Pieris napi chromosome 5, ilPieNapi1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nFR997699.1.\nAssembly name: ilPieNapi1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/01/30. The original whole-genome shotgun project has the\naccession CAJQFT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris napi Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
organic cation/carnitine transporter 7-like
COORDINATES: polyA evidence [ECO:0006239]
synaptic vesicle glycoprotein 2C-like, transcript variant X2
synaptic vesicle glycoprotein 2C-like, transcript variant X3
synaptic vesicle glycoprotein 2C-like, transcript variant X1
synaptic vesicle glycoprotein 2C-like isoform X1
uncharacterized protein LOC125049961 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
FAST kinase domain-containing protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
FAST kinase domain-containing protein 4, transcript variant X3
FAST kinase domain-containing protein 4, transcript variant X2
FAST kinase domain-containing protein 4, transcript variant X1
adenomatous polyposis coli protein-like, transcript variant X7
adenomatous polyposis coli protein-like, transcript variant X1
adenomatous polyposis coli protein-like, transcript variant X4
adenomatous polyposis coli protein-like, transcript variant X9
adenomatous polyposis coli protein-like, transcript variant X2
adenomatous polyposis coli protein-like, transcript variant X3
adenomatous polyposis coli protein-like, transcript variant X5
adenomatous polyposis coli protein-like, transcript variant X6
adenomatous polyposis coli protein-like, transcript variant X8
adenomatous polyposis coli protein-like isoform X1
adenomatous polyposis coli protein-like isoform X2
mitochondrial protein C2orf69 homolog, transcript variant X2
mitochondrial protein C2orf69 homolog, transcript variant X4
mitochondrial protein C2orf69 homolog, transcript variant X5
mitochondrial protein C2orf69 homolog, transcript variant X3
mitochondrial protein C2orf69 homolog, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP4, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP4, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP4 isoform X2
BTB/POZ domain-containing protein 17, 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 116 samples with support for all annotated introns
BTB/POZ domain-containing protein 17, 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 164 samples with support for all annotated introns
BTB/POZ domain-containing protein 17 isoform X1
BTB/POZ domain-containing protein 17 isoform X2
BTB/POZ domain-containing protein 17, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 88 samples with support for all annotated introns
BTB/POZ domain-containing protein 17 isoform X3
spore coat polysaccharide biosynthesis protein SpsK
synaptic vesicle glycoprotein 2B-like, transcript variant X2
synaptic vesicle glycoprotein 2B-like, transcript variant X1
uncharacterized protein LOC125049482 isoform X2
synaptic vesicle glycoprotein 2B-like isoform X1
synaptic vesicle glycoprotein 2B-like isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
organic cation/carnitine transporter 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
organic cation/carnitine transporter 7-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 6 samples with support for all annotated introns
organic cation/carnitine transporter 7-like isoform X1
organic cation/carnitine transporter 7-like isoform X2
synaptic vesicle glycoprotein 2C-like isoform X2
synaptic vesicle 2-related protein-like, transcript variant X2
synaptic vesicle 2-related protein-like, transcript variant X1
synaptic vesicle 2-related protein-like isoform X2
synaptic vesicle 2-related protein-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC125049388, transcript variant X1
uncharacterized LOC125049388, transcript variant X2
ER membrane protein complex subunit 2-like
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X2
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X3
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X4
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X1
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X1
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X5
tRNA (guanine(10)-N2)-methyltransferase homolog, transcript variant X6
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X2
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X3
DNA replication licensing factor Mcm3, transcript variant X1
DNA replication licensing factor Mcm3, transcript variant X2
DNA replication licensing factor Mcm3 isoform X1
DNA replication licensing factor Mcm3 isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-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 5 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-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 4 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like, transcript variant X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4-like isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like isoform X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-like isoform X6
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-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 1 sample with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3-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 2 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X5
solute carrier family 22 member 15-like, transcript variant X2
solute carrier family 22 member 15-like, transcript variant X1
solute carrier family 22 member 15-like isoform X1
solute carrier family 22 member 15-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
scavenger receptor class B member 1-like
uncharacterized LOC125049704, transcript variant X2
uncharacterized LOC125049704, transcript variant X1
uncharacterized LOC125049704, transcript variant X3
uncharacterized protein LOC125049704 isoform X2
uncharacterized protein LOC125049704 isoform X1
uncharacterized LOC125049629, 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 59 samples with support for all annotated introns
uncharacterized LOC125049629, 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 43 samples with support for all annotated introns
uncharacterized protein LOC125049629 isoform X1
uncharacterized protein LOC125049629 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125049632, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC125049632 isoform X1
uncharacterized LOC125049632, transcript variant X2
uncharacterized protein LOC125049632 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase G, transcript variant X2
peptidyl-prolyl cis-trans isomerase G, transcript variant X1
peptidyl-prolyl cis-trans isomerase G, transcript variant X3
peptidyl-prolyl cis-trans isomerase G isoform X2
peptidyl-prolyl cis-trans isomerase G isoform X1
peptidyl-prolyl cis-trans isomerase G isoform X3
heterogeneous nuclear ribonucleoprotein F-like
mothers against decapentaplegic homolog 6
lysosome membrane protein 2-like, transcript variant X1
lysosome membrane protein 2-like, transcript variant X4
lysosome membrane protein 2-like, transcript variant X2
lysosome membrane protein 2-like, transcript variant X3
lysosome membrane protein 2-like isoform X1
lysosome membrane protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor class B member 1-like, transcript variant X1
scavenger receptor class B member 1-like, transcript variant X2
scavenger receptor class B member 1-like isoform X1
scavenger receptor class B member 1-like isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1
mitogen-activated protein kinase kinase kinase 4, transcript variant X2
mitogen-activated protein kinase kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase kinase 4, transcript variant X3
mitogen-activated protein kinase kinase kinase 4 isoform X1
mitogen-activated protein kinase kinase kinase 4 isoform X3
mitogen-activated protein kinase kinase kinase 4 isoform 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 52 samples with support for all annotated introns
RNA-binding protein squid, transcript variant X2
RNA-binding protein squid, transcript variant X1
RNA-binding protein squid, transcript variant X5
RNA-binding protein squid, transcript variant X4
RNA-binding protein squid, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00476
ras GTPase-activating protein-binding protein 2
splicing factor 1, transcript variant X1
splicing factor 1, transcript variant X2
splicing factor 1, transcript variant X3
splicing factor 1, transcript variant X4
programmed cell death 6-interacting protein
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1, transcript variant X3
serine/arginine repetitive matrix protein 1, transcript variant X4
serine/arginine repetitive matrix protein 1, transcript variant X5
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X4
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1 isoform X5
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X2
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X1
ATP synthase mitochondrial F1 complex assembly factor 1
cyclin-dependent kinase 2-like, transcript variant X2
cyclin-dependent kinase 2-like, transcript variant X1
cyclin-dependent kinase 2-like isoform X1
cyclin-dependent kinase 2-like isoform X2
cyclin-dependent kinase 2-like, transcript variant X3
cyclin-dependent kinase 2-like isoform X3
cyclin-dependent kinase 2-like, transcript variant X4
cyclin-dependent kinase 2-like isoform X4
lipid storage droplets surface-binding protein 1, transcript variant X8
lipid storage droplets surface-binding protein 1 isoform X8
lipid storage droplets surface-binding protein 1, transcript variant X9
lipid storage droplets surface-binding protein 1, transcript variant X1
lipid storage droplets surface-binding protein 1, transcript variant X2
lipid storage droplets surface-binding protein 1, transcript variant X5
lipid storage droplets surface-binding protein 1, transcript variant X3
lipid storage droplets surface-binding protein 1, transcript variant X4
lipid storage droplets surface-binding protein 1, transcript variant X6
lipid storage droplets surface-binding protein 1, transcript variant X7
lipid storage droplets surface-binding protein 1 isoform X1
lipid storage droplets surface-binding protein 1 isoform X4
lipid storage droplets surface-binding protein 1 isoform X2
lipid storage droplets surface-binding protein 1 isoform X6
lipid storage droplets surface-binding protein 1 isoform X3
lipid storage droplets surface-binding protein 1 isoform X7
lipid storage droplets surface-binding protein 1 isoform X5
lipid storage droplets surface-binding protein 1 isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 162 samples with support for all annotated introns
diacylglycerol kinase theta, transcript variant X4
diacylglycerol kinase theta, transcript variant X3
diacylglycerol kinase theta, transcript variant X2
diacylglycerol kinase theta, transcript variant X1
diacylglycerol kinase theta, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 107 samples with support for all annotated introns
AP-1 complex subunit sigma-2, transcript variant X4
AP-1 complex subunit sigma-2, transcript variant X2
AP-1 complex subunit sigma-2, transcript variant X3
AP-1 complex subunit sigma-2, transcript variant X1
lipid storage droplets surface-binding protein 2, transcript variant X2
lipid storage droplets surface-binding protein 2, transcript variant X1
lipid storage droplets surface-binding protein 2 isoform X2
lipid storage droplets surface-binding protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
nonsense-mediated mRNA decay factor SMG8
cytoplasmic polyadenylation element-binding protein 1-B
eukaryotic translation initiation factor 4E type 2
dihydroceramide fatty acyl 2-hydroxylase FAH2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like, transcript variant X1
leucine-rich melanocyte differentiation-associated protein-like, transcript variant X2
leucine-rich melanocyte differentiation-associated protein-like isoform X1
leucine-rich melanocyte differentiation-associated protein-like isoform X2
CDK5 regulatory subunit-associated protein 3, transcript variant X1
CDK5 regulatory subunit-associated protein 3, transcript variant X2
CDK5 regulatory subunit-associated protein 3 isoform X1
CDK5 regulatory subunit-associated protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125049784, transcript variant X1
uncharacterized LOC125049784, transcript variant X2
uncharacterized protein LOC125049784 isoform X1
uncharacterized protein LOC125049784 isoform X2
protein tramtrack, beta isoform, transcript variant X1
zinc finger and BTB domain-containing protein 34 isoform X1
protein tramtrack, beta isoform, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X34
protein tramtrack, beta isoform, transcript variant X24
protein tramtrack, beta isoform isoform X23
protein tramtrack, beta isoform, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X15
protein tramtrack, beta isoform, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 153 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X14
protein tramtrack, beta isoform, transcript variant X37
protein tramtrack, beta isoform isoform X36
protein tramtrack, beta isoform, transcript variant X42
protein tramtrack, beta isoform isoform X41
protein tramtrack, beta isoform, transcript variant X46
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 144 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X45
protein tramtrack, beta isoform, transcript variant X25
protein tramtrack, beta isoform isoform X24
protein tramtrack, beta isoform, transcript variant X12
protein tramtrack, beta isoform isoform X12
protein tramtrack, beta isoform, transcript variant X41
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 152 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X40
protein tramtrack, beta isoform, transcript variant X34
protein tramtrack, beta isoform isoform X33
protein tramtrack, beta isoform, transcript variant X32
protein tramtrack, beta isoform isoform X31
protein tramtrack, beta isoform, transcript variant X20
protein tramtrack, beta isoform isoform X19
protein tramtrack, beta isoform, transcript variant X38
protein tramtrack, beta isoform isoform X37
protein tramtrack, beta isoform, transcript variant X18
protein tramtrack, beta isoform isoform X17
protein tramtrack, beta isoform, transcript variant X16
protein tramtrack, beta isoform, transcript variant X19
protein tramtrack, beta isoform isoform X18
protein tramtrack, beta isoform, transcript variant X17
protein tramtrack, beta isoform isoform X16
protein tramtrack, beta isoform, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 151 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X35
protein tramtrack, beta isoform, transcript variant X49
protein tramtrack, beta isoform isoform X48
protein tramtrack, beta isoform, transcript variant X45
protein tramtrack, beta isoform isoform X44
protein tramtrack, beta isoform, transcript variant X48
protein tramtrack, beta isoform isoform X47
protein tramtrack, beta isoform, transcript variant X21
protein tramtrack, beta isoform isoform X20
protein tramtrack, beta isoform, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 147 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X29
protein tramtrack, beta isoform, transcript variant X27
protein tramtrack, beta isoform isoform X26
protein tramtrack, beta isoform, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 145 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X21
protein tramtrack, beta isoform, transcript variant X40
protein tramtrack, beta isoform isoform X39
protein tramtrack, beta isoform, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 166 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X27
protein tramtrack, beta isoform, transcript variant X44
protein tramtrack, beta isoform isoform X43
protein tramtrack, beta isoform, transcript variant X43
protein tramtrack, beta isoform isoform X42
protein tramtrack, beta isoform, transcript variant X23
protein tramtrack, beta isoform isoform X22
protein tramtrack, beta isoform, transcript variant X47
protein tramtrack, beta isoform isoform X46
protein tramtrack, beta isoform, transcript variant X50
protein tramtrack, beta isoform isoform X49
protein tramtrack, beta isoform, transcript variant X3
protein tramtrack, beta isoform isoform X3
protein tramtrack, beta isoform, transcript variant X33
protein tramtrack, beta isoform isoform X32
protein tramtrack, beta isoform, transcript variant X29
protein tramtrack, beta isoform isoform X28
protein tramtrack, beta isoform, transcript variant X26
protein tramtrack, beta isoform isoform X25
protein tramtrack, beta isoform, transcript variant X6
protein tramtrack, beta isoform isoform X6
protein tramtrack, beta isoform, transcript variant X13
protein tramtrack, beta isoform isoform X13
protein tramtrack, beta isoform, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 142 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X9
protein tramtrack, beta isoform, transcript variant X31
protein tramtrack, beta isoform isoform X30
protein tramtrack, beta isoform, transcript variant X4
protein tramtrack, beta isoform isoform X4
protein tramtrack, beta isoform, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 157 samples with support for all annotated introns
protein tramtrack, beta isoform isoform X8
protein tramtrack, beta isoform, transcript variant X7
protein tramtrack, beta isoform isoform X7
protein tramtrack, beta isoform, transcript variant X11
protein tramtrack, beta isoform isoform X11
protein tramtrack, beta isoform, transcript variant X39
protein tramtrack, beta isoform isoform X38
protein tramtrack, beta isoform, transcript variant X2
protein tramtrack, beta isoform isoform X2
protein tramtrack, beta isoform, transcript variant X5
protein tramtrack, beta isoform isoform X5
protein tramtrack, beta isoform, transcript variant X10
protein tramtrack, beta isoform isoform X10
fatty acyl-CoA hydrolase precursor, medium chain
uncharacterized protein DDB_G0283357-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 169 samples with support for all annotated introns
phenylalanine--tRNA ligase beta subunit, transcript variant X1
phenylalanine--tRNA ligase beta subunit, transcript variant X2
phenylalanine--tRNA ligase beta subunit isoform X1
phenylalanine--tRNA ligase beta subunit isoform X2
AN1-type zinc finger protein 6, transcript variant X6
AN1-type zinc finger protein 6, transcript variant X2
AN1-type zinc finger protein 6, transcript variant X4
AN1-type zinc finger protein 6, transcript variant X8
AN1-type zinc finger protein 6, transcript variant X5
AN1-type zinc finger protein 6, transcript variant X3
AN1-type zinc finger protein 6, transcript variant X7
AN1-type zinc finger protein 6 isoform X2
AN1-type zinc finger protein 6, transcript variant X1
AN1-type zinc finger protein 6 isoform X1
progestin and adipoQ receptor family member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase Doa, transcript variant X7
serine/threonine-protein kinase Doa, transcript variant X8
serine/threonine-protein kinase Doa isoform X6
serine/threonine-protein kinase Doa isoform X7
serine/threonine-protein kinase Doa, transcript variant X6
dual specificity protein kinase CLK2 isoform X5
serine/threonine-protein kinase Doa, transcript variant X10
serine/threonine-protein kinase Doa, transcript variant X3
serine/threonine-protein kinase Doa, transcript variant X2
serine/threonine-protein kinase Doa, transcript variant X1
serine/threonine-protein kinase Doa, transcript variant X4
probable myosin light chain kinase DDB_G0279831 isoform X1
probable myosin light chain kinase DDB_G0279831 isoform X2
dual specificity protein kinase lkh1 isoform X3
serine/threonine-protein kinase Doa, transcript variant X9
serine/threonine-protein kinase Doa isoform X8
serine/threonine-protein kinase Doa, transcript variant X5
serine/threonine-protein kinase Doa isoform X9
NADP-dependent malic enzyme, transcript variant X4
NADP-dependent malic enzyme, transcript variant X2
NADP-dependent malic enzyme, transcript variant X1
NADP-dependent malic enzyme, transcript variant X3
translation initiation factor eIF-2B subunit alpha
tyrosine-protein kinase Fer, transcript variant X2
tyrosine-protein kinase Fer, transcript variant X1
tyrosine-protein kinase Fer, transcript variant X3
eukaryotic translation initiation factor 4B, transcript variant X1
eukaryotic translation initiation factor 4B, transcript variant X2
eukaryotic translation initiation factor 4B isoform X1
eukaryotic translation initiation factor 4B isoform X2
uncharacterized LOC125049373, transcript variant X2
uncharacterized LOC125049373, transcript variant X1
uncharacterized LOC125049373, transcript variant X3
uncharacterized protein LOC125049373 isoform X2
uncharacterized protein LOC125049373 isoform X1
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X2
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X1
transmembrane and ubiquitin-like domain-containing protein 1, transcript variant X3
transmembrane and ubiquitin-like domain-containing protein 1 isoform X1
transmembrane and ubiquitin-like domain-containing protein 1 isoform X2
transmembrane and ubiquitin-like domain-containing protein 1 isoform X3
60S ribosomal protein L15, transcript variant X1
60S ribosomal protein L15, transcript variant X2
double-strand-break repair protein rad21 homolog, transcript variant X1
double-strand-break repair protein rad21 homolog, transcript variant X3
double-strand-break repair protein rad21 homolog, transcript variant X4
double-strand-break repair protein rad21 homolog, transcript variant X2
double-strand-break repair protein rad21 homolog isoform X1
double-strand-break repair protein rad21 homolog isoform X2
double-strand-break repair protein rad21 homolog isoform X3
ATP synthase lipid-binding protein, mitochondrial, transcript variant X1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X2
ATP synthase lipid-binding protein, mitochondrial, transcript variant X3
ATP synthase lipid-binding protein, mitochondrial
juxtaposed with another zinc finger protein 1
vacuolar protein sorting-associated protein 16 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125049661, 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 14 samples with support for all annotated introns
uncharacterized LOC125049661, 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 21 samples with support for all annotated introns
uncharacterized protein LOC125049661 isoform X2
uncharacterized protein LOC125049661 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 165 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 87F-like
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1-like isoform X1
heterogeneous nuclear ribonucleoprotein A1-like isoform 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 9 samples with support for all annotated introns
mannose-6-phosphate isomerase, transcript variant X1
mannose-6-phosphate isomerase, transcript variant X2
putative uncharacterized protein DDB_G0289963
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC125049292 isoform X2
ras-related C3 botulinum toxin substrate 1
leucine-rich repeat protein soc-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cleavage stimulation factor subunit 2 tau variant
sex determination protein fruitless-like, transcript variant X7
sex determination protein fruitless-like isoform X3
sex determination protein fruitless-like, transcript variant X6
sex determination protein fruitless-like isoform X2
sex determination protein fruitless-like, transcript variant X2
sex determination protein fruitless-like, transcript variant X3
sex determination protein fruitless-like, transcript variant X1
sex determination protein fruitless-like, transcript variant X4
sex determination protein fruitless-like, transcript variant X5
broad-complex core protein isoforms 1/2/3/4/5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ and ubiquitin-like domain-containing protein
homeobox protein abdominal-B-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 6 samples with support for all annotated introns
uncharacterized LOC125049612, 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 5 samples with support for all annotated introns
uncharacterized protein LOC125049612 isoform X2
uncharacterized LOC125049612, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC125049612 isoform X1
homeobox protein abdominal-B-like, transcript variant X1
homeobox protein abdominal-B-like, transcript variant X3
homeobox protein abdominal-B-like isoform X1
homeobox protein abdominal-B-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
homeobox protein abdominal-A homolog, transcript variant X2
homeobox protein abdominal-A homolog, transcript variant X4
homeobox protein abdominal-A homolog, transcript variant X1
homeobox protein abdominal-A homolog, transcript variant X3
homeobox protein abdominal-A homolog isoform X1
homeobox protein abdominal-A homolog isoform X2
homeobox protein abdominal-A homolog isoform X3
homeobox protein abdominal-A homolog isoform X4
homeotic protein antennapedia, transcript variant X5
homeotic protein antennapedia, transcript variant X3
homeotic protein antennapedia, transcript variant X8
homeotic protein antennapedia, transcript variant X4
homeotic protein antennapedia, transcript variant X1
homeotic protein antennapedia, transcript variant X6
homeotic protein antennapedia, transcript variant X7
homeotic protein antennapedia, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 21% 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 8 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X6
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X8
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X2
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X3
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X4
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X7
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X5
LIM and senescent cell antigen-like-containing domain protein 1, transcript variant X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X2
LIM and senescent cell antigen-like-containing domain protein 1 isoform X1
LIM and senescent cell antigen-like-containing domain protein 1 isoform X3
ATPase H(+)-transporting accessory protein 2
protein N-lysine methyltransferase METTL21D-like
E3 ubiquitin-protein ligase RNF181, transcript variant X1
E3 ubiquitin-protein ligase RNF181, 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 17 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 142 samples with support for all annotated introns
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
rab11 family-interacting protein 4, transcript variant X5
rab11 family-interacting protein 4, transcript variant X1
rab11 family-interacting protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
rab11 family-interacting protein 4, transcript variant X3
rab11 family-interacting protein 4, transcript variant X2
rab11 family-interacting protein 4 isoform X1
rab11 family-interacting protein 4 isoform X2
rab11 family-interacting protein 4 isoform X3
rab11 family-interacting protein 4A isoform X4
rab11 family-interacting protein 4 isoform X5
ubiquitin domain-containing protein UBFD1-like
xylosyltransferase oxt, transcript variant X1
xylosyltransferase oxt, transcript variant X2
protein ecdysoneless homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 96 samples with support for all annotated introns
protein ecdysoneless homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 4
zinc finger CCCH domain-containing protein 3
glutamate receptor ionotropic, NMDA 2B, transcript variant X1
glutamate receptor ionotropic, NMDA 2B, transcript variant X2
glutamate receptor ionotropic, NMDA 2B isoform X2
glutamate receptor ionotropic, NMDA 2B isoform X1
ganglioside-induced differentiation-associated protein 1
vacuolar protein sorting-associated protein 8 homolog
leukocyte receptor cluster member 8 homolog, transcript variant X2
leukocyte receptor cluster member 8 homolog, 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 169 samples with support for all annotated introns
leukocyte receptor cluster member 8 homolog isoform X2
leukocyte receptor cluster member 8 homolog isoform X1
uncharacterized protein C16orf52 homolog A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha-like
enoyl-CoA delta isomerase 3, peroxisomal
glycerol-3-phosphate phosphatase, transcript variant X2
glycerol-3-phosphate phosphatase, transcript variant X1
glycerol-3-phosphate phosphatase isoform X1
glycerol-3-phosphate phosphatase isoform X2
tubulin polymerization-promoting protein homolog, transcript variant X2
tubulin polymerization-promoting protein homolog, transcript variant X1
tubulin polymerization-promoting protein homolog isoform X1
tubulin polymerization-promoting protein homolog isoform X2
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
U3 small nucleolar RNA-associated protein 4 homolog
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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
general transcription and DNA repair factor IIH helicase subunit XPB, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 139 samples with support for all annotated introns
general transcription and DNA repair factor IIH helicase subunit XPB, transcript variant X2
chromosome transmission fidelity protein 8 homolog
general transcription and DNA repair factor IIH helicase subunit XPB, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
general transcription and DNA repair factor IIH helicase subunit XPB
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 38 samples with support for all annotated introns
leukocyte receptor cluster member 1 homolog
WASH complex subunit 5, transcript variant X1
WASH complex subunit 5, transcript variant X2
nuclear pore complex protein Nup160 homolog, transcript variant X2
nuclear pore complex protein Nup160 homolog, transcript variant X1
nuclear pore complex protein Nup160 homolog isoform X2
nuclear pore complex protein Nup160 homolog isoform X1
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X1
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X2
cAMP-dependent protein kinase type I regulatory subunit isoform X1
cAMP-dependent protein kinase type I regulatory subunit isoform X2
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X3
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X4
cAMP-dependent protein kinase type I regulatory subunit isoform X3
cAMP-dependent protein kinase type I regulatory subunit isoform 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 113 samples with support for all annotated introns
gamma-aminobutyric acid receptor-associated protein
general transcription factor IIF subunit 1-like
E3 ubiquitin-protein ligase RNF146, transcript variant X1
E3 ubiquitin-protein ligase RNF146, transcript variant X2
E3 ubiquitin-protein ligase RNF146 isoform X1
E3 ubiquitin-protein ligase RNF146 isoform X2
serine/threonine-protein kinase ATR-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
hepatocyte growth factor-regulated tyrosine kinase substrate-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 139 samples with support for all annotated introns
hepatocyte growth factor-regulated tyrosine kinase substrate-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
hepatocyte growth factor-regulated tyrosine kinase substrate-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 104 samples with support for all annotated introns
hepatocyte growth factor-regulated tyrosine kinase substrate-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 169 samples with support for all annotated introns
hepatocyte growth factor-regulated tyrosine kinase substrate-like isoform X4
hepatocyte growth factor-regulated tyrosine kinase substrate-like isoform X3
hepatocyte growth factor-regulated tyrosine kinase substrate-like isoform X2
hepatocyte growth factor-regulated tyrosine kinase substrate-like isoform X1
U6 snRNA-associated Sm-like protein LSm5
inward rectifier potassium channel 2-like
G protein-activated inward rectifier potassium channel 3-like, transcript variant X1
G protein-activated inward rectifier potassium channel 3-like, transcript variant X5
G protein-activated inward rectifier potassium channel 3-like, transcript variant X2
G protein-activated inward rectifier potassium channel 3-like isoform X1
G protein-activated inward rectifier potassium channel 3-like isoform X3
G protein-activated inward rectifier potassium channel 3-like, transcript variant X4
G protein-activated inward rectifier potassium channel 3-like, transcript variant X3
G protein-activated inward rectifier potassium channel 3-like, transcript variant X6
G protein-activated inward rectifier potassium channel 3-like, transcript variant X7
G protein-activated inward rectifier potassium channel 3-like, transcript variant X8
G protein-activated inward rectifier potassium channel 3-like isoform X2
G protein-activated inward rectifier potassium channel 3-like isoform X4
G protein-activated inward rectifier potassium channel 3-like isoform X5
G protein-activated inward rectifier potassium channel 3-like isoform X6
G protein-activated inward rectifier potassium channel 3, transcript variant X2
G protein-activated inward rectifier potassium channel 3, transcript variant X1
G protein-activated inward rectifier potassium channel 3, transcript variant X3
G protein-activated inward rectifier potassium channel 3 isoform X1
G protein-activated inward rectifier potassium channel 3 isoform X2
G protein-activated inward rectifier potassium channel 3 isoform X3
G protein-activated inward rectifier potassium channel 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 3 isoform X4
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 152 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 119 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 74 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 115 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 161 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase nonstop, transcript variant X1
ubiquitin carboxyl-terminal hydrolase nonstop, transcript variant X2
ubiquitin carboxyl-terminal hydrolase nonstop
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 77 samples with support for all annotated introns
cilia- and flagella-associated protein 52
monocarboxylate transporter 9-like, transcript variant X1
monocarboxylate transporter 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
uncharacterized LOC125049923, transcript variant X2
uncharacterized LOC125049923, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ETS-related transcription factor Elf-3-like
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sodium-independent sulfate anion transporter-like, transcript variant X1
sodium-independent sulfate anion transporter-like, transcript variant X2
sodium-independent sulfate anion transporter-like isoform X1
sodium-independent sulfate anion transporter-like isoform X2
myb/SANT-like DNA-binding domain-containing protein 3
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 75 samples with support for all annotated introns
prominin-like protein, transcript variant X2
prominin-like protein, transcript variant X5
prominin-like protein, transcript variant X1
prominin-like protein, transcript variant X4
prominin-like protein, transcript variant X3
prominin-like protein, transcript variant X6
prominin-like protein, transcript variant X7
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125049779, transcript variant X4
uncharacterized LOC125049779, transcript variant X1
uncharacterized LOC125049779, transcript variant X3
uncharacterized LOC125049779, transcript variant X2
uncharacterized protein LOC125049779 isoform X3
uncharacterized protein LOC125049779 isoform X1
uncharacterized protein LOC125049779 isoform X2
nuclear protein localization protein 4 homolog
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X1
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X3
coiled-coil domain-containing protein 137
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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 27 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 135 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like isoform X3
multiple inositol polyphosphate phosphatase 1-like, transcript variant X2
multiple inositol polyphosphate phosphatase 1-like, transcript variant X1
multiple inositol polyphosphate phosphatase 1-like, transcript variant X3
multiple inositol polyphosphate phosphatase 1-like
DNA-directed RNA polymerase III subunit RPC5
dihydropyrimidine dehydrogenase [NADP(+)]
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 151 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 3A1, 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 9 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 3A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 3A1, transcript variant X2
heparan sulfate glucosamine 3-O-sulfotransferase 3A1 isoform X2
heparan sulfate glucosamine 3-O-sulfotransferase 3A1 isoform X3
heparan sulfate glucosamine 3-O-sulfotransferase 3A1 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 12 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
small subunit processome component 20 homolog
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 24 samples with support for all annotated introns
prostaglandin reductase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
prostaglandin reductase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 112 samples with support for all annotated introns
neprilysin-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
neprilysin-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
neprilysin-4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC125049415, transcript variant X3
uncharacterized LOC125049415, transcript variant X1
uncharacterized LOC125049415, transcript variant X2
uncharacterized protein LOC125049415 isoform X1
uncharacterized protein LOC125049415 isoform X3
uncharacterized protein LOC125049415 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
uncharacterized LOC125049509, transcript variant X5
uncharacterized LOC125049509, transcript variant X1
uncharacterized LOC125049509, transcript variant X3
uncharacterized LOC125049509, transcript variant X2
uncharacterized LOC125049509, transcript variant X4
uncharacterized protein LOC125049509 isoform X1
uncharacterized protein LOC125049509 isoform X2
protein CLEC16A homolog, 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 11 samples with support for all annotated introns
protein CLEC16A homolog, 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 33 samples with support for all annotated introns
protein CLEC16A homolog, 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 43 samples with support for all annotated introns
protein CLEC16A 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 50 samples with support for all annotated introns
uncharacterized LOC125049552, 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 31 samples with support for all annotated introns
uncharacterized LOC125049552, 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 94 samples with support for all annotated introns
uncharacterized LOC125049552, transcript variant X2
uncharacterized LOC125049551, 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 83 samples with support for all annotated introns
uncharacterized LOC125049551, 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 143 samples with support for all annotated introns
uncharacterized LOC125049551, 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 146 samples with support for all annotated introns
mitochondrial glycine transporter-like, transcript variant X1
mitochondrial glycine transporter-like, transcript variant X2
mitochondrial glycine transporter-like, transcript variant X3
mitochondrial glycine transporter B-like isoform X1
mitochondrial glycine transporter-like isoform X2
mitochondrial glycine transporter-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 148 samples with support for all annotated introns
uncharacterized LOC125049959, transcript variant X2
uncharacterized LOC125049959, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein NYNRIN-like, transcript variant X1
protein NYNRIN-like, transcript variant X2
uncharacterized protein LOC125049782 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
zinc finger protein 84-like, transcript variant X7
zinc finger protein 84-like, transcript variant X2
zinc finger protein 84-like, transcript variant X8
zinc finger protein 84-like, transcript variant X6
zinc finger protein 84-like, transcript variant X9
zinc finger protein 84-like, transcript variant X4
zinc finger protein 84-like, transcript variant X3
zinc finger protein 84-like, transcript variant X10
zinc finger protein 84-like, transcript variant X5
zinc finger protein 84-like, transcript variant X1
zinc finger protein 420-like isoform X10
extracellular serine/threonine protein CG31145, transcript variant X3
extracellular serine/threonine protein CG31145, transcript variant X1
extracellular serine/threonine protein CG31145 isoform X1
extracellular serine/threonine protein CG31145, transcript variant X2
extracellular serine/threonine protein CG31145 isoform X2
extracellular serine/threonine protein CG31145 isoform 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
uncharacterized LOC125049670, transcript variant X1
uncharacterized protein LOC125049670 isoform X1
uncharacterized LOC125049670, 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 6 samples with support for all annotated introns
uncharacterized protein LOC125049670 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 118 samples with support for all annotated introns
glucose-induced degradation protein 4 homolog
28S ribosomal protein S23, mitochondrial, transcript variant X2
28S ribosomal protein S23, mitochondrial, transcript variant X1
28S ribosomal protein S23, mitochondrial
major facilitator superfamily domain-containing protein 10, transcript variant X2
major facilitator superfamily domain-containing protein 10, transcript variant X1
major facilitator superfamily domain-containing protein 10 isoform X1
major facilitator superfamily domain-containing protein 10 isoform X2
DNA topoisomerase 3-alpha, transcript variant X6
DNA topoisomerase 3-alpha, 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 4 samples with support for all annotated introns
DNA topoisomerase 3-alpha, 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 12 samples with support for all annotated introns
DNA topoisomerase 3-alpha, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
DNA topoisomerase 3-alpha, transcript variant X2
DNA topoisomerase 3-alpha, 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 87 samples with support for all annotated introns
DNA topoisomerase 3-alpha, 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 75 samples with support for all annotated introns
serine hydroxymethyltransferase, transcript variant X1
serine hydroxymethyltransferase, transcript variant X2
serine hydroxymethyltransferase, transcript variant X3
serine hydroxymethyltransferase isoform X1
serine hydroxymethyltransferase isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125049732, transcript variant X2
uncharacterized LOC125049732, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 93-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 60 samples with support for all annotated introns
zinc finger protein 93-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
zinc finger protein 226-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 42 samples with support for all annotated introns
zinc finger protein 226-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 155 samples with support for all annotated introns
uncharacterized LOC125049735, transcript variant X2
uncharacterized LOC125049735, transcript variant X1
zinc finger protein 723-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 58 samples with support for all annotated introns
zinc finger protein 723-like, transcript variant X1
uncharacterized protein LOC125049721 isoform X2
probable basic-leucine zipper transcription factor P
uncharacterized LOC125049727, transcript variant X1
uncharacterized LOC125049727, transcript variant X2
uncharacterized protein LOC125049727 isoform X1
uncharacterized protein LOC125049727 isoform X2
probable isoaspartyl peptidase/L-asparaginase GA20639, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 137 samples with support for all annotated introns
probable isoaspartyl peptidase/L-asparaginase GA20639, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
probable isoaspartyl peptidase/L-asparaginase GA20639, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
probable isoaspartyl peptidase/L-asparaginase GA20639, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 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 73 samples with support for all annotated introns
probable isoaspartyl peptidase/L-asparaginase GA20639, 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 153 samples with support for all annotated introns
probable isoaspartyl peptidase/L-asparaginase GA20639 isoform X1
probable isoaspartyl peptidase/L-asparaginase GA20639 isoform X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X2
rhomboid-related protein 3, transcript variant X1
rhomboid-related protein 3, transcript variant X2
spermatogenesis-associated protein 20, transcript variant X1
spermatogenesis-associated protein 20, transcript variant X2
spermatogenesis-associated protein 20 isoform X1
spermatogenesis-associated protein 20 isoform X2
zinc finger BED domain-containing protein 4-like
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X1
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X2
putative mediator of RNA polymerase II transcription subunit 26
uncharacterized LOC125049658, transcript variant X1
uncharacterized LOC125049658, transcript variant X3
uncharacterized LOC125049658, transcript variant X2
uncharacterized protein LOC125049658 isoform X1
uncharacterized protein LOC125049658 isoform X2
solute carrier family 23 member 2, transcript variant X2
solute carrier family 23 member 2, transcript variant X1
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125049493, 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 16 samples with support for all annotated introns
uncharacterized LOC125049493, 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 52 samples with support for all annotated introns
uncharacterized LOC125049493, transcript variant X5
uncharacterized LOC125049493, 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 63 samples with support for all annotated introns
uncharacterized LOC125049493, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
protein winged eye, transcript variant X1
protein winged eye, transcript variant X2
senecionine N-oxygenase, transcript variant X1
senecionine N-oxygenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 114 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 191 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 119 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
NADH-ubiquinone oxidoreductase subunit 8
pyridoxal-dependent decarboxylase domain-containing protein 1
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 147 samples with support for all annotated introns
lactosylceramide 4-alpha-galactosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
monocarboxylate transporter 14-like, transcript variant X1
monocarboxylate transporter 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC125049655, transcript variant X2
uncharacterized LOC125049655, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 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 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 50 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 41 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 30 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 31 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 43 samples with support for all annotated introns
probable 3-hydroxyisobutyrate dehydrogenase, mitochondrial
sulfotransferase 1E1-like, transcript variant X2
sulfotransferase 1E1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
cytosolic Fe-S cluster assembly factor NUBP2 homolog
54S ribosomal protein L12, mitochondrial
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 168 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X4
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X1
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X3
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X2
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X3
uncharacterized protein LOC125049997 isoform X1
uncharacterized protein LOC125049997 isoform X2
ankyrin repeat and ELMO domain-containing protein D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial isoform X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
17-beta-hydroxysteroid dehydrogenase type 2 isoform X2
nuclear pore complex protein Nup214-like, transcript variant X1
nuclear pore complex protein Nup214-like, transcript variant X2
nuclear pore complex protein Nup214-like, transcript variant X3
nuclear pore complex protein Nup214-like isoform X1
nuclear pore complex protein Nup214-like isoform X2
nuclear pore complex protein Nup214-like isoform X3
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial
uncharacterized LOC125049456, transcript variant X2
uncharacterized LOC125049456, transcript variant X1
transcription initiation factor TFIID subunit 1
polyglutamylase complex subunit TTLL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125049590, transcript variant X2
uncharacterized LOC125049590, transcript variant X1
uncharacterized protein LOC125049590 isoform X1
uncharacterized protein LOC125049590 isoform X2
dynein intermediate chain 3, ciliary-like
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
transcription initiation factor TFIID subunit 2
kynurenine 3-monooxygenase, transcript variant X2
kynurenine 3-monooxygenase, 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 12 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X2
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X1
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X1
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X2
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X3
cilia- and flagella-associated protein 299-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
nitric oxide synthase-like protein, transcript variant X2
nitric oxide synthase-like protein, transcript variant X1
nitric oxide synthase-like protein isoform X2
nitric oxide synthase-like protein isoform X1
UDP-glycosyltransferase UGT5-like, transcript variant X1
UDP-glycosyltransferase UGT5-like isoform X1
UDP-glycosyltransferase UGT5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
UDP-glucosyltransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
NADPH oxidase 4-like, transcript variant X2
NADPH oxidase 4-like, transcript variant X1
protein downstream neighbor of son homolog
chromodomain-helicase-DNA-binding protein Mi-2 homolog, transcript variant X2
chromodomain-helicase-DNA-binding protein Mi-2 homolog, transcript variant X1
chromodomain-helicase-DNA-binding protein Mi-2 homolog isoform X2
chromodomain-helicase-DNA-binding protein Mi-2 homolog isoform X1
TRPL translocation defect protein 14, transcript variant X1
TRPL translocation defect protein 14, transcript variant X2
TRPL translocation defect protein 14, transcript variant X5
TRPL translocation defect protein 14 isoform X2
TRPL translocation defect protein 14 isoform X1
TRPL translocation defect protein 14 isoform X5
TRPL translocation defect protein 14, transcript variant X3
TRPL translocation defect protein 14, transcript variant X4
TRPL translocation defect protein 14 isoform X3
TRPL translocation defect protein 14 isoform X4
protoheme IX farnesyltransferase, mitochondrial, 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 31 samples with support for all annotated introns
protoheme IX farnesyltransferase, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 164 samples with support for all annotated introns
protoheme IX farnesyltransferase, mitochondrial isoform X1
protoheme IX farnesyltransferase, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 88 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X4
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM37-like isoform X1
E3 ubiquitin-protein ligase TRIM37-like isoform X2
E3 ubiquitin-protein ligase TRIM37-like isoform X3
E3 ubiquitin-protein ligase TRIM37-like isoform X4
rho GTPase-activating protein 21, transcript variant X5
rho GTPase-activating protein 21, transcript variant X2
rho GTPase-activating protein 21, transcript variant X6
rho GTPase-activating protein 21, transcript variant X4
rho GTPase-activating protein 21, transcript variant X3
rho GTPase-activating protein 21, transcript variant X1
rho GTPase-activating protein 21, transcript variant X7
rho GTPase-activating protein 21 isoform X2
rho GTPase-activating protein 21 isoform X6
rho GTPase-activating protein 21 isoform X4
rho GTPase-activating protein 21 isoform X3
rho GTPase-activating protein 21 isoform X1
rho GTPase-activating protein 21 isoform X5
rho GTPase-activating protein 21 isoform X7
rho GTPase-activating protein 21, transcript variant X9
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
rho GTPase-activating protein 21, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
rho GTPase-activating protein 21 isoform X8
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform, 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 89 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform, 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 11 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
leucine-rich repeat-containing protein 23-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 5 samples with support for all annotated introns
28S rRNA (cytosine-C(5))-methyltransferase
echinoderm microtubule-associated protein-like CG42247, 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
echinoderm microtubule-associated protein-like CG42247 isoform X2
echinoderm microtubule-associated protein-like CG42247, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
echinoderm microtubule-associated protein-like CG42247 isoform X1
echinoderm microtubule-associated protein-like CG42247, 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 2 samples with support for all annotated introns
echinoderm microtubule-associated protein-like CG42247 isoform X3
echinoderm microtubule-associated protein-like CG42247, transcript variant X4
echinoderm microtubule-associated protein-like CG42247 isoform X4
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4
CD63 antigen-like, transcript variant X2
CD63 antigen-like, transcript variant X1
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X7
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X5
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X2
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X6
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X4
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X1
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X3
ubiquitin-conjugating enzyme E2-24 kDa isoform X1
ubiquitin-conjugating enzyme E2-24 kDa isoform X2
RING-type E3 ubiquitin-protein ligase PPIL2
AP-1 complex subunit gamma-1, transcript variant X7
AP-1 complex subunit gamma-1, transcript variant X4
AP-1 complex subunit gamma-1, transcript variant X3
AP-1 complex subunit gamma-1, transcript variant X6
AP-1 complex subunit gamma-1, transcript variant X2
AP-1 complex subunit gamma-1, transcript variant X5
AP-1 complex subunit gamma-1, transcript variant X1
AP-1 complex subunit gamma-1, transcript variant X10
AP-1 complex subunit gamma-1, transcript variant X9
AP-1 complex subunit gamma-1, transcript variant X8
AP-1 complex subunit gamma-1, transcript variant X11
AP-1 complex subunit gamma-1 isoform X11
AP-1 complex subunit gamma-1 isoform X10
ADP-ribosylation factor-related protein 1
ero1-like protein, transcript variant X2
ero1-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 167 samples with support for all annotated introns
uncharacterized LOC125049855, transcript variant X2
uncharacterized LOC125049855, transcript variant X1
uncharacterized LOC125049855, transcript variant X5
uncharacterized LOC125049855, transcript variant X4
uncharacterized protein LOC125049855 isoform X2
uncharacterized protein LOC125049855 isoform X1
uncharacterized protein LOC125049855 isoform X4
uncharacterized protein LOC125049855 isoform X5
uncharacterized LOC125049855, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized protein LOC125049855 isoform X3
sodium-independent sulfate anion transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 139 samples with support for all annotated introns
uncharacterized LOC125049854, transcript variant X3
uncharacterized LOC125049854, transcript variant X2
uncharacterized LOC125049854, transcript variant X1
uncharacterized protein LOC125049854 isoform X1
uncharacterized protein LOC125049854 isoform X3
uncharacterized protein LOC125049854 isoform X2
superoxide dismutase [Cu-Zn] 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 142 samples with support for all annotated introns
superoxide dismutase [Cu-Zn] 5-like isoform X1
superoxide dismutase [Cu-Zn] 5-like, transcript variant X2
superoxide dismutase [Cu-Zn] 5-like isoform X2
superoxide dismutase [Cu-Zn]-like, transcript variant X2
superoxide dismutase [Cu-Zn]-like, transcript variant X1
superoxide dismutase [Cu-Zn]-like isoform X1
superoxide dismutase [Cu-Zn]-like isoform X2
acyl-CoA-binding protein homolog, transcript variant X2
acyl-CoA-binding protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: Bardet-Biedl syndrome 1 protein
uncharacterized protein LOC125049851 isoform X1
uncharacterized protein LOC125049851 isoform X3
uncharacterized protein LOC125049851 isoform X2
uncharacterized protein LOC125049851 isoform X4
rho guanine nucleotide exchange factor 19 isoform X5
transmembrane emp24 domain-containing protein 5
tRNA pseudouridine synthase-like 1, transcript variant X2
tRNA pseudouridine synthase-like 1, transcript variant X1
tRNA pseudouridine synthase-like 1, transcript variant X3
tRNA pseudouridine synthase-like 1 isoform X2
tRNA pseudouridine synthase-like 1 isoform X1
tRNA pseudouridine synthase-like 1, transcript variant X4
tRNA pseudouridine synthase-like 1 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 137 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 85 samples with support for all annotated introns
mitochondrial E3 ubiquitin protein ligase 1
mediator of RNA polymerase II transcription subunit 9
GTP-binding protein 1, transcript variant X2
GTP-binding protein 1, transcript variant X1
GTP-binding protein 1, transcript variant X4
GTP-binding protein 1, transcript variant X3
fidgetin-like protein 1, transcript variant X1
fidgetin-like protein 1, transcript variant X2
E3 ubiquitin-protein ligase MGRN1, transcript variant X1
E3 ubiquitin-protein ligase MGRN1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
probable cytosolic Fe-S cluster assembly factor GJ13047
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 111 samples with support for all annotated introns
ARF GTPase-activating protein Git, transcript variant X3
ARF GTPase-activating protein Git, transcript variant X2
ARF GTPase-activating protein Git, transcript variant X1
ARF GTPase-activating protein Git isoform X3
ARF GTPase-activating protein Git isoform X2
ARF GTPase-activating protein Git isoform X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit
leucine-rich repeat flightless-interacting protein 2, transcript variant X5
leucine-rich repeat flightless-interacting protein 2, transcript variant X4
leucine-rich repeat flightless-interacting protein 2 isoform X4
leucine-rich repeat flightless-interacting protein 2 isoform X5
leucine-rich repeat flightless-interacting protein 2, transcript variant X3
leucine-rich repeat flightless-interacting protein 2 isoform X3
leucine-rich repeat flightless-interacting protein 2, transcript variant X2
leucine-rich repeat flightless-interacting protein 2, transcript variant X1
leucine-rich repeat flightless-interacting protein 2 isoform X1
leucine-rich repeat flightless-interacting protein 2 isoform X2
leucine-rich repeat flightless-interacting protein 2, transcript variant X6
leucine-rich repeat flightless-interacting protein 2 isoform X6
mediator of RNA polymerase II transcription subunit 19
thioredoxin reductase 1, mitochondrial, transcript variant X2
thioredoxin reductase 1, mitochondrial, transcript variant X3
thioredoxin reductase 1, mitochondrial isoform X2
thioredoxin reductase 1, mitochondrial isoform X3
thioredoxin reductase 1, mitochondrial, transcript variant X1
thioredoxin reductase 1, mitochondrial isoform X1
matrix metalloproteinase-25-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
matrix metalloproteinase-25-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 163 samples with support for all annotated introns
matrix metalloproteinase-25-like isoform X2
matrix metalloproteinase-2-like isoform X1
cilia- and flagella-associated protein 251-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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
B-cell CLL/lymphoma 7 protein family member A
transmembrane GTPase Marf, transcript variant X4
transmembrane GTPase Marf, transcript variant X5
transmembrane GTPase Marf, transcript variant X2
transmembrane GTPase Marf, transcript variant X1
transmembrane GTPase Marf, transcript variant X3
germinal-center associated nuclear protein
uncharacterized LOC125049903, transcript variant X1
uncharacterized LOC125049903, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized serine-rich protein C215.13-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 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
2-oxoglutarate dehydrogenase, mitochondrial-like
COA8 family protein CG14806, mitochondrial
uncharacterized LOC125049985, transcript variant X1
uncharacterized LOC125049985, transcript variant X3
uncharacterized LOC125049985, transcript variant X2
uncharacterized protein LOC125049985 isoform X1
uncharacterized protein LOC125049985 isoform X3
uncharacterized protein LOC125049985 isoform X2
DNA oxidative demethylase ALKBH2-like, transcript variant X1
DNA oxidative demethylase ALKBH2-like, transcript variant X2
rab5 GDP/GTP exchange factor, transcript variant X2
rab5 GDP/GTP exchange factor, transcript variant X1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adhesion G-protein coupled receptor G2-like, transcript variant X1
adhesion G-protein coupled receptor G2-like, transcript variant X2
adhesion G-protein coupled receptor G2-like isoform X1
uncharacterized protein LOC125049981 isoform X2
dynein axonemal assembly factor 3 homolog
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X4
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X3
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X6
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X5
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X8
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X7
disintegrin and metalloproteinase domain-containing protein 11, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 11 isoform X4
disintegrin and metalloproteinase domain-containing protein 11 isoform X3
disintegrin and metalloproteinase domain-containing protein 11 isoform X6
disintegrin and metalloproteinase domain-containing protein 11 isoform X1
disintegrin and metalloproteinase domain-containing protein 11 isoform X5
disintegrin and metalloproteinase domain-containing protein 11 isoform X2
disintegrin and metalloproteinase domain-containing protein 11 isoform X7
disintegrin and metalloproteinase domain-containing protein 11 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
39S ribosomal protein L21, mitochondrial
regulator of telomere elongation helicase 1 homolog
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 39 samples with support for all annotated introns
elongator complex protein 2, transcript variant X2
elongator complex protein 2, transcript variant X1
myeloid differentiation primary response protein MyD88-like
uncharacterized LOC125049667, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized LOC125049667, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125049667, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125049667, 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 11 samples with support for all annotated introns
uncharacterized LOC125049667, 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 46 samples with support for all annotated introns
uncharacterized protein LOC125049667 isoform X2
uncharacterized protein LOC125049667 isoform X1
D-glucuronyl C5-epimerase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
D-glucuronyl C5-epimerase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
post-GPI attachment to proteins factor 3, transcript variant X2
post-GPI attachment to proteins factor 3, transcript variant X1
post-GPI attachment to proteins factor 3 isoform X1
post-GPI attachment to proteins factor 3 isoform X2
post-GPI attachment to proteins factor 3, transcript variant X3
post-GPI attachment to proteins factor 3 isoform X3
lethal(3)malignant brain tumor-like protein 3, transcript variant X1
lethal(3)malignant brain tumor-like protein 3, transcript variant X2
uncharacterized protein LOC125049786 isoform X1
lethal(3)malignant brain tumor-like protein 3 isoform X2
BTB/POZ domain-containing protein 9, transcript variant X1
BTB/POZ domain-containing protein 9, transcript variant X2
BTB/POZ domain-containing protein 9, transcript variant X3
BTB/POZ domain-containing protein 9 isoform X1
BTB/POZ domain-containing protein 9 isoform X2
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like, transcript variant X3
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like, transcript variant X2
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-like, transcript variant X1
U11/U12 small nuclear ribonucleoprotein 48 kDa protein-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
uncharacterized protein LOC125049914 isoform X2
uncharacterized LOC125049298, transcript variant X2
uncharacterized LOC125049298, transcript variant X1
uncharacterized LOC125049298, transcript variant X3
uncharacterized protein LOC125049298 isoform X1
uncharacterized protein LOC125049298 isoform X2
uncharacterized protein LOC125049298 isoform X3
vacuolar protein sorting-associated protein 13D
ester hydrolase C11orf54-like, transcript variant X3
ester hydrolase C11orf54-like, transcript variant X1
ester hydrolase C11orf54-like, transcript variant X2
ester hydrolase C11orf54-like isoform X1
ester hydrolase C11orf54-like isoform X2
ester hydrolase C11orf54-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 88 samples with support for all annotated introns
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC125049485 isoform X1
uncharacterized protein LOC125049485 isoform X2
rhomboid-related protein 2-like, transcript variant X3
rhomboid-related protein 2-like, transcript variant X4
rhomboid-related protein 2-like, transcript variant X2
rhomboid-related protein 2-like, transcript variant X1
probable G-protein coupled receptor Mth-like 1
uncharacterized LOC125049344, transcript variant X4
uncharacterized LOC125049344, transcript variant X1
uncharacterized LOC125049344, transcript variant X2
uncharacterized LOC125049344, 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
uncharacterized protein LOC125049344 isoform X1
uncharacterized protein LOC125049344 isoform X2
uncharacterized protein LOC125049344 isoform X3
protein-tyrosine sulfotransferase, transcript variant X1
protein-tyrosine sulfotransferase, transcript variant X2