Homo sapiens Protein: NLGN4X
Summary
InnateDB Protein IDBP-41666.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NLGN4X
Protein Name neuroligin 4, X-linked
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000370485
InnateDB Gene IDBG-41664 (NLGN4X)
Protein Structure
UniProt Annotation
Function Putative neuronal cell surface protein involved in cell- cell-interactions.
Subcellular Localization Cell membrane; Single-pass type I membrane protein. Cell junction, synapse, postsynaptic cell membrane, postsynaptic density.
Disease Associations Autism, X-linked 2 (AUTSX2) [MIM:300495]: A complex multifactorial, pervasive developmental disorder characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Most individuals with autism also manifest moderate mental retardation. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.Asperger syndrome, X-linked, 2 (ASPGX2) [MIM:300497]: A syndrome with features similar to autism. Affected individuals exhibit qualitative impairment in social interaction, as manifest by impairment in the use of non-verbal behaviors such as eye-to- eye gaze, facial expression, body postures, and gestures, failure to develop appropriate peer relationships, and lack of social sharing or reciprocity. Patients also exhibit restricted, repetitive and stereotyped patterns of behavior, interests, and activities, including abnormal preoccupation with certain activities and inflexible adherence to routines or rituals. Asperger syndrome is primarily distinguished from autism by the higher cognitive abilities and a more normal and timely development of language and communicative phrases. {ECO:0000269PubMed:14963808}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity Expressed at highest levels in heart. Expressed at lower levels in liver, skeletal muscle and pancreas and at very low levels in brain. {ECO:0000269PubMed:11368788}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
Experimentally validated
Total 6 [view]
Protein-Protein 6 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004872 receptor activity
GO:0005515 protein binding
GO:0016787 hydrolase activity
GO:0031404 chloride ion binding
GO:0042043 neurexin family protein binding
GO:0042803 protein homodimerization activity
GO:0050839 cell adhesion molecule binding
Biological Process
GO:0003360 brainstem development
GO:0007158 neuron cell-cell adhesion
GO:0007612 learning
GO:0008152 metabolic process
GO:0021549 cerebellum development
GO:0030182 neuron differentiation
GO:0030534 adult behavior
GO:0035176 social behavior
GO:0035265 organ growth
GO:0045216 cell-cell junction organization
GO:0050808 synapse organization
GO:0071625 vocalization behavior
GO:0090394 negative regulation of excitatory postsynaptic membrane potential
GO:0097105 presynaptic membrane assembly
Cellular Component
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0009986 cell surface
GO:0014069 postsynaptic density
GO:0016021 integral component of membrane
GO:0030054 cell junction
GO:0030425 dendrite
GO:0045202 synapse
GO:0045211 postsynaptic membrane
GO:0060076 excitatory synapse
Protein Structure and Domains
PDB ID
InterPro IPR000460 Neuroligin
IPR002018 Carboxylesterase, type B
IPR013094 Alpha/beta hydrolase fold-3
IPR029058 Alpha/Beta hydrolase fold
PFAM PF00135
PF07859
PRINTS PR01090
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8N0W4
PhosphoSite PhosphoSite-Q8N0W4
TrEMBL B3KMT6
UniProt Splice Variant
Entrez Gene 57502
UniGene Hs.21107
RefSeq NP_851849
HUGO HGNC:14287
OMIM 300427
CCDS CCDS14126
HPRD 02336
IMGT
EMBL AB033086 AF376803 AK022621 AY358562 BC034018 CH471074
GenPept AAH34018 AAM46112 AAQ88925 BAA86574 BAG51098 EAW98738 EAW98739 EAW98741