Penaeus chinensis breed Huanghai No. 1 chromosome 39, ASM1920278v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Dendrobranchiata; Penaeoidea; Penaeidae; Penaeus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032964.1.\nAssembly name: ASM1920278v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2021/07/13. The\noriginal whole-genome shotgun project has the accession\nJAGKSU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Date :: 2020\nAssembly Method :: FALCON-Unzip v. MAY-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 150.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Penaeus chinensis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
conservation base of Haifeng Aquaculture Co., Ltd.
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
nuclear transcription factor Y subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
proline-rich receptor-like protein kinase PERK2
COORDINATES: polyA evidence [ECO:0006239]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein basonuclin-2-like
uncharacterized LOC125046661, 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 39 samples with support for all annotated introns
uncharacterized protein LOC125046661 isoform X3
uncharacterized LOC125046661, transcript variant X1
uncharacterized LOC125046661, 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 17 samples with support for all annotated introns
uncharacterized protein LOC125046661 isoform X1
uncharacterized protein LOC125046661 isoform X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2-like
glycine-rich cell wall structural protein-like
uncharacterized LOC125046864, transcript variant X2
uncharacterized LOC125046864, transcript variant X1
uncharacterized LOC125046865, transcript variant X2
uncharacterized LOC125046865, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
glycine-rich cell wall structural protein 1-like
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: 88% coverage of the annotated genomic feature by RNAseq alignments
neuropeptide-like protein 31, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuropeptide-like protein 31, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01038220.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 194 bases not found in genome assembly; 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 2 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: added 64 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
glyoxylate reductase/hydroxypyruvate reductase-like, transcript variant X1
glyoxylate reductase/hydroxypyruvate reductase-like isoform X1
glyoxylate reductase/hydroxypyruvate reductase-like, transcript variant X2
glyoxylate reductase/hydroxypyruvate reductase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit alpha-like
malate dehydrogenase, mitochondrial-like
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125046933, transcript variant X2
uncharacterized LOC125046933, transcript variant X1
uncharacterized protein LOC125046933 isoform X1
uncharacterized protein LOC125046933 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized LOC125046573, transcript variant X2
uncharacterized LOC125046573, transcript variant X3
uncharacterized LOC125046573, transcript variant X1
uncharacterized LOC125046676, transcript variant X1
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 25 samples with support for all annotated introns
uncharacterized LOC125046676, transcript variant X4
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
uncharacterized LOC125046676, transcript variant X5
uncharacterized LOC125046676, transcript variant X6
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 11 samples with support for all annotated introns
uncharacterized LOC125046676, transcript variant X2
uncharacterized LOC125046676, transcript variant X3
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 19 samples with support for all annotated introns
uncharacterized protein LOC125046676 isoform X1
uncharacterized protein LOC125046676 isoform X4
uncharacterized protein LOC125046676 isoform X5
uncharacterized protein LOC125046676 isoform X6
uncharacterized protein LOC125046676 isoform X2
uncharacterized protein LOC125046676 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125046581, transcript variant X1
uncharacterized LOC125046581, transcript variant X2
uncharacterized protein LOC125046581 isoform X1
uncharacterized protein LOC125046581 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
inactive rhomboid protein 1-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 4 samples with support for all annotated introns
inactive rhomboid protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
inactive rhomboid protein 1-like isoform X1
inactive rhomboid protein 1-like isoform X2
inactive rhomboid protein 1-like, transcript variant X3
inactive rhomboid protein 1-like isoform X3
cytosol aminopeptidase-like, transcript variant X3
cytosol aminopeptidase-like, transcript variant X2
cytosol aminopeptidase-like, transcript variant X1
E3 ubiquitin-protein ligase COP1-like isoform X1
beta,beta-carotene 15,15'-dioxygenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125046403, transcript variant X1
uncharacterized LOC125046403, transcript variant X2
uncharacterized LOC125046403, transcript variant X5
uncharacterized LOC125046403, transcript variant X4
uncharacterized LOC125046403, transcript variant X6
uncharacterized LOC125046403, transcript variant X3
uncharacterized protein LOC125046403 isoform X1
uncharacterized protein LOC125046403 isoform X2
uncharacterized protein LOC125046403 isoform X5
uncharacterized protein LOC125046403 isoform X4
uncharacterized protein LOC125046403 isoform X6
uncharacterized protein LOC125046403 isoform X3
uncharacterized LOC125046403, transcript variant X7
uncharacterized protein LOC125046403 isoform X7
protein mesh-like, transcript variant X1
protein mesh-like, transcript variant X2
protein mesh-like, transcript variant X3
pollen-specific leucine-rich repeat extensin-like protein 2
similar to RNA sequence (same species):INSD:GHUY01009978.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 553 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 443 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
1-aminocyclopropane-1-carboxylate synthase-like protein 1
uncharacterized LOC125046746, 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
uncharacterized LOC125046746, 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 2 samples with support for all annotated introns
uncharacterized LOC125046746, transcript variant X2
glycine-rich cell wall structural protein 1.8-like
glycerophosphocholine choline phosphodiesterase ENPP6-like
bis(5'-adenosyl)-triphosphatase enpp4-like
lysosomal-trafficking regulator-like, 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 13 samples with support for all annotated introns
lysosomal-trafficking regulator-like isoform X2
lysosomal-trafficking regulator-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 14 samples with support for all annotated introns
lysosomal-trafficking regulator-like isoform X1
osteoclast-stimulating factor 1-like, transcript variant X2
osteoclast-stimulating factor 1-like, transcript variant X1
osteoclast-stimulating factor 1-like isoform X1
osteoclast-stimulating factor 1-like isoform X2
long-chain-fatty-acid--CoA ligase 4-like
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: long-chain-fatty-acid--CoA ligase 4-like
splicing factor 3B subunit 2-like, transcript variant X1
splicing factor 3B subunit 2-like, transcript variant X2
splicing factor 3B subunit 2-like isoform X1
splicing factor 3B subunit 2-like isoform X2
DNA mismatch repair protein Mlh3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
DNA mismatch repair protein Mlh3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
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
Hermansky-Pudlak syndrome 1 protein homolog
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 36 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein 27C-like isoform X6
heterogeneous nuclear ribonucleoprotein 27C-like isoform X5
heterogeneous nuclear ribonucleoprotein 27C-like isoform X2
heterogeneous nuclear ribonucleoprotein 27C-like isoform X3
heterogeneous nuclear ribonucleoprotein 27C-like isoform X1
heterogeneous nuclear ribonucleoprotein 27C-like isoform X4
GRB10-interacting GYF protein 2-like, transcript variant X2
GRB10-interacting GYF protein 2-like, transcript variant X1
GRB10-interacting GYF protein 2-like, transcript variant X3
GRB10-interacting GYF protein 2-like, transcript variant X4
GRB10-interacting GYF protein 2-like, transcript variant X6
GRB10-interacting GYF protein 2-like, transcript variant X5
GRB10-interacting GYF protein 2-like isoform X1
GRB10-interacting GYF protein 2-like isoform X2
GRB10-interacting GYF protein 2-like isoform X3
GRB10-interacting GYF protein 2-like isoform X5
GRB10-interacting GYF protein 2-like isoform X4
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X4
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X3
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X1
protein kinase C and casein kinase substrate in neurons protein 2-like isoform X2
protein kinase C and casein kinase substrate in neurons protein 1-like isoform X4
protein kinase C and casein kinase substrate in neurons protein 1-like isoform X3
protein kinase C and casein kinase substrate in neurons protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
serine/threonine/tyrosine-protein kinase HT1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC125046760, 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 23 samples with support for all annotated introns
uncharacterized LOC125046760, 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 15 samples with support for all annotated introns
uncharacterized LOC125046760, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC125046760, 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 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: sepiapterin reductase-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
ras-related protein Rab-34-like, transcript variant X1
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 24 samples with support for all annotated introns
ras-related protein Rab-34-like, transcript variant X2
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 5 samples with support for all annotated introns
ras-related protein Rab-34-like, transcript variant X3
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 1 sample with support for all annotated introns
uncharacterized LOC125046845, transcript variant X2
uncharacterized protein LOC125046845 isoform X2
uncharacterized LOC125046845, transcript variant X1
uncharacterized protein LOC125046845 isoform X1
DNA damage-binding protein 2-like, transcript variant X2
DNA damage-binding protein 2-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 22 samples with support for all annotated introns
DNA damage-binding protein 2-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 9 samples with support for all annotated introns
DNA damage-binding protein 2-like isoform X3
DNA damage-binding protein 2-like isoform X2
DNA damage-binding protein 2-like 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
LOW QUALITY PROTEIN: kelch-like ECH-associated protein 1B
interleukin-1 receptor-associated kinase 4-like
LOW QUALITY PROTEIN: interleukin-1 receptor-associated kinase 4-like
golgin subfamily A member 6-like protein 6, transcript variant X2
golgin subfamily A member 6-like protein 6, transcript variant X3
golgin subfamily A member 6-like protein 6 isoform X2
golgin subfamily A member 6-like protein 6 isoform X3
golgin subfamily A member 6-like protein 6, transcript variant X1
golgin subfamily A member 6-like protein 6 isoform X1
transcription initiation factor TFIID subunit 9-like
uncharacterized protein DDB_G0287625-like
uncharacterized LOC125046585, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125046585, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125046585, transcript variant X14
uncharacterized LOC125046585, transcript variant X11
uncharacterized LOC125046585, transcript variant X8
uncharacterized LOC125046585, transcript variant X9
uncharacterized LOC125046585, transcript variant X13
uncharacterized protein LOC125046585 isoform X4
uncharacterized protein LOC125046585 isoform X3
uncharacterized protein LOC125046585 isoform X5
uncharacterized protein LOC125046585 isoform X6
uncharacterized LOC125046585, transcript variant X5
uncharacterized LOC125046585, 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 7 samples with support for all annotated introns
uncharacterized LOC125046585, transcript variant X1
uncharacterized LOC125046585, transcript variant X2
uncharacterized LOC125046585, transcript variant X6
uncharacterized LOC125046585, transcript variant X4
uncharacterized LOC125046585, transcript variant X3
uncharacterized protein LOC125046585 isoform X2
uncharacterized protein LOC125046585 isoform X1
probable citrate synthase 1, mitochondrial, transcript variant X1
probable citrate synthase 1, mitochondrial, transcript variant X2
probable citrate synthase 1, mitochondrial isoform X1
probable citrate synthase 1, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
leucine zipper transcription factor-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
calcium and integrin-binding protein 1-like
cysteine--tRNA ligase, cytoplasmic-like, transcript variant X2
cysteine--tRNA ligase, cytoplasmic-like, transcript variant X1
probable serine racemase, transcript variant X2
probable serine racemase, transcript variant X1
transcription factor kayak-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
transcription factor kayak-like, transcript variant X4
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 39 samples with support for all annotated introns
transcription factor kayak-like, transcript variant X1
transcription factor kayak-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
transcription factor kayak-like isoform X4
transcription factor kayak-like isoform X2
transcription factor kayak-like isoform X1
transcription factor kayak-like isoform X3
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125046757, transcript variant X2
uncharacterized LOC125046757, transcript variant X1
uncharacterized protein LOC125046757 isoform X2
uncharacterized protein LOC125046757 isoform X1
3-hydroxybutyrate dehydrogenase type 2-like, transcript variant X2
3-hydroxybutyrate dehydrogenase type 2-like, transcript variant X3
3-hydroxybutyrate dehydrogenase type 2-like, transcript variant X4
3-hydroxybutyrate dehydrogenase type 2-like, transcript variant X1
3-hydroxybutyrate dehydrogenase type 2-like isoform X2
3-hydroxybutyrate dehydrogenase type 2-like isoform X1
glycerol-3-phosphate acyltransferase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125046829, transcript variant X1
uncharacterized LOC125046829, transcript variant X3
uncharacterized LOC125046829, transcript variant X2
uncharacterized protein LOC125046829 isoform X1
uncharacterized protein LOC125046829 isoform X2
small G protein signaling modulator 1-like
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
translation initiation factor eIF-2B subunit delta-like, transcript variant X6
translation initiation factor eIF-2B subunit delta-like, transcript variant X4
translation initiation factor eIF-2B subunit delta-like, transcript variant X5
translation initiation factor eIF-2B subunit delta-like, transcript variant X1
translation initiation factor eIF-2B subunit delta-like, transcript variant X2
translation initiation factor eIF-2B subunit delta-like, transcript variant X3
translation initiation factor eIF-2B subunit delta-like isoform X1
translation initiation factor eIF-2B subunit delta-like isoform X3
translation initiation factor eIF-2B subunit delta-like isoform X2
translation initiation factor eIF-2B subunit delta-like isoform X4
translation initiation factor eIF-2B subunit delta-like isoform X5
pancreatic lipase-related protein 2-like
uncharacterized LOC125046578, transcript variant X1
uncharacterized LOC125046578, transcript variant X2
uncharacterized LOC125046693, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized LOC125046693, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
nucleolar protein dao-5-like, transcript variant X4
nucleolar protein dao-5-like, transcript variant X2
nucleolar protein dao-5-like, transcript variant X3
nucleolar protein dao-5-like, transcript variant X1
nucleolar and coiled-body phosphoprotein 1-like isoform X2
nucleolar and coiled-body phosphoprotein 1-like isoform X1
ethanolamine-phosphate cytidylyltransferase-like
transfer RNA arginine (anticodon UCG); 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: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vacuolar protein sorting-associated protein 33A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125046664, transcript variant X6
uncharacterized LOC125046664, transcript variant X1
uncharacterized LOC125046664, transcript variant X4
uncharacterized LOC125046664, transcript variant X3
uncharacterized LOC125046664, transcript variant X5
uncharacterized LOC125046664, transcript variant X7
uncharacterized LOC125046664, transcript variant X2
uncharacterized protein LOC125046664 isoform X1
uncharacterized protein LOC125046664 isoform X3
uncharacterized protein LOC125046664 isoform X5
uncharacterized protein LOC125046664 isoform X2
uncharacterized protein LOC125046664 isoform X4
uncharacterized protein LOC125046664 isoform X6
glycine-rich cell wall structural protein 1.0-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized transmembrane protein DDB_G0289901-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
glycine-rich cell wall structural protein 2-like
iduronate 2-sulfatase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
iduronate 2-sulfatase-like, 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 23 samples with support for all annotated introns
uncharacterized LOC125046603, transcript variant X1
uncharacterized LOC125046603, transcript variant X2
uncharacterized LOC125046603, transcript variant X3
uncharacterized protein LOC125046603 isoform X1
uncharacterized protein LOC125046603 isoform X2
uncharacterized LOC125046607, transcript variant X2
uncharacterized LOC125046607, transcript variant X3
uncharacterized LOC125046607, transcript variant X1
uncharacterized LOC125046607, transcript variant X4
uncharacterized LOC125046607, transcript variant X5
uncharacterized LOC125046613, transcript variant X2
uncharacterized LOC125046613, transcript variant X1
uncharacterized LOC125046613, transcript variant X3
zinc finger protein 614-like, transcript variant X1
zinc finger protein 614-like, transcript variant X2
28S ribosomal protein S21, mitochondrial-like
3-hydroxy-3-methylglutaryl-coenzyme A reductase-like
LOW QUALITY PROTEIN: 3-hydroxy-3-methylglutaryl-coenzyme A reductase-like
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
basic proline-rich protein-like, transcript variant X1
basic proline-rich protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
chondroitin sulfate N-acetylgalactosaminyltransferase 2-like
similar to RNA sequence (same species):INSD:GHUY01009171.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 241 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 226 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein NipSnap-like, transcript variant X2
protein NipSnap-like, 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 39 samples with support for all annotated introns
protein NipSnap-like, transcript variant X3
SET domain-containing protein SmydA-8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
LOW QUALITY PROTEIN: kelch-like protein 18
U4/U6 small nuclear ribonucleoprotein Prp31-like
swi5-dependent recombination DNA repair protein 1 homolog, transcript variant X1
swi5-dependent recombination DNA repair protein 1 homolog, transcript variant X2
swi5-dependent recombination DNA repair protein 1 homolog, transcript variant X3
swi5-dependent recombination DNA repair protein 1 homolog
adenosine 5'-monophosphoramidase HINT3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
adenosine 5'-monophosphoramidase HINT3-like, transcript variant X2
adenosine 5'-monophosphoramidase HINT3-like isoform X1
adenosine 5'-monophosphoramidase HINT3-like isoform X2
major facilitator superfamily domain-containing protein 6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-like isoform X1
major facilitator superfamily domain-containing protein 6-like isoform X2
major facilitator superfamily domain-containing protein 6-like isoform X3
BRISC and BRCA1-A complex member 1-like, transcript variant X2
BRISC and BRCA1-A complex member 1-like, transcript variant X1
BRISC and BRCA1-A complex member 1-like, transcript variant X3
facilitated trehalose transporter Tret1-like
nucleoporin NUP188-like, transcript variant X1
nucleoporin NUP188-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
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
cartilage oligomeric matrix protein-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GHUY01000147.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 146 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 89 bases not found in genome assembly; 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: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X7
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X8
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X6
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X4
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X2
uncharacterized protein LOC125046799 isoform X4
uncharacterized protein LOC125046799 isoform X5
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X5
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like, transcript variant X3
uncharacterized protein LOC125046799 isoform X3
uncharacterized protein LOC125046799 isoform X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial-like isoform X2
uncharacterized LOC125046714, transcript variant X1
uncharacterized LOC125046714, transcript variant X2
uncharacterized LOC125046714, transcript variant X3
pleckstrin homology domain-containing family G member 5-like, transcript variant X1
pleckstrin homology domain-containing family G member 5-like, transcript variant X2
pleckstrin homology domain-containing family G member 5-like isoform X2
pleckstrin homology domain-containing family G member 5-like isoform X1
probable serine/threonine-protein kinase irlF
tetra-peptide repeat homeobox protein 1-like
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein Gfi-1b-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
zinc finger protein Gfi-1b-like isoform X3
zinc finger protein Gfi-1b-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
zinc finger protein Gfi-1b-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
zinc finger protein Gfi-1b-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
zinc finger protein Gfi-1b-like, transcript variant X2
uncharacterized LOC125046808, 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 2 samples with support for all annotated introns
uncharacterized LOC125046808, 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 2 samples with support for all annotated introns
uncharacterized protein LOC125046808 isoform X2
uncharacterized protein LOC125046808 isoform X1
muscle, skeletal receptor tyrosine protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% 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: 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125046643, transcript variant X1
uncharacterized LOC125046643, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
adrenodoxin-like protein 1, mitochondrial, transcript variant X2
adrenodoxin-like protein 1, mitochondrial isoform X2
adrenodoxin-like protein 1, mitochondrial, transcript variant X1
adrenodoxin-like protein 1, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, 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 1 sample with support for all annotated introns
tachykinin-like peptides receptor 99D isoform X1
tachykinin-like peptides receptor 99D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tachykinin-like peptides receptor 99D isoform X2
glycine, alanine and asparagine-rich protein-like
WW domain-containing protein C660.06-like
endonuclease 8-like 3, transcript variant X1
endonuclease 8-like 3, transcript variant X2
endonuclease 8-like 3, transcript variant X3
calmodulin-lysine N-methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat protein 37-like
uncharacterized LOC125046938, transcript variant X2
uncharacterized LOC125046938, transcript variant X1
retinoid-inducible serine carboxypeptidase-like
serine protease HTRA2, mitochondrial-like
importin subunit alpha-9-like, transcript variant X3
importin subunit alpha-9-like, transcript variant X1
importin subunit alpha-9-like, transcript variant X4
importin subunit alpha-9-like, transcript variant X5
importin subunit alpha-9-like, transcript variant X6
importin subunit alpha-9-like, transcript variant X2
importin subunit alpha-9-like, transcript variant X8
importin subunit alpha-9-like, transcript variant X7
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X1
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X3
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X1
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
riboflavin kinase-like, transcript variant X2
riboflavin kinase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
U3 small nucleolar RNA-associated protein 14 homolog A-like
L-threonine 3-dehydrogenase, mitochondrial-like
uncharacterized PE-PGRS family protein PE_PGRS54-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01027422.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 469 bases not found in genome assembly; 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 39 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: added 108 bases not found in genome assembly; 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: 19 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125046614, transcript variant X2
uncharacterized LOC125046614, transcript variant X3
uncharacterized LOC125046614, transcript variant X1
uncharacterized protein LOC125046614 isoform X2
uncharacterized protein LOC125046614 isoform X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5-like
uncharacterized LOC125046708, transcript variant X3
uncharacterized LOC125046708, transcript variant X1
uncharacterized LOC125046708, transcript variant X2
glycerol-3-phosphate acyltransferase 4-like, transcript variant X1
glycerol-3-phosphate acyltransferase 4-like, transcript variant X4
glycerol-3-phosphate acyltransferase 4-like, transcript variant X2
glycerol-3-phosphate acyltransferase 4-like, transcript variant X3
glycerol-3-phosphate acyltransferase 4-like
similar to RNA sequence (same species):INSD:GIYE01017234.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 562 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 6 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: added 280 bases not found in genome assembly; 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: 31 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: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent glycine transporter 2-like, transcript variant X3
sodium- and chloride-dependent glycine transporter 2-like, transcript variant X1
sodium- and chloride-dependent glycine transporter 2-like, transcript variant X2
sodium- and chloride-dependent glycine transporter 2-like isoform X2
sodium- and chloride-dependent glycine transporter 2-like isoform X1
M-phase phosphoprotein 8-like, transcript variant X4
M-phase phosphoprotein 8-like, transcript variant X1
M-phase phosphoprotein 8-like, transcript variant X2
M-phase phosphoprotein 8-like, transcript variant X3
M-phase phosphoprotein 8-like isoform X3
M-phase phosphoprotein 8-like isoform X2
M-phase phosphoprotein 8-like isoform X4
M-phase phosphoprotein 8-like isoform X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X3
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X4
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X5
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like, transcript variant X6
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like isoform X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1-like isoform X3
mitochondrial ribonuclease P catalytic subunit-like
altered inheritance of mitochondria protein 3-like
proline-rich protein HaeIII subfamily 1-like
actin-related protein 2/3 complex subunit 3-like
protein arginine N-methyltransferase 1-like, transcript variant X4
protein arginine N-methyltransferase 1-like, transcript variant X8
protein arginine N-methyltransferase 1-like, transcript variant X7
protein arginine N-methyltransferase 1-like, transcript variant X3
protein arginine N-methyltransferase 1-like, transcript variant X5
protein arginine N-methyltransferase 1-like, transcript variant X2
protein arginine N-methyltransferase 1-like, transcript variant X1
protein arginine N-methyltransferase 1-like, transcript variant X6
protein arginine N-methyltransferase 1-like
glycylpeptide N-tetradecanoyltransferase 2-like
glucose dehydrogenase [FAD, quinone]-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-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 4 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X5
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
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X4
glucose dehydrogenase [FAD, quinone]-like
glucose dehydrogenase [FAD, quinone]-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 4 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X6
diacylglycerol kinase theta-like, 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 7 samples with support for all annotated introns
diacylglycerol kinase theta-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
diacylglycerol kinase theta-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 14 samples with support for all annotated introns
diacylglycerol kinase theta-like, transcript variant X1
diacylglycerol kinase theta-like isoform X3
diacylglycerol kinase theta-like isoform X4
diacylglycerol kinase theta-like isoform X2
diacylglycerol kinase theta-like isoform X1
diacylglycerol kinase theta-like, transcript variant X6
diacylglycerol kinase theta-like, transcript variant X5
diacylglycerol kinase theta-like, transcript variant X7
diacylglycerol kinase theta-like isoform X7
diacylglycerol kinase theta-like isoform X6
diacylglycerol kinase theta-like isoform X5
testis-expressed protein 10-like, transcript variant X2
testis-expressed protein 10-like, transcript variant X3
testis-expressed protein 10-like, transcript variant X1
cyclin-D-binding Myb-like transcription factor 1, transcript variant X4
cyclin-D-binding Myb-like transcription factor 1, transcript variant X2
cyclin-D-binding Myb-like transcription factor 1, transcript variant X3
cyclin-D-binding Myb-like transcription factor 1, transcript variant X1
cyclin-D-binding Myb-like transcription factor 1 isoform X1
cyclin-D-binding Myb-like transcription factor 1 isoform X2
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial-like isoform X1
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 1, mitochondrial-like isoform X2
uncharacterized LOC125046646, transcript variant X1
uncharacterized LOC125046646, 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 31 samples with support for all annotated introns
U-scoloptoxin(01)-Cw1a-like, transcript variant X2
U-scoloptoxin(01)-Cw1a-like, transcript variant X1
ATP-dependent RNA helicase DDX42-like, transcript variant X2
ATP-dependent RNA helicase DDX42-like, transcript variant X3
ATP-dependent RNA helicase DDX42-like, transcript variant X1
ATP-dependent RNA helicase DDX42-like isoform X1
ATP-dependent RNA helicase DDX42-like isoform X2
protein lap4-like, transcript variant X3
protein lap4-like, transcript variant X1
protein lap4-like, transcript variant X2
protein scribble homolog, transcript variant X1
protein scribble homolog, transcript variant X9
protein scribble homolog, transcript variant X3
protein scribble homolog, transcript variant X10
protein scribble homolog, transcript variant X11
protein scribble homolog, transcript variant X13
protein scribble homolog, transcript variant X12
protein scribble homolog, transcript variant X6
protein scribble homolog, transcript variant X2
protein scribble homolog, transcript variant X4
protein scribble homolog, transcript variant X5
protein scribble homolog, transcript variant X7
protein scribble homolog, transcript variant X8
protein scribble homolog, transcript variant X15
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 31 samples with support for all annotated introns
protein scribble homolog, transcript variant X14
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
palmitoyl-protein thioesterase ABHD10, mitochondrial-like
glutamate receptor ionotropic, kainate 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
presequence protease, mitochondrial-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 19 samples with support for all annotated introns
uncharacterized LOC125046835, transcript variant X1
uncharacterized LOC125046835, transcript variant X2
A-agglutinin anchorage subunit-like, 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 16 samples with support for all annotated introns
A-agglutinin anchorage subunit-like, transcript variant X3
A-agglutinin anchorage subunit-like, transcript variant X1
nuclear receptor subfamily 2 group E member 1-like
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
39S ribosomal protein L42, mitochondrial-like
MICOS complex subunit MIC19-like, transcript variant X2
MICOS complex subunit MIC19-like, transcript variant X1
MICOS complex subunit MIC19-like isoform X2
MICOS complex subunit mic25a-like isoform X1
epidermal growth factor receptor-like, transcript variant X1
epidermal growth factor receptor-like, transcript variant X3
epidermal growth factor receptor-like, transcript variant X2
epidermal growth factor receptor-like, transcript variant X4
epidermal growth factor receptor-like isoform X1
epidermal growth factor receptor-like isoform X3
epidermal growth factor receptor-like isoform X2
epidermal growth factor receptor-like isoform 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 31 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10-like
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
60S ribosomal protein L3-like, transcript variant X1
60S ribosomal protein L3-like, transcript variant X2
60S ribosomal protein L3-like isoform X1
60S ribosomal protein L3-like isoform X2
CLK4-associating serine/arginine rich protein-like
transcription activator BRG1-like, transcript variant X1
transcription activator BRG1-like, transcript variant X2
transcription activator BRG1-like, transcript variant X3
transcription activator BRG1-like isoform X1
transcription activator BRG1-like isoform X2
transcription activator BRG1-like isoform X3
N-acetyltransferase ESCO2-like, transcript variant X2
N-acetyltransferase ESCO2-like, transcript variant X1
N-acetyltransferase ESCO2-like isoform X2
N-acetyltransferase ESCO2-like isoform X1
elongation of very long chain fatty acids protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
elongation of very long chain fatty acids protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
elongation of very long chain fatty acids protein 4-like isoform X1
elongation of very long chain fatty acids protein 4-like isoform X2
uncharacterized LOC125046737, transcript variant X1
uncharacterized LOC125046737, transcript variant X2
uncharacterized protein LOC125046737 isoform X1
uncharacterized protein LOC125046737 isoform X2
cytoplasmic FMR1-interacting protein-like, transcript variant X2
cytoplasmic FMR1-interacting protein-like, transcript variant X1
cytoplasmic FMR1-interacting protein-like, transcript variant X4
cytoplasmic FMR1-interacting protein-like, transcript variant X3
cytoplasmic FMR1-interacting protein-like isoform X2
cytoplasmic FMR1-interacting protein-like isoform X1
cytoplasmic FMR1-interacting protein-like isoform X4
cytoplasmic FMR1-interacting protein-like isoform X3
eukaryotic translation initiation factor 3 subunit G-like
eukaryotic translation initiation factor 3 subunit G-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G-like, transcript variant X5
eukaryotic translation initiation factor 3 subunit G-like, 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 6 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G-like, transcript variant X6
eukaryotic translation initiation factor 3 subunit G-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G-like isoform X1
eukaryotic translation initiation factor 3 subunit G-like isoform X2
ATP-binding cassette sub-family G member 5-like
ATP-binding cassette sub-family G member 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
ATP-binding cassette sub-family G member 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATP-binding cassette sub-family G member 8-like isoform X1
ATP-binding cassette sub-family G member 8-like isoform X2
similar to RNA sequence (same species):INSD:GHUY01000134.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 962 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 929 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
techylectin-5A-like, transcript variant X1
techylectin-5A-like, transcript variant X2
repetitive proline-rich cell wall protein 1-like
microtubule-associated proteins 1A/1B light chain 3A-like
dehydrogenase/reductase SDR family member 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 11-like
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 22 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 11-like, transcript variant X5
dehydrogenase/reductase SDR family member 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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 30 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 11-like isoform X1
dehydrogenase/reductase SDR family member 11-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
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
putative uncharacterized protein YGR160W
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
abscisic acid and environmental stress-inducible protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
cell surface glycoprotein 1-like, transcript variant X1
cell surface glycoprotein 1-like, transcript variant X4
cell surface glycoprotein 1-like, transcript variant X2
cell surface glycoprotein 1-like isoform X1
cell surface glycoprotein 1-like isoform X4
cell surface glycoprotein 1-like, transcript variant X3
cell surface glycoprotein 1-like isoform X3
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like
nuclear pore complex protein DDB_G0274915-like
pollen-specific leucine-rich repeat extensin-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
cold and drought-regulated protein CORA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
glycine-rich cell wall structural protein 2-like, transcript variant X1
glycine-rich cell wall structural protein 2-like, transcript variant X2
receptor-interacting serine/threonine-protein kinase 1-like
uncharacterized LOC125046931, transcript variant X1
uncharacterized LOC125046931, transcript variant X2
coiled-coil domain-containing protein 43-like
protein bric-a-brac 2-like, transcript variant X1
protein bric-a-brac 2-like, transcript variant X2
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X2
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X4
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X1
longitudinals lacking protein, isoforms A/B/D/L-like isoform X3
protein tramtrack, beta isoform-like isoform X1
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X3
protein tramtrack, beta isoform-like isoform X2
rho-related BTB domain-containing protein 1-like, transcript variant X4
rho-related BTB domain-containing protein 1-like, transcript variant X2
rho-related BTB domain-containing protein 1-like, transcript variant X1
rho-related BTB domain-containing protein 1-like, transcript variant X5
rho-related BTB domain-containing protein 1-like, transcript variant X3
rho-related BTB domain-containing protein 1-like isoform X2
rho-related BTB domain-containing protein 1-like isoform X1
rho-related BTB domain-containing protein 1-like isoform X3
protein pellino-like, transcript variant X1
protein pellino-like, transcript variant X2
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X5
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X6
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X7
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X9
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X4
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X1
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X2
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X8
nucleoside diphosphate phosphatase ENTPD5-like, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 5-like isoform X5
ectonucleoside triphosphate diphosphohydrolase 5-like isoform X4
nucleoside diphosphate phosphatase ENTPD5-like isoform X2
ectonucleoside triphosphate diphosphohydrolase 5-like isoform X1
ectonucleoside triphosphate diphosphohydrolase 5-like isoform X3
ectonucleoside triphosphate diphosphohydrolase 5-like isoform X6
polyadenylate-binding protein-interacting protein 2-like
mediator of RNA polymerase II transcription subunit 22-like
phosphatidylinositide phosphatase SAC2-like, transcript variant X2
phosphatidylinositide phosphatase SAC2-like isoform X2
phosphatidylinositide phosphatase SAC2-like, transcript variant X1
phosphatidylinositide phosphatase SAC2-like, transcript variant X3
phosphatidylinositide phosphatase SAC2-like isoform X1
phosphatidylinositide phosphatase SAC2-like isoform X3
bestrophin-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
bestrophin-2-like, transcript variant X2
bestrophin-2-like, transcript variant X3
uncharacterized LOC125046819, transcript variant X5
uncharacterized LOC125046819, transcript variant X6
uncharacterized LOC125046819, transcript variant X4
uncharacterized LOC125046819, transcript variant X3
uncharacterized LOC125046819, transcript variant X7
uncharacterized LOC125046819, transcript variant X1
uncharacterized LOC125046819, transcript variant X2
uncharacterized protein LOC125046819 isoform X1
uncharacterized protein LOC125046819 isoform X2
uncharacterized protein LOC125046819 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
receptor-mediated endocytosis protein 6 homolog, transcript variant X1
receptor-mediated endocytosis protein 6 homolog, transcript variant X2
GTPase-activating protein and VPS9 domain-containing protein 1-like isoform X1
GTPase-activating protein and VPS9 domain-containing protein 1-like isoform X2
receptor-mediated endocytosis protein 6 homolog, transcript variant X3
receptor-mediated endocytosis protein 6 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125046827, transcript variant X2
uncharacterized LOC125046827, 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 18 samples with support for all annotated introns
uncharacterized protein LOC125046827 isoform X1
uncharacterized protein LOC125046827 isoform X2
protein transport protein Sec61 subunit beta-like
probable methyltransferase-like protein 23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
acyl-CoA-binding domain-containing protein 6-like
transcription factor Sp8-like, transcript variant X4
transcription factor Sp8-like, transcript variant X6
transcription factor Sp8-like, transcript variant X3
transcription factor Sp8-like, transcript variant X1
transcription factor Sp8-like, transcript variant X2
transcription factor Sp8-like, transcript variant X5
transcription factor Sp4-like isoform X6
transcription factor Sp8-like isoform X2
transcription factor Sp4-like isoform X4
transcription factor Sp4-like isoform X3
transcription factor Sp4-like isoform X1
transcription factor Sp4-like isoform X5
transcription factor E2F8-like, transcript variant X2
transcription factor E2F8-like, transcript variant X1
transcription factor E2F8-like isoform X1
uncharacterized protein LOC125046691 isoform X2
dual specificity mitogen-activated protein kinase kinase hemipterous-like, transcript variant X2
dual specificity mitogen-activated protein kinase kinase hemipterous-like, transcript variant X1
dual specificity mitogen-activated protein kinase kinase hemipterous-like isoform X2
dual specificity mitogen-activated protein kinase kinase hemipterous-like isoform X1
uncharacterized LOC125046918, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC125046918, 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 19 samples with support for all annotated introns
uncharacterized protein LOC125046918 isoform X2
uncharacterized protein LOC125046918 isoform X1
enhancer of mRNA-decapping protein 4-like, transcript variant X2
enhancer of mRNA-decapping protein 4-like, transcript variant X1
enhancer of mRNA-decapping protein 4-like isoform X1
enhancer of mRNA-decapping protein 4-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein conundrum-like
segmentation protein Runt-like, transcript variant X1
segmentation protein Runt-like, transcript variant X2
segmentation protein Runt-like isoform X1
segmentation protein Runt-like isoform X2
beta-1,3-galactosyltransferase 1-like, transcript variant X1
beta-1,3-galactosyltransferase 1-like, transcript variant X2
beta-1,3-galactosyltransferase 1-like, transcript variant X3
beta-1,3-galactosyltransferase 1-like isoform X1
beta-1,3-galactosyltransferase 1-like isoform X2
beta-1,3-galactosyltransferase 1-like, transcript variant X4
beta-1,3-galactosyltransferase 1-like isoform X3
uncharacterized LOC125046628, transcript variant X2
uncharacterized LOC125046628, transcript variant X1
uncharacterized LOC125046628, transcript variant X3
coiled-coil domain-containing protein 12-like
graves disease carrier protein-like, transcript variant X1
graves disease carrier protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
graves disease carrier protein-like isoform X1
graves disease carrier protein-like isoform 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
piggyBac transposable element-derived protein 3-like
transfer RNA alanine (anticodon UGC); 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: 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
pyroglutamylated RF-amide peptide receptor-like
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: 1 Protein, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% 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 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable inactive protein kinase DDB_G0270444
calcium-activated potassium channel subunit alpha-1-like, transcript variant X1
calcium-activated potassium channel subunit alpha-1-like, transcript variant X3
calcium-activated potassium channel subunit alpha-1-like, transcript variant X2
calcium-activated potassium channel subunit alpha-1-like isoform X1
calcium-activated potassium channel subunit alpha-1-like isoform X2
calcium-activated potassium channel slowpoke-like, transcript variant X1
calcium-activated potassium channel slowpoke-like isoform X1
calcium-activated potassium channel slowpoke-like, transcript variant X2
calcium-activated potassium channel slowpoke-like isoform X2