Protein detail

NTNG2

Netrin-G2 (Laminet-2)

Entry name
NTNG2
UniProt ID
EVMP score
0.38
Frequency
3
Transmembrane count
Protein classification
Disease related genesHuman disease related genesPredicted intracellular proteins
EVMP score: annotation confidence score.
Extremely high >= 0.85High >= 0.70Medium >= 0.55Low >= 0.40
Basic Information
Protein Names
Netrin-G2 (Laminet-2)
Protein Class
Disease related genesHuman disease related genesPredicted intracellular proteins
Protein Function
  • Disease related genes
  • Human disease related genes:Congenital malformations:Congenital malformations of the nervous system
  • Predicted intracellular proteins
Entrez Gene Symbol
Gene Synonym
KIAA1857Lmnt2NTNG1
Gene Description
Netrin G2
Chromosome
9
Position
132162058-132244526
Frequency
3
EVMP Score
0.38
Fluorescence & Localization
NTNG2 fluorescence
Tissue SpecificbrainCell SpecificBrain excitatory neurons
Function & Pathway
Relations & Evidence

Enzyme-Mediated Modification

0 records.

Ligand-Receptor Signaling

35 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
cell_adhesioncell_adhesionCellinkerYesYesYesNoNo
adhesionadhesionOmniPathYesYesYesNoNo
cell_adhesioncell_adhesionOmniPathYesYesYesNoNo
peripheralperipheralUniProt_locationNoNoYesNoNo
peripheralperipheralOmniPathNoNoYesNoNo
plasma_membraneplasma_membraneUniProt_locationNoNoYesNoNo
plasma_membraneplasma_membraneCellinkerNoNoYesNoNo
plasma_membraneplasma_membraneOmniPathNoNoYesNoNo
secretedsecretedconnectomeDB2020NoNoYesNoNo
secretedsecretedOmniPathNoNoYesNoNo
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Regulatory Interaction Network

1 record.

Source Protein SymbolSource UniProt IDTarget Protein SymbolTarget UniProt IDIs DirectedIs StimulationIs InhibitionDatabaseReferences
NTNG2Q96CW9LRRC4Q9HBW1YesYesNoFantom5_LRdbCellTalkDBiTALKtalklrRamilowski2015_Baccin2019SIGNORconnectomeDB2020HINTBaccin2019IntActLit-BM-17CellinkerLRdbSTRING_talklrEMBRACERamilowski2015Lit-BM-17:21946559LRdb:17973922IntAct:21946559Ramilowski2015:17973922SIGNOR:19467332HINT:21946559connectomeDB2020:17973922Cellinker:25411505talklr:17973922CellTalkDB:17973922

Protein Complex Composition

2 records.

Component NameComponent Gene SymbolsComponent UniProt IDStoichiometryDatabaseDatabase IDsReferences
NTNG2Q96CW92PDBPDB:3zyg
LRRC4NTNG2Q96CW9Q9HBW11:1PDBPDB:3zyi

Isolation & Detection Technology

1 record.

EV Isolation MethodDetection MethodNumber of ReferencesReferences
Differential UltracentrifugationDensity Gradient CentrifugationSize Exclusion ChromatographyImmunoaffinity CaptureMass spectrometryWestern blottingELISA424505114376863664009834631588238
Sequence, Structure & Domains

Sequences

Length
530
Mass
59,799
Sequence
MLHLLALFLHCLPLASGDYDICKSWVTTDEGPTWEFYACQPKVMRLKDYVKVKVEPSGITCGDPPERFCSHENPYLCSNECDASNPDLAHPPRLMFDKEEEGLATYWQSITWSRYPSPLEANITLSWNKTVELTDDVVMTFEYGRPTVMVLEKSLDNGRTWQPYQFYAEDCMEAFGMSARRARDMSSSSAHRVLCTEEYSRWAGSKKEKHVRFEVRDRFAIFAGPDLRNMDNLYTRLESAKGLKEFFTLTDLRMRLLRPALGGTYVQRENLYKYFYAISNIEVIGRCKCNLHANLCSMREGSLQCECEHNTTGPDCGKCKKNFRTRSWRAGSYLPLPHGSPNACATAGSFGNCECYGHSNRCSYIDFLNVVTCVSCKHNTRGQHCQHCRLGYYRNGSAELDDENVCIECNCNQIGSVHDRCNETGFCECREGAAGPKCDDCLPTHYWRQGCYPNVCDDDQLLCQNGGTCLQNQRCACPRGYTGVRCEQPRCDPADDDGGLDCDRAPGAAPRPATLLGCLLLLGLAARLGR
Alternative Products
Event=Alternative splicing; Named isoforms=2; Name=1; IsoId=Q96CW9-1; Sequence=Displayed; Name=2; IsoId=Q96CW9-2; Sequence=VSP_013147, VSP_013148
Alternative Sequence
352..422; NCECYGHSNRCSYIDFLNVVTCVSCKHNTRGQHCQHCRLGYYRNGSAELDDENVCIECNCNQIGSVHDRCN -> TLQTPPPGRSPSALRGSRRGLANVKEPAGSRPQISEMLLGCTVTLHQGSVGPHIPPKLSLPDPGGPWLGSQ (in isoform 2); 423..530; Missing (in isoform 2)

3D Structural Models

Turn
74..76; 86..88; 113..116; 198..204; 224..227; 336..338
Helix
46..49; 92..95; 171..175; 182..184; 187..189; 216..223; 230..239; 243..246; 271..273
Beta Strand
22..28; 31..36; 51..56; 66..68; 71..73; 79..81; 83..85; 107..109; 121..133; 137..143; 147..156; 162..170; 205..207; 210..213; 248..258; 277..282; 284..287; 296..299; 302..305; 311..313; 324..326
3D Structure
X-ray crystallography (3)

Domain & Motif Annotations

Domain (CC)
The laminin N-terminal domain mediates 1:1 binding to NGL ligand with sub-micromolar affinity. Three NGL-binding loops mediate discrimination for LRRC4C/NGL1 among other NGLs by binding specifically to its LRR repeats. This specificity drives the sorting of a mixed population of molecules into discrete cell surface subdomains.
Domain (FT)
35..286; Laminin N-terminal; 287..346; Laminin EGF-like 1; 353..408; Laminin EGF-like 2; 409..453; Laminin EGF-like 3
Region
69..88; NGL discriminant loop I; 201..203; NGL discriminant loop II; 264..267; NGL discriminant loop III
Clinical Relevance
Disease Involvement
Autism spectrum disorderDisease variantIntellectual disability