Gene Details:
- Gene ID: AT3G18780
- Gene Symbol: ACT2, DER1, ENL2, FIZ2, LSR2
- Gene Name: actin 2, DEFORMED ROOT HAIRS 1, ENHANCER OF LRX1 2, FRIZZY AND KINKED SHOOTS 2, LIGHT STRESS-REGULATED 2
- Description: actin 2;(source:Araport11)
- TAIR Accession:
- Genome: Araport11_genome_release
- Species: Arabidopsis thaliana
Transcripts:
Plant Ontology Annotations:
- PO:0004006 — mesophyll cell — célula del mesófilo (Spanish, exact), 葉肉細胞 (Japanese, exact)
- PO:0004013 — plant epidermal cell — célula epidérmica (Spanish, exact), 表皮細胞 (Japanese, exact)
- PO:0025281 — pollen — polen (Spanish, exact), pollen grain (exact), 花粉 (Japanese, exact)
- PO:0025195 — pollen tube cell — célula del tubo polínico (Spanish, exact), 花粉管細胞 (Japanese, exact)
- PO:0009006 — shoot system — sistema de epiblasto (epiblastema) (Spanish, exact), シュート系、苗条系 (Japanese, exact), Poaceae crown (related), shoot (related), thalli (related), thallus (related), tree crown (narrow)
Germplasm Phenotype:
- CS25244 — Impaired root hair development; the site selection of the initial bulge, the positioning of the tip-growth machinery at the bulge, and the process of tip growth per se are affected; displays a weak phenotype with the lower one-half of the root hair proper being enlarged, whereas the upper one-half of the root hair seemed to develop normally; root hairs are consistently shorter than in wild type; the initiating bulge forms sometimes rather in the middle than at the distal end of the trichoblast cell; a thin root hair without an enlarged basis can be developed; structure of these root hairs is irregular with a varying diameter; in an alternate manner, the lower one-half of the root hair was strongly enlarged, whereas the upper part was thinner but again very irregular; very often, the enlarged part of the root hair formed, but did not develop further, resulting in a stump-like structure; in some cases, two root hairs developed from the initial bulge; many times, the initially restricted area of bulge formation grew bigger along the epidermal surface of the trichoblast, and tip growth seemed to initiate at two different positions, although it did not proceed any further.
- CS25245 — Impaired root hair development; the site selection of the initial bulge, the positioning of the tip-growth machinery at the bulge, and the process of tip growth per se are strongly affected; displays stronger phenotype than der1-1; basis of the root hair is often enlarged and the root hair structure is very short compared to wild type; the initiating bulge forms sometimes rather in the middle than at the distal end of the trichoblast cell; root hairs frequently had a strongly enlarged basis, implying a severely affected bulge-formation and tip-growth process; root hairs develop the strongly enlarged basis at a higher frequency than der1-3.
- CS25246 — Impaired root hair development; the site selection of the initial bulge, the positioning of the tip-growth machinery at the bulge, and the process of tip growth per se are strongly affected; displays stronger phenotype than der1-1; basis of the root hair is often enlarged and the root hair structure is very short compared to wild type; the initiating bulge forms sometimes rather in the middle than at the distal end of the trichoblast cell; root hairs frequently had a strongly enlarged basis, implying a severely affected bulge-formation and tip-growth process; root hair structures more often remain thin, compared to der1-2.
- CS25256 — Impaired root hair development; develops root hairs that are very short and often have a radially enlarged root hair proper; this enlargement is not confined to the root hair base, but extends further to the tip.
- CS25495 — Resistant to Agrobacterium tumefaciens root transformation; observed tumorigenesis is less than 25% of wild-type; phosphinothricin (ppt) resistance is less than 25% of wild-type; transient GUS activity is less than 33% of wild-type; kanamycin resistant.
- CS6958 — Defects in initiation and elongation of root hair, root cell expansion, trichome development, and growth of aerial parts. Polymerlization of actin microfilaments is disturbed.
- CS6959 — Defects in root hair elongation.
- act2-1 — Mutants have abnormal root hairs that are stunted, bulging or may be branched. The orientation of microtubules is abnormal.
- act2-1/act7-4 — Plants are dwarf and reach only 15% of the height of wild type. Roots lack root hairs- the initiate but do not develop further than a bulge. Leaves are small with reduced surface area and fewer lobes. Leaf trichomes are abnormal and contain fewer branches. Also defects in flower morphology, reduced fertility, abnormal inflorescence structure and abnormal silique development.
- act2-1/act8-2 — Lacks root hairs.Root hairs initiate but do not develop further.
Function-related keywords:
Literature:
- Strong, constitutive expression of the Arabidopsis ACT2/ACT8 actin subclass in vegetative tissues. DOI: 10.1046/j.1365-313x.1996.10010107.x ; PMID: 8758981
- Identification of genes expressed in response to light stress in leaves of Arabidopsis thaliana using RNA differential display. DOI: 10.1046/j.1432-1033.2001.02471.x ; PMID: 11683875
- Functional nonequivalency of actin isovariants in Arabidopsis. DOI: 10.1091/mbc.01-07-0342 ; PMID: 11809837
- Distribution of actin gene isoforms in the Arabidopsis leaf measured in microsamples from intact individual cells. DOI: 10.1007/s00425-001-0732-y ; PMID: 12029478
- Both vegetative and reproductive actin isovariants complement the stunted root hair phenotype of the Arabidopsis act2-1 mutation. DOI: 10.1104/pp.014068 ; PMID: 12481103
- Gene expression in response to endoplasmic reticulum stress in Arabidopsis thaliana. DOI: 10.1111/j.1742-4658.2005.04770.x ; PMID: 15978049
- Immediate-early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome-wide expression profiling reveal novel cytokinin-sensitive processes and suggest cytokinin action through transcriptional cascades. DOI: 10.1111/j.1365-313X.2005.02530.x ; PMID: 16212609
- phyA dominates in transduction of red-light signals to rapidly responding genes at the initiation of Arabidopsis seedling de-etiolation. DOI: 10.1111/j.1365-313X.2006.02914.x ; PMID: 17076805
- Class-specific interaction of profilin and ADF isovariants with actin in the regulation of plant development. DOI: 10.1105/tpc.107.052621 ; PMID: 17933902
- Global analysis of Arabidopsis gene expression uncovers a complex array of changes impacting pathogen response and cell cycle during geminivirus infection. DOI: 10.1104/pp.108.121038 ; PMID: 18650403
- Transcriptome analyses show changes in gene expression to accompany pollen germination and tube growth in Arabidopsis. DOI: 10.1104/pp.108.126375 ; PMID: 18775970
- Transcriptomic analysis of Arabidopsis developing stems: a close-up on cell wall genes. DOI: 10.1186/1471-2229-9-6 ; PMID: 19149885
- A single vegetative actin isovariant overexpressed under the control of multiple regulatory sequences is sufficient for normal Arabidopsis development. DOI: 10.1105/tpc.108.061960 ; PMID: 19304937
- SUMO E3 ligase HIGH PLOIDY2 regulates endocycle onset and meristem maintenance in Arabidopsis. DOI: 10.1105/tpc.109.068072 ; PMID: 19666737
- The Arabidopsis nitrate transporter NRT1.8 functions in nitrate removal from the xylem sap and mediates cadmium tolerance. DOI: 10.1105/tpc.110.075242 ; PMID: 20501909
- DAY NEUTRAL FLOWERING represses CONSTANS to prevent Arabidopsis flowering early in short days. DOI: 10.1105/tpc.109.066605 ; PMID: 20435904
- Identification and testing of superior reference genes for a starting pool of transcript normalization in Arabidopsis. DOI: 10.1093/pcp/pcq128 ; PMID: 20798276
- Differential sublocalization of actin variants within the nucleus. DOI: 10.1002/cm.20484 ; PMID: 20862689
- AGD1, a class 1 ARF-GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity. DOI: 10.1111/j.1365-313X.2011.04856.x ; PMID: 22098134
- Vacuolar nicotianamine has critical and distinct roles under iron deficiency and for zinc sequestration in Arabidopsis. DOI: 10.1105/tpc.111.095042 ; PMID: 22374397
- Plant vegetative and animal cytoplasmic actins share functional competence for spatial development with protists. DOI: 10.1105/tpc.111.095281 ; PMID: 22589468
- A vacuolar β-glucosidase homolog that possesses glucose-conjugated abscisic acid hydrolyzing activity plays an important role in osmotic stress responses in Arabidopsis. DOI: 10.1105/tpc.112.095935 ; PMID: 22582100
- Proanthocyanidins inhibit seed germination by maintaining a high level of abscisic acid in Arabidopsis thaliana. DOI: 10.1111/j.1744-7909.2012.01142.x ; PMID: 22765383
- A survey of dominant mutations in Arabidopsis thaliana. DOI: 10.1016/j.tplants.2012.08.006 ; PMID: 22995285
- Characterization of a NADH-dependent glutamate dehydrogenase mutant of Arabidopsis demonstrates the key role of this enzyme in root carbon and nitrogen metabolism. DOI: 10.1105/tpc.112.103689 ; PMID: 23054470
- Arabidopsis acyl-CoA-binding protein ACBP1 participates in the regulation of seed germination and seedling development. DOI: 10.1111/tpj.12121 ; PMID: 23448237
- Arabidopsis BPM proteins function as substrate adaptors to a cullin3-based E3 ligase to affect fatty acid metabolism in plants. DOI: 10.1105/tpc.112.107292 ; PMID: 23792371
- An extracellular subtilase switch for immune priming in Arabidopsis. DOI: 10.1371/journal.ppat.1003445 ; PMID: 23818851
- Overlapping and divergent signaling pathways for ARK1 and AGD1 in the control of root hair polarity in Arabidopsis thaliana. DOI: 10.3389/fpls.2013.00528 ; PMID: 24400013
- Strigolactone analog GR24 triggers changes in PIN2 polarity, vesicle trafficking and actin filament architecture. DOI: 10.1111/nph.12744 ; PMID: 24571327
- Abscisic acid uridine diphosphate glucosyltransferases play a crucial role in abscisic acid homeostasis in Arabidopsis. DOI: 10.1104/pp.114.239210 ; PMID: 24676855
- Ascomycete fungal actins differentially support plant spatial cell and organ development. DOI: 10.1002/cm.21198 ; PMID: 25428798
- Proteasome-mediated degradation of FRIGIDA modulates flowering time in Arabidopsis during vernalization. DOI: 10.1105/tpc.114.132738 ; PMID: 25538183
- Fibrillin 5 Is Essential for Plastoquinone-9 Biosynthesis by Binding to Solanesyl Diphosphate Synthases in Arabidopsis. DOI: 10.1105/tpc.15.00707 ; PMID: 26432861
- Distinct Biochemical Properties of Arabidopsis thaliana Actin Isoforms. DOI: 10.1093/pcp/pcv176 ; PMID: 26578694
- Interplay between ABA and GA Modulates the Timing of Asymmetric Cell Divisions in the Arabidopsis Root Ground Tissue. DOI: 10.1016/j.molp.2016.02.009 ; PMID: 26970019
- Natural Variation of Cold Deacclimation Correlates with Variation of Cold-Acclimation of the Plastid Antioxidant System in Arabidopsis thaliana Accessions. DOI: 10.3389/fpls.2016.00305 ; PMID: 27014325
- The Nonspecific Lipid Transfer Protein AtLtpI-4 Is Involved in Suberin Formation of Arabidopsis thaliana Crown Galls. DOI: 10.1104/pp.16.01486 ; PMID: 27688623
- Arabidopsis small nucleolar RNA monitors the efficient pre-rRNA processing during ribosome biogenesis. DOI: 10.1073/pnas.1614852113 ; PMID: 27708161
- Correction: An Extracellular Subtilase Switch for Immune Priming in Arabidopsis. DOI: 10.1371/journal.ppat.1006003 ; PMID: 27806116
- Acetolactate synthase regulatory subunits play divergent and overlapping roles in branched-chain amino acid synthesis and Arabidopsis development. DOI: 10.1186/s12870-017-1022-6 ; PMID: 28388946
- Tonoplast-localized nitrate uptake transporters involved in vacuolar nitrate efflux and reallocation in Arabidopsis. DOI: 10.1038/s41598-017-06744-5 ; PMID: 28743909
- Measurement of enzymatic and motile activities of Arabidopsis myosins by using Arabidopsis actins. DOI: 10.1016/j.bbrc.2017.12.071 ; PMID: 29248727
- Genetic dissection of cyclic pyranopterin monophosphate biosynthesis in plant mitochondria. DOI: 10.1042/BCJ20170559 ; PMID: 29247140
- STRESS INDUCED FACTOR 2, a Leucine-Rich Repeat Kinase Regulates Basal Plant Pathogen Defense. DOI: 10.1104/pp.17.01266 ; PMID: 29463771
- METHIONINE ADENOSYLTRANSFERASE4 Mediates DNA and Histone Methylation. DOI: 10.1104/pp.18.00183 ; PMID: 29572390
- Hydrogen Sulfide Disturbs Actin Polymerization via S-Sulfhydration Resulting in Stunted Root Hair Growth. DOI: 10.1104/pp.18.00838 ; PMID: 30166418
- Manipulating mRNA splicing by base editing in plants. DOI: 10.1007/s11427-018-9392-7 ; PMID: 30267262
- ANGUSTIFOLIA Regulates Actin Filament Alignment for Nuclear Positioning in Leaves. DOI: 10.1104/pp.18.01150 ; PMID: 30404821
- Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls. DOI: 10.1111/tpj.14301 ; PMID: 30821050
- OPENER Is a Nuclear Envelope and Mitochondria Localized Protein Required for Cell Cycle Progression in Arabidopsis. DOI: 10.1105/tpc.19.00033 ; PMID: 31023726
- ACTIN7 Is Required for Perinuclear Clustering of Chloroplasts during Arabidopsis Protoplast Culture. DOI: 10.3390/plants9020225 ; PMID: 32050601
- FATTY ACID DESATURASE5 Is Required to Induce Autoimmune Responses in Gigantic Chloroplast Mutants of Arabidopsis. DOI: 10.1105/tpc.20.00016 ; PMID: 32796124
- Arabidopsis NF-YCs play dual roles in repressing brassinosteroid biosynthesis and signaling during light-regulated hypocotyl elongation. DOI: 10.1093/plcell/koab112 ; PMID: 33871651
- Polygalacturonase45 cleaves pectin and links cell proliferation and morphogenesis to leaf curvature in Arabidopsis thaliana. DOI: 10.1111/tpj.15308 ; PMID: 33960548
- Arabidopsis thaliana subclass I ACTIN DEPOLYMERIZING FACTORs and vegetative ACTIN2/8 are novel regulators of endoreplication. DOI: 10.1007/s10265-021-01333-0 ; PMID: 34282484
- Stress response proteins NRP1 and NRP2 are pro-survival factors that inhibit cell death during ER stress. DOI: 10.1093/plphys/kiab335 ; PMID: 34618053
- The U1 snRNP component RBP45d regulates temperature-responsive flowering in Arabidopsis. DOI: 10.1093/plcell/koab273 ; PMID: 34791475
- Mechanical stress effects on transcriptional regulation of genes encoding and actin-associated proteins. DOI: 10.1007/s12298-021-01123-x ; PMID: 35210715
- The Arabidopsis cyclophilin CYP18-1 facilitates PRP18 dephosphorylation and the splicing of introns retained under heat stress. DOI: 10.1093/plcell/koac084 ; PMID: 35262729
- Phytocytokine signalling reopens stomata in plant immunity and water loss. DOI: 10.1038/s41586-022-04684-3 ; PMID: 35508659
- ADP-ribosylation factor D1 modulates Golgi morphology, cell plate formation, and plant growth in Arabidopsis. DOI: 10.1093/plphys/kiac329 ; PMID: 35876822
- Analysis of the Arabidopsis nuclear proteome and its response to cold stress. DOI: 10.1046/j.1365-313x.2003.01907.x ; PMID: 14617066
- Immediate-early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome-wide expression profiling reveal novel cytokinin-sensitive processes and suggest cytokinin action through transcriptional cascades. DOI: 10.1111/j.1365-313X.2005.02530.x ; PMID: 16212609
- Proteome mapping of mature pollen of Arabidopsis thaliana. DOI: 10.1002/pmic.200402011 ; PMID: 16247729
- phyA dominates in transduction of red-light signals to rapidly responding genes at the initiation of Arabidopsis seedling de-etiolation. DOI: 10.1111/j.1365-313X.2006.02914.x ; PMID: 17076805
- Membrane proteomic analysis of Arabidopsis thaliana using alternative solubilization techniques. DOI: 10.1021/pr060525b ; PMID: 17432890
- Arabidopsis PEROXIN11c-e, FISSION1b, and DYNAMIN-RELATED PROTEIN3A cooperate in cell cycle-associated replication of peroxisomes. DOI: 10.1105/tpc.107.057679 ; PMID: 18539750
- A single vegetative actin isovariant overexpressed under the control of multiple regulatory sequences is sufficient for normal Arabidopsis development. DOI: 10.1105/tpc.108.061960 ; PMID: 19304937
- Analysis of the Arabidopsis cytosolic proteome highlights subcellular partitioning of central plant metabolism. DOI: 10.1021/pr1009433 ; PMID: 21166475
- Analysis of the Arabidopsis nuclear proteome and its response to cold stress. DOI: 10.1046/j.1365-313x.2003.01907.x ; PMID: 14617066
- Proteome mapping of mature pollen of Arabidopsis thaliana. DOI: 10.1002/pmic.200402011 ; PMID: 16247729
- phyA dominates in transduction of red-light signals to rapidly responding genes at the initiation of Arabidopsis seedling de-etiolation. DOI: 10.1111/j.1365-313X.2006.02914.x ; PMID: 17076805
- Membrane proteomic analysis of Arabidopsis thaliana using alternative solubilization techniques. DOI: 10.1021/pr060525b ; PMID: 17432890
- Arabidopsis PEROXIN11c-e, FISSION1b, and DYNAMIN-RELATED PROTEIN3A cooperate in cell cycle-associated replication of peroxisomes. DOI: 10.1105/tpc.107.057679 ; PMID: 18539750
- A single vegetative actin isovariant overexpressed under the control of multiple regulatory sequences is sufficient for normal Arabidopsis development. DOI: 10.1105/tpc.108.061960 ; PMID: 19304937
- Analysis of the Arabidopsis cytosolic proteome highlights subcellular partitioning of central plant metabolism. DOI: 10.1021/pr1009433 ; PMID: 21166475
- Analysis of protein complexes in Arabidopsis leaves using size exclusion chromatography and label-free protein correlation profiling. DOI: 10.1016/j.jprot.2017.06.004 ; PMID: 28627464
Sequences:
cDNA Sequence
- >AT3G18780.1
AAACCCGCCTATATAAATTCATATATTTTCCTCTCCGCTTTGAATTGTCTCGTTGTCCTCCTCACTTTCATCAGCCGTTTTGAATCTCCGGCGACTTGACAGAGAAGAACAAGGAAGAAGACTAAGAGAGAAAGTAAGAGATAATCCAGGAGATTCATTCTCCGTTTTGAATCTTCCTCAATCTCATCTTCTTCCGCTCTTTCTTTCCAAGGTAATAGGAACTTTCTGGATCTACTTTATTTGCTGGATCTCGATCTTGTTTTCTCAATTTCCTTGAGATCTGGAATTCGTTTAATTTGGATCTGTGAACCTCCACTAAATCTTTTGGTTTTACTAGAATCGATCTAAGTTGACCGATCAGTTAGCTCGATTATAGCTACCAGAATTTGGCTTGACCTTGATGGAGAGATCCATGTTCATGTTACCTGGGAAATGATTTGTATATGTGAATTGAAATCTGAACTGTTGAAGTTAGATTGAATCTGAACACTGTCAATGTTAGATTGAATCTGAACACTGTTTAAGCTCATAAAAAATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGAAATCAAAGGCTGATTATTTATGTATATGTTGGTTACAGATGTGGATCTCCAAGGCCGAGTATGATGAGGCAGGTCCAGGAATCGTTCACAGAAAATGTTTCTAAGCTCTCAAGATCAAAGGCTTAAAAAGCTGGGGTTTTATGAATGGGATCAAAGTTTCTTTTTTTCTTTTATATTTGCTTCTCCATTTGTTTGTTTCATTTCCCTTTTTGTTTTCGTTTCTATGATGCACTTGTGTGTGACAAACTCTCTGGGTTTTTACTTACGTCTGCGTTTCAAAAAAAAAAACCGCTTTCGTTTTGCGTTTTAGTCCCATTGTTTTGTAGCTCTGAGTGATCGAATTGATGCCTCTTTATTCCTTTTGTTCCCTATAATTTCTTTCAAAACTCAGAAGAAAAACCTTGAAACTCTTTGCAATGTTAATATAAGTATTGTATAAGATTTTTATTGATTTGGTTATTAGTCTTACTTTTGCT - >AT3G18780.3
AAACCCGCCTATATAAATTCATATATTTTCCTCTCCGCTTTGAATTGTCTCGTTGTCCTCCTCACTTTCATCAGCCGTTTTGAATCTCCGGCGACTTGACAGAGAAGAACAAGGAAGAAGACTAAGAGAGAAAGTAAGAGATAATCCAGGAGATTCATTCTCCGTTTTGAATCTTCCTCAATCTCATCTTCTTCCGCTCTTTCTTTCCAAGGTAATAGGAACTTTCTGGATCTACTTTATTTGCTGGATCTCGATCTTGTTTTCTCAATTTCCTTGAGATCTGGAATTCGTTTAATTTGGATCTGTGAACCTCCACTAAATCTTTTGGTTTTACTAGAATCGATCTAAGTTGACCGATCAGTTAGCTCGATTATAGCTACCAGAATTTGGCTTGACCTTGATGGAGAGATCCATGTTCATGTTACCTGGGAAATGATTTGTATATGTGAATTGAAATCTGAACTGTTGAAGTTAGATTGAATCTGAACACTGTCAATGTTAGATTGAATCTGAACACTGTTTAAGCTCATAAAAAATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGAAATCAAAGGCTGATTATTTATGTATATGTTGGTTACAGATGTGGATCTCCAAGGCCGAGTATGATGAGGCAGGTCCAGGAATCGTTCACAGAAAATGTTTCTAAGCTCTCAAGATCAAAGGCTTAAAAAGCTGGGGTTTTATGAATGGGATCAAAGTTTCTTTTTTTCTTTTATATTTGCTTCTCCATTTGTTTGTTTCATTTCCCTTTTTGTTTTCGTTTCTATGATGCACTTGTGTGTGACAAACTCTCTGGGTTTTTACTTACGTCTGCGTTTCAAAAAAAAAAACCGCTTTCGTTTTGCGTTTTAGTCCCATTGTTTTGTAGCTCTGAGTGATCGAATTGATGCCTCTTTATTCCTTTTGTTCCCTATAATTTCTTTCAAAACTCAGAAGAAAAACCTTGAAACTCTTTGCAATGTTAATATAAGTATTGTATAAGATTTTTATTGATTTGGTTATTAGTCTTACTTTTGCT - >AT3G18780.2
AAACCCGCCTATATAAATTCATATATTTTCCTCTCCGCTTTGAATTGTCTCGTTGTCCTCCTCACTTTCATCAGCCGTTTTGAATCTCCGGCGACTTGACAGAGAAGAACAAGGAAGAAGACTAAGAGAGAAAGTAAGAGATAATCCAGGAGATTCATTCTCCGTTTTGAATCTTCCTCAATCTCATCTTCTTCCGCTCTTTCTTTCCAAGGTAATAGGAACTTTCTGGATCTACTTTATTTGCTGGATCTCGATCTTGTTTTCTCAATTTCCTTGAGATCTGGAATTCGTTTAATTTGGATCTGTGAACCTCCACTAAATCTTTTGGTTTTACTAGAATCGATCTAAGTTGACCGATCAGTTAGCTCGATTATAGCTACCAGAATTTGGCTTGACCTTGATGGAGAGATCCATGTTCATGTTACCTGGGAAATGATTTGTATATGTGAATTGAAATCTGAACTGTTGAAGTTAGATTGAATCTGAACACTGTCAATGTTAGATTGAATCTGAACACTGTTTAAGCTCATAAAAAATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGAAATCAAAGGCTGATTATTTATGTATATGTTGGTTACAGATGTGGATCTCCAAGGCCGAGTATGATGAGGCAGGTCCAGGAATCGTTCACAGAAAATGTTTCTAAGCTCTCAAGATCAAAGGCTTAAAAAGCTGGGGTTTTATGAATGGGATCAAAGTTTCTTTTTTTCTTTTATATTTGCTTCTCCATTTGTTTGTTTCATTTCCCTTTTTGTTTTCGTTTCTATGATGCACTTGTGTGTGACAAACTCTCTGGGTTTTTACTTACGTCTGCGTTTCAAAAAAAAAAACCGCTTTCGTTTTGCGTTTTAGTCCCATTGTTTTGTAGCTCTGAGTGATCGAATTGATGCCTCTTTATTCCTTTTGTTCCCTATAATTTCTTTCAAAACTCAGAAGAAAAACCTTGAAACTCTTTGCAATGTTAATATAAGTATTGTATAAGATTTTTATTGATTTGGTTATTAGTCTTACTTTTGCT
CDS Sequence
- >AT3G18780.1
ATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGA - >AT3G18780.3
ATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGA - >AT3G18780.2
ATGGCTGAGGCTGATGATATTCAACCAATCGTGTGTGACAATGGTACCGGTATGGTGAAGGCTGGATTTGCAGGAGATGATGCTCCCAGGGCTGTTTTTCCCAGTGTTGTTGGTAGGCCAAGACATCATGGTGTCATGGTTGGGATGAACCAGAAGGATGCATATGTTGGTGATGAAGCACAATCCAAGAGAGGTATTCTTACCTTGAAGTATCCTATTGAGCATGGTGTTGTTAGCAACTGGGATGATATGGAAAAGATCTGGCATCACACTTTCTACAATGAGCTTCGTATTGCTCCTGAAGAGCACCCTGTTCTTCTTACCGAGGCTCCTCTTAACCCAAAGGCCAACAGAGAGAAGATGACTCAAATCATGTTTGAGACCTTTAACTCTCCCGCTATGTATGTCGCCATCCAAGCTGTTCTCTCCTTGTACGCCAGTGGTCGTACAACCGGTATTGTGCTGGATTCTGGTGATGGTGTGTCTCACACTGTGCCAATCTACGAGGGTTTCTCTCTTCCTCATGCCATCCTCCGTCTTGACCTTGCTGGACGTGACCTTACTGATTACCTCATGAAGATCCTTACAGAGAGAGGTTACATGTTCACCACAACAGCAGAGCGGGAAATTGTAAGAGACATCAAGGAGAAGCTCTCCTTTGTTGCTGTTGACTACGAGCAGGAGATGGAAACCTCAAAGACCAGCTCTTCCATCGAGAAGAACTATGAATTACCCGATGGGCAAGTCATCACGATTGGTGCTGAGAGATTCAGATGCCCAGAAGTCTTGTTCCAGCCCTCGTTTGTGGGAATGGAAGCTGCTGGAATCCACGAGACAACCTATAACTCAATCATGAAGTGTGATGTGGATATCAGGAAGGATCTGTACGGTAACATTGTGCTCAGTGGTGGAACCACTATGTTCTCAGGTATCGCTGACCGTATGAGCAAAGAAATCACAGCACTTGCACCAAGCAGCATGAAGATTAAGGTCGTTGCACCACCTGAAAGGAAGTACAGTGTCTGGATCGGTGGTTCCATTCTTGCTTCCCTCAGCACATTCCAGCAGGTAAAAATTGATCAGATTTTGTTTCGAATTCTCTTACATGCAAATTGA
Protein Sequence
- >AT3G18780.1
MAEADDIQPIVCDNGTGMVKAGFAGDDAPRAVFPSVVGRPRHHGVMVGMNQKDAYVGDEAQSKRGILTLKYPIEHGVVSNWDDMEKIWHHTFYNELRIAPEEHPVLLTEAPLNPKANREKMTQIMFETFNSPAMYVAIQAVLSLYASGRTTGIVLDSGDGVSHTVPIYEGFSLPHAILRLDLAGRDLTDYLMKILTERGYMFTTTAEREIVRDIKEKLSFVAVDYEQEMETSKTSSSIEKNYELPDGQVITIGAERFRCPEVLFQPSFVGMEAAGIHETTYNSIMKCDVDIRKDLYGNIVLSGGTTMFSGIADRMSKEITALAPSSMKIKVVAPPERKYSVWIGGSILASLSTFQQVKIDQILFRILLHAN - >AT3G18780.3
MAEADDIQPIVCDNGTGMVKAGFAGDDAPRAVFPSVVGRPRHHGVMVGMNQKDAYVGDEAQSKRGILTLKYPIEHGVVSNWDDMEKIWHHTFYNELRIAPEEHPVLLTEAPLNPKANREKMTQIMFETFNSPAMYVAIQAVLSLYASGRTTGIVLDSGDGVSHTVPIYEGFSLPHAILRLDLAGRDLTDYLMKILTERGYMFTTTAEREIVRDIKEKLSFVAVDYEQEMETSKTSSSIEKNYELPDGQVITIGAERFRCPEVLFQPSFVGMEAAGIHETTYNSIMKCDVDIRKDLYGNIVLSGGTTMFSGIADRMSKEITALAPSSMKIKVVAPPERKYSVWIGGSILASLSTFQQVKIDQILFRILLHAN - >AT3G18780.2
MAEADDIQPIVCDNGTGMVKAGFAGDDAPRAVFPSVVGRPRHHGVMVGMNQKDAYVGDEAQSKRGILTLKYPIEHGVVSNWDDMEKIWHHTFYNELRIAPEEHPVLLTEAPLNPKANREKMTQIMFETFNSPAMYVAIQAVLSLYASGRTTGIVLDSGDGVSHTVPIYEGFSLPHAILRLDLAGRDLTDYLMKILTERGYMFTTTAEREIVRDIKEKLSFVAVDYEQEMETSKTSSSIEKNYELPDGQVITIGAERFRCPEVLFQPSFVGMEAAGIHETTYNSIMKCDVDIRKDLYGNIVLSGGTTMFSGIADRMSKEITALAPSSMKIKVVAPPERKYSVWIGGSILASLSTFQQVKIDQILFRILLHAN