CNTNAP4
Contactin-associated protein-like 4
Also known as: CASPR4, CNTP4_HUMAN, KIAA1763
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9C0A0
- Gene
- CNTNAP4
- Ensembl
- ENSG00000152910
- Chromosome
- 16
- Canonical length
- 1308 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a member of the neurexin protein family. Members of this family function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. This protein may also play a role in proper neurotransmission in the dopaminergic and GABAergic systems and mutations in this gene may be associated with certain psychiatric illnesses. A polymorphism in an intron of this gene may be associated with longevity. [provided by RefSeq, Apr 2016]
Canonical amino-acid sequenceUniProt
1308 residues, UniProt reviewed canonical sequence.
>Q9C0A0|CNTNAP4
1 MGSVTGAVLK TLLLLSTQNW NRVEAGNSYD CDDPLVSALP QASFSSSSEL SSSHGPGFAR
61 LNRRDGAGGW SPLVSNKYQW LQIDLGERME VTAVATQGGY GSSNWVTSYL LMFSDSGWNW
121 KQYRQEDSIW GFSGNANADS VVYYRLQPSI KARFLRFIPL EWNPKGRIGM RIEVFGCAYR
181 SEVVDLDGKS SLLYRFDQKS LSPIKDIISL KFKTMQSDGI LLHREGPNGD HITLQLRRAR
241 LFLLINSGEA KLPSTSTLVN LTLGSLLDDQ HWHSVLIQRL GKQVNFTVDE HRHHFHARGE
301 FNLMNLDYEI SFGGIPAPGK SVSFPHRNFH GCLENLYYNG VDIIDLAKQQ KPQIIAMGNV
361 SFSCSQPQSM PVTFLSSRSY LALPDFSGEE EVSATFQFRT WNKAGLLLFS ELQLISGGIL
421 LFLSDGKLKS NLYQPGKLPS DITAGVELND GQWHSVSLSA KKNHLSVAVD GQMASAAPLL
481 GPEQIYSGGT YYFGGCPDKS FGSKCKSPLG GFQGCMRLIS ISGKVVDLIS VQQGSLGNFS
541 DLQIDSCGIS DRCLPNYCEH GGECSQSWST FHCNCTNTGY RGATCHNSIY EQSCEAYKHR
601 GNTSGFYYID SDGSGPLEPF LLYCNMTETA WTIIQHNGSD LTRVRNTNPE NPYAGFFEYV
661 ASMEQLQATI NRAEHCEQEF TYYCKKSRLV NKQDGTPLSW WVGRTNETQT YWGGSSPDLQ
721 KCTCGLEGNC IDSQYYCNCD ADRNEWTNDT GLLAYKEHLP VTKIVITDTG RLHSEAAYKL
781 GPLLCQGDRS FWNSASFDTE ASYLHFPTFH GELSADVSFF FKTTASSGVF LENLGIADFI
841 RIELRSPTVV TFSFDVGNGP FEISVQSPTH FNDNQWHHVR VERNMKEASL QVDQLTPKTQ
901 PAPADGHVLL QLNSQLFVGG TATRQRGFLG CIRSLQLNGM TLDLEERAQV TPEVQPGCRG
961 HCSSYGKLCR NGGKCRERPI GFFCDCTFSA YTGPFCSNEI SAYFGSGSSV IYNFQENYLL
1021 SKNSSSHAAS FHGDMKLSRE MIKFSFRTTR TPSLLLFVSS FYKEYLSVII AKNGSLQIRY
1081 KLNKYQEPDV VNFDFKNMAD GQLHHIMINR EEGVVFIEID DNRRRQVHLS SGTEFSAVKS
1141 LVLGRILEHS DVDQDTALAG AQGFTGCLSA VQLSHVAPLK AALHPSHPDP VTVTGHVTES
1201 SCMAQPGTDA TSRERTHSFA DHSGTIDDRE PLANAIKSDS AVIGGLIAVV IFILLCITAI
1261 AVRIYQQKRL YKRSEAKRSE NVDSAEAVLK SELNIQNAVN ENQKEYFFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CNTNAP4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 95 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 95 nTPM
- midbrain: 37 nTPM
- hippocampal formation: 22 nTPM
- cerebral cortex: 21 nTPM
- hypothalamus: 19 nTPM
- cerebellum: 16 nTPM
Single-cell type
- early spermatids: 8.4 nCPM
- late primary spermatocytes: 3.5 nCPM
- late spermatids: 2.7 nCPM
- distal convoluted tubule cells: 2.2 nCPM
- renal collecting duct principal cells: 1.9 nCPM
- renal connecting tubule cells: 1.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 245 nTPM
- medulla oblongata: 160 nTPM
- pons: 124 nTPM
- basal ganglia: 119 nTPM
- thalamus: 111 nTPM
- cerebral cortex: 100 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.52
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.24
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell adhesion
- nervous system development
- regulation of grooming behavior
- regulation of synaptic transmission, dopaminergic
- regulation of synaptic transmission, GABAergic
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coagulation factor 5/8, C-terminal domain
- EGF-like domain
- Laminin G domain
- Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain
- Galactose-binding-like domain superfamily
- Concanavalin A-like lectin/glucanase domain superfamily
- Fibrinogen-like, C-terminal
- Neurexin-related cell adhesion and synaptic protein
- F5/8 type C domain
- Laminin G domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CNTNAP4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CNTNAP4 as an antibody target. Whether an autoantibody or antibody against CNTNAP4 could matter depends on whether native CNTNAP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CNTNAP4 is annotated at the cell surface, where native CNTNAP4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CNTNAP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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