Portunus trituberculatus isolate SZX2019 chromosome 11, ASM1759143v1, whole genome shotgun sequence.
Portunus trituberculatus (swimming crab)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Brachyura; Eubrachyura; Portunoidea; Portunidae; Portunus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM030081.1.\nAssembly name: ASM1759143v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Center for Ecological and\nEnvironmental Sciences on 2021/03/30. The original whole-genome\nshotgun project has the accession JAGGDN000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Center for Ecological and Environmental\n Sciences\nAssembly Method :: Wtdbg v. 2.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 54.74x\nSequencing Technology :: Oxford Nanopore; Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Portunus trituberculatus Annotation\n Release 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.
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 6 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123502249, 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 8 samples with support for all annotated introns
uncharacterized LOC123502249, transcript variant X1
uncharacterized LOC123502254, 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 4 samples with support for all annotated introns
uncharacterized LOC123502254, transcript variant X1
uncharacterized LOC123502251, transcript variant X4
uncharacterized LOC123502251, 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 36 samples with support for all annotated introns
uncharacterized LOC123502251, 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 15 samples with support for all annotated introns
uncharacterized LOC123502251, transcript variant X3
uncharacterized LOC123502255, transcript variant X3
uncharacterized LOC123502255, transcript variant X4
uncharacterized LOC123502255, transcript variant X2
uncharacterized LOC123502255, transcript variant X1
uncharacterized LOC123502255, transcript variant X7
uncharacterized LOC123502255, transcript variant X8
uncharacterized LOC123502255, transcript variant X9
uncharacterized LOC123502255, transcript variant X10
uncharacterized LOC123502255, transcript variant X5
uncharacterized LOC123502255, transcript variant X6
uncharacterized protein LOC123502255 isoform X1
uncharacterized protein LOC123502255 isoform X3
uncharacterized protein LOC123502255 isoform 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 18 samples with support for all annotated introns
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, including 3 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 40% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC123502270, transcript variant X1
uncharacterized LOC123502270, 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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
neurogenic locus protein delta-like, transcript variant X1
neurogenic locus protein delta-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 1 sample with support for all annotated introns
neurogenic locus protein delta-like isoform X1
neurogenic locus protein delta-like isoform 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 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
trihelix transcription factor ASIL2-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 7 samples with support for all annotated introns
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 3 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 16 samples with support for all annotated introns
uncharacterized LOC123502322, transcript variant X1
uncharacterized LOC123502322, transcript variant X5
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 LOC123502322, transcript variant X3
uncharacterized LOC123502322, transcript variant X2
uncharacterized LOC123502322, 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 28 samples with support for all annotated introns
uncharacterized LOC123502285, transcript variant X5
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
uncharacterized LOC123502285, transcript variant X8
uncharacterized LOC123502285, transcript variant X6
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 protein LOC123502285 isoform X1
uncharacterized LOC123502285, transcript variant X4
uncharacterized LOC123502285, transcript variant X7
uncharacterized protein LOC123502285 isoform X2
uncharacterized LOC123502285, transcript variant X2
uncharacterized LOC123502285, transcript variant X9
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
uncharacterized LOC123502285, transcript variant X3
uncharacterized protein LOC123502285 isoform X3
uncharacterized LOC123502285, transcript variant X1
uncharacterized LOC123502285, transcript variant X13
uncharacterized LOC123502285, transcript variant X12
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 LOC123502285, transcript variant X14
uncharacterized LOC123502285, transcript variant X11
uncharacterized LOC123502285, transcript variant X10
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 LOC123502329, 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 29 samples with support for all annotated introns
uncharacterized LOC123502329, 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 35 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 34 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 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123502334, transcript variant X1
uncharacterized LOC123502334, transcript variant X2
uncharacterized LOC123502308, transcript variant X2
uncharacterized LOC123502308, 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 13 samples with support for all annotated introns
uncharacterized LOC123502308, transcript variant X1
uncharacterized LOC123502308, transcript variant X4
uncharacterized LOC123502308, transcript variant X5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123502306, transcript variant X1
uncharacterized LOC123502306, 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 24 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123502313, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123502286, transcript variant X1
uncharacterized LOC123502286, transcript variant X2
uncharacterized protein LOC123502286 isoform X2
uncharacterized protein LOC123502286 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123502273, transcript variant X3
uncharacterized protein LOC123502273 isoform X3
uncharacterized LOC123502274, transcript variant X2
uncharacterized LOC123502274, transcript variant X1
uncharacterized protein LOC123502274 isoform X2
uncharacterized protein LOC123502274 isoform X1
uncharacterized LOC123502273, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123502273, transcript variant X1
uncharacterized protein LOC123502273 isoform X1
uncharacterized protein LOC123502273 isoform X2
uncharacterized LOC123502296, transcript variant X1
uncharacterized LOC123502296, transcript variant X2
uncharacterized LOC123502284, transcript variant X2
uncharacterized LOC123502284, transcript variant X1
uncharacterized LOC123502279, transcript variant X3
uncharacterized LOC123502279, transcript variant X5
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 LOC123502279, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized LOC123502279, transcript variant X4
uncharacterized LOC123502279, transcript variant X1
uncharacterized LOC123502294, transcript variant X2
uncharacterized LOC123502294, transcript variant X1
uncharacterized LOC123502295, transcript variant X3
uncharacterized LOC123502295, transcript variant X2
uncharacterized LOC123502295, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized LOC123502295, 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 LOC123502278, transcript variant X2
uncharacterized LOC123502278, transcript variant X1
uncharacterized LOC123502281, transcript variant X3
uncharacterized LOC123502281, transcript variant X1
uncharacterized LOC123502281, transcript variant X4
uncharacterized LOC123502281, transcript variant X2
uncharacterized protein LOC123502281 isoform X1
uncharacterized protein LOC123502281 isoform X2
GPI mannosyltransferase 2-like, transcript variant X2
GPI mannosyltransferase 2-like, transcript variant X1
GPI mannosyltransferase 2-like isoform X1
GPI mannosyltransferase 2-like isoform X2
GPI mannosyltransferase 2-like, transcript variant X3
GPI mannosyltransferase 2-like isoform X3
uncharacterized LOC123502293, transcript variant X1
uncharacterized LOC123502293, transcript variant X2
uncharacterized LOC123502293, transcript variant X4
uncharacterized LOC123502293, transcript variant X5
uncharacterized LOC123502293, transcript variant X3
uncharacterized LOC123502275, transcript variant X4
uncharacterized LOC123502275, transcript variant X5
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: 70% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123502289, transcript variant X1
uncharacterized LOC123502289, transcript variant X5
uncharacterized LOC123502289, transcript variant X4
uncharacterized LOC123502289, transcript variant X3
uncharacterized protein LOC123502289 isoform X1
uncharacterized LOC123502289, transcript variant X6
uncharacterized LOC123502289, transcript variant X2
uncharacterized protein LOC123502289 isoform X2
uncharacterized LOC123502302, transcript variant X1
uncharacterized LOC123502302, transcript variant X2
uncharacterized LOC123502297, transcript variant X2
uncharacterized LOC123502297, transcript variant X1
uncharacterized LOC123502297, transcript variant X3
uncharacterized LOC123502275, transcript variant X2
uncharacterized LOC123502275, transcript variant X6
uncharacterized LOC123502275, transcript variant X3
uncharacterized protein LOC123502275 isoform X2
uncharacterized LOC123502275, transcript variant X1
uncharacterized protein LOC123502275 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123502290, transcript variant X1
uncharacterized LOC123502290, transcript variant X2
uncharacterized protein LOC123502290 isoform X1
uncharacterized protein LOC123502290 isoform X2
uncharacterized LOC123502290, transcript variant X5
uncharacterized LOC123502290, transcript variant X4
uncharacterized LOC123502290, transcript variant X3
uncharacterized LOC123502288, transcript variant X1
uncharacterized LOC123502288, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
uncharacterized LOC123502288, transcript variant X2
uncharacterized LOC123502300, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized LOC123502300, 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 33 samples with support for all annotated introns
uncharacterized LOC123502300, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 88% 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: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
DNA repair protein REV1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA repair protein REV1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DNA repair protein REV1-like, transcript variant X3
uncharacterized LOC123502384, transcript variant X1
uncharacterized protein LOC123502384 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
vegetative cell wall protein gp1-like, transcript variant X2
vegetative cell wall protein gp1-like, transcript variant X1
vegetative cell wall protein gp1-like isoform X1
vegetative cell wall protein gp1-like isoform X2
uncharacterized LOC123502386, transcript variant X3
uncharacterized LOC123502386, transcript variant X2
uncharacterized LOC123502386, transcript variant X1
uncharacterized protein LOC123502386 isoform X2
uncharacterized protein LOC123502386 isoform X1
uncharacterized LOC123502393, transcript variant X2
uncharacterized LOC123502393, transcript variant X1
uncharacterized protein LOC123502393 isoform X2
uncharacterized protein LOC123502393 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123502384, transcript variant X2
uncharacterized protein LOC123502384 isoform X2
uncharacterized LOC123502403, transcript variant X2
uncharacterized LOC123502403, transcript variant X1
uncharacterized LOC123502403, transcript variant X3
uncharacterized LOC123502403, transcript variant X4
uncharacterized LOC123502403, transcript variant X5
uncharacterized LOC123502385, transcript variant X5
uncharacterized protein LOC123502385 isoform X3
uncharacterized LOC123502385, transcript variant X4
uncharacterized LOC123502385, transcript variant X2
uncharacterized LOC123502385, transcript variant X3
uncharacterized protein LOC123502385 isoform X2
uncharacterized LOC123502385, transcript variant X1
uncharacterized protein LOC123502385 isoform X1
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
uncharacterized LOC123502440, transcript variant X2
uncharacterized LOC123502440, transcript variant X3
uncharacterized LOC123502440, 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 9 samples with support for all annotated introns
uncharacterized LOC123502434, transcript variant X3
uncharacterized LOC123502434, transcript variant X2
uncharacterized LOC123502434, transcript variant X1
uncharacterized LOC123502434, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123502450, transcript variant X1
uncharacterized LOC123502450, transcript variant X2
uncharacterized LOC123502380, transcript variant X4
uncharacterized LOC123502380, transcript variant X1
uncharacterized LOC123502380, transcript variant X2
uncharacterized LOC123502380, 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 26 samples with support for all annotated introns
uncharacterized protein LOC123502380 isoform X2
uncharacterized protein LOC123502380 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% 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 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
piggyBac transposable element-derived protein 3-like
uncharacterized LOC123502411, transcript variant X2
uncharacterized LOC123502411, transcript variant X1
uncharacterized LOC123502428, transcript variant X2
uncharacterized LOC123502428, transcript variant X1
uncharacterized LOC123502394, transcript variant X5
uncharacterized LOC123502394, transcript variant X12
uncharacterized LOC123502394, transcript variant X10
uncharacterized LOC123502394, transcript variant X9
uncharacterized LOC123502394, transcript variant X8
uncharacterized LOC123502394, transcript variant X3
uncharacterized LOC123502394, transcript variant X4
uncharacterized LOC123502394, transcript variant X2
uncharacterized LOC123502394, transcript variant X11
uncharacterized LOC123502394, transcript variant X7
uncharacterized LOC123502394, transcript variant X6
uncharacterized LOC123502394, transcript variant X1
uncharacterized LOC123502390, transcript variant X11
uncharacterized LOC123502390, transcript variant X10
uncharacterized LOC123502390, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC123502390, transcript variant X5
uncharacterized LOC123502390, transcript variant X7
uncharacterized LOC123502390, transcript variant X8
uncharacterized LOC123502390, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
uncharacterized LOC123502390, transcript variant X1
uncharacterized LOC123502390, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC123502390, transcript variant X6
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
uncharacterized LOC123502390, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized LOC123502445, transcript variant X1
uncharacterized LOC123502445, transcript variant X2
uncharacterized LOC123502406, transcript variant X3
uncharacterized LOC123502406, transcript variant X2
uncharacterized LOC123502406, transcript variant X1
uncharacterized LOC123502406, transcript variant X6
uncharacterized LOC123502406, transcript variant X4
uncharacterized LOC123502406, transcript variant X5
uncharacterized LOC123502389, transcript variant X1
uncharacterized LOC123502389, transcript variant X3
uncharacterized LOC123502389, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
uncharacterized LOC123502388, transcript variant X2
uncharacterized LOC123502388, transcript variant X1
uncharacterized protein LOC123502388 isoform X1
uncharacterized protein LOC123502388 isoform X2
uncharacterized LOC123502388, transcript variant X5
uncharacterized LOC123502388, transcript variant X4
uncharacterized LOC123502388, transcript variant X3
uncharacterized LOC123502382, transcript variant X4
uncharacterized LOC123502382, transcript variant X1
uncharacterized LOC123502382, transcript variant X2
uncharacterized LOC123502382, transcript variant X5
uncharacterized LOC123502382, transcript variant X6
uncharacterized protein LOC123502382 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 89% 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 long SRA read, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
uncharacterized LOC123502382, transcript variant X3
uncharacterized LOC123502382, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC123502382 isoform X1
uncharacterized LOC123502401, transcript variant X1
uncharacterized LOC123502401, transcript variant X2
uncharacterized LOC123502401, transcript variant X3
uncharacterized LOC123502401, transcript variant X4
repressor of RNA polymerase III transcription MAF1 homolog, transcript variant X1
repressor of RNA polymerase III transcription MAF1 homolog, transcript variant X2
repressor of RNA polymerase III transcription MAF1 homolog isoform X2
repressor of RNA polymerase III transcription MAF1 homolog isoform X1
uncharacterized LOC123502375, transcript variant X1
uncharacterized LOC123502375, transcript variant X2
palmitoyltransferase akr1-like, transcript variant X4
palmitoyltransferase akr1-like, transcript variant X3
palmitoyltransferase akr1-like, transcript variant X5
palmitoyltransferase akr1-like, transcript variant X2
palmitoyltransferase akr1-like, transcript variant X1
palmitoyltransferase akr1-like isoform X2
palmitoyltransferase akr1-like isoform X3
palmitoyltransferase akr1-like isoform X1
uncharacterized LOC123502374, transcript variant X2
uncharacterized LOC123502374, 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 2 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X1
membrane metallo-endopeptidase-like 1 isoform X6
membrane metallo-endopeptidase-like 1 isoform X5
membrane metallo-endopeptidase-like 1 isoform X4
membrane metallo-endopeptidase-like 1 isoform X2
membrane metallo-endopeptidase-like 1 isoform X3
membrane metallo-endopeptidase-like 1 isoform X1
uncharacterized LOC123502399, transcript variant X1
uncharacterized LOC123502399, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
uncharacterized LOC123502460, transcript variant X3
uncharacterized LOC123502460, transcript variant X1
uncharacterized LOC123502460, transcript variant X4
uncharacterized LOC123502460, transcript variant X2
uncharacterized LOC123502466, transcript variant X2
uncharacterized LOC123502466, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC123502465, transcript variant X3
uncharacterized LOC123502465, 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 44 samples with support for all annotated introns
uncharacterized LOC123502465, transcript variant X1
uncharacterized LOC123502464, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC123502464, transcript variant X3
uncharacterized LOC123502464, transcript variant X4
uncharacterized LOC123502464, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 85% 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: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123502472, transcript variant X1
uncharacterized LOC123502472, transcript variant X2
uncharacterized protein LOC123502472 isoform X2
uncharacterized protein LOC123502472 isoform X1
uncharacterized LOC123502472, transcript variant X4
uncharacterized LOC123502472, transcript variant X3
uncharacterized LOC123502476, transcript variant X2
uncharacterized LOC123502476, transcript variant X1
uncharacterized LOC123502473, transcript variant X1
uncharacterized LOC123502473, transcript variant X3
uncharacterized LOC123502473, transcript variant X13
uncharacterized LOC123502473, transcript variant X9
uncharacterized LOC123502473, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123502473, transcript variant X12
uncharacterized LOC123502473, transcript variant X11
uncharacterized LOC123502473, transcript variant X8
uncharacterized LOC123502473, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123502473, transcript variant X10
uncharacterized LOC123502473, transcript variant X7
uncharacterized LOC123502473, transcript variant X4
uncharacterized protein LOC123502473 isoform X1
uncharacterized protein LOC123502473 isoform X3
uncharacterized LOC123502473, transcript variant X2
uncharacterized protein LOC123502473 isoform X2
uncharacterized LOC123502479, transcript variant X1
uncharacterized LOC123502479, transcript variant X2
uncharacterized protein LOC123502479 isoform X1
uncharacterized protein LOC123502479 isoform X2
uncharacterized LOC123502479, transcript variant X11
uncharacterized LOC123502479, transcript variant X10
uncharacterized LOC123502479, transcript variant X5
uncharacterized LOC123502479, transcript variant X9
uncharacterized LOC123502479, transcript variant X6
uncharacterized LOC123502479, transcript variant X8
uncharacterized LOC123502479, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC123502479, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
uncharacterized LOC123502479, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 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: 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: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns