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Neuroligin-4, X-linked (NLGN4X)

Homo sapiens — UniProt Q8N0W4

Gene: NLGN4XHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Neuroligin-4, X-linked (NLGN4X) is a protein from Homo sapiens identified by UniProt accession Q8N0W4, 816 residues long. MolForge cross-references it against 0 known binders and 83 disease associations.

  • UniProt accession: Q8N0W4; gene symbol NLGN4X.
  • Organism: Homo sapiens.
  • Length: 816 amino acids.
  • Top disease associations (Open Targets): autism, neurodegenerative disease and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameNeuroligin-4, X-linked
UniProt accessionQ8N0W4
GeneNLGN4X
OrganismHomo sapiens
Length816 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (83)

Diseases linked to this target (Open Targets).

  • autism · score 0.59
  • neurodegenerative disease · score 0.49
  • genetic disorder · score 0.47
  • X-linked intellectual disability · score 0.42
  • X-linked complex neurodevelopmental disorder · score 0.37
  • Crohn's disease · score 0.31
  • vaginal discharge · score 0.30
  • Asperger syndrome · score 0.16
  • Intellectual disability · score 0.15
  • autism spectrum disorder · score 0.12

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8N0W4-F1alphafoldPREDICTED79.09—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8N0W4.

Amino-acid sequence (816 residues)

MSRPQGLLWL PLLFTPVCVM LNSNVLLWLT ALAIKFTLID SQAQYPVVNT NYGKIRGLRT PLPNEILGPV EQYLGVPYAS PPTGERRFQP PEPPSSWTGI RNTTQFAAVC PQHLDERSLL HDMLPIWFTA NLDTLMTYVQ DQNEDCLYLN IYVPTEDDIH DQNSKKPVMV YIHGGSYMEG TGNMIDGSIL ASYGNVIVIT INYRLGILGF LSTGDQAAKG NYGLLDQIQA LRWIEENVGA FGGDPKRVTI FGSGAGASCV SLLTLSHYSE GLFQKAIIQS GTALSSWAVN YQPAKYTRIL ADKVGCNMLD TTDMVECLRN KNYKELIQQT ITPATYHIAF GPVIDGDVIP DDPQILMEQG EFLNYDIMLG VNQGEGLKFV DGIVDNEDGV TPNDFDFSVS NFVDNLYGYP EGKDTLRETI KFMYTDWADK ENPETRRKTL VALFTDHQWV APAVATADLH AQYGSPTYFY AFYHHCQSEM KPSWADSAHG DEVPYVFGIP MIGPTELFSC NFSKNDVMLS AVVMTYWTNF AKTGDPNQPV PQDTKFIHTK PNRFEEVAWS KYNPKDQLYL HIGLKPRVRD HYRATKVAFW LELVPHLHNL NEIFQYVSTT TKVPPPDMTS FPYGTRRSPA KIWPTTKRPA ITPANNPKHS KDPHKTGPED TTVLIETKRD YSTELSVTIA VGASLLFLNI LAFAALYYKK DKRRHETHRR PSPQRNTTND IAHIQNEEIM SLQMKQLEHD HECESLQAHD TLRLTCPPDY TLTLRRSPDD IPLMTPNTIT MIPNTLTGMQ PLHTFNTFSG GQNSTNLPHG HSTTRV

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with NLGN4X?

The strongest Open Targets associations for NLGN4X are autism, neurodegenerative disease, genetic disorder, X-linked intellectual disability and X-linked complex neurodevelopmental disorder.

How long is the NLGN4X protein?

The Homo sapiens NLGN4X protein (UniProt Q8N0W4) is 816 amino acids long.

Browse: Targets: N · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ8N0W4
GeneNLGN4X
OrganismHomo sapiens
Length816
Binders0
Diseases83
View on UniProt