0 sources retrieved · Most recent: April 2026 · Index updated 16 days ago
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69PubMed Papers
21Diseases
0Drugs
12Pathogenic Variants
CLINICALOMIM Disease Gene
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
vocalization behaviorlearningsynapse organizationexcitatory synapseautismautism spectrum disordergenetic disorderIntellectual disability
AI summary not yet available. Showing NCBI Gene summary.
neuroligin 3
⚠Limited data available — This gene has 0 indexed publications. Summary and analysis may be incomplete.
autism spectrum disorderOpen Targets
genetic disorderOpen Targets
Intellectual disabilityOpen Targets
neurodegenerative diseaseOpen Targets
Asperger syndromeOpen Targets
X-linked complex neurodevelopmental disorderOpen Targets
Autistic behaviorOpen Targets
hypogonadotropic hypogonadismOpen Targets
complex neurodevelopmental disorderOpen Targets
attention deficit hyperactivity disorderOpen Targets
glioblastoma multiformeOpen Targets
hereditary attention deficit-hyperactivity disorderOpen Targets
attention deficit-hyperactivity disorder 8Open Targets
schizophrenia 15Open Targets
intellectual disability, autosomal recessive 59Open Targets
Tourette syndromeOpen Targets
intellectual disability, autosomal dominant 50Open Targets
Potocki-Lupski syndromeOpen Targets
Autism, X-linked 1UniProt
NM_181303.2(NLGN3):c.422_423del (p.Cys141fs)Likely pathogenic
Autism, susceptibility to, X-linked 1
★☆☆☆2024→ Residue 141
NM_181303.2(NLGN3):c.622G>A (p.Gly208Arg)Likely pathogenic
Autism, susceptibility to, X-linked 1|Melanoma
★☆☆☆2024→ Residue 208
NM_181303.2(NLGN3):c.1978C>T (p.Arg660Cys)Likely pathogenic
X-linked complex neurodevelopmental disorder
★☆☆☆2023→ Residue 660
NM_181303.2(NLGN3):c.366G>A (p.Trp122Ter)Pathogenic
Hypogonadotropic hypogonadism
★☆☆☆2023→ Residue 122
NM_181303.2(NLGN3):c.2222T>G (p.Leu741Arg)Likely pathogenic
Autism, susceptibility to, X-linked 1
★☆☆☆2022→ Residue 741
NM_181303.2(NLGN3):c.1600C>T (p.Pro534Ser)Pathogenic
Intellectual disability;Autistic behavior
★☆☆☆2019→ Residue 534
NM_181303.2(NLGN3):c.214dup (p.Val72fs)Pathogenic
Inborn genetic diseases
★☆☆☆2016→ Residue 72
NM_181303.2(NLGN3):c.577+1G>ALikely pathogenic
Inborn genetic diseases
★☆☆☆2014
NM_181303.2(NLGN3):c.1849C>T (p.Arg617Trp)Likely pathogenic
Intellectual disability
★☆☆☆2014→ Residue 617
NM_181303.2(NLGN3):c.913+1G>ALikely pathogenic
Autism, susceptibility to, X-linked 1
☆☆☆☆2022
NM_181303.2(NLGN3):c.1672A>G (p.Met558Val)Likely pathogenic
Autism, susceptibility to, X-linked 1
☆☆☆☆→ Residue 558
NM_181303.2(NLGN3):c.611T>C (p.Val204Ala)Pathogenic
Autism, susceptibility to, X-linked 1
☆☆☆☆→ Residue 204