Transcript: Human NM_001368771.2

Homo sapiens septin 4 (SEPTIN4), transcript variant 11, mRNA.

Source:
NCBI, updated 2019-09-05
Taxon:
Homo sapiens (human)
Gene:
SEPTIN4 (5414)
Length:
3303
CDS:
143..3133

Additional Resources:

NCBI RefSeq record:
NM_001368771.2
NBCI Gene record:
SEPTIN4 (5414)

sgRNA constructs matching this transcript (CRISPRko, NGG PAM)

This list includes CRISPRko constructs with 100% (20mer + NGG) sequence match to the coding regions of this transcript.

No results found.

shRNA constructs matching this transcript with 100% SDR[?] match

This list includes all shRNAs that have a perfect SDR[?] match to Human NM_001368771.2, regardless of what transcript they were originally designed to target. For example, this list can include shRNAs that were originally designed to target: (i) a different isoform or obsolete version of this transcript (as annotated by NCBI), (ii) a transcript of an orthologous gene (in this collection, generally human-to-mouse or mouse-to-human), or (iii) a transcript of a different gene (from the same or different taxon).

Clone ID Target Seq Vector Match Position Match Region[?] SDR Match %[?] Intrinsic Score[?] Adjusted Score[?] Matches Other Human Gene?[?] Orig. Target Gene[?] Addgene[?]
1 TRCN0000282743 CAGGTCCTTACGGTCCAATTC pLKO_005 891 CDS 100% 10.800 15.120 N n/a
2 TRCN0000263658 TGATGGTGTACACCGAGTTTC pLKO_005 985 CDS 100% 10.800 15.120 N n/a
3 TRCN0000164795 CCCTAAAGGAAAGCATCCCAT pLKO.1 2706 CDS 100% 2.640 3.696 N SEPTIN4 n/a
4 TRCN0000165287 GTGGACCACAAGAAACGCAAA pLKO.1 2591 CDS 100% 4.050 3.240 N SEPTIN4 n/a
5 TRCN0000441026 AGGAACGGAATCGCAACAAAC pLKO_005 2958 CDS 100% 10.800 7.560 N Sept4 n/a
6 TRCN0000161166 GAGCAAGTTCGTGAAGGATTT pLKO.1 1798 CDS 100% 10.800 7.560 N SEPTIN4 n/a
7 TRCN0000282745 GGGTCTGAGGTTACTACTAAC pLKO_005 194 CDS 100% 10.800 7.560 N n/a
8 TRCN0000161680 GCAAGCTTGATCCCTATGATT pLKO.1 2025 CDS 100% 5.625 3.938 N SEPTIN4 n/a
9 TRCN0000164742 CATTGTGGACACACCAGGTTT pLKO.1 2311 CDS 100% 4.950 3.465 N SEPTIN4 n/a
10 TRCN0000101736 CCTAAAGGAAAGCATCCCATT pLKO.1 2707 CDS 100% 4.050 2.835 N Sept4 n/a
11 TRCN0000160749 CCTAAAGGAAAGCATCCCATT pLKO.1 2707 CDS 100% 4.050 2.835 N SEPTIN4 n/a
12 TRCN0000165540 GCTGAAGAGAGGATCATGCAA pLKO.1 2228 CDS 100% 3.000 2.100 N SEPTIN4 n/a
13 TRCN0000101737 CCGGCCATTGGATGTTGAATT pLKO.1 2497 CDS 100% 0.000 0.000 N Sept4 n/a
14 TRCN0000161444 CGTGAAGGATTTCTCAGGAAA pLKO.1 1807 CDS 100% 4.950 2.970 N SEPTIN4 n/a
15 TRCN0000165317 GATGCAGGAGATGCTACACAA pLKO.1 3082 CDS 100% 4.950 2.970 N SEPTIN4 n/a
16 TRCN0000164663 CTGAGCAAGTTCGTGAAGGAT pLKO.1 1796 CDS 100% 3.000 1.800 N SEPTIN4 n/a
17 TRCN0000433206 TGCATCAGCGGGTCAACATTG pLKO_005 2529 CDS 100% 10.800 7.560 N Sept4 n/a
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shRNA constructs with at least a near match to this transcript

This list includes shRNAs that have at least a >84% (16 of 19 bases) SDR[?] match to the transcript NM_001368771.2, regardless of what transcript they were originally designed to target. For example, this list can include shRNAs that were originally designed to target: (i) a different isoform or obsolete version of this transcript (as annotated by NCBI), (ii) a transcript of an orthologous gene (in this collection, generally human-to-mouse or mouse-to-human), or (iii) a transcript of a different gene (from the same or different taxon). NOTE: this download is a superset of the above result set.

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All ORF constructs matching this transcript

Clone ID DNA Barcode Vector Sequenced %[?] Nuc. Match %[?] Prot. Match %[?] Epitope Tag Match Diffs[?] Addgene[?]
1 ccsbBroadEn_09951 pDONR223 100% 55.3% 52.3% None (many diffs) n/a
2 ccsbBroad304_09951 pLX_304 0% 55.3% 52.3% V5 (many diffs) n/a
3 TRCN0000465614 CCCGACAGTAGCACTCATTGCTGG pLX_317 21.6% 55.3% 52.3% V5 (many diffs) n/a
4 ccsbBroadEn_01233 pDONR223 100% 47.1% 45.8% None (many diffs) n/a
5 ccsbBroad304_01233 pLX_304 0% 47.1% 45.8% V5 (many diffs) n/a
6 TRCN0000481592 ATGCAACTCATTTCAGGTCCTCCG pLX_317 29.2% 44.8% 40% V5 (not translated due to prior stop codon) (many diffs) n/a
7 TRCN0000476347 CCATTTCCAACTATGATTTCGGGC pLX_317 25.8% 44.8% 40% V5 (not translated due to prior stop codon) (many diffs) n/a
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