Bombus pyrosoma isolate SC7728 linkage group LG13, ASM1482585v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Apoidea; Apidae; Bombus; Melanobombus.
Genus-wide characterization of bumblebee genomes provides insights into their evolution and variation in ecological and behavioral traits
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM026137.1.\nAssembly name: ASM1482585v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Chinese Academy of\nAgricultural Sciences on 2020/10/02. The original whole-genome\nshotgun project has the accession JACXIN000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Chinese Academy of Agricultural Sciences\nAssembly Date :: DEC-2017\nAssembly Method :: DISCOVAR de novo v. 52488\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Bombus pyrosoma 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: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 1 Protein
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, and 86% 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 2 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122574179, 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 2 samples with support for all annotated introns
uncharacterized LOC122574179, 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 protein LOC122574179 isoform X1
uncharacterized protein LOC122574179 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 4 samples with support for all annotated introns
piggyBac transposable element-derived protein 1-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: piggyBac transposable element-derived protein 1-like
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
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
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: uncharacterized protein LOC122574355
uncharacterized LOC122574153, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC122574153, transcript variant X2
signal recognition particle receptor subunit beta, transcript variant X1
signal recognition particle receptor subunit beta, transcript variant X2
signal recognition particle receptor subunit beta isoform X1
signal recognition particle receptor subunit beta 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC122574022, transcript variant X5
uncharacterized LOC122574022, transcript variant X4
uncharacterized LOC122574022, transcript variant X8
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 LOC122574022, transcript variant X1
uncharacterized LOC122574022, transcript variant X6
uncharacterized protein LOC122574022 isoform X4
uncharacterized protein LOC122574022 isoform X1
uncharacterized protein LOC122574022 isoform X5
uncharacterized LOC122574022, transcript variant X3
uncharacterized protein LOC122574022 isoform 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 6 samples with support for all annotated introns
uncharacterized LOC122574022, transcript variant X7
uncharacterized LOC122574022, transcript variant X2
uncharacterized protein LOC122574022 isoform X6
uncharacterized protein LOC122574022 isoform X2
uncharacterized LOC122574024, transcript variant X3
uncharacterized LOC122574024, transcript variant X2
uncharacterized LOC122574022, transcript variant X12
uncharacterized LOC122574024, 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 5 samples with support for all annotated introns
uncharacterized LOC122574021, transcript variant X2
uncharacterized LOC122574021, 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 7 samples with support for all annotated introns
uncharacterized protein LOC122574021 isoform X2
uncharacterized protein LOC122574021 isoform X1
uncharacterized LOC122574021, transcript variant X4
uncharacterized LOC122574021, transcript variant X3
uncharacterized protein LOC122574021 isoform X4
uncharacterized protein LOC122574021 isoform X3
uncharacterized LOC122574022, transcript variant X9
uncharacterized LOC122574022, transcript variant X10
uncharacterized LOC122574022, transcript variant X11
uncharacterized LOC122574088, transcript variant X8
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 8 samples with support for all annotated introns
uncharacterized LOC122574088, transcript variant X2
uncharacterized LOC122574088, transcript variant X6
uncharacterized LOC122574088, transcript variant X1
uncharacterized LOC122574088, transcript variant X3
uncharacterized LOC122574088, transcript variant X5
uncharacterized LOC122574088, transcript variant X4
uncharacterized LOC122574088, transcript variant X7
EF-hand calcium-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
POU domain, class 6, transcription factor 1, transcript variant X3
POU domain, class 6, transcription factor 1, transcript variant X1
POU domain, class 6, transcription factor 1, transcript variant X2
POU domain, class 6, transcription factor 1 isoform X1
POU domain, class 6, transcription factor 1 isoform X3
POU domain, class 6, transcription factor 1 isoform X2
POU domain, class 6, transcription factor 1, transcript variant X4
POU domain, class 6, transcription factor 1 isoform X4
UNC93-like protein, transcript variant X1
UNC93-like protein, transcript variant X2
retinol dehydrogenase 12-like, transcript variant X2
retinol dehydrogenase 12-like, transcript variant X1
retinol dehydrogenase 12-like isoform X2
retinol dehydrogenase 12-like isoform X1
cytochrome P450 302a1, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 302a1, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 302a1, mitochondrial isoform X2
cytochrome P450 302a1, mitochondrial isoform X1
uncharacterized LOC122574177, transcript variant X1
uncharacterized LOC122574177, transcript variant X2
endocuticle structural glycoprotein SgAbd-2-like
endocuticle structural glycoprotein SgAbd-1-like
larval cuticle protein LCP-17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
larval cuticle protein LCP-17-like, transcript variant X4
larval cuticle protein LCP-17-like, transcript variant X3
larval cuticle protein LCP-17-like, transcript variant X2
uncharacterized LOC122574063, transcript variant X2
uncharacterized LOC122574063, transcript variant X1
uncharacterized LOC122574063, transcript variant X3
uncharacterized LOC122574063, transcript variant X4
uncharacterized protein LOC122574063 isoform X1
uncharacterized protein LOC122574063 isoform X2
uncharacterized LOC122574063, transcript variant X6
uncharacterized LOC122574063, transcript variant X7
uncharacterized LOC122574063, transcript variant X5
uncharacterized protein LOC122574063 isoform X3
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 4 samples with support for all annotated introns
elongation of very long chain fatty acids protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
endocuticle structural glycoprotein ABD-4-like, transcript variant X14
endocuticle structural glycoprotein ABD-4-like, transcript variant X15
endocuticle structural glycoprotein ABD-4-like, transcript variant X12
endocuticle structural glycoprotein ABD-4-like, transcript variant X18
endocuticle structural glycoprotein ABD-4-like, transcript variant X20
endocuticle structural glycoprotein ABD-4-like, transcript variant X16
endocuticle structural glycoprotein ABD-4-like, transcript variant X17
endocuticle structural glycoprotein ABD-4-like, transcript variant X24
endocuticle structural glycoprotein ABD-4-like, transcript variant X25
endocuticle structural glycoprotein ABD-4-like, transcript variant X26
endocuticle structural glycoprotein ABD-4-like, transcript variant X13
endocuticle structural glycoprotein ABD-4-like, transcript variant X23
endocuticle structural glycoprotein ABD-4-like, transcript variant X22
endocuticle structural glycoprotein ABD-4-like, transcript variant X21
endocuticle structural glycoprotein ABD-4-like, transcript variant X27
endocuticle structural glycoprotein ABD-4-like, transcript variant X19
endocuticle structural glycoprotein ABD-4-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
endocuticle structural glycoprotein ABD-4-like, transcript variant X9
endocuticle structural glycoprotein ABD-4-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
endocuticle structural glycoprotein ABD-4-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
endocuticle structural glycoprotein ABD-4-like, transcript variant X5
endocuticle structural glycoprotein ABD-4-like, transcript variant X4
endocuticle structural glycoprotein ABD-4-like, transcript variant X10
endocuticle structural glycoprotein ABD-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
endocuticle structural glycoprotein ABD-4-like, transcript variant X2
endocuticle structural glycoprotein ABD-4-like, transcript variant X3
endocuticle structural glycoprotein ABD-4-like, transcript variant X11
endocuticle structural glycoprotein ABD-4-like
uncharacterized LOC122574414, transcript variant X2
uncharacterized LOC122574414, transcript variant X1
uncharacterized protein LOC122574414 isoform X2
uncharacterized protein LOC122574414 isoform X1
uncharacterized LOC122574517, transcript variant X1
uncharacterized LOC122574517, transcript variant X2
uncharacterized LOC122574138, transcript variant X3
uncharacterized LOC122574138, transcript variant X2
uncharacterized LOC122574138, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 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: 2 Proteins
glucose dehydrogenase [FAD, quinone]-like, transcript variant X3
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 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: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122574392, transcript variant X1
uncharacterized protein LOC122574392 isoform X1
uncharacterized LOC122574392, transcript variant X3
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 8 samples with support for all annotated introns
uncharacterized protein LOC122574392 isoform X3
uncharacterized LOC122574394, transcript variant X1
uncharacterized LOC122574394, transcript variant X2
uncharacterized LOC122574392, transcript variant X2
uncharacterized protein LOC122574392 isoform X2
uncharacterized LOC122574393, transcript variant X4
uncharacterized LOC122574393, transcript variant X3
uncharacterized LOC122574393, transcript variant X6
uncharacterized LOC122574393, transcript variant X7
uncharacterized LOC122574393, transcript variant X8
uncharacterized LOC122574393, transcript variant X11
uncharacterized LOC122574393, transcript variant X9
uncharacterized LOC122574393, transcript variant X5
uncharacterized LOC122574393, 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
uncharacterized LOC122574393, transcript variant X1
uncharacterized LOC122574393, transcript variant X10
uncharacterized LOC122574515, transcript variant X5
uncharacterized LOC122574515, transcript variant X3
uncharacterized LOC122574515, transcript variant X2
uncharacterized LOC122574515, transcript variant X6
uncharacterized LOC122574515, transcript variant X4
uncharacterized LOC122574515, transcript variant X9
uncharacterized LOC122574515, transcript variant X1
uncharacterized LOC122574515, transcript variant X7
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 4-like
uncharacterized LOC122574515, transcript variant X8
uncharacterized LOC122574515, transcript variant X11
uncharacterized LOC122574515, transcript variant X10
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
COP9 signalosome complex subunit 7b, transcript variant X2
COP9 signalosome complex subunit 7b, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 isoform X2
paired amphipathic helix protein Sin3a, transcript variant X2
paired amphipathic helix protein Sin3a, transcript variant X3
paired amphipathic helix protein Sin3a, transcript variant X1
paired amphipathic helix protein Sin3a isoform X2
paired amphipathic helix protein Sin3a isoform X3
paired amphipathic helix protein Sin3a isoform X1
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X5
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X2
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X1
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X7
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X6
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X3
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X4
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X9
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X10
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X8
mitochondrial tRNA-specific 2-thiouridylase 1 isoform X1
mitochondrial tRNA-specific 2-thiouridylase 1 isoform X2
mitochondrial tRNA-specific 2-thiouridylase 1 isoform X3
neprilysin-4-like, transcript variant X1
neprilysin-4-like, transcript variant X3
neprilysin-4-like, transcript variant X2
neprilysin-4-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 7 samples with support for all annotated introns
neprilysin-4-like, transcript variant X5
neprilysin-4-like, transcript variant X4
neprilysin-4-like, transcript variant X6
segment polarity protein dishevelled homolog DVL-3, transcript variant X7
segment polarity protein dishevelled homolog DVL-3, transcript variant X6
segment polarity protein dishevelled homolog DVL-3, transcript variant X8
segment polarity protein dishevelled homolog DVL-3, transcript variant X5
segment polarity protein dishevelled homolog DVL-3, transcript variant X2
segment polarity protein dishevelled homolog DVL-3, transcript variant X1
segment polarity protein dishevelled homolog DVL-3, transcript variant X4
segment polarity protein dishevelled homolog DVL-3, transcript variant X3
segment polarity protein dishevelled homolog DVL-3
uncharacterized LOC122574243, transcript variant X10
uncharacterized LOC122574243, transcript variant X8
uncharacterized LOC122574243, transcript variant X7
uncharacterized LOC122574243, transcript variant X4
uncharacterized LOC122574243, transcript variant X6
uncharacterized LOC122574243, transcript variant X3
uncharacterized LOC122574243, transcript variant X1
uncharacterized LOC122574243, transcript variant X5
uncharacterized LOC122574243, transcript variant X2
uncharacterized LOC122574243, transcript variant X9
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
structural maintenance of chromosomes protein 5, transcript variant X3
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 7 samples with support for all annotated introns
structural maintenance of chromosomes protein 5, transcript variant X5
structural maintenance of chromosomes protein 5, transcript variant X1
structural maintenance of chromosomes protein 5, transcript variant X2
structural maintenance of chromosomes protein 5, transcript variant X4
structural maintenance of chromosomes protein 5
uncharacterized LOC122574234, transcript variant X2
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 5 samples with support for all annotated introns
uncharacterized LOC122574234, transcript variant X1
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
uncharacterized protein LOC122574234 isoform X1
uncharacterized protein LOC122574234 isoform X2
uncharacterized LOC122574235, transcript variant X2
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 1 sample with support for all annotated introns
uncharacterized LOC122574235, transcript variant X1
uncharacterized LOC122574235, transcript variant X4
uncharacterized LOC122574235, transcript variant X3
uncharacterized protein LOC122574235 isoform X1
uncharacterized protein LOC122574235 isoform X3
uncharacterized protein LOC122574235 isoform X2
uncharacterized LOC122574239, transcript variant X2
uncharacterized LOC122574239, transcript variant X1
uncharacterized protein LOC122574239 isoform X1
uncharacterized protein LOC122574239 isoform X2
uncharacterized LOC122574108, transcript variant X2
uncharacterized LOC122574108, transcript variant X1
uncharacterized protein LOC122574108 isoform X2
uncharacterized protein LOC122574108 isoform X1
uncharacterized LOC122574389, transcript variant X2
uncharacterized LOC122574389, transcript variant X1
uncharacterized protein LOC122574389 isoform X1
uncharacterized LOC122574391, transcript variant X1
uncharacterized LOC122574391, transcript variant X2
uncharacterized LOC122574389, transcript variant X3
uncharacterized protein LOC122574389 isoform X2
uncharacterized LOC122574390, transcript variant X1
uncharacterized LOC122574390, transcript variant X8
uncharacterized LOC122574390, transcript variant X12
uncharacterized LOC122574390, transcript variant X10
uncharacterized LOC122574390, transcript variant X11
uncharacterized LOC122574390, transcript variant X5
uncharacterized LOC122574390, transcript variant X7
uncharacterized LOC122574390, transcript variant X6
uncharacterized LOC122574390, transcript variant X3
uncharacterized LOC122574390, transcript variant X2
uncharacterized LOC122574390, transcript variant X4
uncharacterized LOC122574390, transcript variant X9
uncharacterized protein LOC122574390 isoform X1
uncharacterized protein LOC122574390 isoform X2
uncharacterized protein LOC122574390 isoform X3
uncharacterized protein LOC122574390 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, 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 Protein, and 31% coverage of the annotated genomic feature by RNAseq alignments
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X1
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X2
EGF domain-specific O-linked N-acetylglucosamine transferase, transcript variant X3
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X1
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X2
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X3
ATPase WRNIP1-like, transcript variant X2
ATPase WRNIP1-like, transcript variant X1
ATPase WRNIP1-like, transcript variant X3
ATPase WRNIP1-like, transcript variant X4
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
uncharacterized LOC122574046, transcript variant X1
uncharacterized LOC122574046, transcript variant X2
uncharacterized protein LOC122574046 isoform X1
uncharacterized protein LOC122574046 isoform X2
39S ribosomal protein L10, mitochondrial, transcript variant X1
39S ribosomal protein L10, mitochondrial, transcript variant X2
39S ribosomal protein L10, mitochondrial isoform X1
39S ribosomal protein L10, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
UBX domain-containing protein 4, transcript variant X1
UBX domain-containing protein 4, transcript variant X2
UBX domain-containing protein 4 isoform X1
UBX domain-containing protein 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); 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: 13 Proteins, and 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC122574492, transcript variant X3
uncharacterized LOC122574492, transcript variant X2
uncharacterized LOC122574492, transcript variant X1
uncharacterized protein LOC122574492 isoform X2
uncharacterized protein LOC122574492 isoform X1
uncharacterized LOC122574155, transcript variant X1
uncharacterized LOC122574155, transcript variant X2
homeotic protein distal-less, transcript variant X4
homeotic protein distal-less, transcript variant X2
homeotic protein distal-less, transcript variant X1
homeotic protein distal-less, transcript variant X3
uncharacterized LOC122574403, transcript variant X2
uncharacterized LOC122574403, transcript variant X5
uncharacterized LOC122574403, transcript variant X3
uncharacterized LOC122574403, transcript variant X4
uncharacterized protein LOC122574403 isoform X2
homeotic protein distal-less, transcript variant X6
homeotic protein distal-less, transcript variant X5
homeotic protein distal-less, transcript variant X7
uncharacterized LOC122574403, transcript variant X1
uncharacterized protein LOC122574403 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
SIFamide-related peptide, transcript variant X3
SIFamide-related peptide, transcript variant X4
SIFamide-related peptide, transcript variant X1
SIFamide-related peptide, transcript variant X2
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 8 samples with support for all annotated introns
glutamate decarboxylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fas apoptotic inhibitory molecule 1, transcript variant X1
fas apoptotic inhibitory molecule 1, 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
fas apoptotic inhibitory molecule 1 isoform X2
fas apoptotic inhibitory molecule 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 65% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 113
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122574039, transcript variant X2
uncharacterized LOC122574039, transcript variant X1
uncharacterized LOC122574039, transcript variant X3
uncharacterized LOC122574039, transcript variant X4
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X7
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X6
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X4
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X5
voltage-dependent L-type calcium channel subunit beta-2 isoform X3
voltage-dependent L-type calcium channel subunit beta-2 isoform X1
voltage-dependent L-type calcium channel subunit beta-2 isoform X4
voltage-dependent L-type calcium channel subunit beta-2 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5 isoform X5
broad-complex core protein isoforms 1/2/3/4/5 isoform X3
putative sodium-dependent multivitamin transporter
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% 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: 46 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase B-like
piezo-type mechanosensitive ion channel component, transcript variant X1
piezo-type mechanosensitive ion channel component, transcript variant X5
piezo-type mechanosensitive ion channel component, transcript variant X11
piezo-type mechanosensitive ion channel component, transcript variant X4
piezo-type mechanosensitive ion channel component, transcript variant X2
piezo-type mechanosensitive ion channel component, transcript variant X3
piezo-type mechanosensitive ion channel component, transcript variant X6
piezo-type mechanosensitive ion channel component, transcript variant X8
piezo-type mechanosensitive ion channel component, transcript variant X7
piezo-type mechanosensitive ion channel component, transcript variant X9
piezo-type mechanosensitive ion channel component, transcript variant X10
piezo-type mechanosensitive ion channel component isoform X1
piezo-type mechanosensitive ion channel component isoform X5
piezo-type mechanosensitive ion channel component isoform X11
piezo-type mechanosensitive ion channel component isoform X4
piezo-type mechanosensitive ion channel component isoform X2
piezo-type mechanosensitive ion channel component isoform X3
piezo-type mechanosensitive ion channel component isoform X6
piezo-type mechanosensitive ion channel component isoform X8
piezo-type mechanosensitive ion channel component isoform X7
piezo-type mechanosensitive ion channel component isoform X9
piezo-type mechanosensitive ion channel component isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fez family zinc finger protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fez family zinc finger protein 2-like isoform X1
fez family zinc finger protein 2-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
fez family zinc finger protein 2-like isoform X2
uncharacterized LOC122574151, 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 8 samples with support for all annotated introns
uncharacterized LOC122574151, 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 6 samples with support for all annotated introns
uncharacterized LOC122574151, transcript variant X3
uncharacterized protein LOC122574151 isoform X1
uncharacterized protein LOC122574151 isoform X2
uncharacterized LOC122574425, transcript variant X4
uncharacterized LOC122574425, transcript variant X1
uncharacterized LOC122574425, transcript variant X2
uncharacterized LOC122574425, transcript variant X3
uncharacterized protein LOC122574425 isoform X1
uncharacterized protein LOC122574425 isoform X2
uncharacterized protein LOC122574425 isoform X3
uncharacterized protein LOC122574425 isoform X4
carcinine transporter, transcript variant X1
carcinine transporter, transcript variant X2
importin subunit beta-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
importin subunit beta-1, transcript variant X2
importin subunit beta-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
probable nuclear hormone receptor HR38, transcript variant X5
probable nuclear hormone receptor HR38, transcript variant X6
probable nuclear hormone receptor HR38, transcript variant X8
probable nuclear hormone receptor HR38, transcript variant X2
probable nuclear hormone receptor HR38, transcript variant X1
probable nuclear hormone receptor HR38, transcript variant X7
probable nuclear hormone receptor HR38, transcript variant X4
probable nuclear hormone receptor HR38, transcript variant X3
nuclear receptor subfamily 4 group A member 2 isoform X5
probable nuclear hormone receptor HR38 isoform X6
probable nuclear hormone receptor HR38 isoform X8
nuclear receptor subfamily 4 group A member 2 isoform X2
nuclear receptor subfamily 4 group A member 2 isoform X1
nuclear receptor subfamily 4 group A member 2 isoform X4
probable nuclear hormone receptor HR38 isoform X3
probable nuclear hormone receptor HR38 isoform X7
ras-related protein Rab-6.2, transcript variant X2
ras-related protein Rab-6.2, transcript variant X1
cysteine desulfurase, mitochondrial, transcript variant X4
cysteine desulfurase, mitochondrial, transcript variant X3
cysteine desulfurase, mitochondrial, transcript variant X1
cysteine desulfurase, mitochondrial, transcript variant X2
cysteine desulfurase, mitochondrial isoform X2
cysteine desulfurase, mitochondrial isoform X1
transmembrane protein 45B-like, transcript variant X5
transmembrane protein 45B-like, transcript variant X3
transmembrane protein 45B-like, transcript variant X2
transmembrane protein 45B-like, transcript variant X4
transmembrane protein 45B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dual serine/threonine and tyrosine protein kinase, transcript variant X5
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 6 samples with support for all annotated introns
dual serine/threonine and tyrosine protein kinase, transcript variant X3
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 5 samples with support for all annotated introns
dual serine/threonine and tyrosine protein kinase isoform X2
dual serine/threonine and tyrosine protein kinase, transcript variant X4
dual serine/threonine and tyrosine protein kinase, transcript variant X1
dual serine/threonine and tyrosine protein kinase, transcript variant X2
dual serine/threonine and tyrosine protein kinase isoform X1
forkhead box protein P1-like, transcript variant X17
forkhead box protein P1-like, transcript variant X23
forkhead box protein P1-like, transcript variant X4
forkhead box protein P1-like, transcript variant X5
forkhead box protein P1-like, transcript variant X29
forkhead box protein P1-like, transcript variant X15
forkhead box protein P1-like, transcript variant X1
forkhead box protein P1-like, transcript variant X2
forkhead box protein P1-like, transcript variant X10
forkhead box protein P1-like, transcript variant X3
forkhead box protein P1-like, transcript variant X7
forkhead box protein P1-like, transcript variant X9
forkhead box protein P1-like, transcript variant X6
forkhead box protein P1-like, transcript variant X8
forkhead box protein P1-like, transcript variant X11
forkhead box protein P1-like isoform X10
forkhead box protein P2-like isoform X11
forkhead box protein P1-like, transcript variant X18
forkhead box protein P1-like, transcript variant X20
forkhead box protein P1-like, transcript variant X22
forkhead box protein P1-like, transcript variant X14
forkhead box protein P1-like, transcript variant X12
forkhead box protein P1-like, transcript variant X16
forkhead box protein P1-like, transcript variant X19
forkhead box protein P1-like, transcript variant X13
forkhead box protein P1-like, transcript variant X21
forkhead box protein P1-like, transcript variant X24
forkhead box protein P1-like isoform X12
forkhead box protein P1-like, transcript variant X30
forkhead box protein P1-like, transcript variant X26
forkhead box protein P1-like, transcript variant X25
forkhead box protein P1-like isoform X13
forkhead box protein P1-like, transcript variant X28
forkhead box protein P1-like isoform X15
forkhead box protein P1-like, transcript variant X27
forkhead box protein P1-like isoform X14
forkhead box protein P1-like isoform X16
protein tyrosine phosphatase domain-containing protein 1-like
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 6 samples with support for all annotated introns
secretory carrier-associated membrane protein 5A, transcript variant X11
secretory carrier-associated membrane protein 5A, transcript variant X3
secretory carrier-associated membrane protein 5A, transcript variant X10
secretory carrier-associated membrane protein 5A, transcript variant X8
secretory carrier-associated membrane protein 5A, transcript variant X4
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 8 samples with support for all annotated introns
secretory carrier-associated membrane protein 5A, transcript variant X1
secretory carrier-associated membrane protein 5A, transcript variant X7
secretory carrier-associated membrane protein 5A, transcript variant X2
secretory carrier-associated membrane protein 5A, transcript variant X9
secretory carrier-associated membrane protein 5A, transcript variant X6
secretory carrier-associated membrane protein 5A, transcript variant X5
secretory carrier-associated membrane protein 5A
uncharacterized LOC122574255, transcript variant X1
uncharacterized LOC122574255, transcript variant X2
uncharacterized LOC122574255, transcript variant X3
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC122574255 isoform X1
uncharacterized protein LOC122574255 isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X3
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X8
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X9
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X11
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X1
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X12
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X10
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X13
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X2
zwei Ig domain protein zig-8-like isoform X3
zwei Ig domain protein zig-8-like isoform X5
zwei Ig domain protein zig-8-like isoform X4
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X1
uncharacterized LOC122574257, transcript variant X3
uncharacterized LOC122574257, transcript variant X2
uncharacterized LOC122574257, transcript variant X1
uncharacterized LOC122574254, transcript variant X1
uncharacterized LOC122574254, transcript variant X2
uncharacterized LOC122574254, transcript variant X3
ankyrin repeat and death domain-containing protein 1A-like, transcript variant 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 8 samples with support for all annotated introns
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X3
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X4
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X2
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 4 samples with support for all annotated introns
ankyrin repeat and death domain-containing protein 1A-like isoform X1
ankyrin repeat and death domain-containing protein 1A-like isoform X2
ankyrin repeat and death domain-containing protein 1A-like isoform X3
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein 27C-like isoform X4
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein 27C-like isoform X5
heterogeneous nuclear ribonucleoprotein 27C-like isoform X1
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein 27C-like isoform X2
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein 27C-like isoform X3
chondroitin sulfate synthase 1, transcript variant X7
chondroitin sulfate synthase 1, transcript variant X2
chondroitin sulfate synthase 1, transcript variant X4
chondroitin sulfate synthase 1, transcript variant X1
chondroitin sulfate synthase 1, transcript variant X5
chondroitin sulfate synthase 1, transcript variant X3
chondroitin sulfate synthase 1, transcript variant X8
chondroitin sulfate synthase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
immediate early response 3-interacting protein 1, transcript variant X3
immediate early response 3-interacting protein 1, transcript variant X1
immediate early response 3-interacting protein 1, transcript variant X2
immediate early response 3-interacting protein 1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X2
neuropeptide CCHamide-2 receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuropeptide CCHamide-2 receptor-like, transcript variant X2
neuropeptide CCHamide-2 receptor-like, transcript variant X4
neuropeptide CCHamide-2 receptor-like, transcript variant X1
neuropeptide CCHamide-2 receptor-like, transcript variant X5
neuropeptide CCHamide-2 receptor-like, transcript variant X6
neuropeptide CCHamide-2 receptor-like isoform X1
neuropeptide CCHamide-2 receptor-like isoform X2
neuropeptide CCHamide-1 receptor-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuropeptide CCHamide-1 receptor-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuropeptide CCHamide-1 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neuropeptide CCHamide-1 receptor-like, transcript variant X6
neuropeptide CCHamide-1 receptor-like, transcript variant X2
neuropeptide CCHamide-1 receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuropeptide CCHamide-1 receptor-like, transcript variant X7
neprilysin-1-like, transcript variant X2
neprilysin-1-like, transcript variant X3
neprilysin-1-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 1 sample with support for all annotated introns
5-hydroxytryptamine receptor-like, transcript variant X12
5-hydroxytryptamine receptor-like, transcript variant X5
5-hydroxytryptamine receptor-like, transcript variant X6
5-hydroxytryptamine receptor-like, transcript variant X4
5-hydroxytryptamine receptor-like, transcript variant X2
5-hydroxytryptamine receptor-like, transcript variant X3
5-hydroxytryptamine receptor-like, transcript variant X1
5-hydroxytryptamine receptor-like, transcript variant X10
5-hydroxytryptamine receptor-like, transcript variant X7
5-hydroxytryptamine receptor-like, transcript variant X9
5-hydroxytryptamine receptor-like, transcript variant X13
5-hydroxytryptamine receptor-like, transcript variant X11
5-hydroxytryptamine receptor-like, transcript variant X8
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122574142, transcript variant X2
uncharacterized LOC122574142, transcript variant X1
RING finger protein nhl-1, transcript variant X5
RING finger protein nhl-1, transcript variant X3
RING finger protein nhl-1, transcript variant X1
RING finger protein nhl-1, transcript variant X8
RING finger protein nhl-1, transcript variant X6
RING finger protein nhl-1, transcript variant X7
RING finger protein nhl-1, transcript variant X2
RING finger protein nhl-1, transcript variant X4
serine-rich adhesin for platelets isoform X1
serine-rich adhesin for platelets isoform X2
calmodulin-binding transcription activator 2-like, transcript variant X6
calmodulin-binding transcription activator 2-like, transcript variant X3
calmodulin-binding transcription activator 2-like, transcript variant X1
calmodulin-binding transcription activator 2-like, transcript variant X4
calmodulin-binding transcription activator 2-like, transcript variant X2
calmodulin-binding transcription activator 2-like, transcript variant X7
calmodulin-binding transcription activator 2-like isoform X5
calmodulin-binding transcription activator 2-like isoform X2
calmodulin-binding transcription activator 2-like isoform X1
calmodulin-binding transcription activator 2-like isoform X6
calmodulin-binding transcription activator 2-like isoform X3
calmodulin-binding transcription activator 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calmodulin-binding transcription activator 2-like isoform X4
AP-2 complex subunit mu, transcript variant X1
AP-2 complex subunit mu, transcript variant X2
CTD nuclear envelope phosphatase 1 homolog, transcript variant X2
CTD nuclear envelope phosphatase 1 homolog, transcript variant X1
CTD nuclear envelope phosphatase 1 homolog, transcript variant X3
CTD nuclear envelope phosphatase 1 homolog isoform X2
CTD nuclear envelope phosphatase 1 homolog, transcript variant X4
CTD nuclear envelope phosphatase 1 homolog isoform X3
CTD nuclear envelope phosphatase 1 homolog isoform X1
BMP and activin membrane-bound inhibitor homolog
uncharacterized LOC122574458, transcript variant X3
uncharacterized protein LOC122574458 isoform X2
uncharacterized LOC122574458, transcript variant X2
uncharacterized LOC122574458, transcript variant X1
uncharacterized protein LOC122574458 isoform X1
biogenesis of lysosome-related organelles complex 1 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 89% 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 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor Or1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
odorant receptor Or1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
odorant receptor Or1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
odorant receptor Or1-like, transcript variant X1
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
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
odorant receptor 2a-like, transcript variant 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 1 sample with support for all annotated introns
odorant receptor 2a-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 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: 19 Proteins, and 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: 54 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16, transcript variant X2
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16, transcript variant X1
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 isoform X2
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 isoform X1
F-box/LRR-repeat protein 2, transcript variant X2
F-box/LRR-repeat protein 2, transcript variant X1
F-box/LRR-repeat protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
chitin-binding domain protein cbd-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
serine protease filzig, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine protease filzig, transcript variant X3
serine protease filzig, transcript variant X1
T-complex protein 1 subunit epsilon, transcript variant X2
T-complex protein 1 subunit epsilon, transcript variant X1
unconventional myosin-Va, transcript variant X2
unconventional myosin-Va, transcript variant X3
unconventional myosin-Va, transcript variant X1
unconventional myosin-Va, transcript variant X6
unconventional myosin-Va, transcript variant X4
unconventional myosin-Va, transcript variant X5
calponin homology domain-containing protein DDB_G0272472-like
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
succinate dehydrogenase assembly factor 3, mitochondrial
nucleoside diphosphate-linked moiety X motif 19-like, transcript variant X1
nucleoside diphosphate-linked moiety X motif 19-like, transcript variant X2
nucleoside diphosphate-linked moiety X motif 19-like isoform X1
nucleoside diphosphate-linked moiety X motif 19-like isoform X2
L-threonine 3-dehydrogenase, mitochondrial, transcript variant X2
L-threonine 3-dehydrogenase, mitochondrial, transcript variant X1
L-threonine 3-dehydrogenase, mitochondrial isoform X2
L-threonine 3-dehydrogenase, mitochondrial isoform X1
protein artichoke, transcript variant X5
protein artichoke, transcript variant X4
protein artichoke, transcript variant X3
protein artichoke, transcript variant X2
protein artichoke, transcript variant X1
26S proteasome non-ATPase regulatory subunit 7
inosine triphosphate pyrophosphatase, transcript variant X1
inosine triphosphate pyrophosphatase, transcript variant X2
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor Sox-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 144 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transcription factor Sox-2-like, transcript variant X4
transcription factor Sox-2-like isoform X1
transcription factor Sox-2-like, transcript variant X1
transcription factor Sox-2-like, transcript variant X5
transcription factor Sox-2-like, transcript variant X3
transcription factor Sox-2-like isoform X2
transcription factor Sox-2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription factor Sox-2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription factor Sox-2-like isoform X3
uncharacterized LOC122574345, transcript variant X2
uncharacterized LOC122574345, 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 3 samples with support for all annotated introns
uncharacterized protein LOC122574345 isoform X2
uncharacterized protein LOC122574345 isoform X1
uncharacterized LOC122574103, transcript variant X3
uncharacterized LOC122574103, transcript variant X2
uncharacterized LOC122574103, transcript variant X1
uncharacterized protein LOC122574103 isoform X1
uncharacterized protein LOC122574103 isoform X2
serine/arginine repetitive matrix protein 2, transcript variant X2
serine/arginine repetitive matrix protein 2, transcript variant X1
serine/arginine repetitive matrix protein 2, transcript variant X3
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 isoform X3
mannose-P-dolichol utilization defect 1 protein homolog
tubulin glycylase 3A-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 4 samples with support for all annotated introns
tubulin glycylase 3A-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 3 samples with support for all annotated introns
tubulin glycylase 3A-like, transcript variant X3
tubulin glycylase 3A-like, transcript variant X4
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 4 samples with support for all annotated introns
UPF0430 protein CG31712-like, transcript variant X3
UPF0430 protein CG31712-like, transcript variant X4
UPF0430 protein CG31712-like, transcript variant X1
UPF0430 protein CG31712-like, transcript variant X2
serine/threonine-protein kinase 25, transcript variant X3
serine/threonine-protein kinase 25, transcript variant X5
serine/threonine-protein kinase 25 isoform X3
serine/threonine-protein kinase 25, transcript variant X4
serine/threonine-protein kinase 25 isoform X2
serine/threonine-protein kinase 25, transcript variant X1
serine/threonine-protein kinase 25, transcript variant X2
serine/threonine-protein kinase 25 isoform X1
uncharacterized LOC122574197, transcript variant X2
uncharacterized LOC122574197, transcript variant X5
uncharacterized LOC122574197, transcript variant X1
uncharacterized LOC122574197, transcript variant X3
uncharacterized LOC122574197, transcript variant X4
uncharacterized LOC122574197, transcript variant X6
prolyl 3-hydroxylase OGFOD1, transcript variant X2
prolyl 3-hydroxylase OGFOD1, transcript variant X1
uncharacterized LOC122574208, transcript variant X1
uncharacterized LOC122574208, transcript variant X2
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X4
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X3
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X6
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X1
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X8
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X7
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X5
LHFPL tetraspan subfamily member 2a protein-like, transcript variant X2
LHFPL tetraspan subfamily member 2a protein-like
putative gamma-glutamylcyclotransferase CG2811, transcript variant X1
putative gamma-glutamylcyclotransferase CG2811, transcript variant X2
putative gamma-glutamylcyclotransferase CG2811 isoform X2
putative gamma-glutamylcyclotransferase CG2811 isoform X1
putative gamma-glutamylcyclotransferase CG2811, transcript variant X3
putative gamma-glutamylcyclotransferase CG2811 isoform X3
protein CDV3 homolog, transcript variant X2
protein CDV3 homolog, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X2
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X2
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X1
uncharacterized protein LOC122574114 isoform X3
translation machinery-associated protein 7 homolog
dihydrofolate reductase, transcript variant X2
dihydrofolate reductase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
histidine triad nucleotide-binding protein 1
cyclin-dependent kinase 4-like, transcript variant X10
cyclin-dependent kinase 4-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cyclin-dependent kinase 4-like, transcript variant X13
cyclin-dependent kinase 4-like, transcript variant X6
cyclin-dependent kinase 4-like, transcript variant X2
cyclin-dependent kinase 4-like, transcript variant X3
cyclin-dependent kinase 4-like, transcript variant X1
cyclin-dependent kinase 4-like, transcript variant X7
cyclin-dependent kinase 4-like, transcript variant X14
cyclin-dependent kinase 4-like, transcript variant X12
cyclin-dependent kinase 4-like, transcript variant X5
cyclin-dependent kinase 4-like, transcript variant X11
cyclin-dependent kinase 4-like, transcript variant X9
cyclin-dependent kinase 4-like, transcript variant X4
uncharacterized LOC122574115, transcript variant X3
uncharacterized protein LOC122574115 isoform X3
uncharacterized LOC122574115, transcript variant X1
uncharacterized LOC122574115, transcript variant X2
uncharacterized protein LOC122574115 isoform X2
uncharacterized protein LOC122574115 isoform X1
protein N-terminal glutamine amidohydrolase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
isochorismatase domain-containing protein 2-like
uncharacterized LOC122574123, transcript variant X1
uncharacterized protein LOC122574123 isoform X1
uncharacterized LOC122574123, transcript variant X2
uncharacterized protein LOC122574123 isoform X2
transcription factor CP2-like protein 1, transcript variant X3
transcription factor CP2-like protein 1, transcript variant X4
transcription factor CP2-like protein 1, transcript variant X2
transcription factor CP2-like protein 1, transcript variant X1
transcription factor CP2-like protein 1 isoform X3
transcription factor CP2-like protein 1 isoform X4
transcription factor CP2-like protein 1 isoform X2
transcription factor CP2-like protein 1 isoform X1
probable inactive tRNA-specific adenosine deaminase-like protein 3, transcript variant X2
probable inactive tRNA-specific adenosine deaminase-like protein 3, transcript variant X1
probable inactive tRNA-specific adenosine deaminase-like protein 3
receptor-type tyrosine-protein phosphatase mu-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase mu-like, transcript variant X2
receptor-type tyrosine-protein phosphatase mu-like isoform X2
receptor-type tyrosine-protein phosphatase mu-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: chromatin-remodeling ATPase INO80-like
putative WEB family protein At1g65010, chloroplastic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122574312, transcript variant X2
uncharacterized LOC122574312, transcript variant X5
uncharacterized LOC122574312, transcript variant X6
uncharacterized LOC122574312, transcript variant X13
uncharacterized LOC122574312, transcript variant X3
uncharacterized LOC122574312, transcript variant X4
uncharacterized LOC122574312, transcript variant X1
uncharacterized LOC122574312, transcript variant X11
uncharacterized LOC122574312, transcript variant X9
uncharacterized LOC122574312, transcript variant X10
uncharacterized LOC122574312, transcript variant X7
uncharacterized LOC122574312, transcript variant X8
uncharacterized LOC122574312, transcript variant X12
cyclic AMP-dependent transcription factor ATF-2, transcript variant X3
cyclic AMP-dependent transcription factor ATF-2, transcript variant X2
cyclic AMP-dependent transcription factor ATF-2, transcript variant X1
cyclic AMP-dependent transcription factor ATF-2 isoform X2
cyclic AMP-dependent transcription factor ATF-2 isoform X1
39S ribosomal protein L16, mitochondrial, transcript variant X2
39S ribosomal protein L16, mitochondrial, transcript variant X1
39S ribosomal protein L16, mitochondrial
transmembrane protein 132C, transcript variant X1
transmembrane protein 132C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related protein M-Ras-like, transcript variant X2
ras-related protein M-Ras-like, transcript variant X1
116 kDa U5 small nuclear ribonucleoprotein component
polycomb group protein Psc-like, transcript variant X1
polycomb group protein Psc-like, transcript variant X2
serine-rich adhesin for platelets-like, transcript variant X1
serine-rich adhesin for platelets-like, transcript variant X2
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 5 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X3
leucine-rich repeat-containing protein 51-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Hermansky-Pudlak syndrome 3 protein homolog, transcript variant X1
Hermansky-Pudlak syndrome 3 protein homolog, transcript variant X2
uncharacterized protein LOC122574210 isoform X1
Hermansky-Pudlak syndrome 3 protein homolog isoform X2
peroxisomal targeting signal 1 receptor, transcript variant X3
peroxisomal targeting signal 1 receptor, transcript variant X2
peroxisomal targeting signal 1 receptor, transcript variant X1
peroxisomal targeting signal 1 receptor isoform X1
peroxisomal targeting signal 1 receptor, transcript variant X4
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 8 samples with support for all annotated introns
peroxisomal targeting signal 1 receptor isoform X2
G patch domain-containing protein 4, transcript variant X2
G patch domain-containing protein 4, transcript variant X1
G patch domain-containing protein 4 isoform X2
G patch domain-containing protein 4 isoform X1
beta-1,3-galactosyltransferase 1-like, transcript variant X2
beta-1,3-galactosyltransferase 1-like, transcript variant X4
beta-1,3-galactosyltransferase 1-like, transcript variant X1
beta-1,3-galactosyltransferase 1-like, transcript variant X3
beta-1,3-galactosyltransferase 1-like isoform X3
beta-1,3-galactosyltransferase 1-like isoform X1
beta-1,3-galactosyltransferase 1-like isoform X2
GATA zinc finger domain-containing protein 1
uncharacterized LOC122574211, transcript variant X1
uncharacterized LOC122574211, transcript variant X8
uncharacterized LOC122574211, transcript variant X2
uncharacterized LOC122574211, transcript variant X3
uncharacterized LOC122574211, 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 4 samples with support for all annotated introns
uncharacterized LOC122574211, transcript variant X4
uncharacterized LOC122574211, transcript variant X7
uncharacterized LOC122574211, transcript variant X10
uncharacterized LOC122574211, transcript variant X11
uncharacterized LOC122574211, transcript variant X12
uncharacterized LOC122574211, transcript variant X5
uncharacterized LOC122574211, transcript variant X9
uncharacterized LOC122574211, transcript variant X14
uncharacterized LOC122574211, transcript variant X13
uncharacterized LOC122574211, transcript variant X15
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 7 samples with support for all annotated introns
uncharacterized protein LOC122574211 isoform X2
uncharacterized protein LOC122574211 isoform X1
uncharacterized protein LOC122574211 isoform X3
uncharacterized protein LOC122574211 isoform X4
uncharacterized LOC122574220, transcript variant X2
uncharacterized LOC122574220, transcript variant X3
uncharacterized LOC122574220, transcript variant X1
broad-complex core protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
broad-complex core protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
broad-complex core protein-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
broad-complex core protein-like, transcript variant X8
broad-complex core protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
broad-complex core protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
broad-complex core protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
broad-complex core protein-like, transcript variant X2
broad-complex core protein isoforms 1/2/3/4/5-like isoform X3
broad-complex core protein-like isoform X4
broad-complex core protein isoforms 1/2/3/4/5-like isoform X1
broad-complex core protein isoforms 1/2/3/4/5-like isoform X2
broad-complex core protein isoforms 1/2/3/4/5-like
neo-calmodulin-like, transcript variant X3
neo-calmodulin-like, transcript variant X4
neo-calmodulin-like, transcript variant X1
neo-calmodulin-like, transcript variant X5
neo-calmodulin-like, transcript variant X2
neo-calmodulin-like, transcript variant X6
endoplasmic reticulum resident protein 44, transcript variant X1
endoplasmic reticulum resident protein 44, transcript variant X2
endoplasmic reticulum resident protein 44 isoform X2
endoplasmic reticulum resident protein 44 isoform X1
transcription factor Sp3-like, transcript variant X2
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 1 sample with support for all annotated introns
transcription factor Sp3-like isoform X2
transcription factor Sp3-like, transcript variant X4
transcription factor Sp3-like, transcript variant X1
transcription factor Sp3-like, transcript variant X3
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 2 samples with support for all annotated introns
transcription factor Sp3-like isoform X1
transcription factor Sp3-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
obg-like ATPase 1, transcript variant X3
obg-like ATPase 1, transcript variant X4
obg-like ATPase 1, transcript variant X1
obg-like ATPase 1, transcript variant X2
uronyl 2-sulfotransferase-like, transcript variant X3
uronyl 2-sulfotransferase-like isoform X2
obg-like ATPase 1, transcript variant X5
uronyl 2-sulfotransferase-like, transcript variant X1
uronyl 2-sulfotransferase-like, transcript variant X2
uronyl 2-sulfotransferase-like isoform X1
potassium voltage-gated channel subfamily H member 8, transcript variant X1
potassium voltage-gated channel subfamily H member 8, transcript variant X2
potassium voltage-gated channel subfamily H member 8, transcript variant X3
potassium voltage-gated channel subfamily H member 8 isoform X1
potassium voltage-gated channel subfamily H member 8 isoform X2
potassium voltage-gated channel subfamily H member 8 isoform X3
mitochondrial 2-oxoglutarate/malate carrier protein-like
cytochrome b5 domain-containing protein 1
probable malate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 34% 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 97% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase 17B-like, transcript variant X1
serine/threonine-protein kinase 17B-like isoform X1
serine/threonine-protein kinase 17B-like, transcript variant X2
serine/threonine-protein kinase 17A-like isoform X2
probable serine/threonine-protein kinase MARK-A
ATP-dependent RNA helicase DDX42, transcript variant X1
ATP-dependent RNA helicase DDX42, transcript variant X2
cationic amino acid transporter 4, transcript variant X1
cationic amino acid transporter 4, transcript variant X3
cationic amino acid transporter 4, transcript variant X5
cationic amino acid transporter 4, transcript variant X2
cationic amino acid transporter 4, transcript variant X4
cationic amino acid transporter 4, transcript variant X7
cationic amino acid transporter 4, transcript variant X8
cationic amino acid transporter 4, transcript variant X6
host cell factor 2-like, transcript variant X4
uncharacterized LOC122574280, transcript variant X1
uncharacterized LOC122574280, transcript variant X3
uncharacterized LOC122574280, transcript variant X2
uncharacterized protein LOC122574280 isoform X2
uncharacterized protein LOC122574280 isoform X1
host cell factor 2-like, transcript variant X1
host cell factor 2-like, transcript variant X5
host cell factor 2-like, transcript variant X2
host cell factor 2-like, transcript variant X3
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X5
CKLF-like MARVEL transmembrane domain-containing protein 4 isoform X2
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X3
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X4
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X1
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 3 samples with support for all annotated introns
dynein axonemal intermediate chain 3-like isoform X1
uncharacterized LOC122574078, transcript variant X1
uncharacterized LOC122574078, transcript variant X3
uncharacterized LOC122574078, transcript variant X2
uncharacterized LOC122574077, transcript variant X2
uncharacterized LOC122574077, transcript variant X1
uncharacterized LOC122574077, transcript variant X3
uncharacterized LOC122574077, transcript variant X4
pyridoxine/pyridoxamine 5'-phosphate oxidase
atrial natriuretic peptide-converting enzyme, transcript variant X1
atrial natriuretic peptide-converting enzyme, transcript variant X3
atrial natriuretic peptide-converting enzyme, transcript variant X4
atrial natriuretic peptide-converting enzyme, transcript variant X2
atrial natriuretic peptide-converting enzyme isoform X1
atrial natriuretic peptide-converting enzyme isoform X3
atrial natriuretic peptide-converting enzyme isoform X2
armadillo segment polarity protein, transcript variant X1
armadillo segment polarity protein, transcript variant X2
armadillo segment polarity protein isoform X1
armadillo segment polarity protein, transcript variant X4
armadillo segment polarity protein, transcript variant X3
armadillo segment polarity protein isoform X2
zinc finger protein 600, transcript variant X3
zinc finger protein 600, 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 2 samples with support for all annotated introns
zinc finger protein 600, 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 5 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGGP01033967.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 354 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 354 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like, transcript variant X1
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like, transcript variant X2
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 306a1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome P450 306a1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytochrome P450 306a1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 18a1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 18a1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
LOW QUALITY PROTEIN: uncharacterized protein LOC122574502
glycolipid transfer protein, transcript variant X1
glycolipid transfer protein, transcript variant X2
transmembrane protein 17-like, transcript variant X2
transmembrane protein 17-like isoform X2
transmembrane protein 17-like, transcript variant X1
transmembrane protein 17-like isoform X1
26S proteasome non-ATPase regulatory subunit 11
serine proteinase stubble-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X8
serine proteinase stubble-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine proteinase stubble-like, transcript variant X3
serine proteinase stubble-like, transcript variant X6
serine proteinase stubble-like, transcript variant X7
serine proteinase stubble-like, transcript variant X10
serine proteinase stubble-like, transcript variant X5
uncharacterized protein LOC122574500 isoform X3
transmembrane protease serine 13-like isoform X6
uncharacterized protein LOC122574500 isoform X4
serine proteinase stubble-like isoform X9
serine proteinase stubble-like isoform X13
transmembrane protease serine 13-like isoform X5
serine proteinase stubble-like isoform X11
serine proteinase stubble-like, transcript variant X12
serine proteinase stubble-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X17
serine proteinase stubble-like, transcript variant X13
transmembrane protease serine 13-like isoform X7
serine proteinase stubble-like isoform X12
uncharacterized protein LOC122574500 isoform X1
uncharacterized protein LOC122574500 isoform X2
serine proteinase stubble-like isoform X8
serine proteinase stubble-like, transcript variant X15
serine proteinase stubble-like isoform X10
myosin-2 essential light chain, transcript variant X2
myosin-2 essential light chain, transcript variant X1
myosin-2 essential light chain isoform X2
myosin-2 essential light chain isoform X1
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X1
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X3
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X2
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X4
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X5
WD repeat, SAM and U-box domain-containing protein 1-like isoform X1
WD repeat, SAM and U-box domain-containing protein 1-like isoform X2
protein regulator of cytokinesis 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein regulator of cytokinesis 1-like, transcript variant X2
protein regulator of cytokinesis 1-like isoform X1
protein regulator of cytokinesis 1-like isoform X2
sphingomyelin phosphodiesterase, transcript variant X2
sphingomyelin phosphodiesterase, transcript variant X1
sphingomyelin phosphodiesterase, transcript variant X5
sphingomyelin phosphodiesterase, transcript variant X8
sphingomyelin phosphodiesterase, transcript variant X7
sphingomyelin phosphodiesterase, transcript variant X9
sphingomyelin phosphodiesterase, transcript variant X4
sphingomyelin phosphodiesterase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sphingomyelin phosphodiesterase, transcript variant X3
sphingomyelin phosphodiesterase, transcript variant X10
sphingomyelin phosphodiesterase isoform X2
sphingomyelin phosphodiesterase isoform X5
sphingomyelin phosphodiesterase isoform X4
sphingomyelin phosphodiesterase isoform X6
sphingomyelin phosphodiesterase isoform X1
sphingomyelin phosphodiesterase isoform X3
multiple coagulation factor deficiency protein 2 homolog, transcript variant X6
multiple coagulation factor deficiency protein 2 homolog, transcript variant X2
multiple coagulation factor deficiency protein 2 homolog, transcript variant X1
multiple coagulation factor deficiency protein 2 homolog, transcript variant X3
multiple coagulation factor deficiency protein 2 homolog, transcript variant X4
multiple coagulation factor deficiency protein 2 homolog, transcript variant X5
multiple coagulation factor deficiency protein 2 homolog, transcript variant X7
multiple coagulation factor deficiency protein 2 homolog, transcript variant X8
multiple coagulation factor deficiency protein 2 homolog
protein argonaute-2, transcript variant X1
protein argonaute-2, transcript variant X2
39S ribosomal protein L53, mitochondrial
proteasomal ubiquitin receptor ADRM1-A, transcript variant X2
proteasomal ubiquitin receptor ADRM1-A, transcript variant X1
proteasomal ubiquitin receptor ADRM1 homolog isoform X2
proteasomal ubiquitin receptor ADRM1-A isoform X1
arrestin domain-containing protein 17-like, transcript variant X3
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 3 samples with support for all annotated introns
arrestin domain-containing protein 17-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 6 samples with support for all annotated introns
arrestin domain-containing protein 17-like, transcript variant X2
arrestin domain-containing protein 17-like, transcript variant X4
arrestin domain-containing protein 17-like isoform X1
arrestin domain-containing protein 17-like isoform X2
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X7
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X8
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X3
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X6
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X5
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X4
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X2
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X3
trichohyalin-like, transcript variant X3
trichohyalin-like, transcript variant X1
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X5
golgin subfamily A member 6-like protein 22 isoform X1
trichohyalin-like, transcript variant X4
uncharacterized LOC122574083, transcript variant X1
uncharacterized LOC122574083, transcript variant X2
uncharacterized LOC122574083, transcript variant X3
uncharacterized LOC122574083, transcript variant X4
uncharacterized protein LOC122574083 isoform X2
uncharacterized protein LOC122574083 isoform X1
uncharacterized protein LOC122574083 isoform X4
uncharacterized protein LOC122574083 isoform X3
uncharacterized LOC122574332, transcript variant X2
uncharacterized LOC122574332, transcript variant X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X3
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X3
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X6
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X5
PAN2-PAN3 deadenylation complex catalytic subunit PAN2, transcript variant X4
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X4
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X5
integrin alpha-PS2, transcript variant X2
integrin alpha-PS2, transcript variant X1
integrin alpha-PS2, transcript variant X3
uncharacterized LOC122574333, transcript variant X2
uncharacterized LOC122574333, transcript variant X1
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 8 samples with support for all annotated introns
pyruvate carboxylase, mitochondrial, transcript variant X1
pyruvate carboxylase, mitochondrial, transcript variant X2
pyruvate carboxylase, mitochondrial isoform X1
pyruvate carboxylase, mitochondrial isoform X2
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X4
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X2
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X3
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X5
bumetanide-sensitive sodium-(potassium)-chloride cotransporter
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X3
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X6
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X5
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X4
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X7
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X2
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X3
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X2
probable cytochrome P450 6a14, transcript variant X1
probable cytochrome P450 6a14, transcript variant X3
probable cytochrome P450 6a14, transcript variant X2
cytochrome P450 6a2-like, transcript variant X5
cytochrome P450 6a2-like, transcript variant X3
cytochrome P450 6a2-like, transcript variant X2
cytochrome P450 6a2-like, transcript variant X1
cytochrome P450 6a2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 152 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
PAT complex subunit CCDC47-like, transcript variant X5
kinesin-like protein KIF3B, transcript variant X1
PAT complex subunit CCDC47-like, transcript variant X4
PAT complex subunit CCDC47-like isoform X3
PAT complex subunit CCDC47-like, transcript variant X7
PAT complex subunit CCDC47-like, transcript variant X8
PAT complex subunit CCDC47-like, transcript variant X6
PAT complex subunit CCDC47-like, transcript variant X3
PAT complex subunit CCDC47-like isoform X2
PAT complex subunit CCDC47-like isoform X4
kinesin-like protein KIF3B, transcript variant X2
PAT complex subunit CCDC47-like, transcript variant X1
PAT complex subunit CCDC47-like, transcript variant X2
uncharacterized protein CG7065-like isoform 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
potassium voltage-gated channel protein Shaw, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel protein Shaw, transcript variant X3
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 1 sample with support for all annotated introns
potassium voltage-gated channel protein Shaw, transcript variant X2
potassium voltage-gated channel protein Shaw isoform X3
potassium voltage-gated channel protein Shaw isoform X1
potassium voltage-gated channel protein Shaw isoform X2
potassium voltage-gated channel protein Shaw-like, transcript variant X4
potassium voltage-gated channel protein Shaw-like, transcript variant X3
potassium voltage-gated channel protein Shaw-like, transcript variant X5
potassium voltage-gated channel protein Shaw-like, transcript variant X1
potassium voltage-gated channel protein Shaw-like, transcript variant X2
potassium voltage-gated channel protein Shaw-like isoform X1
potassium voltage-gated channel protein Shaw-like isoform X2
potassium voltage-gated channel protein Shaw-like isoform X3
potassium voltage-gated channel protein Shaw-like, transcript variant X6
potassium voltage-gated channel protein Shaw-like isoform X4
uncharacterized LOC122574494, transcript variant X7
uncharacterized protein LOC122574494 isoform X7
uncharacterized LOC122574494, transcript variant X1
uncharacterized LOC122574494, transcript variant X3
uncharacterized LOC122574494, transcript variant X2
uncharacterized LOC122574494, transcript variant X4
uncharacterized LOC122574494, transcript variant X6
uncharacterized LOC122574494, transcript variant X5
uncharacterized protein LOC122574494 isoform X1
uncharacterized protein LOC122574494 isoform X4
uncharacterized protein LOC122574494 isoform X2
uncharacterized protein LOC122574494 isoform X5
uncharacterized protein LOC122574494 isoform X3
uncharacterized protein LOC122574494 isoform X6
protein drumstick, transcript variant X2
protein drumstick, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 94% 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin receptor substrate 1, transcript variant X4
insulin receptor substrate 1, transcript variant X1
insulin receptor substrate 1, transcript variant X3
insulin receptor substrate 1, transcript variant X2
piwi-like protein Ago3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
piwi-like protein Ago3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
piwi-like protein Ago3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
piwi-like protein Ago3, transcript variant X1
piwi-like protein Ago3, transcript variant X2
piwi-like protein Ago3, transcript variant X6
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X1
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X3
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X1
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X2
cGMP-dependent protein kinase, isozyme 2 forms cD5/T2 isoform X3
paired mesoderm homeobox protein 2B, transcript variant X1
paired mesoderm homeobox protein 2B, transcript variant X5
paired mesoderm homeobox protein 2B, transcript variant X3
paired mesoderm homeobox protein 2B, transcript variant X4
paired mesoderm homeobox protein 2B, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
microsomal triglyceride transfer protein large subunit, transcript variant X4
microsomal triglyceride transfer protein large subunit, transcript variant X2
microsomal triglyceride transfer protein large subunit, transcript variant X1
microsomal triglyceride transfer protein large subunit, transcript variant X3
microsomal triglyceride transfer protein large subunit, transcript variant X5
microsomal triglyceride transfer protein large subunit isoform X1
microsomal triglyceride transfer protein large subunit isoform X2
microsomal triglyceride transfer protein large subunit, transcript variant X6
microsomal triglyceride transfer protein large subunit isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X2
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X5
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X3
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X4
vesicle transport through interaction with t-SNAREs homolog 1A-like, transcript variant X1
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X2
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X1
vesicle transport through interaction with t-SNAREs homolog 1A-like isoform X3
uncharacterized LOC122574453, transcript variant X2
uncharacterized LOC122574453, transcript variant X1
uncharacterized protein LOC122574453 isoform X2
uncharacterized protein LOC122574453 isoform X1
spermidine synthase, transcript variant X2
spermidine synthase, transcript variant X1
J domain-containing protein DDB_G0295729, transcript variant X2
J domain-containing protein DDB_G0295729, transcript variant X1
transcriptional regulator ATRX isoform X1
J domain-containing protein DDB_G0295729 isoform X2
translational activator of cytochrome c oxidase 1
uncharacterized LOC122574450, transcript variant X2
uncharacterized LOC122574450, transcript variant X1
uncharacterized protein LOC122574450 isoform X2
uncharacterized protein LOC122574450 isoform X1
uncharacterized LOC122574455, transcript variant X2
uncharacterized LOC122574455, transcript variant X1
uncharacterized LOC122574447, transcript variant X2
uncharacterized LOC122574447, transcript variant X1
uncharacterized protein LOC122574447 isoform X2
uncharacterized protein LOC122574447 isoform X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X2
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X3
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X4
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X7
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X5
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X6
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X2
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X3
mRNA decay activator protein ZFP36L3, transcript variant X2
mRNA decay activator protein ZFP36L3, transcript variant X3
mRNA decay activator protein ZFP36L3, transcript variant X4
mRNA decay activator protein ZFP36L3, transcript variant X1
mRNA decay activator protein ZFP36L3, transcript variant X5
mRNA decay activator protein ZFP36L3 isoform X3
mRNA decay activator protein ZFP36L3 isoform X2
mRNA decay activator protein ZFP36L3 isoform X1
mRNA decay activator protein ZFP36L3 isoform X4
uncharacterized LOC122574195, transcript variant X1
uncharacterized LOC122574195, transcript variant X2
echinoderm microtubule-associated protein-like 2, transcript variant X3
echinoderm microtubule-associated protein-like 2, transcript variant X14
echinoderm microtubule-associated protein-like 2, transcript variant X10
echinoderm microtubule-associated protein-like 2, transcript variant X13
echinoderm microtubule-associated protein-like 2, transcript variant X5
echinoderm microtubule-associated protein-like 2, transcript variant X7
echinoderm microtubule-associated protein-like 2, transcript variant X6
echinoderm microtubule-associated protein-like 2, transcript variant X12
echinoderm microtubule-associated protein-like 2, transcript variant X2
echinoderm microtubule-associated protein-like 2, transcript variant X1
echinoderm microtubule-associated protein-like 2, transcript variant X4
echinoderm microtubule-associated protein-like 2, transcript variant X11
echinoderm microtubule-associated protein-like 2, transcript variant X8
echinoderm microtubule-associated protein-like 2, transcript variant X9
echinoderm microtubule-associated protein-like 2, transcript variant X15
echinoderm microtubule-associated protein-like 2 isoform X11
echinoderm microtubule-associated protein-like 2 isoform X4
echinoderm microtubule-associated protein-like 2 isoform X6
echinoderm microtubule-associated protein-like 2 isoform X5
echinoderm microtubule-associated protein-like 2 isoform X10
echinoderm microtubule-associated protein-like 2 isoform X2
echinoderm microtubule-associated protein-like 2 isoform X1
echinoderm microtubule-associated protein-like 2 isoform X12
echinoderm microtubule-associated protein-like 2 isoform X9
echinoderm microtubule-associated protein-like 2 isoform X3
echinoderm microtubule-associated protein-like 2 isoform X7
echinoderm microtubule-associated protein-like 2 isoform X8
echinoderm microtubule-associated protein-like 2 isoform X13
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
MD-2-related lipid-recognition protein-like
similar to RNA sequence (same species):INSD:GGGP01024071.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 105 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 105 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
breast cancer metastasis-suppressor 1-like protein
facilitated trehalose transporter Tret1-like, transcript variant X9
facilitated trehalose transporter Tret1-like isoform X3
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like, transcript variant X4
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like, transcript variant X5
facilitated trehalose transporter Tret1-like, transcript variant X6
facilitated trehalose transporter Tret1-like, transcript variant X7
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X10
facilitated trehalose transporter Tret1-2 homolog isoform X1
facilitated trehalose transporter Tret1-like, transcript variant X8
facilitated trehalose transporter Tret1-like isoform X2
facilitated trehalose transporter Tret1-like isoform X4
LOW QUALITY PROTEIN: uncharacterized protein LOC122574388
uncharacterized LOC122574160, transcript variant X7
uncharacterized LOC122574160, transcript variant X6
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 3 samples with support for all annotated introns
uncharacterized LOC122574160, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC122574160, transcript variant X5
uncharacterized LOC122574160, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC122574160, transcript variant X4
uncharacterized LOC122574160, transcript variant X3
uncharacterized LOC122574160, transcript variant X8
uncharacterized LOC122574160, transcript variant X9
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
GATOR complex protein Iml1, transcript variant X11
GATOR complex protein Iml1, transcript variant X4
GATOR complex protein Iml1, transcript variant X1
GATOR complex protein Iml1, transcript variant X7
GATOR complex protein Iml1, transcript variant X9
GATOR complex protein Iml1, transcript variant X12
GATOR complex protein Iml1, transcript variant X13
GATOR complex protein Iml1, transcript variant X2
GATOR complex protein Iml1, transcript variant X3
GATOR complex protein Iml1, transcript variant X6
GATOR complex protein Iml1, transcript variant X14
GATOR complex protein Iml1, transcript variant X10
GATOR complex protein Iml1, transcript variant X15
GATOR complex protein Iml1, transcript variant X8
GATOR complex protein Iml1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC4
F-box only protein 43-like, transcript variant X1
F-box only protein 43-like, transcript variant X2
uncharacterized protein LOC122574174 isoform X2
threonylcarbamoyladenosine tRNA methylthiotransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
threonylcarbamoyladenosine tRNA methylthiotransferase, transcript variant X2
threonylcarbamoyladenosine tRNA methylthiotransferase
glucose dehydrogenase [FAD, quinone]-like isoform X1
glucose dehydrogenase [FAD, quinone]-like isoform X2