalia
Stereotypic Movement Disorder

Stereotypy Habit Disorder

Stereotyped Repetitive Movements

Stereotyped Disorder

Stereotypes Nos

Stereotype Habit Disorder

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder

ADHD

Attention Deficit Disorder

Attention Deficit-Hyperactivity Disorder, Susceptibility To

Attention Deficit Disorder With Hyperactivity

Hyperkinetic Disorder

Hyperactivity Of Childhood

Attention-Deficit/Hyperactivity Disorder

Add

Addh

Attention Deficit

Attention Deficit Disorder Of Childhood With Hyperactivity

Attention Deficit Disorder With Hyperactivity Syndrome

Hyperkinetic Syndrome

Attention-Deficit Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

Disturbance Of Activity And Attention

Disorder Of Activity And Attention

Adhd - [Attention Deficit Hyperactivity Disorder]

Hyperkinetic Disorders

Disorder Of Activity And Attention With Hyperkinesia

Attention Deficit Syndrome With Hyperactivity

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus SLITRK1 VGNC VGNC:65454
Rattus norvegicus SLITRK1 RGD RGD:1308858
Mus musculus SLITRK1 MGD MGI:2679446
Bos taurus SLITRK1 VGNC VGNC:34962
Canis familiaris SLITRK1 VGNC VGNC:46506
Macaca mulatta SLITRK1 VGNC VGNC:77744
Others SLITRK1 NCBI