Penaeus chinensis breed Huanghai No. 1 chromosome 4, 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\nCM032929.1.\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.
protein N-terminal glutamine amidohydrolase-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
protein N-terminal glutamine amidohydrolase-like, transcript variant X2
protein N-terminal glutamine amidohydrolase-like isoform X1
protein N-terminal glutamine amidohydrolase-like isoform X2
protein N-terminal glutamine amidohydrolase-like, transcript variant X3
protein N-terminal glutamine amidohydrolase-like isoform 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 19 samples with support for all annotated introns
serine/threonine-protein kinase PAK 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase PAK 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase PAK 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine/threonine-protein kinase PAK 2-like isoform X2
serine/threonine-protein kinase PAK 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125025106, 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 2 samples with support for all annotated introns
uncharacterized LOC125025106, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125025106, transcript variant X3
uncharacterized LOC125025106, 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 1 sample with support for all annotated introns
uncharacterized protein LOC125025106 isoform X3
uncharacterized protein LOC125025106 isoform X1
uncharacterized protein LOC125025106 isoform X4
uncharacterized protein LOC125025106 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cytochrome P450 2J4-like, transcript variant X1
cytochrome P450 2J4-like, transcript variant X2
serine/threonine-protein kinase PAK 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 25-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 25-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 25-like isoform X1
mediator of RNA polymerase II transcription subunit 25-like isoform X2
protein CIP2A homolog, transcript variant X3
protein CIP2A homolog, transcript variant X1
protein CIP2A homolog, transcript variant X2
protein CIP2A homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 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: 5 Proteins, 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% 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
kinesin-like protein KIF21A, transcript variant X3
kinesin-like protein KIF21A, transcript variant X4
kinesin-like protein KIF21A, transcript variant X1
kinesin-like protein KIF21A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
G-protein coupled receptor 143-like, transcript variant X2
G-protein coupled receptor 143-like, transcript variant X3
G-protein coupled receptor 143-like, transcript variant X1
G-protein coupled receptor 143-like, transcript variant X4
thiamine transporter 1-like, transcript variant X2
thiamine transporter 1-like, transcript variant X1
thiamine transporter 1-like, transcript variant X4
thiamine transporter 1-like, transcript variant X3
thiamine transporter 1-like, transcript variant X5
thiamine transporter 1-like, transcript variant X6
thiamine transporter 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
cofilin/actin-depolymerizing factor homolog
uncharacterized LOC125025148, transcript variant X1
uncharacterized LOC125025148, transcript variant X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X5
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X3
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X6
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X4
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X1
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like, transcript variant X7
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like isoform X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like isoform X1
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like isoform X4
adenosine 3'-phospho 5'-phosphosulfate transporter 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 84% 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
uncharacterized LOC125024933, transcript variant X3
uncharacterized LOC125024933, transcript variant X2
uncharacterized LOC125024933, transcript variant X1
DNA-dependent metalloprotease dvc-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
DNA-dependent metalloprotease dvc-1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA-dependent metalloprotease dvc-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
DNA-dependent metalloprotease dvc-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
DNA-dependent metalloprotease dvc-1-like, 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 30 samples with support for all annotated introns
DNA-dependent metalloprotease dvc-1-like isoform X1
DNA-dependent metalloprotease dvc-1-like isoform X2
DNA-dependent metalloprotease dvc-1-like isoform X3
fibroblast growth factor receptor substrate 3-like
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 37 samples with support for all annotated introns
small subunit processome component 20 homolog
uncharacterized LOC125046999, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125046999, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125046999, 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 4 samples with support for all annotated introns
uncharacterized protein LOC125046999 isoform X2
uncharacterized protein LOC125046999 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dehydrogenase/reductase SDR family member 7-like, transcript variant X5
dehydrogenase/reductase SDR family member 7-like, transcript variant X2
dehydrogenase/reductase SDR family member 7-like, transcript variant X3
dehydrogenase/reductase SDR family member 7-like, transcript variant X1
dehydrogenase/reductase SDR family member 7-like, transcript variant X4
dehydrogenase/reductase SDR family member 7-like isoform X1
dehydrogenase/reductase SDR family member 7-like isoform X2
6-phosphogluconate dehydrogenase, decarboxylating-like, transcript variant X2
6-phosphogluconate dehydrogenase, decarboxylating-like isoform X2
6-phosphogluconate dehydrogenase, decarboxylating-like, transcript variant X1
6-phosphogluconate dehydrogenase, decarboxylating-like isoform X1
uncharacterized LOC125046790, 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 3 samples with support for all annotated introns
uncharacterized LOC125046790, 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 32 samples with support for all annotated introns
uncharacterized LOC125046790, 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 5 samples with support for all annotated introns
catenin delta-2-like, transcript variant X16
catenin delta-2-like, transcript variant X14
catenin delta-2-like, transcript variant X17
catenin delta-2-like, transcript variant X18
catenin delta-2-like, transcript variant X15
catenin delta-2-like, transcript variant X19
catenin delta-2-like, transcript variant X3
catenin delta-2-like, transcript variant X4
catenin delta-2-like, transcript variant X2
catenin delta-2-like, transcript variant X1
catenin delta-2-like, transcript variant X6
catenin delta-2-like, transcript variant X5
catenin delta-2-like, transcript variant X13
uncharacterized protein LOC125046679 isoform X9
uncharacterized protein LOC125046679 isoform X6
uncharacterized protein LOC125046679 isoform X5
uncharacterized protein LOC125046679 isoform X4
uncharacterized protein LOC125046679 isoform X2
uncharacterized protein LOC125046679 isoform X3
uncharacterized protein LOC125046679 isoform X1
catenin delta-2-like, transcript variant X10
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
catenin delta-2-like, transcript variant X7
catenin delta-2-like, transcript variant X11
catenin delta-2-like, transcript variant X8
catenin delta-2-like, transcript variant X12
catenin delta-2-like, transcript variant X9
uncharacterized protein LOC125046679 isoform X8
uncharacterized protein LOC125046679 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
myocardin-related transcription factor B-like, transcript variant X6
myocardin-related transcription factor B-like, transcript variant X1
myocardin-related transcription factor B-like, transcript variant X4
myocardin-related transcription factor B-like, transcript variant X7
myocardin-related transcription factor B-like, transcript variant X2
myocardin-related transcription factor B-like, transcript variant X3
myocardin-related transcription factor B-like, transcript variant X5
transcription factor mef2A-like isoform X6
myocardin-related transcription factor B-like isoform X1
myocardin-related transcription factor B-like isoform X2
myocardin-related transcription factor B-like isoform X4
myocardin-related transcription factor B-like isoform X3
myocardin-related transcription factor B-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
40S ribosomal protein S10-like, transcript variant X1
40S ribosomal protein S10-like, transcript variant X2
40S ribosomal protein S10-like isoform X1
40S ribosomal protein S10-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
plasma membrane calcium-transporting ATPase 3-like, transcript variant X9
plasma membrane calcium-transporting ATPase 3-like, transcript variant X8
plasma membrane calcium-transporting ATPase 2-like isoform X4
plasma membrane calcium-transporting ATPase 2-like isoform X3
plasma membrane calcium-transporting ATPase 3-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 38 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-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 36 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-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 35 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-like, transcript variant X7
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 15 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-like, transcript variant X1
plasma membrane calcium-transporting ATPase 3-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 34 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-like, transcript variant X6
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 29 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 2-like isoform X2
plasma membrane calcium-transporting ATPase 2-like isoform X1
plasma membrane calcium-transporting ATPase 3-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3-like isoform X5
elongation factor-like GTPase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
elongation factor-like GTPase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tRNA-uridine aminocarboxypropyltransferase 1-like, transcript variant X1
tRNA-uridine aminocarboxypropyltransferase 1-like, transcript variant X3
tRNA-uridine aminocarboxypropyltransferase 1-like, transcript variant X2
tRNA-uridine aminocarboxypropyltransferase 1-like
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
apolipoprotein D-like, transcript variant X1
apolipoprotein D-like, transcript variant X2
alanine--glyoxylate aminotransferase 2, mitochondrial-like
RNA-binding region-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
RNA-binding region-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RNA-binding region-containing protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
RNA-binding region-containing protein 3-like isoform X1
RNA-binding region-containing protein 3-like isoform X2
similar to RNA sequence (same species):INSD:GIYE01046864.1
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 355 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 304 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
G protein-activated inward rectifier potassium channel 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
S1 RNA-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like
putative uncharacterized protein DDB_G0286901
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
probable serine/threonine-protein kinase cdc7
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: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable serine/threonine-protein kinase cdc7
keratin, type II cytoskeletal 2 epidermal-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
sodium-dependent multivitamin transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
sodium-dependent multivitamin transporter-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 23 samples with support for all annotated introns
sodium-dependent multivitamin transporter-like, transcript variant X2
sodium-dependent multivitamin transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 37 Proteins
saccharopine dehydrogenase-like oxidoreductase, transcript variant X1
saccharopine dehydrogenase-like oxidoreductase, transcript variant X5
saccharopine dehydrogenase-like oxidoreductase, transcript variant X2
saccharopine dehydrogenase-like oxidoreductase, transcript variant X4
saccharopine dehydrogenase-like oxidoreductase, transcript variant X3
saccharopine dehydrogenase-like oxidoreductase isoform X1
saccharopine dehydrogenase-like oxidoreductase isoform X2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
crustacyanin-A2 subunit-like, transcript variant X1
crustacyanin-A2 subunit-like, transcript variant X2
crustacyanin-A2 subunit-like, transcript variant X3
uncharacterized LOC125025098, transcript variant X1
uncharacterized LOC125025098, transcript variant X2
uncharacterized protein LOC125025098 isoform X1
uncharacterized protein LOC125025098 isoform X2
sodium- and chloride-dependent transporter XTRP3A-like, transcript variant X3
sodium- and chloride-dependent transporter XTRP3A-like, transcript variant X5
sodium- and chloride-dependent transporter XTRP3A-like, transcript variant X1
sodium- and chloride-dependent transporter XTRP3A-like, transcript variant X2
sodium- and chloride-dependent transporter XTRP3A-like isoform X2
sodium- and chloride-dependent transporter XTRP3A-like isoform X1
sodium- and chloride-dependent transporter XTRP3A-like isoform X5
sodium- and chloride-dependent transporter XTRP3A-like, transcript variant X4
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
sodium- and chloride-dependent transporter XTRP3A-like isoform X4
sodium- and chloride-dependent transporter XTRP3A-like isoform X3
serine/threonine-protein kinase stk11-like, 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 4 samples with support for all annotated introns
serine/threonine-protein kinase stk11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
serine/threonine-protein kinase stk11-like
DEP domain-containing protein 1A-like, transcript variant X1
DEP domain-containing protein 1A-like, transcript variant X2
DEP domain-containing protein 1A-like, transcript variant X3
DEP domain-containing protein 1A-like isoform X1
DEP domain-containing protein 1A-like isoform X2
DEP domain-containing protein 1A-like isoform X3
CDK5 regulatory subunit-associated protein 3-like
ankyrin repeat domain-containing protein 65-like
mediator of DNA damage checkpoint protein 1-like
putative uncharacterized protein DDB_G0271982
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport protein 52 homolog, transcript variant X1
intraflagellar transport protein 52 homolog, transcript variant X2
intraflagellar transport protein 52 homolog
uncharacterized LOC125025121, transcript variant X4
uncharacterized LOC125025121, transcript variant X2
uncharacterized LOC125025121, transcript variant X1
uncharacterized LOC125025121, transcript variant X3
uncharacterized protein LOC125025121 isoform X2
uncharacterized protein LOC125025121 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
innexin inx2-like, transcript variant X4
innexin inx2-like, transcript variant X5
innexin inx2-like, transcript variant X8
innexin inx2-like, transcript variant X6
innexin inx2-like, transcript variant X2
innexin inx2-like, transcript variant X9
innexin inx2-like, transcript variant X7
innexin inx2-like, transcript variant X3
innexin inx2-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable cytosolic iron-sulfur protein assembly protein CIAO1, transcript variant X2
probable cytosolic iron-sulfur protein assembly protein CIAO1, transcript variant X3
probable cytosolic iron-sulfur protein assembly protein CIAO1, transcript variant X1
probable cytosolic iron-sulfur protein assembly protein CIAO1, transcript variant X4
probable cytosolic iron-sulfur protein assembly protein CIAO1 isoform X4
thioredoxin domain-containing protein 6-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
dynein intermediate chain 2, ciliary-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
nuclear pore complex protein Nup160-like
glycine-rich cell wall structural protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glycine-rich cell wall structural protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
protein HID1-like, transcript variant X1
protein HID1-like, transcript variant X2
carbonic anhydrase-related protein 10-like
leucine-rich repeat-containing protein 14-like, transcript variant X6
leucine-rich repeat-containing protein 14-like, transcript variant X4
leucine-rich repeat-containing protein 14-like, transcript variant X5
leucine-rich repeat-containing protein 14-like, transcript variant X2
leucine-rich repeat-containing protein 14-like, transcript variant X9
leucine-rich repeat-containing protein 14-like, transcript variant X1
leucine-rich repeat-containing protein 14-like, transcript variant X3
leucine-rich repeat-containing protein 14-like, transcript variant X7
leucine-rich repeat-containing protein 14-like, transcript variant X8
leucine-rich repeat-containing protein 14-like isoform X1
leucine-rich repeat-containing protein 14-like isoform X2
gastrula zinc finger protein XlCGF57.1-like
adenosylhomocysteinase-like 1, transcript variant X9
adenosylhomocysteinase-like 1, transcript variant X8
adenosylhomocysteinase-like 1, transcript variant X5
adenosylhomocysteinase-like 1, transcript variant X4
adenosylhomocysteinase-like 1, transcript variant X1
adenosylhomocysteinase-like 1, transcript variant X2
adenosylhomocysteinase-like 1, transcript variant X3
adenosylhomocysteinase-like 1, transcript variant X6
adenosylhomocysteinase-like 1, transcript variant X10
adenosylhomocysteinase-like 1, transcript variant X7
adenosylhomocysteinase-like 1, transcript variant X11
adenosylhomocysteinase-like 1 isoform X8
adenosylhomocysteinase-like 1 isoform X7
adenosylhomocysteinase-like 1 isoform X5
adenosylhomocysteinase-like 1 isoform X4
adenosylhomocysteinase-like 1 isoform X2
adenosylhomocysteinase-like 1 isoform X3
adenosylhomocysteinase-like 1 isoform X1
adenosylhomocysteinase-like 1 isoform X9
adenosylhomocysteinase-like 1 isoform X6
adenosylhomocysteinase-like 1 isoform X10
required for excision 1-B domain-containing protein-like, transcript variant X1
required for excision 1-B domain-containing protein-like isoform X1
required for excision 1-B domain-containing protein-like, transcript variant X2
required for excision 1-B domain-containing protein-like isoform X2
non-structural maintenance of chromosomes element 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 1A-B-like, transcript variant X1
actin-related protein 2/3 complex subunit 1A-B-like, transcript variant X2
actin-related protein 2/3 complex subunit 1A-B-like
tubulin-specific chaperone A-like, transcript variant X3
tubulin-specific chaperone A-like, transcript variant X2
tubulin-specific chaperone A-like, transcript variant X1
uncharacterized protein DDB_G0284459-like
uncharacterized LOC125047386, transcript variant X2
uncharacterized LOC125047386, transcript variant X5
uncharacterized LOC125047386, transcript variant X3
uncharacterized LOC125047386, transcript variant X4
uncharacterized LOC125047386, transcript variant X1
uncharacterized protein LOC125047386 isoform X2
uncharacterized protein LOC125047386 isoform X4
uncharacterized protein LOC125047386 isoform X3
uncharacterized protein LOC125047386 isoform X1
probable 28S ribosomal protein S26, mitochondrial
sorting nexin-25-like, transcript variant X2
sorting nexin-25-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 8 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 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125025004, transcript variant X2
uncharacterized LOC125025004, transcript variant X1
uncharacterized protein LOC125025004 isoform X2
uncharacterized protein LOC125025004 isoform X1
CBP80/20-dependent translation initiation factor-like
uncharacterized LOC125047492, transcript variant X2
uncharacterized LOC125047492, transcript variant X1
Fanconi anemia core complex-associated protein 24-like
mitochondrial uncoupling protein 4-like, transcript variant X4
mitochondrial uncoupling protein 4-like, transcript variant X6
mitochondrial uncoupling protein 4-like, transcript variant X2
mitochondrial uncoupling protein 4-like, transcript variant X7
mitochondrial uncoupling protein 4-like, transcript variant X3
mitochondrial uncoupling protein 4-like, transcript variant X1
mitochondrial uncoupling protein 4-like, transcript variant X5
mitochondrial uncoupling protein 4-like isoform X1
mitochondrial uncoupling protein 4-like isoform X2
mitochondrial uncoupling protein 4-like isoform X3
dual specificity protein phosphatase 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
proline-rich receptor-like protein kinase PERK9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 61% 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
bromodomain adjacent to zinc finger domain protein 1A-like, transcript variant X2
bromodomain adjacent to zinc finger domain protein 1A-like, transcript variant X1
bromodomain adjacent to zinc finger domain protein 1A-like isoform X2
bromodomain adjacent to zinc finger domain protein 1A-like 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 6 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-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 18 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-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 17 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-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 16 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-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 13 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
prostaglandin E2 receptor EP4 subtype-like isoform X1
prostaglandin E2 receptor EP4 subtype-like isoform X2
prostaglandin E2 receptor EP4 subtype-like isoform X3
prostaglandin E2 receptor EP4 subtype-like isoform X4
probable cyclin-dependent serine/threonine-protein kinase DDB_G0292550
putative uncharacterized protein DDB_G0282133
uncharacterized LOC125025074, transcript variant X2
uncharacterized LOC125025074, transcript variant X3
uncharacterized LOC125025074, 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
mothers against decapentaplegic homolog 3-like
uncharacterized LOC125024984, transcript variant X1
uncharacterized protein LOC125024984 isoform X1
uncharacterized LOC125024984, transcript variant X2
uncharacterized protein LOC125024984 isoform X2
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
similar to RNA sequence, mRNA (same species):INSD:MW051504.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 216 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 216 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
cAMP-specific 3',5'-cyclic phosphodiesterase-like
similar to RNA sequence (same species):INSD:GIYE01008311.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 167 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 167 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125048115, 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 LOC125048115, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
LOW QUALITY PROTEIN: uncharacterized protein LOC125025202
SH3 domain-containing protein C23A1.17-like
similar to RNA sequence (same species):INSD:GHUY01009495.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 496 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 129 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125047250, transcript variant X1
uncharacterized LOC125047250, transcript variant X2
uncharacterized protein LOC125047250 isoform X1
uncharacterized protein LOC125047250 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acanthoscurrin-2-like, transcript variant X5
acanthoscurrin-2-like, transcript variant X4
acanthoscurrin-2-like, transcript variant X1
acanthoscurrin-2-like, transcript variant X2
acanthoscurrin-2-like, transcript variant X6
acanthoscurrin-2-like, transcript variant X9
acanthoscurrin-2-like, transcript variant X3
acanthoscurrin-2-like, transcript variant X8
acanthoscurrin-2-like, transcript variant X7
acanthoscurrin-2-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
KRR1 small subunit processome component homolog, transcript variant X2
KRR1 small subunit processome component homolog, transcript variant X1
KRR1 small subunit processome component homolog isoform X1
KRR1 small subunit processome component homolog isoform X2
uncharacterized LOC125025056, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC125025056, transcript variant X3
uncharacterized LOC125025056, transcript variant X1
uncharacterized protein LOC125025056 isoform X1
uncharacterized protein LOC125025056 isoform X2
uncharacterized protein LOC125025056 isoform X3
molybdenum cofactor biosynthesis protein 1-like
ferrochelatase, mitochondrial-like, transcript variant X1
ferrochelatase, mitochondrial-like isoform X1
ferrochelatase, mitochondrial-like, transcript variant X2
ferrochelatase, mitochondrial-like isoform X2
condensin-2 complex subunit G2-like, transcript variant X3
condensin-2 complex subunit G2-like, transcript variant X1
condensin-2 complex subunit G2-like, transcript variant X2
condensin-2 complex subunit G2-like isoform X2
condensin-2 complex subunit G2-like isoform X1
uncharacterized LOC125025063, transcript variant X3
uncharacterized protein LOC125025063 isoform X2
uncharacterized LOC125025063, transcript variant X1
uncharacterized LOC125025063, transcript variant X2
uncharacterized protein LOC125025063 isoform X1
rap1 GTPase-activating protein 1-like, transcript variant X1
uncharacterized protein LOC125024913 isoform X1
rap1 GTPase-activating protein 1-like, transcript variant X2
rap1 GTPase-activating protein 1-like isoform X2
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X3
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X2
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X1
protein-cysteine N-palmitoyltransferase HHAT-like
zinc finger protein 300-like, transcript variant X1
zinc finger protein 300-like, transcript variant X2
zinc finger protein 300-like, transcript variant X3
glutamate receptor ionotropic, delta-2-like
patched domain-containing protein 3-like, transcript variant X7
patched domain-containing protein 3-like, transcript variant X6
patched domain-containing protein 3-like isoform X3
patched domain-containing protein 3-like, transcript variant X4
patched domain-containing protein 3-like, transcript variant X1
patched domain-containing protein 3-like, transcript variant X3
patched domain-containing protein 3-like, transcript variant X2
patched domain-containing protein 3-like, transcript variant X10
patched domain-containing protein 3-like isoform X1
patched domain-containing protein 3-like, transcript variant X9
patched domain-containing protein 3-like, transcript variant X8
patched domain-containing protein 3-like, transcript variant X5
patched domain-containing protein 3-like isoform X2
patched domain-containing protein 3-like isoform X4
bone morphogenetic protein receptor type-1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
protein roadkill-like, transcript variant X1
protein roadkill-like, transcript variant X2
protein roadkill-like, transcript variant X3
speckle-type POZ protein B-like isoform X1
speckle-type POZ protein B-like isoform X2
speckle-type POZ protein B-like isoform X3
protein roadkill-like, transcript variant X4
uncharacterized LOC125025088, transcript variant X2
uncharacterized LOC125025088, transcript variant X1
uncharacterized LOC125025088, transcript variant X4
uncharacterized LOC125025088, transcript variant X3
uncharacterized protein LOC125025088 isoform X2
uncharacterized protein LOC125025088 isoform X1
uncharacterized LOC125025122, transcript variant X1
uncharacterized LOC125025122, transcript variant X3
uncharacterized LOC125025122, transcript variant X2
uncharacterized protein LOC125025122 isoform X1
uncharacterized protein LOC125025122 isoform X3
uncharacterized protein LOC125025122 isoform X2
microfibril-associated glycoprotein 4-like
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.
uncharacterized LOC125048136, transcript variant X3
uncharacterized LOC125048136, transcript variant X2
uncharacterized LOC125048136, transcript variant X1
uncharacterized protein LOC125048136 isoform X2
uncharacterized protein LOC125048136 isoform X1
uncharacterized protein LOC125048136 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein 63, mitochondrial-like
GTP:AMP phosphotransferase AK3, mitochondrial-like
39S ribosomal protein L44, mitochondrial-like
forkhead box protein K2-like, transcript variant X3
forkhead box protein K2-like, transcript variant X5
forkhead box protein K2-like, transcript variant X2
forkhead box protein K2-like, transcript variant X6
forkhead box protein K2-like, transcript variant X4
forkhead box protein K2-like, transcript variant X1
LOW QUALITY PROTEIN: protein flightless-1-like
mothers against decapentaplegic homolog 6-like
glutenin, high molecular weight subunit DX5-like
carotenoid-cleaving dioxygenase, mitochondrial-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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein DDB_G0271670-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
GATA zinc finger domain-containing protein 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
coiled-coil domain-containing protein 85C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
coiled-coil domain-containing protein 85C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
coiled-coil domain-containing protein 85C-like
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X3
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X5
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X4
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X2
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X1
threonine--tRNA ligase 1, cytoplasmic-like isoform X5
threonine--tRNA ligase 1, cytoplasmic-like isoform X4
threonine--tRNA ligase 1, cytoplasmic-like isoform X2
threonine--tRNA ligase 1, cytoplasmic-like isoform X1
threonine--tRNA ligase 1, cytoplasmic-like isoform X3
hrp65 protein-like, transcript variant X4
hrp65 protein-like, transcript variant X6
hrp65 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
hrp65 protein-like, transcript variant X5
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 30 samples with support for all annotated introns
hrp65 protein-like, transcript variant X7
hrp65 protein-like, transcript variant X1
hrp65 protein-like, transcript variant X2
uncharacterized LOC125025027, transcript variant X1
similar to RNA sequence (same species):INSD:GHUY01004809.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2610 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 28 samples with support for all annotated introns
uncharacterized LOC125025027, transcript variant X2
uncharacterized LOC125025027, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2610 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 11 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 1271 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein argonaute-2-like, transcript variant X2
protein argonaute-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transmembrane emp24 domain-containing protein 1-like
ubiquinol-cytochrome-c reductase complex assembly factor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 69% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125025032, transcript variant X2
uncharacterized LOC125025032, transcript variant X1
uncharacterized protein LOC125025032 isoform X2
uncharacterized protein LOC125025032 isoform X1
glyoxalase domain-containing protein 4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
glyoxalase domain-containing protein 4-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 20 samples with support for all annotated introns
glyoxalase domain-containing protein 4-like, transcript variant X3
glyoxalase domain-containing protein 4-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 35 samples with support for all annotated introns
glyoxalase domain-containing protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
glyoxalase domain-containing protein 4-like isoform X1
glyoxalase domain-containing protein 4-like isoform X3
glyoxalase domain-containing protein 4-like isoform X2
similar to RNA sequence (same species):INSD:GHUY01002105.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 758 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 4 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 599 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
rRNA methyltransferase 1, mitochondrial-like, transcript variant X2
rRNA methyltransferase 1, mitochondrial-like, transcript variant X1
rRNA methyltransferase 1, mitochondrial-like isoform X1
rRNA methyltransferase 1, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
glycine receptor subunit beta-type 4-like
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
calcium-activated chloride channel regulator 1-like
activating signal cointegrator 1 complex subunit 2 homolog
uncharacterized LOC125025044, transcript variant X2
uncharacterized LOC125025044, transcript variant X1
uncharacterized protein LOC125025044 isoform X2
uncharacterized protein LOC125025044 isoform X1
dual specificity protein phosphatase 14-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 37 samples with support for all annotated introns
dual specificity protein phosphatase 14-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 9 samples with support for all annotated introns
uncharacterized LOC125025034, transcript variant X1
uncharacterized LOC125025034, transcript variant X2
uncharacterized protein LOC125025034 isoform X1
uncharacterized protein LOC125025034 isoform X2
mannosyl-oligosaccharide glucosidase-like, transcript variant X1
mannosyl-oligosaccharide glucosidase-like, transcript variant X2
mannosyl-oligosaccharide glucosidase-like isoform X1
mannosyl-oligosaccharide glucosidase-like isoform X2
mitochondrial intermediate peptidase-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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
copper-transporting ATPase 2-like, transcript variant X7
copper-transporting ATPase 2-like, transcript variant X6
copper-transporting ATPase 2-like, transcript variant X10
copper-transporting ATPase 2-like, transcript variant X8
copper-transporting ATPase 2-like, transcript variant X1
copper-transporting ATPase 2-like, transcript variant X9
copper-transporting ATPase 2-like, transcript variant X3
copper-transporting ATPase 2-like, transcript variant X2
copper-transporting ATPase 2-like, transcript variant X5
copper-transporting ATPase 2-like, transcript variant X4
copper-transporting ATPase 2-like isoform X6
copper-transporting ATPase 2-like isoform X4
copper-transporting ATPase 2-like isoform X5
copper-transporting ATPase 2-like isoform X3
copper-transporting ATPase 2-like isoform X2
copper-transporting ATPase 2-like isoform X1
thioredoxin domain-containing protein 2-like
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
dehydrogenase/reductase SDR family member 12-like
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
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 25 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
regulator of MON1-CCZ1 complex-like, transcript variant X1
regulator of MON1-CCZ1 complex-like, transcript variant X3
regulator of MON1-CCZ1 complex-like, transcript variant X5
regulator of MON1-CCZ1 complex-like, transcript variant X2
regulator of MON1-CCZ1 complex-like isoform X1
regulator of MON1-CCZ1 complex-like isoform X3
regulator of MON1-CCZ1 complex-like isoform X5
regulator of MON1-CCZ1 complex-like isoform X2
regulator of MON1-CCZ1 complex-like, transcript variant X4
regulator of MON1-CCZ1 complex-like isoform X4
N-terminal kinase-like protein, transcript variant X2
N-terminal kinase-like protein, transcript variant X1
N-terminal kinase-like protein isoform X1
N-terminal kinase-like protein isoform X2
innexin unc-9-like, transcript variant X1
innexin unc-9-like, transcript variant X2
arylsulfatase I-like, transcript variant X2
arylsulfatase I-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DDB_G0287625-like
solute carrier organic anion transporter family member 74D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger HIT domain-containing protein 3-like
cortactin-binding protein 2-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 32 samples with support for all annotated introns
cortactin-binding protein 2-like, transcript variant X5
cortactin-binding protein 2-like, 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 17 samples with support for all annotated introns
cortactin-binding protein 2-like, transcript variant X6
cortactin-binding protein 2-like, transcript variant X3
cortactin-binding protein 2-like, transcript variant X2
cortactin-binding protein 2-like isoform X1
cortactin-binding protein 2-like isoform X2
glutaminase liver isoform, mitochondrial-like, transcript variant X2
glutaminase liver isoform, mitochondrial-like, transcript variant X1
glutaminase liver isoform, mitochondrial-like, transcript variant X3
glutaminase liver isoform, mitochondrial-like, transcript variant X5
glutaminase liver isoform, mitochondrial-like isoform X2
glutaminase liver isoform, mitochondrial-like isoform X3
glutaminase liver isoform, mitochondrial-like isoform X1
glutaminase liver isoform, mitochondrial-like isoform X5
glutaminase liver isoform, mitochondrial-like, transcript variant X4
glutaminase liver isoform, mitochondrial-like isoform X4
NADPH azoreductase-like, transcript variant X1
NADPH azoreductase-like, transcript variant X2
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
MAGUK p55 subfamily member 7-like, transcript variant X3
MAGUK p55 subfamily member 7-like, transcript variant X2
MAGUK p55 subfamily member 7-like, transcript variant X1
MAGUK p55 subfamily member 7-like isoform X3
MAGUK p55 subfamily member 7-like isoform X2
MAGUK p55 subfamily member 7-like isoform X1
similar to RNA sequence (same species):INSD:GHUY01005092.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 85 bases not found in genome assembly; 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
polycystic kidney disease protein 1-like 2
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
MAPK regulated corepressor interacting protein 2-like
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like, transcript variant X1
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like, transcript variant X2
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like, transcript variant X4
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like, transcript variant X3
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like isoform X3
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like isoform X1
inhibitor of nuclear factor kappa-B kinase subunit epsilon-like isoform X2
acyl-coenzyme A diphosphatase FITM2-like, transcript variant X3
acyl-coenzyme A diphosphatase FITM2-like, transcript variant X4
acyl-coenzyme A diphosphatase FITM2-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 36 samples with support for all annotated introns
acyl-coenzyme A diphosphatase FITM2-like, transcript variant X2
acyl-coenzyme A diphosphatase FITM2-like isoform X1
acyl-coenzyme A diphosphatase FITM2-like isoform X3
acyl-coenzyme A diphosphatase FITM2-like isoform X4
acyl-coenzyme A diphosphatase FITM2-like isoform X2
glycerophosphocholine cholinephosphodiesterase ENPP6-like
glycerophosphocholine cholinephosphodiesterase ENPP6-like, transcript variant X1
glycerophosphocholine cholinephosphodiesterase ENPP6-like, transcript variant X2
uncharacterized protein LOC125024560 isoform X4
transforming acidic coiled-coil-containing protein 3-like
sialic acid synthase-like, transcript variant X1
sialic acid synthase-like, transcript variant X2
AT-rich interactive domain-containing protein 2-like, transcript variant X1
AT-rich interactive domain-containing protein 2-like, transcript variant X2
AT-rich interactive domain-containing protein 2-like, transcript variant X3
AT-rich interactive domain-containing protein 2-like isoform X1
AT-rich interactive domain-containing protein 2-like isoform X2
AT-rich interactive domain-containing protein 2-like isoform X3
similar to RNA sequence (same species):INSD:GIYE01013805.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 126 bases not found in genome assembly; 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 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 126 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
myosin light chain kinase, smooth muscle-like
uncharacterized protein LOC125046299 isoform X1
DNA-directed RNA polymerase II subunit RPB1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 21, 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 6 samples with support for all annotated introns
probable G-protein coupled receptor 21, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable G-protein coupled receptor 21, 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 4 samples with support for all annotated introns
probable G-protein coupled receptor 21, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
probable G-protein coupled receptor 21, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like
zinc finger FYVE domain-containing protein 9-like, transcript variant X1
zinc finger FYVE domain-containing protein 9-like, transcript variant X2
zinc finger FYVE domain-containing protein 9-like, transcript variant X3
zinc finger FYVE domain-containing protein 9-like, transcript variant X4
zinc finger FYVE domain-containing protein 9-like, transcript variant X5
zinc finger FYVE domain-containing protein 9-like isoform X1
zinc finger FYVE domain-containing protein 9-like isoform X2
zinc finger FYVE domain-containing protein 9-like isoform X3
zinc finger FYVE domain-containing protein 9-like isoform X4
zinc finger FYVE domain-containing protein 9-like isoform X5
3'(2'),5'-bisphosphate nucleotidase 1-like, transcript variant X1
3'(2'),5'-bisphosphate nucleotidase 1-like, transcript variant X2
3'(2'),5'-bisphosphate nucleotidase 1-like isoform X1
3'(2'),5'-bisphosphate nucleotidase 1-like isoform X2
cysteine-rich hydrophobic domain-containing protein 2-like
26S proteasome non-ATPase regulatory subunit 1-like
WAS/WASL-interacting protein family member 1-like
integrator complex subunit 2-like, transcript variant X1
integrator complex subunit 2-like, transcript variant X3
integrator complex subunit 2-like, transcript variant X2
integrator complex subunit 2-like isoform X1
integrator complex subunit 2-like isoform X3
integrator complex subunit 2-like isoform X2
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: nitric oxide synthase-like protein
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
nuclear apoptosis-inducing factor 1-like, transcript variant X2
nuclear apoptosis-inducing factor 1-like, transcript variant X1
nuclear apoptosis-inducing factor 1-like isoform X2
nuclear apoptosis-inducing factor 1-like isoform X1
mitochondrial ribosome-associated GTPase 2-like, transcript variant X3
mitochondrial ribosome-associated GTPase 2-like, transcript variant X1
uncharacterized protein LOC125025129 isoform X1
mitochondrial ribosome-associated GTPase 2-like, transcript variant X2
mitochondrial ribosome-associated GTPase 2-like, transcript variant X4
mitochondrial ribosome-associated GTPase 2-like, transcript variant X5
mitochondrial ribosome-associated GTPase 2-like isoform X2
mitochondrial ribosome-associated GTPase 2-like isoform X3
mitochondrial ribosome-associated GTPase 2-like isoform 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 2 samples with support for all annotated introns
solute carrier family 35 member C2-like, transcript variant X1
solute carrier family 35 member C2-like isoform X1
solute carrier family 35 member C2-like, transcript variant X2
solute carrier family 35 member C2-like isoform X2
solute carrier family 35 member C2-like, transcript variant X5
solute carrier family 35 member C2-like isoform X5
solute carrier family 35 member C2-like, transcript variant X3
solute carrier family 35 member C2-like, transcript variant X4
solute carrier family 35 member C2-like isoform X4
solute carrier family 35 member C2-like isoform X3
solute carrier family 35 member C2-like, transcript variant X6
solute carrier family 35 member C2-like, transcript variant X8
solute carrier family 35 member C2-like, transcript variant X7
solute carrier family 35 member C2-like, transcript variant X9
solute carrier family 35 member C2-like isoform X6
solute carrier family 35 member C2-like isoform X7
biogenesis of lysosome-related organelles complex 1 subunit 6-like
choline transporter-like protein 4, transcript variant X3
choline transporter-like protein 4 isoform X3
choline transporter-like protein 4, transcript variant X4
choline transporter-like protein 4 isoform X4
choline transporter-like protein 4, transcript variant X5
choline transporter-like protein 4 isoform X5
choline transporter-like protein 4, transcript variant X2
choline transporter-like protein 4, transcript variant X1
choline transporter-like protein 4 isoform X1
choline transporter-like protein 2 isoform X2
peritrophin-1-like, transcript variant X1
peritrophin-1-like, transcript variant X2
glutamate receptor ionotropic, kainate 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor 4, transcript variant X1
ADP-ribosylation factor 4, transcript variant X2
zinc finger protein 808-like, transcript variant X1
zinc finger protein 808-like, transcript variant X2
PX domain-containing protein kinase-like protein, transcript variant X1
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein, transcript variant X2
PX domain-containing protein kinase-like protein isoform X2
splicing regulatory glutamine/lysine-rich protein 1-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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized protein LOC125047997 isoform X3
uncharacterized protein LOC125047997 isoform X2
uncharacterized protein LOC125047997 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
heparan sulfate 2-O-sulfotransferase 1-like, transcript variant X1
heparan sulfate 2-O-sulfotransferase 1-like, transcript variant X3
heparan sulfate 2-O-sulfotransferase 1-like, transcript variant X5
heparan sulfate 2-O-sulfotransferase 1-like, transcript variant X4
heparan sulfate 2-O-sulfotransferase 1-like, transcript variant X2
heparan sulfate 2-O-sulfotransferase 1-like isoform X1
heparan sulfate 2-O-sulfotransferase 1-like isoform X2
calcium-binding mitochondrial carrier protein Aralar1-like
uncharacterized LOC125047604, transcript variant X1
uncharacterized LOC125047604, transcript variant X2
uncharacterized LOC125047604, transcript variant X4
uncharacterized LOC125047604, transcript variant X3
uncharacterized protein LOC125047604 isoform X1
uncharacterized protein LOC125047604 isoform X2
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial import inner membrane translocase subunit Tim22-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
sodium/calcium exchanger 3-like, transcript variant X1
sodium/calcium exchanger 3-like, transcript variant X2
sodium/calcium exchanger 3-like isoform X1
sodium/calcium exchanger 3-like isoform X2
cilia- and flagella-associated protein 52-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 4
membrane-associated progesterone receptor component 1-like
40-kDa huntingtin-associated protein-like
uncharacterized LOC125024943, transcript variant X1
uncharacterized LOC125024943, transcript variant X2
4-coumarate--CoA ligase 1-like, transcript variant X2
4-coumarate--CoA ligase 1-like, transcript variant X1
4-coumarate--CoA ligase 1-like isoform X2
4-coumarate--CoA ligase 1-like isoform X1
probable low-specificity L-threonine aldolase 2, transcript variant X1
probable low-specificity L-threonine aldolase 2, transcript variant X2
probable low-specificity L-threonine aldolase 2 isoform X1
probable low-specificity L-threonine aldolase 2 isoform X2
vesicle-trafficking protein SEC22b-B-like, transcript variant X1
vesicle-trafficking protein SEC22b-B-like, transcript variant X2
vesicle-trafficking protein SEC22b-B-like isoform X1
vesicle-trafficking protein SEC22b-B-like isoform X2
popeye domain-containing protein 3-like, transcript variant X2
popeye domain-containing protein 3-like, transcript variant X3
popeye domain-containing protein 3-like, transcript variant X5
popeye domain-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
popeye domain-containing protein 3-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 28 samples with support for all annotated introns
blood vessel epicardial substance-like isoform X4
popeye domain-containing protein 3-like isoform X2
popeye domain-containing protein 3-like isoform X1
popeye domain-containing protein 3-like isoform X3
gem-associated protein 5-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 30 samples with support for all annotated introns
gem-associated protein 5-like, transcript variant X1
gem-associated protein 5-like isoform X2
gem-associated protein 5-like isoform X1
spectrin beta chain-like, transcript variant X8
spectrin beta chain-like, transcript variant X10
spectrin beta chain-like, transcript variant X7
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 22 samples with support for all annotated introns
spectrin beta chain-like, transcript variant X4
spectrin beta chain-like, transcript variant X5
spectrin beta chain-like, transcript variant X6
spectrin beta chain-like, transcript variant X1
spectrin beta chain-like, transcript variant X3
spectrin beta chain-like, transcript variant X2
spectrin beta chain-like, transcript variant X9
sorting nexin-29-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sorting nexin-29-like, transcript variant X5
sorting nexin-29-like, transcript variant X1
sorting nexin-29-like, transcript variant X2
sorting nexin-29-like, transcript variant X3
sorting nexin-29-like, transcript variant X9
sorting nexin-29-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sorting nexin-29-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sorting nexin-29-like, transcript variant X7
sorting nexin-29-like, transcript variant X10
sorting nexin-29-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
UDP-xylose and UDP-N-acetylglucosamine transporter-like, transcript variant X2
UDP-xylose and UDP-N-acetylglucosamine transporter-like, transcript variant X1
UDP-xylose and UDP-N-acetylglucosamine transporter-like
signal recognition particle subunit SRP72-like
LOW QUALITY PROTEIN: signal recognition particle subunit SRP72-like
uncharacterized LOC125047328, transcript variant X2
uncharacterized LOC125047328, transcript variant X1
transmembrane protein 245-like, transcript variant X2
transmembrane protein 245-like, transcript variant X3
transmembrane protein 245-like, transcript variant X5
transmembrane protein 245-like, transcript variant X1
transmembrane protein 245-like, transcript variant X4
transmembrane protein 245-like isoform X3
transmembrane protein 245-like isoform X1
transmembrane protein 245-like isoform X2
tetratricopeptide repeat protein 33-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
corticotropin-releasing factor-binding protein-like
heme-binding protein 2-like, transcript variant X1
heme-binding protein 2-like, transcript variant X2
uncharacterized LOC125046639, transcript variant X1
uncharacterized LOC125046639, transcript variant X2
uncharacterized LOC125046639, transcript variant X3
uncharacterized protein LOC125046639 isoform X1
uncharacterized protein LOC125046639 isoform X2
uncharacterized protein LOC125046639 isoform X3
small G protein signaling modulator 3 homolog, 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 6 samples with support for all annotated introns
small G protein signaling modulator 3 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small G protein signaling modulator 3 homolog
gametogenetin-binding protein 2-like, transcript variant X2
gametogenetin-binding protein 2-like, transcript variant X1
gametogenetin-binding protein 2-like isoform X1
gametogenetin-binding protein 2-like isoform X2
solute carrier organic anion transporter family member 74D-like, transcript variant X1
solute carrier organic anion transporter family member 74D-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 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 74D-like, transcript variant X5
solute carrier organic anion transporter family member 74D-like, transcript variant X4
solute carrier organic anion transporter family member 74D-like, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 2-like
dihydropteridine reductase-like, transcript variant X3
dihydropteridine reductase-like, transcript variant X5
dihydropteridine reductase-like, transcript variant X4
dihydropteridine reductase-like, transcript variant X2
dihydropteridine reductase-like, transcript variant X1
dihydropteridine reductase-like isoform X2
dihydropteridine reductase-like isoform X3
dihydropteridine reductase-like isoform X1
SPEG neighbor protein-like, transcript variant X4
SPEG neighbor protein-like, transcript variant X1
SPEG neighbor protein-like, transcript variant X2
SPEG neighbor protein-like, transcript variant X3
uncharacterized protein LOC125047634 isoform X1
uncharacterized protein LOC125047634 isoform X2
double-stranded RNA-specific editase 1-like, transcript variant X3
double-stranded RNA-specific editase 1-like, transcript variant X2
double-stranded RNA-specific editase 1-like, transcript variant X1
double-stranded RNA-specific editase 1-like isoform X3
double-stranded RNA-specific editase 1-like isoform X2
double-stranded RNA-specific editase 1-like isoform X1
protein sax-3-like, transcript variant X1
protein sax-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
deoxyribonuclease-1-like, transcript variant X1
deoxyribonuclease-1-like, transcript variant X2
1-aminocyclopropane-1-carboxylate synthase-like protein 1, transcript variant X3
1-aminocyclopropane-1-carboxylate synthase-like protein 1, transcript variant X1
1-aminocyclopropane-1-carboxylate synthase-like protein 1, transcript variant X2
1-aminocyclopropane-1-carboxylate synthase-like protein 1, transcript variant X4
1-aminocyclopropane-1-carboxylate synthase-like protein 1
protein numb-like, transcript variant X4
protein numb-like, transcript variant X5
protein numb-like, transcript variant X1
protein numb-like, transcript variant X3
protein numb-like, transcript variant X2
keratin, type I cytoskeletal 9-like, transcript variant X1
keratin, type I cytoskeletal 9-like, transcript variant X3
keratin, type I cytoskeletal 9-like, transcript variant X2
ubiquinone biosynthesis protein COQ9, mitochondrial-like, transcript variant X2
ubiquinone biosynthesis protein COQ9, mitochondrial-like isoform X2
ubiquinone biosynthesis protein COQ9, mitochondrial-like, transcript variant X1
putative GPI-anchored protein pfl2, transcript variant X1
putative GPI-anchored protein pfl2, transcript variant X3
putative GPI-anchored protein pfl2, 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 4 samples with support for all annotated introns
putative GPI-anchored protein pfl2 isoform X1
putative GPI-anchored protein pfl2 isoform X3
putative GPI-anchored protein pfl2 isoform X2
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007, transcript variant X3
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007, 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 22 samples with support for all annotated introns
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007, transcript variant X1
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007 isoform X3
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007 isoform X2
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007 isoform X1
signal recognition particle receptor subunit beta-like
adenylate kinase-like, transcript variant X1
adenylate kinase-like, transcript variant X2
sorting nexin-17-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 23 samples with support for all annotated introns
sorting nexin-17-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 1 sample with support for all annotated introns
sorting nexin-17-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
inorganic pyrophosphatase-like, transcript variant X2
inorganic pyrophosphatase-like, transcript variant X1
inorganic pyrophosphatase-like isoform X2
inorganic pyrophosphatase-like isoform X1
folylpolyglutamate synthase, mitochondrial-like
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X2
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
sodium-coupled monocarboxylate transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
nuclear pore complex protein DDB_G0274915-like, transcript variant X5
nuclear pore complex protein DDB_G0274915-like, transcript variant X4
nuclear pore complex protein DDB_G0274915-like, transcript variant X3
nuclear pore complex protein DDB_G0274915-like, transcript variant X2
nuclear pore complex protein DDB_G0274915-like, transcript variant X1
nuclear pore complex protein DDB_G0274915-like isoform X5
nuclear pore complex protein DDB_G0274915-like isoform X4
nuclear pore complex protein DDB_G0274915-like isoform X3
nuclear pore complex protein Nup214-like isoform X2
nuclear pore complex protein Nup214-like isoform 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 7 samples with support for all annotated introns
uncharacterized LOC125025018, transcript variant X2
uncharacterized LOC125025018, transcript variant X1
uncharacterized LOC125025018, transcript variant X3
uncharacterized protein LOC125025018 isoform X2
uncharacterized protein LOC125025018 isoform X1
uncharacterized protein LOC125025018 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
motile sperm domain-containing protein 1-like, transcript variant X3
motile sperm domain-containing protein 1-like, transcript variant X5
motile sperm domain-containing protein 1-like, transcript variant X1
motile sperm domain-containing protein 1-like, transcript variant X4
motile sperm domain-containing protein 1-like, transcript variant X2
motile sperm domain-containing protein 1-like isoform X1
motile sperm domain-containing protein 1-like isoform X2
motile sperm domain-containing protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125024998, 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 24 samples with support for all annotated introns
uncharacterized LOC125024998, transcript variant X2
uncharacterized LOC125024998, transcript variant X1
uncharacterized protein LOC125024998 isoform X1
uncharacterized protein LOC125024998 isoform X2
uncharacterized LOC125024999, transcript variant X2
uncharacterized protein LOC125024999 isoform X2
uncharacterized LOC125024999, transcript variant X1
uncharacterized protein LOC125024999 isoform X1
similar to RNA sequence (same species):INSD:GIYE01044609.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 187 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 187 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
nascent polypeptide-associated complex subunit alpha-like
beta-1,3-galactosyltransferase 5-like, transcript variant X1
beta-1,3-galactosyltransferase 5-like, transcript variant X2
beta-1,3-galactosyltransferase 5-like isoform X1
beta-1,3-galactosyltransferase 5-like, transcript variant X3
beta-1,3-galactosyltransferase 5-like isoform X2
progestin and adipoQ receptor family member 4-like, transcript variant X2
progestin and adipoQ receptor family member 4-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 29 samples with support for all annotated introns
progestin and adipoQ receptor family member 4-like isoform X1
progestin and adipoQ receptor family member 4-like isoform X2
HIG1 domain family member 1C-like, transcript variant X2
HIG1 domain family member 1C-like, transcript variant X1
HIG1 domain family member 1C-like isoform X1
HIG1 domain family member 1C-like isoform X2
ankyrin repeat and LEM domain-containing protein 2-like, transcript variant X2
ankyrin repeat and LEM domain-containing protein 2-like, transcript variant X1
ankyrin repeat and LEM domain-containing protein 2-like
carbohydrate sulfotransferase 11-like, transcript variant X1
carbohydrate sulfotransferase 11-like, transcript variant X2
carbohydrate sulfotransferase 11-like isoform X1
carbohydrate sulfotransferase 11-like isoform X2
uncharacterized LOC125047803, transcript variant X2
uncharacterized LOC125047803, transcript variant X1
uncharacterized protein LOC125047803 isoform X2
uncharacterized protein LOC125047803 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myotubularin-related protein 2-like, transcript variant X4
myotubularin-related protein 2-like, transcript variant X3
myotubularin-related protein 2-like, transcript variant X1
myotubularin-related protein 2-like, transcript variant X2
myotubularin-related protein 2-like isoform X3
myotubularin-related protein 2-like isoform X2
myotubularin-related protein 2-like isoform X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like, transcript variant X2
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X1
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X3
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X2
ATP-binding cassette sub-family B member 10, mitochondrial-like
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
brahma-associated protein of 60 kDa-like, transcript variant X3
brahma-associated protein of 60 kDa-like, transcript variant X2
brahma-associated protein of 60 kDa-like, transcript variant X1
brahma-associated protein of 60 kDa-like isoform X3
brahma-associated protein of 60 kDa-like isoform X2
brahma-associated protein of 60 kDa-like isoform X1
hepatocyte nuclear factor 4-gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hepatocyte nuclear factor 4-gamma-like, transcript variant X3
hepatocyte nuclear factor 4-gamma-like, transcript variant X2
hepatocyte nuclear factor 4-gamma-like isoform X1
hepatocyte nuclear factor 4-gamma-like isoform X2
mitochondrial amidoxime reducing component 2-like, transcript variant X1
mitochondrial amidoxime reducing component 2-like, transcript variant X2
mitochondrial amidoxime reducing component 2-like
cytosolic carboxypeptidase-like protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5, transcript variant X2
cytosolic carboxypeptidase-like protein 5
probable helicase with zinc finger domain
sideroflexin-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
sideroflexin-2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sideroflexin-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns