Penaeus chinensis breed Huanghai No. 1 chromosome 13, 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\nCM032938.1.\nAssembly name: ASM1920278v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2021/07/13. The\noriginal whole-genome shotgun project has the accession\nJAGKSU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Date :: 2020\nAssembly Method :: FALCON-Unzip v. MAY-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 150.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Penaeus chinensis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
conservation base of Haifeng Aquaculture Co., Ltd.
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
COORDINATES: polyA evidence [ECO:0006239]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: chorion peroxidase-like
mitochondrial enolase superfamily member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial enolase superfamily member 1-like, transcript variant X6
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 7 samples with support for all annotated introns
mitochondrial enolase superfamily member 1-like, transcript variant X3
mitochondrial enolase superfamily member 1-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 8 samples with support for all annotated introns
mitochondrial enolase superfamily member 1-like, transcript variant X5
mitochondrial enolase superfamily member 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial enolase superfamily member 1-like
CD151 antigen-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 3 samples with support for all annotated introns
CD151 antigen-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 17 samples with support for all annotated introns
CD151 antigen-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
general transcription factor II-I repeat domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
WW domain-containing protein C660.06-like, transcript variant X1
WW domain-containing protein C660.06-like, transcript variant X3
WW domain-containing protein C660.06-like isoform X1
ATP-dependent RNA helicase DBP2-A-like isoform X3
WW domain-containing protein C660.06-like, transcript variant X2
WW domain-containing protein C660.06-like isoform X2
protein white-like, transcript variant X2
protein white-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
relaxin receptor 1-like, transcript variant X2
relaxin receptor 1-like, transcript variant X1
uncharacterized LOC125031504, transcript variant X1
uncharacterized LOC125031504, transcript variant X2
uncharacterized LOC125031504, transcript variant X3
uncharacterized protein LOC125031504 isoform X1
uncharacterized protein LOC125031504 isoform X2
leucine-rich repeat extensin-like protein 2
LOW QUALITY PROTEIN: leucine-rich repeat extensin-like protein 2
glycine-rich cell wall structural protein 1-like
putative uncharacterized protein YHR217C
tubulin alpha-3 chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tubulin alpha-3 chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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
heat shock protein 75 kDa, mitochondrial-like
probable G-protein coupled receptor No18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
protein Mo25-like, transcript variant X1
protein Mo25-like, transcript variant X3
protein Mo25-like, transcript variant X2
LITAF domain-containing protein-like, transcript variant X1
LITAF domain-containing protein-like, transcript variant X3
LITAF domain-containing protein-like, transcript variant X2
LITAF domain-containing protein-like, transcript variant X4
LITAF domain-containing protein-like isoform X1
LITAF domain-containing protein-like isoform X2
uncharacterized LOC125031538, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125031538, transcript variant X1
uncharacterized protein LOC125031538 isoform X2
uncharacterized protein LOC125031538 isoform X1
uncharacterized aarF domain-containing protein kinase 5-like
LOW QUALITY PROTEIN: uncharacterized aarF domain-containing protein kinase 5-like
LOW QUALITY PROTEIN: uncharacterized protein LOC125031876
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125031408, transcript variant X3
uncharacterized LOC125031408, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125031408, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125031408, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 4H-like, transcript variant X3
eukaryotic translation initiation factor 4H-like, transcript variant X1
eukaryotic translation initiation factor 4H-like, transcript variant X2
eukaryotic translation initiation factor 4H-like isoform X2
eukaryotic translation initiation factor 4H-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 27 samples with support for all annotated introns
28S ribosomal protein S2, mitochondrial-like, transcript variant X1
28S ribosomal protein S2, mitochondrial-like isoform X1
28S ribosomal protein S2, mitochondrial-like, transcript variant X3
uncharacterized protein LOC125031470 isoform X3
28S ribosomal protein S2, mitochondrial-like, transcript variant X4
28S ribosomal protein S2, mitochondrial-like, transcript variant X2
28S ribosomal protein S2, mitochondrial-like isoform X2
28S ribosomal protein S2, mitochondrial-like isoform X4
cytochrome b-c1 complex subunit 6, mitochondrial-like
S-formylglutathione hydrolase-like, transcript variant X1
S-formylglutathione hydrolase-like, transcript variant X4
S-formylglutathione hydrolase-like, transcript variant X3
S-formylglutathione hydrolase-like, transcript variant X2
S-formylglutathione hydrolase-like isoform X1
S-formylglutathione hydrolase-like isoform X2
S-formylglutathione hydrolase-like isoform X3
kinase suppressor of Ras 2-like, transcript variant X2
kinase suppressor of Ras 2-like, transcript variant X1
kinase suppressor of Ras 2-like, transcript variant X3
kinase suppressor of Ras 2-like, transcript variant X4
kinase suppressor of Ras 2-like, transcript variant X5
kinase suppressor of Ras 2-like, transcript variant X6
kinase suppressor of Ras 2-like isoform X1
kinase suppressor of Ras 2-like isoform X2
kinase suppressor of Ras 2-like isoform X3
kinase suppressor of Ras 2-like isoform X5
kinase suppressor of Ras 2-like isoform X4
zinc finger CCCH domain-containing protein 13-like
uncharacterized LOC125031519, transcript variant X2
uncharacterized LOC125031519, transcript variant X1
uncharacterized protein LOC125031519 isoform X2
uncharacterized protein LOC125031519 isoform X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X4
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X5
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X7
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X8
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X6
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 isoform X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 isoform X1
cytochrome P450 3A29-like, transcript variant X1
cytochrome P450 3A29-like, transcript variant X2
X-linked retinitis pigmentosa GTPase regulator-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: X-linked retinitis pigmentosa GTPase regulator-like
palmitoyltransferase ZDHHC18-like, transcript variant X1
palmitoyltransferase ZDHHC18-like, transcript variant X2
palmitoyltransferase ZDHHC18-like, transcript variant X3
palmitoyltransferase ZDHHC18-like isoform X1
palmitoyltransferase ZDHHC18-like isoform X2
uncharacterized LOC125031428, transcript variant X4
uncharacterized LOC125031428, transcript variant X5
uncharacterized LOC125031428, transcript variant X6
uncharacterized LOC125031428, transcript variant X3
uncharacterized LOC125031428, transcript variant X2
uncharacterized LOC125031428, transcript variant X7
uncharacterized LOC125031428, transcript variant X1
uncharacterized LOC125031428, transcript variant X8
uncharacterized protein LOC125031428 isoform X2
uncharacterized protein LOC125031428 isoform X3
uncharacterized protein LOC125031428 isoform X1
uncharacterized protein LOC125031428 isoform X4
uncharacterized LOC125031428, transcript variant X9
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X3
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X4
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X5
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X6
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X7
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X1
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X9
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X8
longitudinals lacking protein, isoforms H/M/V-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 7 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X11
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 9 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X4
longitudinals lacking protein, isoforms H/M/V-like isoform X5
longitudinals lacking protein, isoforms H/M/V-like isoform X7
longitudinals lacking protein, isoforms H/M/V-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X6
longitudinals lacking protein, isoforms H/M/V-like isoform X2
longitudinals lacking protein, isoforms H/M/V-like isoform X8
longitudinals lacking protein, isoforms H/M/V-like isoform X9
longitudinals lacking protein, isoforms H/M/V-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 14 samples with support for all annotated introns
amidophosphoribosyltransferase-like, transcript variant X2
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 16 samples with support for all annotated introns
amidophosphoribosyltransferase-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 17 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like, transcript variant X5
serine/arginine repetitive matrix protein 1-like, transcript variant X4
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like, transcript variant X7
serine/arginine repetitive matrix protein 1-like, transcript variant X3
serine/arginine repetitive matrix protein 1-like, transcript variant X6
serine/arginine repetitive matrix protein 1-like isoform X2
serine/arginine repetitive matrix protein 2-like isoform X3
serine/arginine repetitive matrix protein 2-like isoform X1
dual specificity mitogen-activated protein kinase kinase 1-like
aarF domain-containing protein kinase 1-like, transcript variant X1
aarF domain-containing protein kinase 1-like, transcript variant X2
aarF domain-containing protein kinase 1-like isoform X1
aarF domain-containing protein kinase 1-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: protein disulfide-isomerase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat extensin-like protein 3
vesicular integral-membrane protein VIP36-like
LOW QUALITY PROTEIN: peroxisome biogenesis factor 2-like
post-GPI attachment to proteins factor 3-like
cilia- and flagella-associated protein 45-like
GTP-binding protein Di-Ras2-like, transcript variant X2
GTP-binding protein Di-Ras2-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs adt-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
crustacean calcium-binding protein 23-like
serine/arginine repetitive matrix protein 1-like isoform X4
serine/arginine repetitive matrix protein 1-like isoform X3
serine/arginine repetitive matrix protein 1-like isoform X1
polymerase delta-interacting protein 2-like
NADPH--cytochrome P450 reductase-like, transcript variant X1
NADPH--cytochrome P450 reductase-like, transcript variant X2
NADPH--cytochrome P450 reductase-like, transcript variant X3
NADPH--cytochrome P450 reductase-like isoform X1
NADPH--cytochrome P450 reductase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
NADPH--cytochrome P450 reductase-like isoform X2
uncharacterized LOC125031724, transcript variant X1
uncharacterized LOC125031724, transcript variant X2
uncharacterized LOC125031724, transcript variant X3
palmitoyltransferase akr1-like, transcript variant X2
palmitoyltransferase akr1-like, transcript variant X3
palmitoyltransferase akr1-like, transcript variant X1
palmitoyltransferase akr1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GHUY01009407.1
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 549 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 261 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
proline-rich protein 36-like, transcript variant X2
proline-rich protein 36-like, transcript variant X1
28S ribosomal protein S31, mitochondrial-like
LOW QUALITY PROTEIN: 28S ribosomal protein S31, mitochondrial-like
uncharacterized LOC125031786, transcript variant X2
uncharacterized protein LOC125031786 isoform X2
uncharacterized LOC125031786, transcript variant X1
uncharacterized protein LOC125031786 isoform X1
uncharacterized LOC125031910, transcript variant X1
uncharacterized LOC125031910, transcript variant X2
uncharacterized protein LOC125031910 isoform X1
uncharacterized protein LOC125031910 isoform X2
uncharacterized LOC125031889, transcript variant X1
uncharacterized LOC125031889, transcript variant X2
probable serine/threonine-protein kinase kinX, transcript variant X5
probable serine/threonine-protein kinase kinX, transcript variant X2
probable serine/threonine-protein kinase kinX, transcript variant X4
probable serine/threonine-protein kinase kinX, transcript variant X1
probable serine/threonine-protein kinase kinX, transcript variant X3
uncharacterized protein LOC125031710 isoform X5
probable serine/threonine-protein kinase kinX isoform X2
probable serine/threonine-protein kinase kinX isoform X4
probable serine/threonine-protein kinase kinX isoform X1
probable serine/threonine-protein kinase kinX isoform X3
protein gustavus-like, transcript variant X2
protein gustavus-like, transcript variant X1
uncharacterized protein LOC125031438 isoform X1
protein kinase C-binding protein NELL2-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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
stAR-related lipid transfer protein 13-like, transcript variant X2
stAR-related lipid transfer protein 13-like, transcript variant X1
stAR-related lipid transfer protein 13-like isoform X2
stAR-related lipid transfer protein 13-like isoform X1
aspartate aminotransferase, cytoplasmic-like
BSD domain-containing protein 1-like, transcript variant X1
BSD domain-containing protein 1-like, transcript variant X4
BSD domain-containing protein 1-like, transcript variant X3
BSD domain-containing protein 1-like isoform X1
BSD domain-containing protein 1-like isoform X3
BSD domain-containing protein 1-B-like isoform X4
BSD domain-containing protein 1-like, transcript variant X2
BSD domain-containing protein 1-like isoform X2
POU domain, class 4, transcription factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
glycine, alanine and asparagine-rich protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CCR4-NOT transcription complex subunit 1-like, transcript variant X5
CCR4-NOT transcription complex subunit 1-like, transcript variant X1
CCR4-NOT transcription complex subunit 1-like, transcript variant X3
CCR4-NOT transcription complex subunit 1-like, transcript variant X6
CCR4-NOT transcription complex subunit 1-like, transcript variant X4
CCR4-NOT transcription complex subunit 1-like, transcript variant X2
CCR4-NOT transcription complex subunit 1-like, transcript variant X8
CCR4-NOT transcription complex subunit 1-like isoform X1
CCR4-NOT transcription complex subunit 1-like isoform X3
CCR4-NOT transcription complex subunit 1-like isoform X6
CCR4-NOT transcription complex subunit 1-like isoform X4
CCR4-NOT transcription complex subunit 1-like isoform X2
CCR4-NOT transcription complex subunit 1-like isoform X8
CCR4-NOT transcription complex subunit 1-like isoform X5
CCR4-NOT transcription complex subunit 1-like, transcript variant X7
CCR4-NOT transcription complex subunit 1-like isoform X7
hippocampus abundant transcript-like protein 1
similar to RNA sequence (same species):INSD:GHUY01000461.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1769 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 1425 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: 29 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
LOW QUALITY PROTEIN: 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase-like
serine/threonine-protein phosphatase 2B catalytic subunit 3-like
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 15 samples with support for all annotated introns
tudor and KH domain-containing protein homolog
uncharacterized LOC125031729, transcript variant X1
uncharacterized LOC125031729, transcript variant X2
uncharacterized protein LOC125031729 isoform X1
uncharacterized protein LOC125031729 isoform X2
serine/threonine-protein kinase rio2-like
LOW QUALITY PROTEIN: serine/threonine-protein kinase rio2-like
LOW QUALITY PROTEIN: oligopeptidase A-like
grpE protein homolog 1, mitochondrial-like
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X3
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X1
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X2
ELKS/Rab6-interacting/CAST family member 1-like
spindle and kinetochore-associated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
similar to RNA sequence (same species):INSD:GHUY01007305.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 122 bases not found in genome assembly
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
translocon-associated protein subunit gamma-like
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 4 samples with support for all annotated introns
nicotinamide phosphoribosyltransferase-like
aldehyde dehydrogenase, dimeric NADP-preferring-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 75% 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: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
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 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 5C-like isoform X1
zinc finger protein ZFAT-like isoform X4
transcription factor GAGA-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 19 samples with support for all annotated introns
transcription factor GAGA-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
male-specific lethal 1 homolog, 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 16 samples with support for all annotated introns
male-specific lethal 1 homolog, 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 26 samples with support for all annotated introns
male-specific lethal 1 homolog isoform X1
male-specific lethal 1 homolog isoform X2
UV radiation resistance-associated protein-like, transcript variant X1
UV radiation resistance-associated protein-like, transcript variant X3
UV radiation resistance-associated protein-like, transcript variant X2
UV radiation resistance-associated protein-like isoform X2
uncharacterized protein LOC125031452 isoform X1
ATP synthase mitochondrial F1 complex assembly factor 1-like
neuronal acetylcholine receptor subunit alpha-7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
acetylcholine receptor subunit alpha-type unc-63-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
acetylcholine receptor subunit beta-like 1, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01001584.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 787 bases not found in genome assembly
acetylcholine receptor subunit beta-like 1, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 401 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
acetylcholine receptor subunit beta-like 1 isoform X2
acetylcholine receptor subunit beta-like 1 isoform X1
acetylcholine receptor subunit beta-like 1, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 787 bases not found in genome assembly; 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, including 1 sample with support for all annotated introns
acetylcholine receptor subunit beta-like 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 50% 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 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
adhesion G-protein coupled receptor D1-like, transcript variant X3
adhesion G-protein coupled receptor D1-like, transcript variant X1
adhesion G-protein coupled receptor D1-like, transcript variant X2
adhesion G-protein coupled receptor D1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-coupled receptor kinase 2-like
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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125031759, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125031759, transcript variant X3
uncharacterized LOC125031759, transcript variant X1
uncharacterized protein LOC125031759 isoform X1
uncharacterized protein LOC125031759 isoform X2
uncharacterized protein LOC125031759 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 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: 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: 67% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125031443, transcript variant X3
uncharacterized LOC125031443, transcript variant X2
uncharacterized LOC125031443, transcript variant X1
uncharacterized protein LOC125031443 isoform X1
uncharacterized protein LOC125031443 isoform X2
uncharacterized protein LOC125031443 isoform X3
cyclin-dependent kinase inhibitor 1C-like
1,4-alpha-glucan-branching enzyme-like, transcript variant X1
1,4-alpha-glucan-branching enzyme-like, transcript variant X2
1,4-alpha-glucan-branching enzyme-like isoform X2
1,4-alpha-glucan-branching enzyme-like isoform X1
nicotinamide phosphoribosyltransferase-like, transcript variant X2
nicotinamide phosphoribosyltransferase-like, transcript variant X1
nicotinamide phosphoribosyltransferase-like, transcript variant X3
nicotinamide phosphoribosyltransferase-like isoform X1
nicotinamide phosphoribosyltransferase-like isoform X3
nicotinamide phosphoribosyltransferase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
leptin receptor gene-related protein-like, transcript variant X1
leptin receptor gene-related protein-like isoform X1
leptin receptor gene-related protein-like, transcript variant X2
leptin receptor gene-related protein-like isoform X2
rho family-interacting cell polarization regulator 2-like, transcript variant X1
rho family-interacting cell polarization regulator 2-like, transcript variant X2
rho family-interacting cell polarization regulator 2-like isoform X1
rho family-interacting cell polarization regulator 2-like isoform X2
rho family-interacting cell polarization regulator 2-like, transcript variant X3
rho family-interacting cell polarization regulator 2-like isoform X3
developmentally-regulated GTP-binding protein 2-like
palmitoyltransferase ZDHHC23-like, transcript variant X1
palmitoyltransferase ZDHHC23-like, transcript variant X3
palmitoyltransferase ZDHHC23-like, transcript variant X2
palmitoyltransferase ZDHHC23-like isoform X1
palmitoyltransferase ZDHHC23-B-like isoform X2
PR domain zinc finger protein 15-like, transcript variant X1
PR domain zinc finger protein 15-like, transcript variant X3
PR domain zinc finger protein 15-like, transcript variant X2
PR domain zinc finger protein 15-like isoform X1
PR domain zinc finger protein 15-like isoform X2
sodium- and chloride-dependent glycine transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125031758, transcript variant X2
uncharacterized LOC125031758, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
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 2 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 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 33% 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 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 41% 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 33% coverage of the annotated genomic feature by RNAseq alignments
biogenesis of lysosome-related organelles complex 1 subunit 5-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 38 samples with support for all annotated introns
biogenesis of lysosome-related organelles complex 1 subunit 5-like isoform X1
biogenesis of lysosome-related organelles complex 1 subunit 5-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 12 samples with support for all annotated introns
biogenesis of lysosome-related organelles complex 1 subunit 5-like isoform X2
nucleolar protein 58-like, transcript variant X1
nucleolar protein 58-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DDB_G0271670-like
ankyrin repeat domain-containing protein 17-like, transcript variant X1
ankyrin repeat domain-containing protein 17-like, transcript variant X2
ankyrin repeat domain-containing protein 17-like isoform X1
ankyrin repeat domain-containing protein 17-like isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs adt-1-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs adt-1-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs adt-1-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs adt-1-like isoform X2
aquaporin-11-like, transcript variant X2
aquaporin-11-like, transcript variant X1
WW domain-containing adapter protein with coiled-coil-like, transcript variant X4
WW domain-containing adapter protein with coiled-coil-like, transcript variant X3
WW domain-containing adapter protein with coiled-coil-like, transcript variant X2
WW domain-containing adapter protein with coiled-coil-like, transcript variant X1
WW domain-containing adapter protein with coiled-coil-like isoform X2
WW domain-containing adapter protein with coiled-coil-like isoform X1
tRNA (cytosine(38)-C(5))-methyltransferase-like, transcript variant X1
tRNA (cytosine(38)-C(5))-methyltransferase-like, transcript variant X2
tRNA (cytosine(38)-C(5))-methyltransferase-like
integrator complex subunit 12-like, transcript variant X1
integrator complex subunit 12-like, transcript variant X3
integrator complex subunit 12-like, transcript variant X2
integrator complex subunit 12-like isoform X1
integrator complex subunit 12-like isoform X2
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription elongation factor S-II-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
putative E3 ubiquitin-protein ligase UBR7
equilibrative nucleobase transporter 1-like, transcript variant X2
equilibrative nucleobase transporter 1-like, transcript variant X1
equilibrative nucleobase transporter 1-like, transcript variant X3
equilibrative nucleobase transporter 1-like, transcript variant X4
equilibrative nucleobase transporter 1-like isoform X1
equilibrative nucleobase transporter 1-like isoform X2
glucose-6-phosphatase catalytic subunit 1-like
uncharacterized LOC125031746, transcript variant X1
uncharacterized LOC125031746, transcript variant X2
uncharacterized LOC125031927, transcript variant X3
uncharacterized LOC125031927, transcript variant X4
uncharacterized LOC125031927, transcript variant X2
uncharacterized LOC125031927, transcript variant X1
uncharacterized protein LOC125031927 isoform X1
uncharacterized protein LOC125031927 isoform X3
uncharacterized protein LOC125031927 isoform X4
uncharacterized protein LOC125031927 isoform X2
discoidin domain-containing receptor 2-like, transcript variant X1
discoidin domain-containing receptor 2-like, transcript variant X3
discoidin domain-containing receptor 2-like, transcript variant X2
discoidin domain-containing receptor 2-like isoform X1
discoidin domain-containing receptor 2-like isoform X3
discoidin domain-containing receptor 2-like isoform X2
myeloid zinc finger 1-like, transcript variant X34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X31
myeloid zinc finger 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X2
myeloid zinc finger 1-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 28 samples with support for all annotated introns
myeloid zinc finger 1-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
myeloid zinc finger 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X1
myeloid zinc finger 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X5
myeloid zinc finger 1-like, transcript variant X6
myeloid zinc finger 1-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
myeloid zinc finger 1-like, transcript variant X32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7A-like isoform X29
myeloid zinc finger 1-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X7
myeloid zinc finger 1-like, transcript variant X26
protein tramtrack, beta isoform-like isoform X24
myeloid zinc finger 1-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X15
myeloid zinc finger 1-like, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X21
myeloid zinc finger 1-like, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X23
myeloid zinc finger 1-like, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X20
myeloid zinc finger 1-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X11
myeloid zinc finger 1-like, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X22
myeloid zinc finger 1-like, transcript variant X31
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7A-like isoform X28
myeloid zinc finger 1-like, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X18
myeloid zinc finger 1-like, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
myeloid zinc finger 1-like, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7A-like isoform X26
myeloid zinc finger 1-like, transcript variant X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger protein 236-like isoform X19
myeloid zinc finger 1-like, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X17
myeloid zinc finger 1-like, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7A-like isoform X27
myeloid zinc finger 1-like, transcript variant X33
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 22 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X30
myeloid zinc finger 1-like, transcript variant X11
myeloid zinc finger 1-like, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X25
myeloid zinc finger 1-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
myeloid zinc finger 1-like, transcript variant X18
protein tramtrack, beta isoform-like isoform X16
myeloid zinc finger 1-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
zinc finger protein 467-like isoform X10
myeloid zinc finger 1-like, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X13
myeloid zinc finger 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7A-like isoform X3
myeloid zinc finger 1-like, transcript variant X14
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 33 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X12
myeloid zinc finger 1-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
protein tramtrack, alpha isoform-like isoform X14
myeloid zinc finger 1-like, transcript variant X38
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 23 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X35
myeloid zinc finger 1-like, transcript variant X37
protein tramtrack, beta isoform-like isoform X34
myeloid zinc finger 1-like, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myeloid zinc finger 1-like, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X33
protein tramtrack, alpha isoform-like isoform X32
casein kinase I-like, transcript variant X1
casein kinase I-like, transcript variant X4
casein kinase I-like, transcript variant X5
casein kinase I-like, transcript variant X2
casein kinase I-like, transcript variant X3
longitudinals lacking protein, isoforms A/B/D/L-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 27 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X1
longitudinals lacking protein, isoforms A/B/D/L-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 22 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X9
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X8
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X16
longitudinals lacking protein, isoforms A/B/D/L-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 36 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X11
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X18
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X21
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 22 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X20
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X15
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X13
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X30
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X32
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 32 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X37
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 21 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X35
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X34
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X33
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X29
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X24
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 30 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X25
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X28
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X22
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 38 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X39
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X27
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X26
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X40
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 27 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X36
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X45
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 33 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X41
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X42
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 30 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X31
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X44
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 27 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X43
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X46
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X47
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X2
longitudinals lacking protein, isoforms H/M/V-like isoform X17
longitudinals lacking protein, isoforms H/M/V-like isoform X14
longitudinals lacking protein, isoforms H/M/V-like isoform X25
longitudinals lacking protein, isoforms H/M/V-like isoform X41
longitudinals lacking protein, isoforms H/M/V-like isoform X39
longitudinals lacking protein, isoforms H/M/V-like isoform X10
longitudinals lacking protein, isoforms H/M/V-like isoform X34
longitudinals lacking protein, isoforms H/M/V-like isoform X12
longitudinals lacking protein, isoforms H/M/V-like isoform X27
longitudinals lacking protein, isoforms H/M/V-like isoform X32
longitudinals lacking protein, isoforms H/M/V-like isoform X30
longitudinals lacking protein, isoforms H/M/V-like isoform X29
longitudinals lacking protein, isoforms H/M/V-like isoform X28
longitudinals lacking protein, isoforms H/M/V-like isoform X15
longitudinals lacking protein, isoforms H/M/V-like isoform X33
longitudinals lacking protein, isoforms A/B/D/L-like isoform X16
longitudinals lacking protein, isoforms A/B/D/L-like isoform X13
longitudinals lacking protein, isoforms H/M/V-like isoform X24
longitudinals lacking protein, isoforms H/M/V-like isoform X19
longitudinals lacking protein, isoforms H/M/V-like isoform X20
longitudinals lacking protein, isoforms A/B/D/L-like isoform X22
longitudinals lacking protein, isoforms H/M/V-like isoform X36
longitudinals lacking protein, isoforms H/M/V-like isoform X38
longitudinals lacking protein, isoforms H/M/V-like isoform X40
longitudinals lacking protein, isoforms H/M/V-like isoform X37
longitudinals lacking protein, isoforms H/M/V-like isoform X11
longitudinals lacking protein, isoforms H/M/V-like isoform X26
longitudinals lacking protein, isoforms H/M/V-like isoform X35
longitudinals lacking protein, isoforms H/M/V-like isoform X31
longitudinals lacking protein, isoforms H/M/V-like isoform X23
longitudinals lacking protein, isoforms H/M/V-like isoform X18
uncharacterized LOC125031464, transcript variant X3
uncharacterized LOC125031464, transcript variant X1
uncharacterized LOC125031464, transcript variant X2
uncharacterized protein LOC125031464 isoform X1
uncharacterized protein LOC125031464 isoform X2
polyamine-transporting ATPase 13A3-like, transcript variant X1
polyamine-transporting ATPase 13A3-like, transcript variant X3
polyamine-transporting ATPase 13A3-like, transcript variant X2
polyamine-transporting ATPase 13A3-like isoform X1
polyamine-transporting ATPase 13A3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
endocuticle structural glycoprotein SgAbd-1-like
cuticle protein AMP4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cuticle protein AMP4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized protein LOC125031743 isoform X1
cuticle protein AMP1A-like, transcript variant X3
cuticle protein AMP1A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cuticle protein AMP1A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
putative sodium-coupled neutral amino acid transporter 11
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X3
YTH domain-containing family protein 3-like
BTB/POZ domain-containing protein KCTD5-like
nuclear transcription factor Y subunit alpha-like, transcript variant X1
nuclear transcription factor Y subunit alpha-like, transcript variant X4
nuclear transcription factor Y subunit alpha-like, transcript variant X5
nuclear transcription factor Y subunit alpha-like, transcript variant X6
nuclear transcription factor Y subunit alpha-like, transcript variant X7
nuclear transcription factor Y subunit alpha-like, transcript variant X2
nuclear transcription factor Y subunit alpha-like, transcript variant X3
nuclear transcription factor Y subunit alpha-like isoform X1
nuclear transcription factor Y subunit alpha-like isoform X4
nuclear transcription factor Y subunit alpha-like isoform X2
nuclear transcription factor Y subunit alpha-like isoform X3
nuclear transcription factor Y subunit alpha-like isoform X5
protein draper-like, transcript variant X1
protein draper-like, transcript variant X5
protein draper-like, transcript variant X4
protein draper-like, transcript variant X6
protein draper-like, transcript variant X2
protein draper-like, transcript variant X3
uncharacterized LOC125031789, transcript variant X1
uncharacterized LOC125031789, transcript variant X2
uncharacterized LOC125031936, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125031936, transcript variant X2
uncharacterized protein LOC125031936 isoform X1
uncharacterized protein LOC125031936 isoform X2
low-density lipoprotein receptor-related protein-like
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
uncharacterized LOC125031875, transcript variant X2
uncharacterized LOC125031875, transcript variant X3
uncharacterized LOC125031875, transcript variant X1
BRCA2-interacting transcriptional repressor EMSY-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 7 samples with support for all annotated introns
BRCA2-interacting transcriptional repressor EMSY-like, transcript variant X3
BRCA2-interacting transcriptional repressor EMSY-like, transcript variant X2
BRCA2-interacting transcriptional repressor EMSY-like isoform X1
BRCA2-interacting transcriptional repressor EMSY-like isoform X3
BRCA2-interacting transcriptional repressor EMSY-like isoform X2
transcription factor A, mitochondrial-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 39 samples with support for all annotated introns
zinc finger protein 629-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein 629-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 2 samples with support for all annotated introns
zinc finger protein 629-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 629-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 629-like, transcript variant X9
zinc finger protein 629-like, transcript variant X6
zinc finger protein 629-like, transcript variant X5
zinc finger protein 629-like, transcript variant X15
zinc finger protein 629-like, transcript variant X12
zinc finger protein 629-like, transcript variant X10
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
zinc finger protein 629-like, transcript variant X11
zinc finger protein 629-like, transcript variant X8
zinc finger protein 629-like, transcript variant X7
zinc finger protein 629-like, transcript variant X14
zinc finger protein 629-like, transcript variant X13
zinc finger and BTB domain-containing protein 24-like isoform X1
zinc finger and BTB domain-containing protein 24-like isoform X4
zinc finger and BTB domain-containing protein 24-like isoform X5
uncharacterized LOC125031721, transcript variant X4
uncharacterized LOC125031721, transcript variant X1
uncharacterized LOC125031721, transcript variant X3
uncharacterized LOC125031721, transcript variant X2
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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein rotund-like
ubiquitin carboxyl-terminal hydrolase 26-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 26-like, transcript variant X2
uncharacterized protein LOC125031720 isoform X1
uncharacterized protein LOC125031720 isoform X2
ubiquitin carboxyl-terminal hydrolase 26-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 26-like isoform X3
similar to RNA sequence (same species):INSD:GHUY01001679.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 703 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 617 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
amiloride-sensitive sodium channel subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
tRNA (guanine(37)-N1)-methyltransferase-like, transcript variant X2
tRNA (guanine(37)-N1)-methyltransferase-like isoform X2
tRNA (guanine(37)-N1)-methyltransferase-like, transcript variant X1
tRNA (guanine(37)-N1)-methyltransferase-like, transcript variant X3
tRNA (guanine(37)-N1)-methyltransferase-like isoform X1
protein kibra-like, transcript variant X2
protein kibra-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 39 samples with support for all annotated introns
pistil-specific extensin-like protein, transcript variant X1
pistil-specific extensin-like protein, transcript variant X2
actin cytoskeleton-regulatory complex protein PAN1-like isoform X1
pistil-specific extensin-like protein isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coagulation factor IX-like
ubiquitin-conjugating enzyme E2 E1-like, transcript variant X2
ubiquitin-conjugating enzyme E2 E1-like, transcript variant X1
ubiquitin-conjugating enzyme E2 E1-like, transcript variant X3
gelsolin, cytoplasmic-like, transcript variant X6
gelsolin, cytoplasmic-like, transcript variant X3
gelsolin, cytoplasmic-like, transcript variant X5
gelsolin, cytoplasmic-like, transcript variant X2
gelsolin, cytoplasmic-like, transcript variant X1
gelsolin, cytoplasmic-like, transcript variant X4
gelsolin, cytoplasmic-like, transcript variant X7
locomotion-related protein Hikaru genki-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase II subunit RPB1-like
bifunctional protein GlmU-like, transcript variant X1
bifunctional protein GlmU-like, transcript variant X2
protocadherin-like wing polarity protein stan
GTP cyclohydrolase 1-like, transcript variant X1
GTP cyclohydrolase 1-like, transcript variant X2
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like, transcript variant X2
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like, transcript variant X1
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like, transcript variant X3
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like isoform X2
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like isoform X1
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial-like isoform X3
piggyBac transposable element-derived protein 4-like, transcript variant X2
piggyBac transposable element-derived protein 4-like, transcript variant X1
piggyBac transposable element-derived protein 4-like
similar to RNA sequence (same species):INSD:GHUY01007299.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1992 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 1992 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA repair and recombination protein RAD54B-like, transcript variant X2
DNA repair and recombination protein RAD54B-like, transcript variant X6
DNA repair and recombination protein RAD54B-like, transcript variant X1
DNA repair and recombination protein RAD54B-like, transcript variant X5
DNA repair and recombination protein RAD54B-like, transcript variant X4
DNA repair and recombination protein RAD54B-like, transcript variant X3
DNA repair and recombination protein RAD54B-like isoform X2
DNA repair and recombination protein RAD54B-like isoform X3
DNA repair and recombination protein RAD54B-like isoform X1
NADPH oxidase 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NADPH oxidase 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NADPH oxidase 5-like, transcript variant X2
NADPH oxidase 5-like, transcript variant X4
uncharacterized LOC125031834, transcript variant X1
uncharacterized LOC125031834, transcript variant X2
uncharacterized LOC125031834, transcript variant X3
uncharacterized LOC125031834, transcript variant X4
uncharacterized LOC125031834, transcript variant X6
uncharacterized LOC125031834, transcript variant X7
uncharacterized LOC125031834, 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 28 samples with support for all annotated introns
uncharacterized protein LOC125031834 isoform X3
uncharacterized protein LOC125031834 isoform X1
uncharacterized protein LOC125031834 isoform X2
uncharacterized protein LOC125031834 isoform X4
uncharacterized LOC125031834, transcript variant X8
chloride intracellular channel exc-4-like
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 39 samples with support for all annotated introns
regulator of chromosome condensation-like
genetic suppressor element 1-like, transcript variant X3
genetic suppressor element 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 22 samples with support for all annotated introns
genetic suppressor element 1-like, transcript variant X1
genetic suppressor element 1-like isoform X3
genetic suppressor element 1-like isoform X2
genetic suppressor element 1-like isoform X1
glycosyltransferase 1 domain-containing protein 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 26 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 1-like, transcript variant X8
glycosyltransferase 1 domain-containing protein 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 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 11 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 1-like, transcript variant X1
glycosyltransferase 1 domain-containing protein 1-like, transcript variant X2
glycosyltransferase 1 domain-containing protein 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 9 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 1-like, transcript variant X7
glycosyltransferase 1 domain-containing protein 1-like isoform X2
glycosyltransferase 1 domain-containing protein 1-like isoform X1
bromodomain-containing protein 4-like, transcript variant X4
bromodomain-containing protein 4-like, transcript variant X1
bromodomain-containing protein 4-like, transcript variant X3
bromodomain-containing protein 4-like, transcript variant X2
bromodomain-containing protein 4-like isoform X2
bromodomain-containing protein 4-like isoform X1
regulator of nonsense transcripts 2-like, transcript variant X1
regulator of nonsense transcripts 2-like, transcript variant X3
regulator of nonsense transcripts 2-like, transcript variant X2
regulator of nonsense transcripts 2-like, transcript variant X4
regulator of nonsense transcripts 2-like
long-chain-fatty-acid--CoA ligase ACSBG2-like, transcript variant X1
long-chain-fatty-acid--CoA ligase ACSBG2-like isoform X1
long-chain-fatty-acid--CoA ligase ACSBG2-like, transcript variant X2
long-chain-fatty-acid--CoA ligase ACSBG2-like isoform X2
uncharacterized LOC125031537, transcript variant X2
uncharacterized LOC125031537, transcript variant X1
RING finger protein 37-like, transcript variant X1
RING finger protein 37-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 466 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like isoform X1
piggyBac transposable element-derived protein 4-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 238 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 230 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 474 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 249 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 231 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat extensin-like protein 5
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: high mobility group protein B1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: Gnomon. Supporting evidence includes similarity to: 50% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125031471, transcript variant X1
uncharacterized LOC125031471, transcript variant X2