 
    | RGAP LOCUS ID | LOC_Os08g06480 | ||||
| RAP-DB ID | Os08g0162100 | ||||
| Function | lissencephaly type-1-like homology motif, putative, expressed | ||||
| Sub-cellular Localization Predictions | |||||
| 1) WoLF-PSORT Prediction | |||||
| localization | chlo | ||||
| score | 6 | ||||
| 2) CELLO Prediction | |||||
| localization | PlasmaMembrane | ||||
| score | 1.248 | ||||
| 3) NUCPRED Prediction | |||||
| localization | Non Nuclear | ||||
| score | 0.53 | ||||
| 4) Y-Loc Prediction | |||||
| localization | Cytoplasm | ||||
| score | 67 | ||||
| confidence value | 0.5 | ||||
| Number Of Software Predicting Nucleus | 0 | ||||
| Seed Specific | No | ||||
| Transcription factor category | |||||
| Experimental evidence for subcellular localization | |||||
| Published gene name (updated 1 January 2020) | OsTPL|ASP1|OsLIS-L1 | ||||
| Function assigned as per literature | OsLIS-L1 plays an important role in male gametophyte formation and the first internode elongation in rice | ||||
| Subcellular localization as per literature | Nucleus | ||||
| Cells used for localization experiment | Arabidopsis mesophyll protoplasts | ||||
| NUCLEAR or Not Nuclear | NOT NUCLEAR | ||||
| PMID | 22020753 | ||||
| Reference of localization | https://link.springer.com/article/10.1007%2Fs00425-011-1532-7 | ||||
| Is Subcellular localization evidence by author available ? | No | ||||
| Sequence Analysis | |||||
| Number of PAT4 | 0 | ||||
| Number of PAT7 | 0 | ||||
| Number of Bipartite | 0 | ||||
| Basic residues % | 0.102 | ||||
| NLS score | -0.47 | ||||
| Protein Sequence | >LOC_Os08g06480.1 protein MSSLSRELVFLILQFLDEEKFKETVHKLEQESAFYFNMKHFEDLVQGGEWDEVEKYLSGFTKVEDNRYSMKIFFEIRKQKYLEALDRHDRAKAVEILVKD LKVFASFNEELFKEITQLLTLENFRQNEQLSKYGDTKSARNIMLMELKKLIEANPLFRDKLNFPPFKVSRLRTLINQSLNWQHQLCKNPRPNPDIKTLFT DHSCAAPTNGARAPPPANGPLVGPIPKSAAFPPMGAHAPFQPVVSPSPNAIAGWMTNANPSLPHAAVAQGPPGLVQPPNTAAFLKHPRTPTSAPAIDYQS ADSEHLMKRMRVGQPDEVSFSGASHPANIYTQDDLPKQVVRNLNQGSNVMSLDFHPVQQTILLVGTNVGDIGIWEVGSRERIAHKTFKVWDISSCTLPLQ AALMKDAAISVNRCLWSPDGSILGVAFSKHIVQTYAFVLNGELRQQAEIDAHIGGVNDIAFSHPNKTLSIITCGDDKLIKVWDAQTGQKQYTFEGHEAPV YSVCPHYKESIQFIFSTAIDGKIKAWLYDCLGSRVDYDAPGHWCTTMAYSADGTRLFSCGTSKDGDSHLVEWNETEGAIKRTYNGFRKRSLGVVQFDTTR NRFLAAGDEFVVKFWDMDNTNILTTTDCDGGLPASPRLRFNREGSLLAVTANENGIKILANTDGQRLLRMLESRAYEGSRGPPQQINTKPPIVNTLGSVS NVSSPMAVNSERPDRALPTVSMSGLAPMDVSRTPDVKPRITDESEKVKTWKLADIGDSGHLRALRMPDTSATSSKVVRLLYTNNGVALLALGSNAVHKLW KWQRTDRNPNGKSTASFTPQMWQPANGILMANDTSDGNPEEATACIALSKNDSYVMSASGGKVSLFNMMTFKVMTTFMAPPPAATFLAFHPQDNNIIAIG MEDSTIQIYNVRVDEVKSKLKGHSKKITGLAFSQSMNMLVSSGADAQLCAWSIDGWEKKKSRYIQSPANRSGALVGDTRVQFHNDQTHILVVHESQLAIY DAKLECLRSWSPREALPAPISSAIYSCDGLLIYAGFCDGAIGVFEAESLRLRCRIAPSAYIPPSMSSGGSVYPMVVAAHPLEPNQIAVGMSDGAVHVVEP LDSDPKWGVAPPQDNGTHPTISAAPAAANKPEV | ||||
| GO Analysis | |||||
| 1 | 
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| 2 | 
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| 3 | 
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| 4 | 
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| 5 | 
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| 6 | 
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| 7 | 
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| 8 | 
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| 9 | 
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| 10 | 
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| 11 | 
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| 12 | 
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| Presence of Splice variants | No | ||||