Gene
NLGN3
neuroligin 3
- HGNC 14289↗(opens in a new tab)
- Ensembl gene ENSG00000196338↗(opens in a new tab)
- NCBI Gene 54413↗(opens in a new tab)
Summary
- Cytogenetic location
- Xq13.1
- Coordinates
- Chromosome X: 71,144,841–71,171,201 (GRCh38)
- Exons
- 8 exons across 26.4 kb
- Protein
- 848 amino acids
- Also known as
- HNL3, KIAA1480, ASPGX1, AUTSX1
- MANE Select transcript
- ENST00000358741.4NM_181303.2
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome TestCurated reports relevant to this gene
Autism Spectrum Disorder
- Autism, susceptibility to (single-gene forms)
Single-gene contributions to autism, including variants in NLGN3, NLGN4X, PTCHD1, SHANK2, TBR1 and CHD8.
- 1 GenCC submitter rates it definitive or strong
Epilepsy (Full Panel)
- X-Linked Complex Neurodevelopmental Disorder
A complex neurodevelopmental disorder that is transmitted via X-linked inheritance, and is characterized by intellectual disability, autism and epilepsy.
- ClinGen rates the link moderate
- 1 GenCC submitter rates it definitive or strong
How NLGN3 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 4 kb of the gene's 26.4 kb; 2,547 of those bases code for the protein.
How a genome test reads NLGN3
3
positions in NLGN3 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 26.4 kb of NLGN3, introns included, not only the 4 kb of exons.
Genes linked to the same conditions
- NLGN4Xneuroligin 4 X-linkedShares 2 conditions
- PTCHD1patched domain containing 1Shares 2 conditions
- ARHGEF9Cdc42 guanine nucleotide exchange factor 9Shares 1 condition
- ARXaristaless related homeoboxShares 1 condition
- CHD8chromodomain helicase DNA binding protein 8Shares 1 condition
- CLCN4Cl-/H+ antiporter 4Shares 1 condition
- CNKSR2connector enhancer of kinase suppressor of Ras 2Shares 1 condition
- FRMPD4FERM and PDZ domain containing 4Shares 1 condition
- FTSJ1FtsJ RNA 2'-O-methyltransferase 1Shares 1 condition
- GRIA3glutamate ionotropic receptor AMPA type subunit 3Shares 1 condition
- HNRNPH2heterogeneous nuclear ribonucleoprotein H2Shares 1 condition
- IL1RAPL1interleukin 1 receptor accessory protein like 1Shares 1 condition
Traits linked to NLGN3
The Human Phenotype Ontology lists these as features of the rare conditions NLGN3 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). NLGN3 gene: neuroligin 3. Retrieved 17 October 2026, from https://dantelabs.com/genes/nlgn3
Dante Labs. NLGN3 gene: neuroligin 3 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/nlgn3
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