Citations for
1CNTN4, CNTN5
Members of the vertebrate contactin and amyloid precursor protein families interact through a conserved interface
Karuppan SJ, Vogt A, Fischer Z, Ladutska A, Swiastyn J, McGraw HF, Bouyain S.
J Biol Chem. Feb;298(2):101541. doi: 10.1016/j.jbc.2021.101541. Epub 2021 Dec 25. 2022
2CNTN4
The autism risk gene CNTN4 modulates dendritic spine formation.
Zhao R, Zhu T, Liu Q, Tian Q, Wang M, Chen J, Tong D, Yu B, Guo H, Xia K, Qiu Z, Hu Z.
Hum Mol Genet. Dec 27;31(2):207-218. doi: 10.1093/hmg/ddab233. 2021
3CNTN4, DEL3PD
Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder.
Gandawijaya J, Bamford RA, Burbach JPH, Oguro-Ando A.
Front Cell Neurosci Jan 13;14:611379. doi: 10.3389/fncel.2020.611379. eCollection 2020. 2021
4CHL1, CNTN4, CNTN6
Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations
Tassano E, Uccella S, Giacomini T, Severino M, Fiorio P, Gimelli G, Ronchetto P.
Cytogenet Genome Res. 156(3):144-149. doi: 10.1159/000494152. Epub 2018 Dec 4. 2018
5CNTN4, MMP2, SNTB1
Single nucleotide polymorphisms in an Indian cohort and association of CNTN4, MMP2 and SNTB1 variants with oral cancer.
Yete S, Pradhan S, Saranath D.
Cancer Genet 214-215:16-25. doi: 10.1016/j.cancergen.2017.03.006. Epub 2017 Mar 23. 2017
6CNTN4, CNTN5, CNTN6
A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders
Oguro-Ando A, Zuko A, Kleijer KTE, Burbach JPH.
Mol Cell Neurosci. Jun;81:72-83. doi: 10.1016/j.mcn.2016.12.004. Epub 2017 Jan 5. 2017
7CNTN4
Investigating the effect of different transducer stiffness values on the contactin complex detachment by steered molecular dynamics.
Kianfar P, Abolfathi N, Karimi NZ.
J Mol Graph Model. Aug;75:340-346. doi: 10.1016/j.jmgm.2017.05.015. Epub 2017 Jun 2. 2017
8ARHGEF26, CNTN4, ITPR1, TGM4
GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
Chittoor G, Kent JW Jr, Almeida M, Puppala S, Farook VS, Cole SA, Haack K, Göring HH, MacCluer JW, Curran JE, Carless MA, Johnson MP, Moses EK, Almasy L, Mahaney MC, Lehman DM, Duggirala R, Comuzzie AG, Blangero J, Voruganti VS.
BMC Genomics 17:276. doi: 10.1186/s12864-016-2594-5. 2016
9CNTN4
Contactin-4 mediates axon-target specificity and functional development of the accessory optic system.
Osterhout JA, Stafford BK, Nguyen PL, Yoshihara Y, Huberman AD.
Neuron. May 20;86(4):985-999. doi: 10.1016/j.neuron.2015.04.005. Epub 2015 May 7. 2015
10CNTN4, CNTN5, CNTN6
Contactins in the neurobiology of autism
Zuko A, Kleijer KTE, Oguro-Ando A, Kas MJH, van Daalen E, van der Zwaag B, Burbach JPH.
Eur J Pharmacol. Nov 5;719(1-3):63-74. doi: 10.1016/j.ejphar.2013.07.016. Epub 2013 Jul 17. 2013
11CNTN1, CNTN3, CNTN4, CNTN5, CNTN6, PTPRG, PTPRZ1, PTPRZ2
The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules.
Bouyain S, Watkins DJ.
Proc Natl Acad Sci U S A 107(6):2443-8. Epub 2010 Jan 21.PMID: 20133774 2010
12CNTN4
Disruption of contactin 4 in three subjects with autism spectrum disorder.
Roohi J, Montagna C, Tegay DH, Palmer LE, Devincent C, Pomeroy JC, Christian SL, Nowak N, Hatchwell E.
J Med Genet 46(3):176-82. Epub 2008 Mar 18. 2009
13ASDT1, AUTS1, CNTN4, CNTNAP2
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.
Am J Hum Genet 82(1):165-73. 2008
14CNTN4, DEL3PD
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
Fernandez TV, García-González IJ, Mason CE, Hernández-Zaragoza G, Ledezma-Rodríguez VC, Anguiano-Alvarez VM, E'Vega R, Gutiérrez-Angulo M, Maya ML, García-Bejarano HE, González-Cruz M, Barrios S, Atorga R, López-Cardona MG, Armendariz-Borunda J, State MW, Dávalos NO.
Am J Med Genet A 146A(21):2746-52. 2008
15CNTN4, CRBN , DEL3PD, DUP3PD
FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions.
Dijkhuizen T, van Essen T, van der Vlies P, Verheij JB, Sikkema-Raddatz B, van der Veen AY, Gerssen-Schoorl KB, Buys CH, Kok K.
Am J Med Genet A 140(22):2482-7. 2006
16CNTN4
The contactin 4 gene locus at 3p26 is a candidate gene of SCA16.
Miura S, Shibata H, Furuya H, Ohyagi Y, Osoegawa M, Miyoshi Y, Matsunaga H, Shibata A, Matsumoto N, Iwaki A, Taniwaki T, Kikuchi H, Kira J, Fukumaki Y.
Neurology 67(7):1236-41. 2006
17CNTN4, DEL3PD
Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome.
Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW.
Am J Hum Genet 74(6):1286-93. Epub 2004 Apr 21. 2004
18ARPC4, CHL1, CNTN4
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.
Frints SG, Marynen P, Hartmann D, Fryns JP, Steyaert J, Schachner M, Rolf B, Craessaerts K, Snellinx A, Hollanders K, D'Hooge R, De Deyn PP, Froyen G.
Hum Mol Genet 12(13):1463-74. 2003
19CNTN4
A novel splice variant of the cell adhesion molecule contactin 4 ( CNTN4) is mainly expressed in human brain.
Zeng L, Zhang C, Xu J, Ye X, Wu Q, Dai J, Ji C, Gu S, Xie Y, Mao Y.
J Hum Genet 47(9):497-9. 2002
20CNTN1, CNTN2, CNTN3, CNTN4, CNTN5, CNTN6, CNTNAP1
Contactin-associated protein (Caspr) and contactin form a complex that is targeted to the paranodal junctions during myelination.
Rios JC, Melendez-Vasquez CV, Einheber S, Lustig M, Grumet M, Hemperly J, Peles E, Salzer JL.
J Neurosci 20(22):8354-64.PMID: 11069942 2000
21CNTN3, CNTN2, CNTN4, F3
Overlapping and differential expression of BIG-2, BIG-1, TAG-1, and F3: four members of an axon-associated cell adhesion molecule subgroup of the immunoglobulin superfamily.
Yoshihara Y, Kawasaki M, Tamada A, Nagata S, Kagamiyama H, Mori K.
J Neurobiol 28(1):51-69. 1995