Maniola jurtina chromosome 23, ilManJurt1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Nymphalidae; Satyrinae; Satyrini; Maniolina; Maniola.
REFSEQ INFORMATION: The reference sequence is identical to\nHG995230.1.\nAssembly name: ilManJurt1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/03/19. The original whole-genome shotgun project has the\naccession CAJOSP000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Maniola jurtina Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Down syndrome cell adhesion molecule-like protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual serine/threonine and tyrosine protein kinase-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 1 sample with support for all annotated introns
uncharacterized LOC123877296, 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 4 samples with support for all annotated introns
uncharacterized LOC123877296, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
extracellular matrix-binding protein ebh-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 17 samples with support for all annotated introns
uncharacterized LOC123877211, transcript variant X2
uncharacterized LOC123877211, 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 26 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 27 samples with support for all annotated introns
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X4
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X2
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X1
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X3
gamma-aminobutyric acid type B receptor subunit 2 isoform X4
gamma-aminobutyric acid type B receptor subunit 2 isoform X2
gamma-aminobutyric acid type B receptor subunit 2 isoform X3
gamma-aminobutyric acid type B receptor subunit 2 isoform X1
protein transport protein Sec24D, transcript variant X1
protein transport protein Sec24D, transcript variant X4
protein transport protein Sec24D, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein transport protein Sec24D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein transport protein Sec24D isoform X1
protein transport protein Sec24D isoform X3
protein transport protein Sec24D isoform X2
uncharacterized LOC123877216, transcript variant X3
uncharacterized LOC123877216, transcript variant X4
uncharacterized LOC123877216, transcript variant X1
uncharacterized LOC123877216, transcript variant X2
muscle calcium channel subunit alpha-1-like, transcript variant X9
muscle calcium channel subunit alpha-1-like, transcript variant X1
muscle calcium channel subunit alpha-1-like, transcript variant X7
muscle calcium channel subunit alpha-1-like, transcript variant X3
muscle calcium channel subunit alpha-1-like, transcript variant X6
muscle calcium channel subunit alpha-1-like, transcript variant X8
muscle calcium channel subunit alpha-1-like, transcript variant X2
muscle calcium channel subunit alpha-1-like, transcript variant X10
muscle calcium channel subunit alpha-1-like, transcript variant X11
muscle calcium channel subunit alpha-1-like, transcript variant X4
muscle calcium channel subunit alpha-1-like, transcript variant X12
muscle calcium channel subunit alpha-1-like, transcript variant X5
muscle calcium channel subunit alpha-1-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
muscle calcium channel subunit alpha-1-like isoform X9
muscle calcium channel subunit alpha-1-like isoform X1
muscle calcium channel subunit alpha-1-like isoform X7
muscle calcium channel subunit alpha-1-like isoform X3
muscle calcium channel subunit alpha-1-like isoform X6
muscle calcium channel subunit alpha-1-like isoform X8
muscle calcium channel subunit alpha-1-like isoform X2
muscle calcium channel subunit alpha-1-like isoform X10
muscle calcium channel subunit alpha-1-like isoform X11
muscle calcium channel subunit alpha-1-like isoform X4
muscle calcium channel subunit alpha-1-like isoform X12
muscle calcium channel subunit alpha-1-like isoform X5
mitochondrial import receptor subunit TOM40 homolog 1
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 16 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 22 samples with support for all annotated introns
zinc finger protein 329-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 7 samples with support for all annotated introns
zinc finger protein 329-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 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 41-like isoform X2
zinc finger protein 569-like, transcript variant X2
zinc finger protein 569-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 10 samples with support for all annotated introns
nuclear receptor subfamily 2 group C member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nuclear receptor subfamily 2 group C member 2, 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 7 samples with support for all annotated introns
nuclear receptor subfamily 2 group C member 2 isoform X2
nuclear receptor subfamily 2 group C member 2 isoform X1
U3 small nucleolar ribonucleoprotein protein MPP10
nuclear factor 1 B-type, transcript variant X1
nuclear factor 1 B-type, transcript variant X2
nuclear factor 1 B-type, transcript variant X4
nuclear factor 1 B-type, transcript variant X5
nuclear factor 1 B-type, transcript variant X9
nuclear factor 1 B-type, transcript variant X3
nuclear factor 1 B-type, transcript variant X10
nuclear factor 1 B-type, transcript variant X6
nuclear factor 1 B-type, transcript variant X7
nuclear factor 1 B-type, transcript variant X8
hepatocyte nuclear factor 6, 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 10 samples with support for all annotated introns
hepatocyte nuclear factor 6, 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 7 samples with support for all annotated introns
hepatocyte nuclear factor 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hepatocyte nuclear factor 6, transcript variant X4
potassium voltage-gated channel protein Shal, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel protein Shal, transcript variant X3
potassium voltage-gated channel protein Shal, 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 2 samples with support for all annotated introns
potassium voltage-gated channel protein Shal, 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 3 samples with support for all annotated introns
potassium voltage-gated channel protein Shal isoform X1
potassium voltage-gated channel protein Shal isoform X3
potassium voltage-gated channel protein Shal isoform X2
potassium voltage-gated channel protein Shal isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
wiskott-Aldrich syndrome protein family member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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
muscle calcium channel subunit alpha-1-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 1 sample with support for all annotated introns
muscle calcium channel subunit alpha-1-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscle calcium channel subunit alpha-1-like, transcript variant X16
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 1 sample with support for all annotated introns
muscle calcium channel subunit alpha-1-like, transcript variant X14
muscle calcium channel subunit alpha-1-like, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscle calcium channel subunit alpha-1-like isoform X14
muscle calcium channel subunit alpha-1-like isoform X13
muscle calcium channel subunit alpha-1-like isoform X15
muscle calcium channel subunit alpha-1-like isoform X16
voltage-dependent calcium channel type D subunit alpha-1-like isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123877432, transcript variant X1
uncharacterized LOC123877432, transcript variant X2
uncharacterized protein LOC123877432 isoform X1
uncharacterized protein LOC123877432 isoform X2
ommochrome-binding protein-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 8 samples with support for all annotated introns
ommochrome-binding protein-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
ommochrome-binding protein-like isoform X1
ommochrome-binding protein-like isoform X2
microtubule-associated serine/threonine-protein kinase 3, transcript variant X7
microtubule-associated serine/threonine-protein kinase 3, transcript variant X5
microtubule-associated serine/threonine-protein kinase 3, transcript variant X4
microtubule-associated serine/threonine-protein kinase 3, transcript variant X2
microtubule-associated serine/threonine-protein kinase 3, transcript variant X6
microtubule-associated serine/threonine-protein kinase 3, transcript variant X3
microtubule-associated serine/threonine-protein kinase 3, transcript variant X1
microtubule-associated serine/threonine-protein kinase 3 isoform X7
microtubule-associated serine/threonine-protein kinase 3 isoform X5
microtubule-associated serine/threonine-protein kinase 3 isoform X4
microtubule-associated serine/threonine-protein kinase 3 isoform X2
microtubule-associated serine/threonine-protein kinase 3 isoform X6
microtubule-associated serine/threonine-protein kinase 3 isoform X3
microtubule-associated serine/threonine-protein kinase 3 isoform X1
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X1
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X2
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X1
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X3
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X3
formin-like protein 6, 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
formin-like protein 6, transcript variant X2
tubulin alpha chain, transcript variant X1
tubulin alpha chain, transcript variant X2
protein MON2 homolog, transcript variant X2
protein MON2 homolog, transcript variant X1
nuclear receptor coactivator 6, transcript variant X8
nuclear receptor coactivator 6, transcript variant X5
nuclear receptor coactivator 6, transcript variant X7
nuclear receptor coactivator 6, transcript variant X10
nuclear receptor coactivator 6, transcript variant X6
nuclear receptor coactivator 6, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor coactivator 6, transcript variant X2
nuclear receptor coactivator 6, transcript variant X1
nuclear receptor coactivator 6, transcript variant X4
nuclear receptor coactivator 6, transcript variant X3
uncharacterized protein LOC123877422 isoform X1
uncharacterized protein LOC123877422 isoform X5
uncharacterized protein LOC123877422 isoform X2
uncharacterized protein LOC123877422 isoform X4
uncharacterized protein LOC123877422 isoform X7
uncharacterized protein LOC123877422 isoform X3
nuclear receptor coactivator 6 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1
zinc finger protein rotund-like, transcript variant X3
zinc finger protein rotund-like, transcript variant X2
zinc finger protein rotund-like, transcript variant X1
zinc finger protein rotund-like isoform X2
zinc finger protein rotund-like isoform X1
zinc finger protein 135-like, transcript variant X3
zinc finger protein 135-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 135-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 135-like, transcript variant X8
zinc finger protein 135-like, transcript variant X5
zinc finger protein 135-like, transcript variant X7
zinc finger protein 135-like, transcript variant X1
zinc finger protein 135-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 135-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123877456 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% 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 6 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 6 samples with support for all annotated introns
two pore potassium channel protein sup-9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor interleukin-3-regulated protein
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
uncharacterized LOC123877244, transcript variant X1
uncharacterized LOC123877244, transcript variant X2
uncharacterized protein LOC123877244 isoform X1
uncharacterized protein LOC123877244 isoform X2
uncharacterized LOC123877364, transcript variant X11
uncharacterized LOC123877364, transcript variant X10
uncharacterized LOC123877364, transcript variant X2
uncharacterized LOC123877364, transcript variant X5
uncharacterized LOC123877364, transcript variant X9
uncharacterized LOC123877364, transcript variant X4
uncharacterized LOC123877364, transcript variant X8
uncharacterized LOC123877364, transcript variant X7
uncharacterized LOC123877364, transcript variant X6
uncharacterized LOC123877364, transcript variant X3
uncharacterized LOC123877364, transcript variant X1
uncharacterized protein LOC123877364 isoform X11
uncharacterized protein LOC123877364 isoform X10
uncharacterized protein LOC123877364 isoform X2
uncharacterized protein LOC123877364 isoform X5
uncharacterized protein LOC123877364 isoform X9
uncharacterized protein LOC123877364 isoform X4
uncharacterized protein LOC123877364 isoform X8
uncharacterized protein LOC123877364 isoform X7
uncharacterized protein LOC123877364 isoform X6
uncharacterized protein LOC123877364 isoform X3
uncharacterized protein LOC123877364 isoform X1
rho GTPase-activating protein 190, transcript variant X8
rho GTPase-activating protein 190, transcript variant X2
rho GTPase-activating protein 190, transcript variant X4
rho GTPase-activating protein 190, transcript variant X1
rho GTPase-activating protein 190, transcript variant X3
rho GTPase-activating protein 190, transcript variant X7
rho GTPase-activating protein 190, transcript variant X6
rho GTPase-activating protein 190, transcript variant X5
rho GTPase-activating protein 190, transcript variant X10
rho GTPase-activating protein 190, transcript variant X9
uncharacterized LOC123877366, transcript variant X1
uncharacterized LOC123877366, transcript variant X2
uncharacterized LOC123877366, transcript variant X3
uncharacterized LOC123877366, transcript variant X5
uncharacterized LOC123877366, transcript variant X4
uncharacterized LOC123877366, transcript variant X6
uncharacterized LOC123877366, transcript variant X11
uncharacterized LOC123877366, transcript variant X10
uncharacterized LOC123877366, transcript variant X8
uncharacterized LOC123877366, transcript variant X9
uncharacterized LOC123877366, transcript variant X7
uncharacterized protein LOC123877366 isoform X6
uncharacterized protein LOC123877366 isoform X5
uncharacterized protein LOC123877366 isoform X2
uncharacterized protein LOC123877366 isoform X4
uncharacterized protein LOC123877366 isoform X3
uncharacterized protein LOC123877366 isoform X1
uncharacterized protein LOC123877366 isoform X11
uncharacterized protein LOC123877366 isoform X10
uncharacterized protein LOC123877366 isoform X8
uncharacterized protein LOC123877366 isoform X9
uncharacterized protein LOC123877366 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
protein pangolin, isoforms A/H/I/S, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, transcript variant X7
protein pangolin, isoforms A/H/I/S, transcript variant X8
protein pangolin, isoforms A/H/I/S, transcript variant X1
protein pangolin, isoforms A/H/I/S, transcript variant X3
protein pangolin, isoforms A/H/I/S, transcript variant X6
protein pangolin, isoforms A/H/I/S, transcript variant X2
protein pangolin, isoforms A/H/I/S isoform X1
protein pangolin, isoforms A/H/I/S isoform X3
protein pangolin, isoforms A/H/I/S isoform X2
protein pangolin, isoforms A/H/I/S isoform X6
protein pangolin, isoforms A/H/I/S isoform X4
protein pangolin, isoforms A/H/I/S isoform X5
protein pangolin, isoforms A/H/I/S isoform X7
protein pangolin, isoforms A/H/I/S isoform X8
dihydropyrimidinase, transcript variant X2
dihydropyrimidinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
endothelin-converting enzyme homolog, transcript variant X3
endothelin-converting enzyme homolog isoform X2
endothelin-converting enzyme homolog, transcript variant X1
endothelin-converting enzyme homolog, transcript variant X2
endothelin-converting enzyme homolog isoform X1
endothelin-converting enzyme homolog, transcript variant X4
endothelin-converting enzyme homolog isoform X3
uncharacterized LOC123877230, transcript variant X2
uncharacterized LOC123877230, 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 20 samples with support for all annotated introns
uncharacterized LOC123877230, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123877230, transcript variant X1
uncharacterized protein LOC123877230 isoform X1
uncharacterized protein LOC123877230 isoform X2
uncharacterized protein LOC123877230 isoform X3
glycine receptor subunit alpha-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
glycine receptor subunit alpha-4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine receptor subunit alpha-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123877361, transcript variant X2
uncharacterized LOC123877361, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon UGG); 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 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA Delta(11) desaturase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-CoA Delta(11) desaturase-like, transcript variant X2
collagen alpha-2(I) chain-like, transcript variant X4
collagen alpha-2(I) chain-like, transcript variant X1
collagen alpha-2(I) chain-like, transcript variant X9
collagen alpha-2(I) chain-like, transcript variant X7
collagen alpha-2(I) chain-like, transcript variant X5
collagen alpha-2(I) chain-like, transcript variant X6
collagen alpha-2(I) chain-like, transcript variant X8
collagen alpha-2(I) chain-like, transcript variant X3
collagen alpha-2(I) chain-like, transcript variant X10
collagen alpha-2(I) chain-like, transcript variant X11
collagen alpha-2(I) chain-like, transcript variant X2
collagen alpha-1(III) chain-like isoform X1
collagen alpha-1(I) chain-like isoform X6
collagen alpha-1(I) chain-like isoform X4
collagen alpha-1(I) chain-like isoform X7
collagen alpha-2(I) chain-like isoform X3
collagen alpha-2(I) chain-like isoform X5
uncharacterized LOC123877333, transcript variant X1
uncharacterized LOC123877333, transcript variant X2
uncharacterized protein LOC123877333 isoform X2
uncharacterized protein LOC123877333 isoform X1
protein lethal(2)essential for life-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123877346, transcript variant X3
uncharacterized LOC123877346, transcript variant X1
uncharacterized LOC123877346, transcript variant X2
uncharacterized protein LOC123877346 isoform X3
uncharacterized protein LOC123877346 isoform X1
uncharacterized protein LOC123877346 isoform X2
dual specificity protein phosphatase CDC14B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
pyrroline-5-carboxylate reductase, transcript variant X1
pyrroline-5-carboxylate reductase, transcript variant X2
pyrroline-5-carboxylate reductase isoform X1
pyrroline-5-carboxylate reductase isoform X2
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polyamine-transporting ATPase 13A3-like, transcript variant X2
polyamine-transporting ATPase 13A3-like, transcript variant X3
polyamine-transporting ATPase 13A3-like, transcript variant X1
polyamine-transporting ATPase 13A3-like isoform X2
polyamine-transporting ATPase 13A3-like isoform X1
DNA-directed RNA polymerases I, II, and III subunit RPABC5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC5, transcript variant X1
DNA-directed RNA polymerases I, II, and III subunit RPABC5
dual specificity tyrosine-phosphorylation-regulated kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane and coiled-coil domains protein 2, transcript variant X1
transmembrane and coiled-coil domains protein 2, transcript variant X2
transmembrane and coiled-coil domains protein 2, transcript variant X3
transmembrane and coiled-coil domains protein 2, transcript variant X5
transmembrane and coiled-coil domains protein 2, transcript variant X6
transmembrane and coiled-coil domains protein 2, transcript variant X4
transmembrane and coiled-coil domains protein 2, transcript variant X7
transmembrane and coiled-coil domains protein 2, transcript variant X8
transmembrane and coiled-coil domains protein 2, transcript variant X9
transmembrane and coiled-coil domains protein 2, transcript variant X10
transmembrane and coiled-coil domains protein 2 isoform X1
transmembrane and coiled-coil domains protein 2 isoform X2
transmembrane and coiled-coil domains protein 2 isoform X3
transmembrane and coiled-coil domains protein 2 isoform X5
transmembrane and coiled-coil domains protein 2 isoform X6
transmembrane and coiled-coil domains protein 2 isoform X4
transmembrane and coiled-coil domains protein 2 isoform X7
transmembrane and coiled-coil domains protein 2 isoform X8
transmembrane and coiled-coil domains protein 2 isoform X9
transmembrane and coiled-coil domains protein 2 isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 185 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-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 5 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like isoform X2
facilitated trehalose transporter Tret1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123877248
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
IQ motif and SEC7 domain-containing protein 2, transcript variant X7
IQ motif and SEC7 domain-containing protein 2, transcript variant X2
IQ motif and SEC7 domain-containing protein 2, transcript variant X6
IQ motif and SEC7 domain-containing protein 2, transcript variant X1
IQ motif and SEC7 domain-containing protein 2, transcript variant X4
IQ motif and SEC7 domain-containing protein 2, transcript variant X5
IQ motif and SEC7 domain-containing protein 2, transcript variant X3
IQ motif and SEC7 domain-containing protein 2 isoform X6
IQ motif and SEC7 domain-containing protein 3 isoform X2
IQ motif and SEC7 domain-containing protein 2 isoform X5
IQ motif and SEC7 domain-containing protein 2 isoform X1
IQ motif and SEC7 domain-containing protein 3 isoform X4
IQ motif and SEC7 domain-containing protein 2 isoform X3
general transcription factor II-I repeat domain-containing protein 2-like
uncharacterized LOC123877262, transcript variant X2
uncharacterized LOC123877262, transcript variant X1
transcriptional activator cubitus interruptus, transcript variant X1
transcriptional activator cubitus interruptus, transcript variant X2
transcriptional activator cubitus interruptus
dual specificity protein phosphatase 22-like, transcript variant X2
dual specificity protein phosphatase 22-like, transcript variant X1
dual specificity protein phosphatase 22-like
dual specificity protein phosphatase 22-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123877463, transcript variant X6
uncharacterized LOC123877463, transcript variant X10
uncharacterized LOC123877463, transcript variant X1
uncharacterized LOC123877463, transcript variant X7
uncharacterized LOC123877463, transcript variant X5
uncharacterized LOC123877463, transcript variant X3
uncharacterized LOC123877463, transcript variant X4
uncharacterized LOC123877463, transcript variant X8
uncharacterized LOC123877463, transcript variant X9
uncharacterized LOC123877463, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC123877463 isoform X1
uncharacterized protein LOC123877463 isoform X2
uncharacterized protein LOC123877463 isoform X4
uncharacterized protein LOC123877463 isoform X5
uncharacterized protein LOC123877463 isoform X6
uncharacterized protein LOC123877463 isoform X8
uncharacterized protein LOC123877463 isoform X3
uncharacterized protein LOC123877463 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123877394, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123877394, transcript variant X1
uncharacterized LOC123877394, transcript variant X3
uncharacterized LOC123877394, transcript variant X4
uncharacterized protein LOC123877394 isoform X2
uncharacterized protein LOC123877394 isoform X1
uncharacterized protein LOC123877394 isoform X3
tyrosine-protein phosphatase 69D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tyrosine-protein phosphatase 69D, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tyrosine-protein phosphatase 69D, transcript variant X2
tyrosine-protein phosphatase 69D, transcript variant X4
tyrosine-protein phosphatase 69D isoform X1
tyrosine-protein phosphatase 69D isoform X3
tyrosine-protein phosphatase 69D isoform X2
tyrosine-protein phosphatase 69D isoform X4
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X1
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X3
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X4
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X2
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X5
calponin homology domain-containing protein DDB_G0272472-like isoform X1
calponin homology domain-containing protein DDB_G0272472-like isoform X3
calponin homology domain-containing protein DDB_G0272472-like isoform X4
calponin homology domain-containing protein DDB_G0272472-like isoform X2
calponin homology domain-containing protein DDB_G0272472-like isoform X5
plasma membrane calcium-transporting ATPase 3, transcript variant X5
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X2
plasma membrane calcium-transporting ATPase 3, transcript variant X7
plasma membrane calcium-transporting ATPase 3, transcript variant X12
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 3, transcript variant X10
plasma membrane calcium-transporting ATPase 3, transcript variant X13
plasma membrane calcium-transporting ATPase 3, transcript variant X8
plasma membrane calcium-transporting ATPase 3, transcript variant X11
plasma membrane calcium-transporting ATPase 3, transcript variant X9
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X8
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 2 isoform X6
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X7
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 3, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X16
plasma membrane calcium-transporting ATPase 3, transcript variant X15
plasma membrane calcium-transporting ATPase 3, transcript variant X14
plasma membrane calcium-transporting ATPase 3 isoform X10
plasma membrane calcium-transporting ATPase 3 isoform X9
plasma membrane calcium-transporting ATPase 3 isoform X11
solute carrier family 41 member 1-like, transcript variant X1
solute carrier family 41 member 1-like, transcript variant X2
solute carrier family 41 member 1-like isoform X1
solute carrier family 41 member 1-like isoform X2
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
acidic repeat-containing protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
acidic repeat-containing protein, transcript variant X2
uncharacterized protein LOC123877400 isoform X1
acidic repeat-containing protein isoform X2
uncharacterized LOC123877398, transcript variant X1
uncharacterized LOC123877398, 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 6 samples with support for all annotated introns
uncharacterized protein LOC123877398 isoform X1
uncharacterized protein LOC123877398 isoform X2
uncharacterized LOC123877402, 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 8 samples with support for all annotated introns
uncharacterized LOC123877402, 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 5 samples with support for all annotated introns
uncharacterized LOC123877402, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123877402, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC123877402 isoform X2
uncharacterized protein LOC123877402 isoform X1
uncharacterized protein LOC123877402 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 7 samples with support for all annotated introns
zinc finger BED domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
CCR4-NOT transcription complex subunit 1-like, transcript variant X2
CCR4-NOT transcription complex subunit 1-like, transcript variant X1
CCR4-NOT transcription complex subunit 1-like, transcript variant X3
CCR4-NOT transcription complex subunit 1-like isoform X2
CCR4-NOT transcription complex subunit 1-like isoform X1
CCR4-NOT transcription complex subunit 1-like isoform X3
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
neuronal acetylcholine receptor subunit beta-4-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
sugar transporter ERD6-like 6 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X5
facilitated trehalose transporter Tret1-like isoform X5
facilitated trehalose transporter Tret1-like, transcript variant X4
sugar transporter ERD6-like 6 isoform X1
sugar transporter ERD6-like 6 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
forkhead box protein P1, transcript variant X3
forkhead box protein P1, transcript variant X2
forkhead box protein P1, transcript variant X1
forkhead box protein P1, transcript variant X4
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
calcium-dependent secretion activator, transcript variant X15
calcium-dependent secretion activator, transcript variant X5
calcium-dependent secretion activator, transcript variant X14
calcium-dependent secretion activator, transcript variant X10
calcium-dependent secretion activator, transcript variant X2
calcium-dependent secretion activator, transcript variant X13
calcium-dependent secretion activator, transcript variant X4
calcium-dependent secretion activator, transcript variant X11
calcium-dependent secretion activator, transcript variant X3
calcium-dependent secretion activator, transcript variant X12
calcium-dependent secretion activator, transcript variant X6
calcium-dependent secretion activator, transcript variant X8
calcium-dependent secretion activator, transcript variant X7
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator, transcript variant X9
calcium-dependent secretion activator isoform X15
calcium-dependent secretion activator isoform X5
calcium-dependent secretion activator isoform X14
calcium-dependent secretion activator isoform X10
calcium-dependent secretion activator isoform X2
calcium-dependent secretion activator isoform X13
calcium-dependent secretion activator isoform X4
calcium-dependent secretion activator isoform X11
calcium-dependent secretion activator isoform X3
calcium-dependent secretion activator isoform X12
calcium-dependent secretion activator isoform X6
calcium-dependent secretion activator isoform X8
calcium-dependent secretion activator isoform X7
calcium-dependent secretion activator isoform X1
calcium-dependent secretion activator isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
MAM and LDL-receptor class A domain-containing protein 1-like
gastrula zinc finger protein XlCGF26.1-like, transcript variant X1
gastrula zinc finger protein XlCGF26.1-like, transcript variant X2
gastrula zinc finger protein XlCGF26.1-like isoform X1
gastrula zinc finger protein XlCGF26.1-like isoform X2
zinc finger protein 100-like, transcript variant X1
zinc finger protein 100-like, transcript variant X3
zinc finger protein 100-like, transcript variant X2
sodium- and chloride-dependent GABA transporter 1, transcript variant X3
sodium- and chloride-dependent GABA transporter 1, transcript variant X1
sodium- and chloride-dependent GABA transporter 1, transcript variant X2
sodium- and chloride-dependent GABA transporter 1, transcript variant X4
sodium- and chloride-dependent GABA transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NACHT and WD repeat domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 9, transcript variant X2
solute carrier family 12 member 9, transcript variant X1
solute carrier family 12 member 9, transcript variant X3
solute carrier family 12 member 9 isoform X1
solute carrier family 12 member 9 isoform X2
solute carrier family 12 member 9 isoform X3
probable small nuclear ribonucleoprotein G
transcription factor EB-like, transcript variant X1
transcription factor EB-like, transcript variant X2
transcription factor EB-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X3
uncharacterized LOC123877178, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123877178, transcript variant X6
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 12 samples with support for all annotated introns
uncharacterized LOC123877178, transcript variant X3
uncharacterized LOC123877178, transcript variant X7
uncharacterized LOC123877178, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC123877178, transcript variant X5
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
uncharacterized LOC123877178, 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 16 samples with support for all annotated introns
uncharacterized LOC123877178, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123877178, transcript variant X9
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 17 samples with support for all annotated introns
uncharacterized protein LOC123877178 isoform X3
uncharacterized protein LOC123877178 isoform X1
uncharacterized protein LOC123877178 isoform X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
ATP-binding cassette sub-family D member, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-binding cassette sub-family D member, transcript variant X3
ATP-binding cassette sub-family D member, 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 8 samples with support for all annotated introns
ATP-binding cassette sub-family D member
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 2 samples with support for all annotated introns
chloride channel protein 2, transcript variant X4
chloride channel protein 2, transcript variant X2
chloride channel protein 2, transcript variant X3
chloride channel protein 2, transcript variant X1
chloride channel protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 7 Proteins, 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: 9 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X2
facilitated trehalose transporter Tret1-2 homolog, transcript variant X1
facilitated trehalose transporter Tret1-2 homolog
uncharacterized LOC123877280, transcript variant X2
uncharacterized LOC123877280, 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 9 samples with support for all annotated introns
uncharacterized protein LOC123877280 isoform X2
uncharacterized protein LOC123877280 isoform X1
uncharacterized LOC123877280, transcript variant X3
uncharacterized protein LOC123877280 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
lysine-specific demethylase lid, transcript variant X6
lysine-specific demethylase lid, transcript variant X3
lysine-specific demethylase lid, transcript variant X2
lysine-specific demethylase lid, transcript variant X5
lysine-specific demethylase lid, transcript variant X4
lysine-specific demethylase lid, transcript variant X1
lysine-specific demethylase lid isoform X4
lysine-specific demethylase lid isoform X3
lysine-specific demethylase lid isoform X2
lysine-specific demethylase lid isoform X1
uncharacterized LOC123877278, transcript variant X1
uncharacterized LOC123877278, transcript variant X2
uncharacterized protein LOC123877278 isoform X1
uncharacterized protein LOC123877278 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
fez family zinc finger protein erm-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fez family zinc finger protein erm-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 15 samples with support for all annotated introns
transcriptional activator protein Pur-alpha, transcript variant X2
transcriptional activator protein Pur-alpha, transcript variant X1
transcriptional activator protein Pur-alpha, transcript variant X6
transcriptional activator protein Pur-alpha, transcript variant X4
transcriptional activator protein Pur-alpha, transcript variant X5
transcriptional activator protein Pur-alpha, transcript variant X3
transcriptional activator protein Pur-alpha isoform X2
transcriptional activator protein Pur-beta isoform X1
transcriptional activator protein Pur-beta isoform X6
transcriptional activator protein Pur-beta isoform X4
transcriptional activator protein Pur-beta isoform X5
transcriptional activator protein Pur-beta isoform X3
trithorax group protein osa, transcript variant X7
trithorax group protein osa, transcript variant X4
trithorax group protein osa, transcript variant X5
trithorax group protein osa, transcript variant X2
trithorax group protein osa, transcript variant X3
trithorax group protein osa, transcript variant X1
trithorax group protein osa, transcript variant X6
hexokinase-2-like, transcript variant X1
hexokinase-2-like, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X3
epidermal growth factor receptor kinase substrate 8-like protein 1, 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 3 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X2
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF2