Ischnura elegans chromosome 13, ioIscEleg1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Palaeoptera; Odonata; Zygoptera; Coenagrionidae; Ischnura.
REFSEQ INFORMATION: The reference sequence is identical to\nOV121113.1.\nAssembly name: ioIscEleg1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/12/05. The original whole-genome shotgun project has the\naccession CAKLCU000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Ischnura elegans Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170369, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124170369, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124170308, transcript variant X3
uncharacterized LOC124170308, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
uncharacterized LOC124170308, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC124170332, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124170332, transcript variant X3
uncharacterized LOC124170332, transcript variant X1
uncharacterized LOC124170329, transcript variant X2
uncharacterized LOC124170329, transcript variant X1
uncharacterized protein LOC124170329 isoform X2
uncharacterized protein LOC124170329 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124170339, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124170339, transcript variant X2
uncharacterized LOC124170343, transcript variant X2
uncharacterized LOC124170343, transcript variant X1
uncharacterized LOC124170331, transcript variant X1
uncharacterized LOC124170331, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC124170279, transcript variant X2
uncharacterized LOC124170279, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC124170178, transcript variant X3
uncharacterized LOC124170178, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124170178, transcript variant X1
uncharacterized LOC124170178, transcript variant X2
uncharacterized LOC124170247, transcript variant X3
uncharacterized LOC124170247, transcript variant X1
uncharacterized LOC124170247, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170233, transcript variant X7
uncharacterized LOC124170233, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC124170233, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC124170233, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC124170233, transcript variant X2
uncharacterized LOC124170233, transcript variant X6
uncharacterized LOC124170233, transcript variant X5
uncharacterized protein LOC124170233 isoform X2
uncharacterized protein LOC124170233 isoform X1
uncharacterized LOC124170228, transcript variant X3
uncharacterized LOC124170228, transcript variant X2
uncharacterized protein LOC124170228 isoform X2
uncharacterized protein LOC124170228 isoform X1
uncharacterized LOC124170228, transcript variant X1
uncharacterized LOC124170239, transcript variant X2
uncharacterized LOC124170239, transcript variant X3
uncharacterized LOC124170239, transcript variant X1
uncharacterized protein LOC124170239 isoform X2
uncharacterized protein LOC124170239 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 583-like, transcript variant X2
zinc finger protein 583-like, transcript variant X1
uncharacterized LOC124170255, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC124170255, transcript variant X3
uncharacterized LOC124170255, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170234, transcript variant X3
uncharacterized protein LOC124170234 isoform X2
uncharacterized LOC124170234, transcript variant X1
uncharacterized LOC124170234, transcript variant X2
uncharacterized LOC124170234, transcript variant X4
uncharacterized protein LOC124170234 isoform X1
uncharacterized LOC124170253, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC124170253, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC124170253, transcript variant X4
uncharacterized LOC124170253, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
gastrula zinc finger protein XlCGF8.2DB-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170242, transcript variant X2
uncharacterized LOC124170242, transcript variant X1
uncharacterized protein LOC124170242 isoform X1
uncharacterized LOC124170242, transcript variant X4
uncharacterized LOC124170242, transcript variant X3
uncharacterized protein LOC124170242 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170277, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124170277, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
uncharacterized LOC124170277, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170222, transcript variant X3
uncharacterized protein LOC124170222 isoform X2
uncharacterized LOC124170222, transcript variant X2
uncharacterized LOC124170222, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein LOC124170222 isoform X1
uncharacterized LOC124170221, transcript variant X5
uncharacterized LOC124170221, transcript variant X3
uncharacterized LOC124170221, transcript variant X4
uncharacterized protein LOC124170221 isoform X2
uncharacterized protein LOC124170221 isoform X3
uncharacterized LOC124170221, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC124170221, transcript variant X2
uncharacterized protein LOC124170221 isoform X1
zinc finger BED domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170320, transcript variant X1
uncharacterized LOC124170320, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
uncharacterized LOC124170190, transcript variant X2
uncharacterized LOC124170190, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized protein LOC124170190 isoform X1
uncharacterized protein LOC124170190 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X2
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
myb/SANT-like DNA-binding domain-containing protein 3 isoform X2
uncharacterized protein LOC124170299 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
recQ-mediated genome instability protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170460, transcript variant X3
uncharacterized LOC124170460, transcript variant X2
uncharacterized LOC124170460, transcript variant X1
uncharacterized LOC124170456, transcript variant X1
uncharacterized LOC124170456, transcript variant X2
uncharacterized LOC124170457, transcript variant X2
uncharacterized LOC124170457, transcript variant X1
uncharacterized LOC124170274, transcript variant X5
uncharacterized protein LOC124170274 isoform X2
uncharacterized LOC124170274, transcript variant X3
uncharacterized LOC124170274, transcript variant X2
uncharacterized LOC124170274, transcript variant X1
uncharacterized LOC124170274, transcript variant X4
uncharacterized protein LOC124170274 isoform X1
uncharacterized LOC124170192, transcript variant X5
uncharacterized LOC124170192, transcript variant X3
uncharacterized LOC124170192, transcript variant X2
uncharacterized LOC124170192, transcript variant X1
uncharacterized LOC124170192, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124170208, transcript variant X15
uncharacterized LOC124170208, transcript variant X9
uncharacterized LOC124170208, transcript variant X6
uncharacterized LOC124170208, transcript variant X13
uncharacterized LOC124170208, transcript variant X12
uncharacterized LOC124170208, transcript variant X7
uncharacterized LOC124170208, transcript variant X5
uncharacterized LOC124170208, transcript variant X2
uncharacterized LOC124170208, transcript variant X4
uncharacterized LOC124170208, transcript variant X14
uncharacterized LOC124170208, transcript variant X11
uncharacterized LOC124170208, transcript variant X8
uncharacterized LOC124170208, transcript variant X3
uncharacterized LOC124170208, transcript variant X1
uncharacterized LOC124170208, transcript variant X17
uncharacterized LOC124170208, transcript variant X16
uncharacterized LOC124170208, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X3
gastrula zinc finger protein XlCGF57.1-like, transcript variant X4
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
gastrula zinc finger protein XlCGF57.1-like isoform X2
gastrula zinc finger protein XlCGF57.1-like isoform X3
zinc finger protein 391-like, transcript variant X1
zinc finger protein 391-like, transcript variant X2
zinc finger protein 391-like, transcript variant X3
uncharacterized LOC124170437, transcript variant X1
uncharacterized LOC124170437, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 551-like, transcript variant X1
zinc finger protein 551-like, transcript variant X2
zinc finger protein 551-like, transcript variant X3
uncharacterized protein LOC124170210 isoform X3
uncharacterized LOC124170313, transcript variant X1
uncharacterized LOC124170313, transcript variant X2
uncharacterized LOC124170313, transcript variant X3
uncharacterized LOC124170153, transcript variant X2
uncharacterized LOC124170153, transcript variant X4
uncharacterized LOC124170153, transcript variant X3
uncharacterized LOC124170153, transcript variant X1
uncharacterized LOC124170153, transcript variant X5
uncharacterized protein LOC124170153 isoform X1
uncharacterized protein LOC124170153 isoform X2
uncharacterized LOC124170152, transcript variant X1
uncharacterized LOC124170152, transcript variant X2
uncharacterized protein LOC124170152 isoform X1
uncharacterized protein LOC124170152 isoform X2
uncharacterized LOC124170158, transcript variant X1
uncharacterized protein LOC124170158 isoform X1
uncharacterized LOC124170158, transcript variant X2
uncharacterized protein LOC124170158 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
armadillo segment polarity protein, transcript variant X2
armadillo segment polarity protein, transcript variant X1
armadillo segment polarity protein, transcript variant X3
armadillo segment polarity protein isoform X2
armadillo segment polarity protein isoform X1
armadillo segment polarity protein isoform X3
uncharacterized LOC124170148, transcript variant X1
uncharacterized LOC124170148, transcript variant X3
uncharacterized LOC124170148, transcript variant X2
uncharacterized protein LOC124170148 isoform X1
uncharacterized protein LOC124170148 isoform X3
uncharacterized protein LOC124170148 isoform X2
uncharacterized LOC124170112, transcript variant X1
uncharacterized LOC124170112, transcript variant X2
uncharacterized LOC124170112, transcript variant X3
uncharacterized LOC124170112, transcript variant X5
uncharacterized LOC124170112, transcript variant X4
uncharacterized protein LOC124170112 isoform X1
uncharacterized protein LOC124170112 isoform X3
uncharacterized protein LOC124170112 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
uncharacterized LOC124170007, transcript variant X2
uncharacterized LOC124170007, transcript variant X1
uncharacterized protein LOC124170007 isoform X2
uncharacterized protein LOC124170007 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124170350, transcript variant X2
uncharacterized LOC124170350, transcript variant X1
uncharacterized protein LOC124170350 isoform X2
uncharacterized protein LOC124170350 isoform X1
uncharacterized LOC124170278, transcript variant X2
uncharacterized LOC124170278, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
uncharacterized protein LOC124170278 isoform X2
uncharacterized protein LOC124170278 isoform X1
uncharacterized LOC124169995, transcript variant X2
uncharacterized LOC124169995, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC124170002, transcript variant X1
uncharacterized LOC124170002, transcript variant X2
uncharacterized protein LOC124170002 isoform X1
uncharacterized protein LOC124170002 isoform X2
uncharacterized LOC124170352, transcript variant X1
uncharacterized LOC124170352, transcript variant X2
26S proteasome non-ATPase regulatory subunit 2
uncharacterized LOC124170124, transcript variant X1
uncharacterized LOC124170124, transcript variant X2
uncharacterized protein LOC124170124 isoform X1
uncharacterized protein LOC124170124 isoform X2
uncharacterized LOC124169987, transcript variant X1
uncharacterized LOC124169987, transcript variant X4
uncharacterized LOC124169987, transcript variant X2
uncharacterized LOC124169987, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tigger transposable element-derived protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170070, transcript variant X8
uncharacterized LOC124170070, transcript variant X7
uncharacterized LOC124170070, transcript variant X6
uncharacterized LOC124170070, transcript variant X3
uncharacterized LOC124170070, transcript variant X2
uncharacterized LOC124170070, transcript variant X1
uncharacterized LOC124170070, transcript variant X4
uncharacterized LOC124170070, transcript variant X5
uncharacterized protein LOC124170070 isoform X2
uncharacterized protein LOC124170070 isoform X1
uncharacterized protein LOC124170070 isoform X6
uncharacterized protein LOC124170070 isoform X4
uncharacterized protein LOC124170070 isoform X5
uncharacterized protein LOC124170070 isoform X3
uncharacterized protein LOC124170070 isoform X7
uncharacterized protein LOC124170070 isoform X8
uncharacterized LOC124170070, transcript variant X9
uncharacterized protein LOC124170070 isoform X9
tetraspanning orphan receptor-like, transcript variant X1
tetraspanning orphan receptor-like, transcript variant X2
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC124170080, transcript variant X2
uncharacterized LOC124170080, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124170099, transcript variant X1
uncharacterized LOC124170099, transcript variant X2
uncharacterized LOC124170090, transcript variant X2
uncharacterized LOC124170090, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
oocyte zinc finger protein XlCOF6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X2
oocyte zinc finger protein XlCOF6-like isoform X1
oocyte zinc finger protein XlCOF6-like isoform X2
uncharacterized LOC124170271, transcript variant X1
uncharacterized LOC124170271, transcript variant X2
uncharacterized protein LOC124170271 isoform X1
uncharacterized protein LOC124170271 isoform X2
uncharacterized LOC124170193, transcript variant X1
uncharacterized LOC124170193, transcript variant X2
uncharacterized protein LOC124170193 isoform X1
uncharacterized protein LOC124170193 isoform X2
oocyte zinc finger protein XlCOF6-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like isoform X4
oocyte zinc finger protein XlCOF6-like isoform X3
oocyte zinc finger protein XlCOF6-like isoform X5
oocyte zinc finger protein XlCOF6-like isoform X6
oocyte zinc finger protein XlCOF6-like isoform X7
uncharacterized LOC124170451, transcript variant X1
uncharacterized LOC124170451, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
CKLF-like MARVEL transmembrane domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 90 samples with support for all annotated introns
uncharacterized LOC124170323, transcript variant X1
uncharacterized LOC124170323, transcript variant X8
uncharacterized LOC124170323, transcript variant X12
uncharacterized LOC124170323, transcript variant X9
uncharacterized LOC124170323, transcript variant X6
uncharacterized LOC124170323, transcript variant X3
uncharacterized LOC124170323, transcript variant X2
uncharacterized LOC124170323, transcript variant X5
uncharacterized LOC124170323, transcript variant X10
uncharacterized LOC124170323, transcript variant X7
uncharacterized LOC124170323, transcript variant X4
uncharacterized LOC124170323, transcript variant X11
uncharacterized protein LOC124170323 isoform X1
uncharacterized protein LOC124170323 isoform X2
uncharacterized protein LOC124170323 isoform X4
uncharacterized protein LOC124170323 isoform X3
transfer RNA threonine (anticodon GGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
myb/SANT-like DNA-binding domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Golgi reassembly-stacking protein 2-like, transcript variant X2
Golgi reassembly-stacking protein 2-like, transcript variant X1
Golgi reassembly-stacking protein 2-like isoform X1
Golgi reassembly-stacking protein 2-like isoform X2
uncharacterized LOC124170440, transcript variant X1
uncharacterized LOC124170440, transcript variant X2
uncharacterized LOC124170440, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized LOC124170439, transcript variant X5
uncharacterized LOC124170439, transcript variant X1
uncharacterized LOC124170439, transcript variant X2
uncharacterized LOC124170439, transcript variant X3
uncharacterized LOC124170439, transcript variant X4
uncharacterized protein LOC124170439 isoform X2
uncharacterized protein LOC124170439 isoform X1
uncharacterized LOC124170443, transcript variant X1
uncharacterized LOC124170443, transcript variant X3
uncharacterized LOC124170443, transcript variant X2
uncharacterized LOC124170443, transcript variant X4
uncharacterized LOC124170445, transcript variant X1
uncharacterized LOC124170445, transcript variant X3
uncharacterized LOC124170445, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 236-like
uncharacterized protein C05D11.13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
uncharacterized protein C05D11.13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
uncharacterized protein C05D11.13-like isoform X1
uncharacterized protein C05D11.13-like isoform X2
gastrula zinc finger protein XlCGF7.1-like, transcript variant X4
gastrula zinc finger protein XlCGF7.1-like, transcript variant X3
gastrula zinc finger protein XlCGF7.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like
uncharacterized LOC124170316, transcript variant X1
uncharacterized LOC124170316, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 468-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
zinc finger protein 468-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124170289, transcript variant X1
uncharacterized LOC124170289, transcript variant X2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124170135, transcript variant X3
uncharacterized protein LOC124170135 isoform X3
uncharacterized LOC124170127, transcript variant X1
uncharacterized LOC124170127, transcript variant X3
uncharacterized LOC124170127, transcript variant X5
uncharacterized LOC124170127, transcript variant X4
uncharacterized LOC124170127, transcript variant X2
uncharacterized LOC124170136, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC124170136, transcript variant X1
uncharacterized LOC124170136, transcript variant X2
uncharacterized LOC124170136, transcript variant X3
uncharacterized LOC124170136, transcript variant X5
uncharacterized LOC124170130, transcript variant X1
uncharacterized LOC124170130, transcript variant X2
uncharacterized LOC124170135, transcript variant X2
uncharacterized LOC124170135, transcript variant X4
uncharacterized protein LOC124170135 isoform X2
uncharacterized LOC124170128, transcript variant X2
uncharacterized LOC124170128, transcript variant X1
uncharacterized LOC124170135, transcript variant X1
uncharacterized protein LOC124170135 isoform X1
uncharacterized LOC124170135, transcript variant X5
uncharacterized LOC124170169, transcript variant X2
uncharacterized LOC124170169, transcript variant X1
Golgi reassembly-stacking protein 2-like, transcript variant X3
Golgi reassembly-stacking protein 2-like
uncharacterized LOC124170220, transcript variant X1
uncharacterized LOC124170220, transcript variant X2
gastrula zinc finger protein xLCGF3.1-like, transcript variant X3
gastrula zinc finger protein xLCGF3.1-like, transcript variant X2
gastrula zinc finger protein xLCGF3.1-like, transcript variant X4
gastrula zinc finger protein xLCGF3.1-like, transcript variant X1
gastrula zinc finger protein xLCGF3.1-like