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31003 vnd

31003

vnd

ventral nervous system defective

protein-coding

Drosophila melanogaster

基因描述

Type Description
Definition ventral nervous system defective

研究结论

Date Results Publications
2017-12-30 11:05:00 NKX2-5 and MLC2v double-positive cells possess ventricular-like properties. The results demonstrate that the NKX2-5(eGFP/w) and MLC2v(mCherry/w) hPSCs provide a powerful model system to capture region-specific cardiac differentiation from early to late stages. Our study would facilitate subtype-specific cardiac development and functional analysis using the hPSC-derived sources. 29175323
2013-07-13 12:18:00 the Neurogenic Ectoderm Enhancer (NEE) at vnd takes additional input from the complementary Dpp, dorsal, twist gradient via a conserved Schnurri/Mad/Medea silencer element (SSE) unlike NEEs at brk, sog, rho, and vn 23499655
2012-01-14 10:40:00 The results obtained from this study indicate that expression of at least four genes, uzip, CG7687, SytIV, and ase, are regulated by Vnd. 19863267
2011-10-08 11:46:00 Tthe vnd/NK-2 gene encodes an additional protein isoform (NK-2B) that differs from the known one (NK-2A) in its N-terminal domain. 21422076
2011-01-22 11:33:00 excludes Meltrin expression from the embryonic ventral neuroectoderm 20705134

名称对应

Type IDs
Synonymous CG6172, Dm vnd, Dm-NK2, Dmel\CG6172, EC6, EG:118B3.1, HDC16822, NK-2, NK2, Nkx2, VND, Vnd, dNK-2, l(1)1Bf, l(1)EA142, l(1)EC6, l(1)GA100, l(1)GA122, l(1)RC24, l(1)VA208, l(1)VE769, lab, nk-2, vnd/NK-2
Gene
UniProtKB-ID: VND_DROME, Q0KHX8_DROME
UniprotKB: P22808, Q0KHX8
UniParc: UPI00004C58FA, UPI0000079E82
EMBL: M27290, X87141, AE014298, S78691, AL031883
EnsemblGenome: FBgn0261930
KO: dme:Dmel_CG6172
Nucleutide sequences
EMBL-CDS: AAA28617.1, AAB34960.1, CAA60619.1, CAA21410.1, AAF45521.1, ABI30961.1
Gene_ORFName: CG6172, CG6172, Dmel_CG6172
EnsemblGenome_TRS: FBtr0070110, FBtr0110929
Protein sequencees
EnsemblGenome_PRO: FBpp0070105, FBpp0110229
RefSeq: NP_476786.2, NP_001036253.1
Others
UniRef100: UniRef100_P22808, UniRef100_Q0KHX8
UniRef90: UniRef90_Q0KHX8, UniRef90_P22808
UniRef50: UniRef50_Q0KHX8, UniRef50_P22808
UniGene: Dm.4713

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