Homo sapiens plasminogen (PLG), transcript variant 1, mRNA.
| RefSeq Version | NM_000301.3, 270132869 |
| Length | 3538 bp |
| Structure | linear |
| Update Date | 01-MAY-2011 |
| Organism | Homo sapiens (human) |
| Definition | Homo sapiens plasminogen (PLG), transcript variant 1, mRNA. |
| Product | plasminogen isoform 1 precursor |
| Comment | Summary: The protein encoded by this gene is a secreted blood zymogen that is activated by proteolysis and converted to plasmin and angiostatin. Plasmin dissolves fibrin in blood clots and is an important protease in many other cellular processes while angiostatin inhibits angiogenesis. Defects in this gene are likely a cause of thrombophilia and ligneous conjunctivitis. Two transcript variants encoding different isoforms have been found for this gene. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. |
| RefSeq | NP_000292.1 |
| CDS | 113..2545 | Exon (1) | 1..161 | Exon (2) | 1..161 | Exon (3) | 162..297 | Exon (4) | 298..404 | Exon (5) | 405..519 | Exon (6) | 520..659 | Exon (7) | 660..780 | Exon (8) | 781..899 | Exon (9) | 900..1062 | Exon (10) | 1063..1208 | Exon (11) | 1209..1368 | Exon (12) | 1369..1550 | Exon (13) | 1551..1699 | Exon (14) | 1700..1793 | Exon (15) | 1794..1914 | Exon (16) | 1915..1989 | Exon (17) | 1990..2130 | Exon (18) | 2131..2237 | Exon (19) | 2238..2383 | Exon (20) | 2384..3538 |
| Translation | MEHKEVVLLLLLFLKSGQGEPLDDYVNTQGASLFSVTKKQLGAGSIEECAAKCEEDEEFT
CRAFQYHSKEQQCVIMAENRKSSIIIRMRDVVLFEKKVYLSECKTGNGKNYRGTMSKTKN
GITCQKWSSTSPHRPRFSPATHPSEGLEENYCRNPDNDPQGPWCYTTDPEKRYDYCDILE
CEEECMHCSGENYDGKISKTMSGLECQAWDSQSPHAHGYIPSKFPNKNLKKNYCRNPDRE
LRPWCFTTDPNKRWELCDIPRCTTPPPSSGPTYQCLKGTGENYRGNVAVTVSGHTCQHWS
AQTPHTHNRTPENFPCKNLDENYCRNPDGKRAPWCHTTNSQVRWEYCKIPSCDSSPVSTE
QLAPTAPPELTPVVQDCYHGDGQSYRGTSSTTTTGKKCQSWSSMTPHRHQKTPENYPNAG
LTMNYCRNPDADKGPWCFTTDPSVRWEYCNLKKCSGTEASVVAPPPVVLLPDVETPSEED
CMFGNGKGYRGKRATTVTGTPCQDWAAQEPHRHSIFTPETNPRAGLEKNYCRNPDGDVGG
PWCYTTNPRKLYDYCDVPQCAAPSFDCGKPQVEPKKCPGRVVGGCVAHPHSWPWQVSLRT
RFGMHFCGGTLISPEWVLTAAHCLEKSPRPSSYKVILGAHQEVNLEPHVQEIEVSRLFLE
PTRKDIALLKLSSPAVITDKVIPACLPSPNYVVADRTECFITGWGETQGTFGAGLLKEAQ
LPVIENKVCNRYEFLNGRVQSTELCAGHLAGGTDSCQGDSGGPLVCFEKDKYILQGVTSW
GLGCARPNKPGVYVRVSRFVTWIEGVMRNN
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| Gene Symbol | PLG |
| Gene Synonym | DKFZp779M0222 |
| Chromosome | 6 |
| Locus Map | 6q26 |
| All Transcripts | NM_000301 , NM_001168338 |
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