Osmia bicornis bicornis chromosome 14, iOsmBic2.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Apoidea; Megachilidae; Megachilinae; Osmia.
REFSEQ INFORMATION: The reference sequence is identical to\nOU015517.1.\nAssembly name: iOsmBic2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/05/17. The original whole-genome shotgun project has the\naccession CAJRAL000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Osmia bicornis bicornis Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123988461, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123988461, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123988461, transcript variant X5
uncharacterized LOC123988461, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123988461, 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 3 samples with support for all annotated introns
uncharacterized LOC123988461, 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 2 samples with support for all annotated introns
uncharacterized LOC123988461, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123988461, 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 19 samples with support for all annotated introns
WD repeat, SAM and U-box domain-containing protein 1-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
WD repeat, SAM and U-box domain-containing protein 1-like isoform X1
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 isoform X2
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 X4
WD repeat, SAM and U-box domain-containing protein 1-like isoform X3
WD repeat, SAM and U-box domain-containing protein 1-like isoform 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 X5
myosin-2 essential light chain, transcript variant X2
myosin-2 essential light chain isoform X2
myosin-2 essential light chain, transcript variant X1
myosin-2 essential light chain isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ornithine decarboxylase antizyme 1
uncharacterized LOC114880486, transcript variant X7
uncharacterized LOC114880486, transcript variant X5
uncharacterized LOC114880486, transcript variant X8
uncharacterized LOC114880486, transcript variant X4
uncharacterized LOC114880486, transcript variant X3
uncharacterized LOC114880486, transcript variant X1
uncharacterized LOC114880486, transcript variant X2
uncharacterized LOC114880486, transcript variant X6
uncharacterized protein LOC114880486 isoform X2
uncharacterized protein LOC114880486 isoform X1
ras-related protein RabJ-like, transcript variant X2
ras-related protein RabJ-like isoform X2
ras-related protein RabJ-like, transcript variant X1
ras-related protein RabJ-like isoform X1
ras-related protein RabJ-like, transcript variant X3
ras-related protein RabJ-like isoform X3
uncharacterized LOC114880487, transcript variant X4
uncharacterized LOC114880487, transcript variant X6
uncharacterized LOC114880487, transcript variant X8
uncharacterized LOC114880487, transcript variant X1
uncharacterized LOC114880487, transcript variant X2
uncharacterized LOC114880487, transcript variant X10
uncharacterized LOC114880487, transcript variant X9
uncharacterized LOC114880487, transcript variant X11
uncharacterized LOC114880487, transcript variant X3
uncharacterized LOC114880487, transcript variant X5
uncharacterized LOC114880487, transcript variant X7
uncharacterized protein LOC114880487 isoform X3
uncharacterized protein LOC114880487 isoform X1
uncharacterized protein LOC114880487 isoform X2
uncharacterized protein LOC114880487 isoform X4
uncharacterized LOC114880487, transcript variant X12
uncharacterized protein LOC114880487 isoform X5
serine proteinase stubble, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
serine proteinase stubble, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 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: 11 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
proteasome activator complex subunit 3, transcript variant X1
proteasome activator complex subunit 3, transcript variant X2
proteasome activator complex subunit 3 isoform X2
proteasome activator complex subunit 3 isoform X1
26S proteasome non-ATPase regulatory subunit 11
transmembrane protein 17-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 9 samples with support for all annotated introns
transmembrane protein 17-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 18 samples with support for all annotated introns
transmembrane protein 17-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transmembrane protein 17-like isoform X1
transmembrane protein 17-like isoform X2
pleckstrin homology domain-containing family A member 8
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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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: 2 mRNAs, 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 306a1, transcript variant X4
cytochrome P450 306a1, transcript variant X1
cytochrome P450 306a1, transcript variant X5
cytochrome P450 306a1, transcript variant X3
cytochrome P450 306a1, transcript variant X2
serine/threonine-protein kinase fused, transcript variant X3
serine/threonine-protein kinase fused isoform 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 16 samples with support for all annotated introns
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 15 samples with support for all annotated introns
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 15 samples with support for all annotated introns
zinc metalloproteinase nas-13 isoform X2
serine/threonine-protein kinase fused, transcript variant X2
serine/threonine-protein kinase fused, transcript variant X1
serine/threonine-protein kinase fused isoform X1
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like
potassium voltage-gated channel protein Shaw
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
uncharacterized LOC114878668, 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 2 samples with support for all annotated introns
uncharacterized LOC114878668, transcript variant X3
uncharacterized LOC114878668, transcript variant X2
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
uncharacterized LOC114878668, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC114878668 isoform X1
uncharacterized protein LOC114878668 isoform X2
uncharacterized protein LOC114878668 isoform X3
protein bowel-like, transcript variant X1
protein bowel-like, transcript variant X2
protein bowel-like, transcript variant X3
protein drumstick, transcript variant X4
protein drumstick, transcript variant X2
protein drumstick, transcript variant X3
protein drumstick, transcript variant X5
protein drumstick, transcript variant X1
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
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 10 samples with support for all annotated introns
insulin receptor substrate 1, transcript variant X4
insulin receptor substrate 1, transcript variant X3
insulin receptor substrate 1, transcript variant X5
insulin receptor substrate 1, transcript variant X1
insulin receptor substrate 1, transcript variant X2
insulin receptor substrate 1, transcript variant X7
insulin receptor substrate 1, transcript variant X6
insulin receptor substrate 1-B isoform X5
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 10 samples with support for all annotated introns
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 isoform 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 isoform X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X3
cGMP-dependent protein kinase, isozyme 2 forms cD5/T2 isoform X3
PAT complex subunit CCDC47-like, transcript variant X7
PAT complex subunit CCDC47-like, transcript variant X1
PAT complex subunit CCDC47-like, transcript variant X2
PAT complex subunit CCDC47-like, transcript variant X4
PAT complex subunit CCDC47-like, transcript variant X5
PAT complex subunit CCDC47-like, transcript variant X3
uncharacterized protein LOC114878680 isoform X4
uncharacterized protein CG7065-like isoform X1
uncharacterized protein CG7065-like isoform X2
PAT complex subunit CCDC47-like, transcript variant X6
PAT complex subunit CCDC47-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; 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 14 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta-1,3-galactosyltransferase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; deleted 7 bases in 5 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; deleted 7 bases in 5 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: peroxisomal targeting signal 1 receptor
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 78% 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: inserted 4 bases in 3 codons; deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
dual specificity protein kinase splA-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 10 bases in 9 codons; deleted 10 bases in 7 codons; 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, including 8 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 10 bases in 9 codons; deleted 10 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dual specificity protein kinase splA-like
polycomb group protein Psc-like, transcript variant X2
polycomb group protein Psc-like, transcript variant X1
116 kDa U5 small nuclear ribonucleoprotein component, 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 19 samples with support for all annotated introns
116 kDa U5 small nuclear ribonucleoprotein component, transcript variant X2
116 kDa U5 small nuclear ribonucleoprotein component
ras-related protein M-Ras-like, transcript variant X1
ras-related protein M-Ras-like, transcript variant X2
ras-related protein M-Ras-like, transcript variant X3
ras-related protein M-Ras-like isoform X1
ras-related protein M-Ras-like isoform X2
transmembrane protein 132E, transcript variant X4
transmembrane protein 132E, transcript variant X2
transmembrane protein 132E, transcript variant X1
transmembrane protein 132E, transcript variant X3
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
39S ribosomal protein L16, mitochondrial
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
uncharacterized LOC114877065, transcript variant X2
uncharacterized LOC114877065, transcript variant X3
uncharacterized LOC114877065, transcript variant X1
uncharacterized LOC114877065, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
broad-complex core protein, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 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, transcript variant X10
broad-complex core protein, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
broad-complex core protein, transcript variant X8
broad-complex core protein, transcript variant X1
broad-complex core protein, transcript variant X5
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 5 samples with support for all annotated introns
broad-complex core protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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, transcript variant X4
broad-complex core protein, transcript variant X3
broad-complex core protein isoforms 1/2/3/4/5 isoform X5
broad-complex core protein isoforms 1/2/3/4/5 isoform X6
neo-calmodulin-like, transcript variant X3
neo-calmodulin-like, transcript variant X4
neo-calmodulin-like, transcript variant X1
neo-calmodulin-like, transcript variant X2
neo-calmodulin-like, transcript variant X5
endoplasmic reticulum resident protein 44, transcript variant X1
endoplasmic reticulum resident protein 44, transcript variant X2
endoplasmic reticulum resident protein 44 isoform X1
endoplasmic reticulum resident protein 44 isoform X2
transcription factor Sp8, transcript variant X12
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
transcription factor Sp8, transcript variant X11
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 6 samples with support for all annotated introns
transcription factor Sp8, transcript variant X8
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
transcription factor Sp8, transcript variant X6
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
transcription factor Sp8, transcript variant X3
transcription factor Sp8, transcript variant X7
transcription factor Sp8, transcript variant X10
transcription factor Sp8, transcript variant X9
transcription factor Sp8, transcript variant X5
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
transcription factor Sp8, 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
transcription factor Sp8, 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 9 samples with support for all annotated introns
transcription factor Sp8, 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 3 samples with support for all annotated introns
obg-like ATPase 1, transcript variant X1
obg-like ATPase 1, transcript variant X2
obg-like ATPase 1, 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 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily H member 8
mitochondrial 2-oxoglutarate/malate carrier protein-like
DNA repair protein REV1, transcript variant X3
DNA repair protein REV1, transcript variant X1
DNA repair protein REV1, transcript variant X2
cytochrome b5 domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
malate dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 17% 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
serine/threonine-protein kinase 17A-like
probable serine/threonine-protein kinase MARK-C
ATP-dependent RNA helicase DDX42, transcript variant X1
ATP-dependent RNA helicase DDX42, transcript variant X3
ATP-dependent RNA helicase DDX42, transcript variant X2
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 19 samples with support for all annotated introns
acetyl-coenzyme A transporter 1, transcript variant X2
acetyl-coenzyme A transporter 1, transcript variant X1
host cell factor 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
host cell factor 2-like, transcript variant X1
host cell factor 2-like, transcript variant X3
uncharacterized protein LOC114880342 isoform X1
dynein axonemal intermediate chain 3, transcript variant X4
uncharacterized protein LOC114879304 isoform X2
dynein axonemal intermediate chain 3, 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 1 sample with support for all annotated introns
dynein axonemal intermediate chain 3, transcript variant X3
dynein axonemal intermediate chain 3, 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 2 samples with support for all annotated introns
dynein axonemal intermediate chain 3 isoform X1
uncharacterized LOC114879308, transcript variant X1
uncharacterized LOC114879308, transcript variant X2
uncharacterized LOC114879308, transcript variant X3
uncharacterized LOC114879303, transcript variant X1
uncharacterized LOC114879303, transcript variant X2
pyridoxine/pyridoxamine 5'-phosphate oxidase-like
atrial natriuretic peptide-converting enzyme-like, transcript variant X1
atrial natriuretic peptide-converting enzyme-like, transcript variant X2
atrial natriuretic peptide-converting enzyme-like
armadillo segment polarity protein, transcript variant X3
armadillo segment polarity protein, transcript variant X1
armadillo segment polarity protein, transcript variant X2
armadillo segment polarity protein isoform X2
armadillo segment polarity protein isoform X1
armadillo segment polarity protein, 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 19 samples with support for all annotated introns
armadillo segment polarity protein isoform X3
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
microsomal triacylglycerol transfer protein
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
long-chain-fatty-acid--CoA ligase 6, transcript variant X1
long-chain-fatty-acid--CoA ligase 1 isoform X1
long-chain-fatty-acid--CoA ligase 6, transcript variant X2
long-chain-fatty-acid--CoA ligase 6 isoform X2
vesicle transport through interaction with t-SNAREs homolog 1A
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 X3
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
neprilysin-4-like, transcript variant X1
neprilysin-4-like, transcript variant X2
neprilysin-4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitochondrial tRNA-specific 2-thiouridylase 1, transcript variant X3
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 X4
mitochondrial tRNA-specific 2-thiouridylase 1
paired amphipathic helix protein Sin3a, transcript variant X3
paired amphipathic helix protein Sin3a, transcript variant X1
paired amphipathic helix protein Sin3a, transcript variant X2
paired amphipathic helix protein Sin3a isoform X1
paired amphipathic helix protein Sin3a isoform X2
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, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 isoform X1
COP9 signalosome complex subunit 7b, transcript variant X1
COP9 signalosome complex subunit 7b, transcript variant X2
COP9 signalosome complex subunit 7b isoform X1
COP9 signalosome complex subunit 7b isoform 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
POU domain, class 6, transcription factor 2, transcript variant X4
POU domain, class 6, transcription factor 2, transcript variant X3
POU domain, class 6, transcription factor 2, transcript variant X8
POU domain, class 6, transcription factor 2, transcript variant X7
POU domain, class 6, transcription factor 2, transcript variant X5
POU domain, class 6, transcription factor 2, transcript variant X2
POU domain, class 6, transcription factor 2, transcript variant X6
POU domain, class 6, transcription factor 2, transcript variant X1
POU domain, class 6, transcription factor 2 isoform X7
POU domain, class 6, transcription factor 1 isoform X5
POU domain, class 6, transcription factor 2 isoform X4
POU domain, class 6, transcription factor 2 isoform X2
POU domain, class 6, transcription factor 1 isoform X6
POU domain, class 6, transcription factor 1 isoform X3
POU domain, class 6, transcription factor 1 isoform X1
POU domain, class 6, transcription factor 2 isoform X8
uncharacterized LOC114872557, transcript variant X3
uncharacterized LOC114872557, transcript variant X1
uncharacterized LOC114872557, transcript variant X7
uncharacterized LOC114872557, transcript variant X5
uncharacterized LOC114872557, transcript variant X2
uncharacterized LOC114872557, transcript variant X11
uncharacterized LOC114872557, transcript variant X6
uncharacterized LOC114872557, transcript variant X4
uncharacterized LOC114872557, transcript variant X9
uncharacterized LOC114872557, transcript variant X10
uncharacterized LOC114872557, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
EF-hand calcium-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC114872567, transcript variant X4
uncharacterized LOC114872567, transcript variant X3
uncharacterized LOC114872567, transcript variant X2
uncharacterized LOC114872567, transcript variant X1
signal recognition particle receptor subunit beta
histidine protein methyltransferase 1 homolog, 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 19 samples with support for all annotated introns
histidine protein methyltransferase 1 homolog, transcript variant X3
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
pyridoxine/pyridoxamine 5'-phosphate oxidase
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 11 samples with support for all annotated introns
histidine protein methyltransferase 1 homolog, transcript variant X2
histidine protein methyltransferase 1 homolog isoform X1
histidine protein methyltransferase 1 homolog isoform X2
peptidoglycan recognition protein 3-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 12 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X6
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 3 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X7
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 3 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X5
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 2 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X3
uncharacterized protein LOC114872566 isoform X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like isoform X3
uncharacterized protein LOC114872566 isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A-like, transcript variant X4
calponin homology domain-containing protein DDB_G0272472
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, including 3 samples with support for all annotated introns
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: calponin homology domain-containing protein DDB_G0272472
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: GATOR complex protein Iml1
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 12 samples with support for all annotated introns
uncharacterized LOC123988451, transcript variant X1
uncharacterized LOC123988451, transcript variant X2
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 X7
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 X4
piezo-type mechanosensitive ion channel component, transcript variant X6
piezo-type mechanosensitive ion channel component isoform X1
piezo-type mechanosensitive ion channel component isoform X5
piezo-type mechanosensitive ion channel component isoform X7
piezo-type mechanosensitive ion channel component isoform X2
piezo-type mechanosensitive ion channel component isoform X3
piezo-type mechanosensitive ion channel component isoform X4
piezo-type mechanosensitive ion channel component isoform X6
lysosomal thioesterase PPT2 homolog, transcript variant X1
lysosomal thioesterase PPT2 homolog, transcript variant X2
lysosomal thioesterase PPT2 homolog isoform X1
lysosomal thioesterase PPT2 homolog isoform 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 9 samples with support for all annotated introns
uncharacterized LOC114880389, 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 2 samples with support for all annotated introns
uncharacterized LOC114880389, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
4-coumarate--CoA ligase 1-like, transcript variant X3
4-coumarate--CoA ligase 1-like, transcript variant X1
4-coumarate--CoA ligase 1-like, transcript variant X2
4-coumarate--CoA ligase 1-like, transcript variant X4
uncharacterized LOC114878998, transcript variant X4
uncharacterized LOC114878998, transcript variant X3
uncharacterized protein LOC114878998 isoform X3
uncharacterized protein LOC114878998 isoform X4
uncharacterized LOC114878998, transcript variant X2
uncharacterized LOC114878998, transcript variant X1
uncharacterized protein LOC114878998 isoform X1
uncharacterized protein LOC114878998 isoform X2
uncharacterized LOC114878998, transcript variant X5
uncharacterized protein LOC114878998 isoform X5
carcinine transporter, transcript variant X3
carcinine transporter, transcript variant X2
carcinine transporter, transcript variant X1
importin subunit beta-1, transcript variant X3
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 17 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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 2, transcript variant X3
nuclear receptor subfamily 4 group A member 2, transcript variant X2
nuclear receptor subfamily 4 group A member 2, transcript variant X1
nuclear receptor subfamily 4 group A member 2 isoform X3
nuclear receptor subfamily 4 group A member 2 isoform X2
nuclear receptor subfamily 4 group A member 2 isoform X1
MPN domain-containing protein CG4751, transcript variant X2
MPN domain-containing protein CG4751, transcript variant X1
uncharacterized protein LOC114878985 isoform X1
MPN domain-containing protein CG4751 isoform X2
transmembrane protein 45B-like, transcript variant X1
transmembrane protein 45B-like, transcript variant 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, including 9 samples with support for all annotated introns
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 isoform X1
EGF domain-specific O-linked N-acetylglucosamine transferase isoform X2
uncharacterized protein At4g17910, transcript variant X2
uncharacterized protein At4g17910, transcript variant X1
ATPase WRNIP1-like, transcript variant X1
ATPase WRNIP1-like, transcript variant X2
diacylglycerol O-acyltransferase 1, transcript variant X3
diacylglycerol O-acyltransferase 1, transcript variant X1
diacylglycerol O-acyltransferase 1, transcript variant X2
39S ribosomal protein L10, mitochondrial
UBX domain-containing protein 4-like, transcript variant X3
UBX domain-containing protein 4-like, transcript variant X2
UBX domain-containing protein 4-like, transcript variant X4
UBX domain-containing protein 4-like, transcript variant X1
UBX domain-containing protein 4-like isoform X1
UBX domain-containing protein 4-like isoform X3
UBX domain-containing protein 4-like isoform X2
UBX domain-containing protein 4-like isoform X4
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 5 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC114876473, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC114876473, transcript variant X1
uncharacterized protein LOC114876473 isoform X1
uncharacterized protein LOC114876473 isoform X2
uncharacterized LOC114878967, transcript variant X2
uncharacterized LOC114878967, transcript variant X1
homeotic protein distal-less, transcript variant X1
homeotic protein distal-less, transcript variant X2
homeotic protein distal-less, transcript variant X3
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 1 sample with support for all annotated introns
keratin, type I cytoskeletal 9 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
SIFamide-related peptide, transcript variant X1
SIFamide-related peptide, transcript variant X3
SIFamide-related peptide, transcript variant X2
glutamate decarboxylase, transcript variant X1
glutamate decarboxylase, transcript variant X2
coiled-coil domain-containing protein 113-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 79% 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: angiotensin-converting enzyme-like
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X6
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X5
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 X8
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X9
voltage-dependent L-type calcium channel subunit beta-2, transcript variant X7
voltage-dependent L-type calcium channel subunit beta-2 isoform X1
voltage-dependent L-type calcium channel subunit beta-2 isoform X3
voltage-dependent L-type calcium channel subunit beta-2 isoform X2
WW domain-containing adapter protein with coiled-coil homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
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 16 samples with support for all annotated introns
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 3 samples with support for all annotated introns
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 18 samples with support for all annotated introns
putative sodium-dependent multivitamin transporter, transcript variant X3
putative sodium-dependent multivitamin transporter, transcript variant X2
putative sodium-dependent multivitamin transporter, transcript variant X4
putative sodium-dependent multivitamin transporter, transcript variant X1
putative sodium-dependent multivitamin transporter isoform X3
putative sodium-dependent multivitamin transporter isoform X4
putative sodium-dependent multivitamin transporter isoform X2
putative sodium-dependent multivitamin transporter isoform X1
carboxypeptidase B-like, transcript variant X2
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
carboxypeptidase B-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 2 samples with support for all annotated introns
carboxypeptidase B-like, 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 2 samples with support for all annotated introns
carboxypeptidase B-like, transcript variant X3
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
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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase 6-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
DC-STAMP domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
unconventional myosin-Va, transcript variant X1
unconventional myosin-Va, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC114872747, 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 13 samples with support for all annotated introns
uncharacterized LOC114872747, transcript variant X2
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
F-box/LRR-repeat protein 20, transcript variant X1
F-box/LRR-repeat protein 20, transcript variant X2
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16
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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 94b-like, transcript variant X1
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
odorant receptor 94b-like, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 46a-like, transcript variant X1
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
odorant receptor 46a-like, transcript variant X2
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
biogenesis of lysosome-related organelles complex 1 subunit 1
uncharacterized LOC114872730, transcript variant X1
uncharacterized LOC114872730, 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 2 samples with support for all annotated introns
BMP and activin membrane-bound inhibitor homolog
CTD nuclear envelope phosphatase 1 homolog, transcript variant X4
CTD nuclear envelope phosphatase 1 homolog, transcript variant X6
CTD nuclear envelope phosphatase 1 homolog, transcript variant X2
CTD nuclear envelope phosphatase 1 homolog, transcript variant X3
CTD nuclear envelope phosphatase 1 homolog, transcript variant X10
CTD nuclear envelope phosphatase 1 homolog, transcript variant X11
CTD nuclear envelope phosphatase 1 homolog, transcript variant X1
CTD nuclear envelope phosphatase 1 homolog, transcript variant X7
CTD nuclear envelope phosphatase 1 homolog, transcript variant X5
CTD nuclear envelope phosphatase 1 homolog, transcript variant X9
CTD nuclear envelope phosphatase 1 homolog isoform X4
CTD nuclear envelope phosphatase 1 homolog isoform X1
CTD nuclear envelope phosphatase 1 homolog isoform X2
CTD nuclear envelope phosphatase 1 homolog, transcript variant X8
CTD nuclear envelope phosphatase 1 isoform X3
calmodulin-binding transcription activator 2, transcript variant X1
calmodulin-binding transcription activator 2, transcript variant X2
calmodulin-binding transcription activator 2, transcript variant X3
calmodulin-binding transcription activator 2, transcript variant X8
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
calmodulin-binding transcription activator 2, transcript variant X5
calmodulin-binding transcription activator 2, transcript variant X4
calmodulin-binding transcription activator 2 isoform X1
calmodulin-binding transcription activator 2 isoform X2
calmodulin-binding transcription activator 2 isoform X3
calmodulin-binding transcription activator 2 isoform X4
calmodulin-binding transcription activator 2 isoform X5
calmodulin-binding transcription activator 2 isoform X8
calmodulin-binding transcription activator 2, transcript variant X6
calmodulin-binding transcription activator 2 isoform X6
calmodulin-binding transcription activator 2, transcript variant X7
calmodulin-binding transcription activator 2 isoform X7
RING finger protein nhl-1, transcript variant X6
RING finger protein nhl-1, transcript variant X5
RING finger protein nhl-1, transcript variant X4
RING finger protein nhl-1, transcript variant X7
RING finger protein nhl-1, 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 19 samples with support for all annotated introns
RING finger protein nhl-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 17 samples with support for all annotated introns
RING finger protein nhl-1, transcript variant X3
hyphally regulated cell wall protein 3 isoform X5
uncharacterized LOC114872721, 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 7 samples with support for all annotated introns
uncharacterized LOC114872721, transcript variant X1
uncharacterized LOC114872721, transcript variant X2
uncharacterized protein LOC114872721 isoform X1
uncharacterized protein LOC114872721 isoform X3
uncharacterized protein LOC114872721 isoform X2
5-hydroxytryptamine receptor 2B-like, transcript variant X1
5-hydroxytryptamine receptor 2B-like, transcript variant X3
5-hydroxytryptamine receptor 2B-like, transcript variant X2
neuropeptide CCHamide-1 receptor-like, transcript variant X4
neuropeptide CCHamide-1 receptor-like, transcript variant X1
neuropeptide CCHamide-1 receptor-like, transcript variant X2
neuropeptide CCHamide-1 receptor-like, transcript variant X3
neuropeptide CCHamide-1 receptor-like isoform X2
neuropeptide CCHamide-1 receptor-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123988448, 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 protein LOC123988448 isoform X2
uncharacterized LOC123988448, 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 LOC123988448 isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X2
immediate early response 3-interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
chondroitin sulfate synthase 1, transcript variant X1
chondroitin sulfate synthase 1, transcript variant X3
chondroitin sulfate synthase 1, transcript variant X2
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X6
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 7 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein 27C-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 19 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X7
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 19 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like isoform X6
heterogeneous nuclear ribonucleoprotein 27C-like isoform X3
heterogeneous nuclear ribonucleoprotein 27C-like isoform X1
heterogeneous nuclear ribonucleoprotein 27C-like isoform X7
heterogeneous nuclear ribonucleoprotein 27C-like isoform X4
heterogeneous nuclear ribonucleoprotein 27C-like isoform X2
heterogeneous nuclear ribonucleoprotein 27C-like isoform X5
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X1
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 isoform X4
ankyrin repeat and death domain-containing protein 1A-like isoform X3
ankyrin repeat and death domain-containing protein 1A-like isoform X2
ankyrin repeat and death domain-containing protein 1A-like isoform X1
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 2 samples with support for all annotated introns
uncharacterized LOC123988486, transcript variant X4
uncharacterized LOC123988486, transcript variant X5
uncharacterized LOC123988486, transcript variant X2
uncharacterized LOC123988486, transcript variant X1
uncharacterized LOC123988486, transcript variant X3
uncharacterized LOC123988486, transcript variant X8
uncharacterized LOC123988486, transcript variant X7
uncharacterized LOC123988486, transcript variant X6
uncharacterized protein LOC123988486 isoform X3
uncharacterized protein LOC123988486 isoform X2
uncharacterized protein LOC123988486 isoform X1
uncharacterized protein LOC123988486 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
DNA helicase MCM9-like, 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 15 samples with support for all annotated introns
DNA helicase MCM9-like, transcript variant X2
secretory carrier-associated membrane protein 5A, transcript variant X3
secretory carrier-associated membrane protein 5A, transcript variant X2
secretory carrier-associated membrane protein 5A, transcript variant X1
secretory carrier-associated membrane protein 5A
protein tyrosine phosphatase domain-containing protein 1-like
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
forkhead box protein P1-like, transcript variant X5
forkhead box protein P1-like, transcript variant X3
forkhead box protein P1-like, transcript variant X11
forkhead box protein P1-like, transcript variant X10
forkhead box protein P1-like, transcript variant X4
forkhead box protein P1-like, transcript variant X2
forkhead box protein P1-like, transcript variant X1
forkhead box protein P1-like, transcript variant X7
forkhead box protein P1-like, transcript variant X15
forkhead box protein P1-like, transcript variant X8
forkhead box protein P1-like, transcript variant X9
forkhead box protein P1-like, transcript variant X6
forkhead box protein P1-like, transcript variant X17
forkhead box protein P1-like, transcript variant X14
forkhead box protein P1-like, transcript variant X12
forkhead box protein P1-like, transcript variant X13
forkhead box protein P1-like, transcript variant X16
forkhead box protein P1-like, transcript variant X18
forkhead box protein P1-like isoform X11
forkhead box protein P1-like isoform X10
forkhead box protein P1-like isoform X12
dual serine/threonine and tyrosine protein kinase-like, transcript variant X2
dual serine/threonine and tyrosine protein kinase-like, transcript variant X4
dual serine/threonine and tyrosine protein kinase-like, transcript variant X3
dual serine/threonine and tyrosine protein kinase-like, transcript variant X5
dual serine/threonine and tyrosine protein kinase-like, transcript variant X7
dual serine/threonine and tyrosine protein kinase-like, transcript variant X1
dual serine/threonine and tyrosine protein kinase-like, transcript variant X6
dual serine/threonine and tyrosine protein kinase-like isoform X2
dual serine/threonine and tyrosine protein kinase-like isoform X1
uncharacterized LOC114875909, transcript variant X2
uncharacterized LOC114875909, transcript variant X1
uncharacterized LOC114875909, transcript variant X3
probable transmembrane reductase CYB561D1
integrin alpha-PS2, transcript variant X1
integrin alpha-PS2, transcript variant X2
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
uncharacterized LOC114875912, transcript variant X5
uncharacterized LOC114875912, transcript variant X3
uncharacterized LOC114875912, transcript variant X4
uncharacterized LOC114875912, transcript variant X2
uncharacterized LOC114875912, transcript variant X1
uncharacterized protein LOC114875912 isoform X2
uncharacterized protein LOC114875912 isoform X3
uncharacterized protein LOC114875912 isoform X1
uncharacterized LOC114875912, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC114875912 isoform X4
uncharacterized LOC114875905, transcript variant X2
uncharacterized LOC114875905, transcript variant X1
uncharacterized protein LOC114875905 isoform X2
uncharacterized protein LOC114875905 isoform X1
proline-rich protein 36-like, transcript variant X3
proline-rich protein 36-like, 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 3 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
proline-rich protein 36-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 4 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X2
serine-enriched protein, transcript variant X1
serine-enriched protein, transcript variant X2
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X6
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X3
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X5
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X2
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X8
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X7
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X4
putative polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
putative polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
putative polypeptide N-acetylgalactosaminyltransferase 9
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; 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, including 15 samples with support for all annotated introns
LOW QUALITY PROTEIN: putative polypeptide N-acetylgalactosaminyltransferase 9
arrestin domain-containing protein 17-like, transcript variant X1
arrestin domain-containing protein 17-like, transcript variant X2
arrestin domain-containing protein 17-like isoform X1
arrestin domain-containing protein 17-like isoform X2
translational activator of cytochrome c oxidase 1
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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LOW QUALITY PROTEIN: translational activator of cytochrome c oxidase 1
TNF receptor-associated factor family protein DDB_G0272098-like
spermidine synthase, transcript variant X1
spermidine synthase, transcript variant X2
spermidine synthase, transcript variant X3
uncharacterized LOC114876842, transcript variant X1
uncharacterized LOC114876842, transcript variant X2
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
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 17 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 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38% 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: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
receptor-type guanylate cyclase gcy-4-like
succinate dehydrogenase assembly factor 3, mitochondrial
acyl-coenzyme A diphosphatase NUDT19-like
L-threonine 3-dehydrogenase, mitochondrial
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 7
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 18 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 4 samples with support for all annotated introns
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor Sox-2, transcript variant X1
transcription factor Sox-2, transcript variant X5
transcription factor Sox-2, transcript variant X3
transcription factor Sox-2, transcript variant X2
transcription factor Sox-2, transcript variant X6
transcription factor Sox-2, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
LOW QUALITY PROTEIN: uncharacterized protein LOC123988472
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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 X3
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X1
mannose-P-dolichol utilization defect 1 protein homolog
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 19 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 58% coverage of the annotated genomic feature by RNAseq alignments
tubulin glycylase 3A-like, transcript variant X2
tubulin glycylase 3A-like, transcript variant X1
UPF0430 protein CG31712-like, transcript variant X1
UPF0430 protein CG31712-like, transcript variant X2
serine/threonine-protein kinase 26, transcript variant X2
serine/threonine-protein kinase 26, transcript variant X3
serine/threonine-protein kinase 26 isoform X3
serine/threonine-protein kinase 26, transcript variant X4
serine/threonine-protein kinase svkA isoform X2
serine/threonine-protein kinase 26, transcript variant X1
serine/threonine-protein kinase svkA isoform X1
CLIP domain-containing serine protease 2-like
uncharacterized LOC114876837, transcript variant X7
uncharacterized LOC114876837, transcript variant X8
uncharacterized LOC114876837, transcript variant X1
uncharacterized LOC114876837, transcript variant X6
uncharacterized LOC114876837, transcript variant X4
uncharacterized LOC114876837, transcript variant X5
uncharacterized LOC114876837, transcript variant X9
uncharacterized LOC114876837, transcript variant X2
uncharacterized LOC114876837, transcript variant X3
uncharacterized protein LOC114876837 isoform X1
uncharacterized protein LOC114876837 isoform X3
uncharacterized protein LOC114876837 isoform X2
uncharacterized protein LOC114876837 isoform X4
uncharacterized protein LOC114876837 isoform X5
prolyl 3-hydroxylase OGFOD1, transcript variant X1
prolyl 3-hydroxylase OGFOD1, transcript variant X2
prolyl 3-hydroxylase OGFOD1, transcript variant X3
LHFPL tetraspan subfamily member 2 protein
leucine-rich repeat-containing protein 71-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
AP-3 complex subunit sigma-2, transcript variant X2
AP-3 complex subunit sigma-2, transcript variant X3
AP-3 complex subunit sigma-2, transcript variant X4
AP-3 complex subunit sigma-2, transcript variant X1
GATA zinc finger domain-containing protein 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 9 samples with support for all annotated introns
GATA zinc finger domain-containing protein 1, transcript variant X1
GATA zinc finger domain-containing protein 1
cyclic AMP-dependent transcription factor ATF-7, 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 3 samples with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-7, transcript variant X2
cyclic AMP-dependent transcription factor ATF-7, transcript variant X3
cyclic AMP-dependent transcription factor ATF-7 isoform X1
cyclic AMP-dependent transcription factor ATF-2 isoform X2
uncharacterized protein DDB_G0287625-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC114879532, transcript variant X1
uncharacterized LOC114879532, transcript variant X2
uncharacterized protein LOC114879532 isoform X1
uncharacterized protein LOC114879532 isoform 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
receptor-type tyrosine-protein phosphatase T-like, transcript variant X1
receptor-type tyrosine-protein phosphatase T-like, transcript variant X2
receptor-type tyrosine-protein phosphatase T-like isoform X1
receptor-type tyrosine-protein phosphatase T-like isoform X2
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
transcription factor CP2-like protein 1, transcript variant X1
transcription factor CP2-like protein 1, transcript variant X2
transcription factor CP2-like protein 1, transcript variant X3
transcription factor CP2-like protein 1 isoform X1
transcription factor CP2-like protein 1 isoform X2
transcription factor CP2-like protein 1 isoform X3
transcription factor CP2-like protein 1, transcript variant X4
transcription factor CP2-like protein 1 isoform X4
uncharacterized LOC114879543, transcript variant X1
uncharacterized LOC114879543, transcript variant X2
uncharacterized protein LOC114879543 isoform X1
uncharacterized protein LOC114879543 isoform X2
protein N-terminal glutamine amidohydrolase-like
isochorismatase domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinase 4, transcript variant X2
cyclin-dependent kinase 4, transcript variant X6
cyclin-dependent kinase 4, transcript variant X1
cyclin-dependent kinase 4, transcript variant X3
cyclin-dependent kinase 4, transcript variant X4
cyclin-dependent kinase 4, transcript variant X5
adenosine 5'-monophosphoramidase HINT1, transcript variant X1
adenosine 5'-monophosphoramidase HINT1, transcript variant X2
adenosine 5'-monophosphoramidase HINT1 isoform X2
adenosine 5'-monophosphoramidase HINT1 isoform X1
translation machinery-associated protein 7 homolog, transcript variant X1
translation machinery-associated protein 7 homolog, transcript variant X2
translation machinery-associated protein 7 homolog, transcript variant X3
translation machinery-associated protein 7 homolog
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X2
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial, transcript variant X3
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X1
pyruvate dehydrogenase (acetyl-transferring) kinase, mitochondrial isoform X2
uncharacterized LOC123988499, 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 6 samples with support for all annotated introns
uncharacterized LOC123988499, 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
protein CDV3 homolog, transcript variant X2
protein CDV3 homolog, transcript variant X1
putative gamma-glutamylcyclotransferase CG2811, transcript variant X4
putative gamma-glutamylcyclotransferase CG2811, transcript variant X3
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 X3
putative gamma-glutamylcyclotransferase CG2811 isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
probable cytochrome P450 6a14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 149 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
probable cytochrome P450 6a14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 149 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cytochrome P450 6A1-like, transcript variant X4
cytochrome P450 6A1-like, transcript variant X3
cytochrome P450 6A1-like, transcript variant X1
cytochrome P450 6A1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytochrome P450 6a2-like, transcript variant X2
cytochrome P450 6a2-like, transcript variant X1
cytochrome P450 6a2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 98% 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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 81% 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: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 24% 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: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ras-related protein RabJ-like
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X2
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X2
uncharacterized LOC114879379, transcript variant X4
uncharacterized LOC114879379, transcript variant X3
uncharacterized LOC114879379, 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 12 samples with support for all annotated introns
uncharacterized LOC114879379, transcript variant X2
uncharacterized LOC114879381, transcript variant X4
uncharacterized LOC114879381, transcript variant X2
uncharacterized LOC114879381, transcript variant X3
uncharacterized LOC114879381, transcript variant X1
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
condensin complex subunit 1-like, transcript variant X1
condensin complex subunit 1-like, transcript variant X5
condensin complex subunit 1-like, transcript variant X2
condensin complex subunit 1-like isoform X3
condensin complex subunit 1-like, transcript variant X3
condensin complex subunit 1-like, transcript variant X4
condensin complex subunit 1-like, transcript variant X6
condensin complex subunit 1-like, transcript variant X8
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 12 samples with support for all annotated introns
condensin complex subunit 1-like, 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 17 samples with support for all annotated introns
condensin complex subunit 1-like, transcript variant X9
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 19 samples with support for all annotated introns
condensin complex subunit 1-like isoform X4
condensin complex subunit 1-like isoform X1
condensin complex subunit 1-like isoform X2
condensin complex subunit 1-like isoform X6
condensin complex subunit 1-like isoform X8
condensin complex subunit 1-like isoform X7
condensin complex subunit 1-like, transcript variant X7
condensin complex subunit 1-like isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 73% 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: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: thiamine transporter 2-like
pyruvate carboxylase, mitochondrial, transcript variant X1
pyruvate carboxylase, mitochondrial, transcript variant X4
pyruvate carboxylase, mitochondrial, transcript variant X3
pyruvate carboxylase, mitochondrial, transcript variant X2
pyruvate carboxylase, mitochondrial isoform X1
pyruvate carboxylase, mitochondrial isoform X2
probable cytochrome P450 6a14, transcript variant X3
probable cytochrome P450 6a14, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable cytochrome P450 6a14 isoform X1
probable cytochrome P450 6a14 isoform X2
uncharacterized LOC114881125, transcript variant X1
uncharacterized LOC114881125, transcript variant X2
4-O-methyl-glucuronoyl methylesterase 1-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
4-O-methyl-glucuronoyl methylesterase 1-like
4-O-methyl-glucuronoyl methylesterase 1-like, transcript variant X2
uncharacterized LOC114881126, transcript variant X1
uncharacterized LOC114881126, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 67 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: 1 mRNA, 67 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 77% 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: substituted 3 bases at 3 genomic stop codons; 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X3
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, 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 16 samples with support for all annotated introns
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X2
bumetanide-sensitive sodium-(potassium)-chloride cotransporter isoform X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
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 X2
tigger transposable element-derived protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 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: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123988502, transcript variant X2
uncharacterized LOC123988502, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 86% 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: 8 Proteins
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: 57 Proteins, and 94% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytochrome P450 6a2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 100 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: 1 mRNA, 100 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC123988443, transcript variant X6
uncharacterized LOC123988443, transcript variant X8
uncharacterized LOC123988443, transcript variant X7
uncharacterized LOC123988443, transcript variant X5
uncharacterized LOC123988443, transcript variant X3
uncharacterized LOC123988443, transcript variant X4
uncharacterized LOC123988443, transcript variant X9
uncharacterized LOC123988443, transcript variant X1
uncharacterized protein LOC123988443 isoform X1
uncharacterized LOC123988443, transcript variant X2
uncharacterized protein LOC123988443 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
SWI5-dependent HO expression protein 3-like
hydroxysteroid dehydrogenase-like protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
LOW QUALITY PROTEIN: uncharacterized protein LOC123988488
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments