| 1 | NTNG2, RETTL2
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| Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia.
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| Heimer G, van Woerden GM, Barel O, Marek-Yagel D, Kol N, Munting JB, Borghei M, Atawneh OM, Nissenkorn A, Rechavi G, Anikster Y, Elgersma Y, Kushner SA, Ben Zeev B.
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| Hum Mutat um Mutat. 2019 Nov 6. doi: 10.1002/humu.23945. [Epub ahead of print]
2019
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| 2 | NTNG2, RETTL2
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| Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
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| Dias CM, Punetha J, Zheng C, Mazaheri N, Rad A, Efthymiou S, Petersen A, Dehghani M, Pehlivan D, Partlow JN, Posey JE, Salpietro V, Gezdirici A, Malamiri RA, Al Menabawy NM, Selim LA, Vahidi Mehrjardi MY, Banu S, Polla DL, Yang E, Rezazadeh Varaghchi J, Mitani T, van Beusekom E, Najafi M, Sedaghat A, Keller-Ramey J, Durham L, Coban-Akdemir Z, Karaca E, Orlova V, Schaeken LLM, Sherafat A, Jhangiani SN, Stanley V, Shariati G, Galehdari H, Gleeson JG, Walsh CA, Lupski JR, Seiradake E, Houlden H, van Bokhoven H, Maroofian R.
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| Am J Hum Genet 105(5):1048-1056. doi: 10.1016/j.ajhg.2019.09.025. Epub 2019 Oct 24.
2019
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| 3 | NTNG2, RETTL2
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| Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features.
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| Abu-Libdeh B, Ashhab M, Shahrour M, Daana M, Dudin A, Elpeleg O, Edvardson S, Harel T.
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| Neurogenetics 20(4):209-213. doi: 10.1007/s10048-019-00583-4. Epub 2019 Aug 2.
2019
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| 4 | NTNG1, NTNG2
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| Diversification of behavior and postsynaptic properties by netrin-G presynaptic adhesion family proteins.
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| Zhang Q, Goto H, Akiyoshi-Nishimura S, Prosselkov P, Sano C, Matsukawa H, Yaguchi K, Nakashiba T, Itohara S.
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| Mol Brain 9:6. doi: 10.1186/s13041-016-0187-5.
2016
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| 5 | LRRC4, LRRC4C, NTNG1, NTNG2
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| Netrin-G/NGL complexes encode functional synaptic diversification.
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| Matsukawa H, Akiyoshi-Nishimura S, Zhang Q, Luján R, Yamaguchi K, Goto H, Yaguchi K, Hashikawa T, Sano C, Shigemoto R, Nakashiba T, Itohara S.
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| J Neurosci 34(47):15779-92. doi: 10.1523/JNEUROSCI.1141-14.2014. 2014
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| 6 | NTNG1, NTNG2
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| Identification of transcriptional regulatory elements for Ntng1 and Ntng2 genes in mice.
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| Yaguchi K, Nishimura-Akiyoshi S, Kuroki S, Onodera T, Itohara S.
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| Mol Brain 7:19. doi: 10.1186/1756-6606-7-19.
2014
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| 7 | GNG2, NTNG2
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| Topography of Gng2- and NetrinG2-expression suggests an insular origin of the human claustrum.
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| Pirone A, Cozzi B, Edelstein L, Peruffo A, Lenzi C, Quilici F, Antonini R, Castagna M.
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| PLoS One 7(9):e44745. doi: 10.1371/journal.pone.0044745. Epub 2012 Sep 5.
2012
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| 8 | NTNG2
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| Abnormal expression of netrin-G2 in temporal lobe epilepsy neurons in humans and a rat model.
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| Pan Y, Liu G, Fang M, Shen L, Wang L, Han Y, Shen D, Wang X.
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| Exp Neurol 224(2):340-6. doi: 10.1016/j.expneurol.2010.04.001. Epub 2010 Apr 9.
2010
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| 9 | NTNG1, NTNG2
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| Decreased mRNA expression of netrin-G1 and netrin-G2 in the temporal lobe in schizophrenia and bipolar disorder.
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| Eastwood SL, Harrison PJ.
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| Neuropsychopharmacology 33(4):933-45. Epub 2007 May 16.PMID: 17507910 2008
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| 10 | NTNG1, NTNG2
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| Human netrin-G1 isoforms show evidence of differential expression.
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| Meerabux JM, Ohba H, Fukasawa M, Suto Y, Aoki-Suzuki M, Nakashiba T, Nishimura S, Itohara S, Yoshikawa T.
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| Genomics 86(1):112-6. 2005
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| 11 | ABLIM2, ACSS1, ATCAY, ATP13A1, BRSK1, CAPRIN2, CCDC132, CDH23, CHAMP1, COL27A1, EHMT1, FBN3, FNDC1, GMPPB, GPR123, GPS2, HHIPL1, IRF2BPL, JPH4, KBTBD8, KIAA1841, KIRREL3, KIRREL3, MEGF10, MEGF11, MLK4, NTNG2, PHF17, PHYHIPL, RANGAP1, SEMA6C, SLX4, SPIRE2, SRRM4, ST6GAL2, SYVN1, TTBK1, VCPIP1, WDR22, ZNF286A, ZNF333, ZNF512, ZNF528
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| Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O.
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| DNA Res 8(2):85-95. 2001
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| 12 | ABCB6, ADCK2, ANAPC7, ANKRD46, ASPHD1, AVPI1, AZIN1, BRINP2, C12orf24, C14orf79, C17orf90, C17orf91, C5orf15, C9orf127, C9orf25, C9orf82, CNIH3, COG3, COG7, CREB3L1, CSRNP2, DHX29, DHX57, DLAT, EIF2B2, ERI3, FAM13C1, FAM35A, FAM54B, FLAD1, GHITM, GRIP2, GRPEL1, HMGCLL1, IP6K2, IP6K2, ITGB1BP1, KCMF1, KIFC2, LRP10, MDM1, MFN1, NAPG, NCALD, NECAB2, NIPAL4, NPTN, NTNG2, PASK, PCDHB10, PDIA6, PHPT1, PI4K2A, PNPLA2, POGK, PTOV1, RNF13, RNF41, SAC3D1, SDCBP2, SELT, SLC38A6, SLC39A3, SMURF1, SPRED2, SUCLG2, TMCO1, TMEM183A, TP53I11, TRPC4AP, TSC22D3, TUBB, TXNDC12, UTP18, WDR40A, WDR77, WSB2, ZMIZ1
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| Large-scale concatenation cDNA sequencing.
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| Yu W, Andersson B, Worley KC, Muzny DM, Ding Y, Liu W, Ricafrente JY,Wentland MA, Lennon G, Gibbs RA.
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| Genome Res 7(4):353-8. 1997
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| 13 | ADCK2, ANAPC7, ARHGAP22, AVPI1, AZIN1, C12orf24, C14orf79, C5orf15, C9orf25, CNIH3, COG3, COG7, CREB3L1, DHX29, DHX57, DLAT, DLGAP3, EIF2B2, EXOC3, FAM13C1, FAM152B, FAM35A, FAM54B, FAM89B, FLAD1, GHITM, GRPEL1, HMGCLL1, IP6K2, IPO4, ITGB1BP1, KCMF1, KIFC2, LRP10, MDM1, MFN1, NAPG, NCALD, NECAB2, NPTN, NTNG2, PASK, PCDHB10, PHPT1, PI4K2A, PNPLA2, POGK, PTOV1, RNF41, SAC3D1, SDCBP2, SELT, SEMA6C, SLC38A6, SLC39A3, SMURF1, SPRED2, STX12, SUCLG2, TAX1BP3, TMEM183A, TP53I11, TRAPPC3, TRPC4AP, TSC22D3, TUBB, TXNDC12, UTP18, WDFY3, WDR40A, WDR77, WSB2, ZMIZ1, ZNF410, ZXDC
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| A double adaptor method for improved shotgun library construction.
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| Andersson B, Wentland MA, Ricafrente JY, Liu W, Gibbs RA.
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| Anal Biochem 236(1):107-13. 1996
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