Protein detail

TM237

Transmembrane protein 237 (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 4 protein)

Entry name
TM237
UniProt ID
EVMP score
0.50
Frequency
1
Transmembrane count
4
Protein classification
Disease related genesHuman disease related genesPotential drug targetsPredicted membrane proteinsTransporters
EVMP score: annotation confidence score.
Extremely high >= 0.85High >= 0.70Medium >= 0.55Low >= 0.40
Basic Information
Protein Names
Transmembrane protein 237 (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 4 protein)
Protein Class
Disease related genesHuman disease related genesPotential drug targetsPredicted membrane proteinsTransporters
Protein Function
  • Disease related genes
  • Human disease related genes:Congenital malformations:Congenital malformations of the nervous system
  • Transporters:Accessory Factors Involved in Transport
  • Potential drug targets
Transmembrane
227..247; Helical; 268..288; Helical; 303..323; Helical; 358..378; Helical
Transmembrane Count
4
Entrez Gene Symbol
Gene Synonym
ALS2CR4JBTS14
Gene Description
Transmembrane protein 237
Chromosome
2
Position
201620184-201643570
Frequency
1
EVMP Score
0.50
Fluorescence & Localization
Function & Pathway
Protein Function
  • Disease related genes
  • Human disease related genes:Congenital malformations:Congenital malformations of the nervous system
  • Transporters:Accessory Factors Involved in Transport
  • Potential drug targets
Molecular Function
Canonical Pathways
M60 Pid nfat tfpathway
Mediation Categories
Receptor-signaling mediation
Relations & Evidence

Enzyme-Mediated Modification

0 records.

Ligand-Receptor Signaling

9 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
intracellularintracellularGO_IntercellNoNoNoNoNo
intracellularintracellularOmniPathNoNoNoNoNo
transmembranetransmembraneUniProt_locationNoNoNoNoNo
transmembranetransmembraneUniProt_topologyNoNoNoNoNo
transmembranetransmembraneUniProt_keywordNoNoNoNoNo
transmembranetransmembraneLOCATENoNoNoNoNo
transmembranetransmembraneRamilowski_locationNoNoNoNoNo
transmembranetransmembraneOmniPathNoNoNoNoNo
transmembranetransmembrane_predictedPhobiusNoNoNoNoNo

Regulatory Interaction Network

0 records.

Protein Complex Composition

Isolation & Detection Technology

1 record.

EV Isolation MethodDetection MethodNumber of ReferencesReferences
Size Exclusion ChromatographyMass spectrometryR Sequencing134265469
Sequence, Structure & Domains

Sequences

Length
408
Mass
45,526
Sequence
MRTDSGARLEEGHLRPPRALPPVPSQDDIPLSRPKKKKPRTKNTPASASLEGLAQTAGRRPSEGNEPSTKELKEHPEAPVQRRQKKTRLPLELETSSTQKKSSSSSLLRNENGIDAEPAEEAVIQKPRRKTKKTQPAELQYANELGVEDEDIITDEQTTVEQQSVFTAPTGISQPVGKVFVEKSRRFQAADRSELIKTTENIDVSMDVKPSWTTRDVALTVHRAFRMIGLFSHGFLAGCAVWNIVVIYVLAGDQLSNLSNLLQQYKTLAYPFQSLLYLLLALSTISAFDRIDFAKISVAIRNFLALDPTALASFLYFTALILSLSQQMTSDRIHLYTPSSVNGSLWEAGIEEQILQPWIVVNLVVALLVGLSWLFLSYRPGMDLSEELMFSSEVEEYPDKEKEIKASS
Alternative Products
Event=Alternative splicing; Named isoforms=5; Name=1; IsoId=Q96Q45-1; Sequence=Displayed; Name=2; IsoId=Q96Q45-2; Sequence=VSP_016628; Name=3; IsoId=Q96Q45-3; Sequence=VSP_042381; Name=4; IsoId=Q96Q45-4; Sequence=VSP_042382; Name=5; IsoId=Q96Q45-5; Sequence=VSP_042383
Alternative Sequence
1..14; MRTDSGARLEEGHL -> MGKNPV (in isoform 2); 1..14; MRTDSGARLEEGHL -> MTHCACARDRAREGWGARCLGARRPPRPAKRRMGKNPV (in isoform 3); 36..130; Missing (in isoform 4); 132; K -> KRPYYR (in isoform 5)

3D Structural Models

Domain & Motif Annotations

Compositional Bias
1..14; Basic and acidic residues; 60..77; Basic and acidic residues; 95..106; Low complexity
Region
1..137; Disordered
Protein Families
TMEM237 family
Sequence Similarities
Belongs to the TMEM237 family.
Clinical Relevance
Disease Involvement
CiliopathyJoubert syndrome