Rhincodon typus isolate 14 chromosome 20, sRhiTyp1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Rhincodontidae; Rhincodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038817.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\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: 2 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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: FMRFamide receptor-like
cell division cycle and apoptosis regulator 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cell division cycle and apoptosis regulator protein 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00607
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
vacuolar protein sorting-associated protein 26A
SUV3-like helicase, transcript variant X1
SUV3-like helicase, transcript variant X2
SUV3-like helicase, transcript variant X3
ATP-dependent RNA helicase SUPV3L1, mitochondrial isoform X1
ATP-dependent RNA helicase SUPV3L1, mitochondrial isoform X2
ATP-dependent RNA helicase SUPV3L1, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 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: 12 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 25 member 16, transcript variant X1
solute carrier family 25 member 16, transcript variant X2
eukaryotic translation initiation factor 4E family member 1c
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
DNA replication ATP-dependent helicase/nuclease DNA2
heterogeneous nuclear ribonucleoprotein H3 (2H9), transcript variant X1
heterogeneous nuclear ribonucleoprotein H3 (2H9), transcript variant X2
heterogeneous nuclear ribonucleoprotein H3 isoform X2
heterogeneous nuclear ribonucleoprotein H3 isoform X1
heterogeneous nuclear ribonucleoprotein H3 (2H9), transcript variant X3
heterogeneous nuclear ribonucleoprotein H3 isoform X3
RUN and FYVE domain containing 2, transcript variant X4
RUN and FYVE domain containing 2, transcript variant X3
RUN and FYVE domain containing 2, transcript variant X2
RUN and FYVE domain containing 2, transcript variant X1
RUN and FYVE domain-containing protein 2 isoform X2
RUN and FYVE domain-containing protein 2 isoform X3
RUN and FYVE domain-containing protein 2 isoform X4
RUN and FYVE domain-containing protein 2 isoform X1
uncharacterized protein LOC100535981 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC100535981 homolog, 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 LOC100535981 homolog, 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 5 samples with support for all annotated introns
uncharacterized protein si:ch211-250c4.3 isoform X3
uncharacterized protein si:ch211-250c4.3 isoform X1
uncharacterized protein si:ch211-250c4.3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
broad substrate specificity ATP-binding cassette transporter ABCG2-like
protein phosphatase 1K, mitochondrial-like
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 2 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 69% coverage of the annotated genomic feature by RNAseq alignments
polycystic kidney disease 2-like 1 protein
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
HECT and RLD domain containing E3 ubiquitin protein ligase 4, transcript variant X1
HECT and RLD domain containing E3 ubiquitin protein ligase 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 11 samples with support for all annotated introns
HECT and RLD domain containing E3 ubiquitin protein ligase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
HECT and RLD domain containing E3 ubiquitin protein ligase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HERC4 isoform X1
probable E3 ubiquitin-protein ligase HERC4 isoform X2
probable E3 ubiquitin-protein ligase HERC4 isoform X3
cytochrome c oxidase subunit 5B, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytochrome c oxidase subunit 5B, mitochondrial
NAD-dependent protein deacetylase sirtuin-1 isoform X2
NAD-dependent protein deacetylase sirtuin-1 isoform X1
DnaJ (Hsp40) homolog, subfamily C, member 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 94% 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: 1 Protein
erythroblast NAD(P)(+)--arginine ADP-ribosyltransferase-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 7 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 22 member 15, transcript variant X3
solute carrier family 22 member 15, transcript variant X2
solute carrier family 22 member 15, transcript variant X1
solute carrier family 22 member 15, transcript variant X4
solute carrier family 22 member 15 isoform X3
solute carrier family 22 member 15 isoform X2
solute carrier family 22 member 15 isoform X1
solute carrier family 22 member 15 isoform X4
receptor accessory protein 3b, transcript variant X1
receptor accessory protein 3b, transcript variant X2
receptor accessory protein 3b, transcript variant X3
receptor expression-enhancing protein 3 isoform X1
receptor expression-enhancing protein 3 isoform X2
probable JmjC domain-containing histone demethylation protein 2C, transcript variant 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, including 1 sample with support for all annotated introns
probable JmjC domain-containing histone demethylation protein 2C
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
probable JmjC domain-containing histone demethylation protein 2C, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125485556, transcript variant X1
uncharacterized LOC125485556, transcript variant X2
uncharacterized LOC125485556, transcript variant X3
2-aminoethanethiol (cysteamine) dioxygenase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% 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: 2 Proteins, and 64% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
AT-rich interaction domain 5B, transcript variant X1
AT-rich interaction domain 5B, transcript variant X2
AT-rich interaction domain 5B, transcript variant X3
AT-rich interactive domain-containing protein 5B isoform X1
AT-rich interactive domain-containing protein 5B isoform X2
ciliary associated calcium binding coiled-coil 1, transcript variant X2
ciliary associated calcium binding coiled-coil 1, transcript variant X5
ciliary associated calcium binding coiled-coil 1, transcript variant X3
ciliary associated calcium binding coiled-coil 1, transcript variant X4
ciliary associated calcium binding coiled-coil 1, transcript variant X1
ciliary-associated calcium-binding coiled-coil protein 1 isoform X2
ciliary-associated calcium-binding coiled-coil protein 1 isoform X5
ciliary-associated calcium-binding coiled-coil protein 1 isoform X3
ciliary-associated calcium-binding coiled-coil protein 1 isoform X4
ciliary-associated calcium-binding coiled-coil protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Rho related BTB domain containing 1, transcript variant X3
Rho related BTB domain containing 1, transcript variant X2
Rho related BTB domain containing 1, transcript variant X1
Rho related BTB domain containing 1, transcript variant X4
rho-related BTB domain-containing protein 1 isoform X1
Rho related BTB domain containing 1, transcript variant X5
rho-related BTB domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
coiled-coil domain-containing protein 6b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
family with sequence similarity 13 member C, transcript variant X1
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 3 samples with support for all annotated introns
family with sequence similarity 13 member C, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 13 member C, transcript variant X2
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 2 samples with support for all annotated introns
family with sequence similarity 13 member C, transcript variant X6
family with sequence similarity 13 member C, transcript variant X5
family with sequence similarity 13 member C, transcript variant X4
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
phytanoyl-CoA 2-hydroxylase interacting protein-like b, 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 2 samples with support for all annotated introns
phytanoyl-CoA hydroxylase-interacting protein-like isoform X1
phytanoyl-CoA 2-hydroxylase interacting protein-like b, 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 3 samples with support for all annotated introns
phytanoyl-CoA hydroxylase-interacting protein-like isoform X2
uncharacterized protein LOC550248 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
protein bicaudal C homolog 1-A isoform X1
uncharacterized protein LOC550248 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC550248 homolog, 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 5 samples with support for all annotated introns
protein bicaudal C homolog 1-A isoform X3
protein bicaudal C homolog 1-A isoform X2
transcription factor A, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 4 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transcription factor A, mitochondrial isoform X2
transcription factor A, mitochondrial, transcript variant X1
transcription factor A, mitochondrial isoform X1
CDGSH iron-sulfur domain-containing protein 1
LOW QUALITY PROTEIN: CDGSH iron-sulfur domain-containing protein 1
inositol polyphosphate multikinase b, transcript variant X1
inositol polyphosphate multikinase isoform X1
inositol polyphosphate multikinase b, transcript variant X2
inositol polyphosphate multikinase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
dickkopf WNT signaling pathway inhibitor 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
apobec1 complementation factor, transcript variant X1
apobec1 complementation factor, transcript variant X3
apobec1 complementation factor, transcript variant X2
apobec1 complementation factor, transcript variant X4
apobec1 complementation factor, transcript variant X5
APOBEC1 complementation factor isoform X1
APOBEC1 complementation factor isoform X3
APOBEC1 complementation factor isoform X2
APOBEC1 complementation factor isoform X4
APOBEC1 complementation factor isoform X5
phosphatidylcholine:ceramide cholinephosphotransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
multiple inositol-polyphosphate phosphatase 1b, transcript variant X1
multiple inositol-polyphosphate phosphatase 1b, transcript variant X2
multiple inositol polyphosphate phosphatase 1b isoform X1
multiple inositol polyphosphate phosphatase 1b isoform X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2-like
ATPase family AAA domain containing 1b, transcript variant X2
ATPase family AAA domain containing 1b, transcript variant X3
ATPase family AAA domain containing 1b, transcript variant X4
ATPase family AAA domain containing 1b, transcript variant X1
ATPase family AAA domain containing 1b, transcript variant X5
outer mitochondrial transmembrane helix translocase isoform X1
outer mitochondrial transmembrane helix translocase isoform X2
outer mitochondrial transmembrane helix translocase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 8 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
STAM binding protein-like 1, transcript variant X1
STAM binding protein-like 1, transcript variant X3
STAM binding protein-like 1, transcript variant X2
tumor necrosis factor receptor superfamily member 6-like, transcript variant X1
tumor necrosis factor receptor superfamily member 6-like, transcript variant X2
tumor necrosis factor receptor superfamily member 6-like, transcript variant X3
tumor necrosis factor receptor superfamily member 6-like isoform X1
tumor necrosis factor receptor superfamily member 6-like isoform X2
tumor necrosis factor receptor superfamily member 6-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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon-induced protein with tetratricopeptide repeats 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
monocarboxylate transporter 12, transcript variant X9
monocarboxylate transporter 12, transcript variant X7
monocarboxylate transporter 12, transcript variant X6
monocarboxylate transporter 12, transcript variant X2
monocarboxylate transporter 12, transcript variant X4
monocarboxylate transporter 12, transcript variant X10
monocarboxylate transporter 12, transcript variant X1
monocarboxylate transporter 12, transcript variant X5
monocarboxylate transporter 12, transcript variant X3
monocarboxylate transporter 12, transcript variant X8
monocarboxylate transporter 12 isoform X1
monocarboxylate transporter 12 isoform X2
monocarboxylate transporter 12 isoform X3
pantothenate kinase 1, transcript variant X3
pantothenate kinase 1, transcript variant X1
pantothenate kinase 1, transcript variant X4
pantothenate kinase 1, transcript variant X2
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease P/MRP 30 subunit, transcript variant X1
ribonuclease P/MRP 30 subunit, transcript variant X3
ribonuclease P/MRP 30 subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
ankyrin repeat domain 1b (cardiac muscle)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ankyrin repeat domain-containing protein 1b
polycomb group ring finger 5b, transcript variant X1
polycomb group ring finger 5b, transcript variant X2
polycomb group ring finger 5b, transcript variant X4
polycomb group ring finger 5b, transcript variant X3
polycomb group ring finger 5b, transcript variant X6
polycomb group ring finger 5b, transcript variant X5
HECT domain containing 2, transcript variant X1
HECT domain containing 2, 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 1 sample with support for all annotated introns
probable E3 ubiquitin-protein ligase HECTD2
protein phosphatase 1, regulatory subunit 3Cb
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 3C-B
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X6
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
poly [ADP-ribose] polymerase tankyrase-2, 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 5 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X2
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X1
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X3
poly [ADP-ribose] polymerase tankyrase-2 isoform X1
poly [ADP-ribose] polymerase tankyrase-2 isoform X3
poly [ADP-ribose] polymerase tankyrase-2 isoform X2
poly [ADP-ribose] polymerase tankyrase-2 isoform X4
poly [ADP-ribose] polymerase tankyrase-2 isoform X6
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X7
poly [ADP-ribose] polymerase tankyrase-2, transcript variant X5
poly [ADP-ribose] polymerase tankyrase-2 isoform X5
poly [ADP-ribose] polymerase tankyrase-2 isoform X7
fibroblast growth factor-binding protein 3-like, transcript variant X4
fibroblast growth factor-binding protein 3-like, transcript variant X2
fibroblast growth factor-binding protein 3-like, transcript variant X1
fibroblast growth factor-binding protein 3-like, transcript variant X3
fibroblast growth factor-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1
solute carrier family 35 member G1, transcript variant X2
solute carrier family 35 member G1, transcript variant X1
solute carrier family 35 member G1 isoform X2
solute carrier family 35 member G1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich glioma-inactivated protein 1b
phosphodiesterase 6C, cGMP-specific, cone, alpha prime
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha'
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 26A1, transcript variant X3
cytochrome P450 26A1, transcript variant X2
cytochrome P450 26A1, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytochrome P450 26C1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hematopoietically-expressed homeobox protein hhex
cytoplasmic polyadenylation element binding protein 3, transcript variant X1
cytoplasmic polyadenylation element binding protein 3, transcript variant X2
cytoplasmic polyadenylation element binding protein 3, transcript variant X3
cytoplasmic polyadenylation element-binding protein 3 isoform X1
cytoplasmic polyadenylation element-binding protein 3 isoform X2
cytoplasmic polyadenylation element-binding protein 3 isoform X3
BTAF1 RNA polymerase II, B-TFIID transcription factor-associated
TATA-binding protein-associated factor 172
RNA/RNP complex-1-interacting phosphatase-like
membrane-associated ring finger (C3HC4) 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
insulin-degrading enzyme, transcript variant X4
insulin-degrading enzyme, transcript variant X3
insulin-degrading enzyme, transcript variant X2
insulin-degrading enzyme, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 13 Proteins, and 97% 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: 4 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
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 2 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 1 sample with support for all annotated introns
zinc finger protein 518A, transcript variant X2
zinc finger protein 518A, transcript variant X1
zinc finger protein 518A, transcript variant X5
zinc finger protein 518A, transcript variant X4
zinc finger protein 518A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
heparan sulfate glucosamine 3-O-sulfotransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
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 12 samples with support for all annotated introns
kinase non-catalytic C-lobe domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G protein-coupled receptor A1, 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 5 samples with support for all annotated introns
adhesion G protein-coupled receptor A1, 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
adhesion G protein-coupled receptor A3 isoform X1
adhesion G protein-coupled receptor A1 isoform X2
cilia- and flagella-associated protein 46
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); 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: 41 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% 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: 1 long SRA read, and 41% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PWWP domain containing 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PWWP domain containing 2B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PWWP domain containing 2B, transcript variant X2
PWWP domain containing 2B, transcript variant X4
PWWP domain containing 2B, transcript variant X3
leucine-rich repeat-containing protein 27
serine/threonine-protein kinase 32C, transcript variant X1
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
serine/threonine-protein kinase 32C isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
serine/threonine-protein kinase 32C, transcript variant X2
serine/threonine-protein kinase 32C isoform X2
dihydropyrimidinase-related protein 2-like
Janus kinase and microtubule interacting protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
janus kinase and microtubule-interacting protein 3
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3
protein phosphatase 2, regulatory subunit B, delta, transcript variant X3
protein phosphatase 2, regulatory subunit B, delta, transcript variant X2
protein phosphatase 2, regulatory subunit B, delta, transcript variant X1
protein phosphatase 2, regulatory subunit B, delta, transcript variant X4
protein phosphatase 2, regulatory subunit B, delta, transcript variant X5
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform isoform X2
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform isoform X3
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform isoform X1
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform isoform X4
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform isoform X5
protein phosphatase 2, regulatory subunit B, delta, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein phosphatase 2, regulatory subunit B, delta, transcript variant X6
transcription elongation regulator 1 like
transcription elongation regulator 1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
EBF transcription factor 3a, transcript variant X1
EBF transcription factor 3a, transcript variant X2
EBF transcription factor 3a, transcript variant X4
EBF transcription factor 3a, transcript variant X3
O-6-methylguanine-DNA methyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
O-6-methylguanine-DNA methyltransferase, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
O-6-methylguanine-DNA methyltransferase, transcript variant X10
O-6-methylguanine-DNA methyltransferase, transcript variant X4
O-6-methylguanine-DNA methyltransferase, transcript variant X7
methylated-DNA--protein-cysteine methyltransferase isoform X1
methylated-DNA--protein-cysteine methyltransferase isoform X4
methylated-DNA--protein-cysteine methyltransferase isoform X2
methylated-DNA--protein-cysteine methyltransferase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type Ea, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type Ea, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type Ea, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type Ea, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein tyrosine phosphatase receptor type Ea, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein tyrosine phosphatase receptor type Ea, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
receptor-type tyrosine-protein phosphatase epsilon isoform X2
receptor-type tyrosine-protein phosphatase epsilon isoform X1
receptor-type tyrosine-protein phosphatase epsilon isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments
uroporphyrinogen III synthase, transcript variant X1
uroporphyrinogen III synthase, transcript variant X2
uroporphyrinogen III synthase, transcript variant X3
uroporphyrinogen III synthase, transcript variant X4
uroporphyrinogen-III synthase isoform X1
uroporphyrinogen-III synthase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fibronectin type 3 and ankyrin repeat domains protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
(E2-independent) E3 ubiquitin-conjugating enzyme FATS
uncharacterized LOC125485594, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125485594, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 77% 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 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 38% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125485610, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485610, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
erythroid differentiation regulatory factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
erythroid differentiation-related factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
C-terminal-binding protein 2, transcript variant X4
C-terminal-binding protein 2, transcript variant X6
C-terminal-binding protein 2, transcript variant X5
C-terminal-binding protein 2, transcript variant X3
C-terminal-binding protein 2, transcript variant X1
C-terminal-binding protein 2, transcript variant X2
uncharacterized protein LOC109934160 isoform X2
uncharacterized protein LOC109934160 isoform X1
uncharacterized protein LOC109934160 isoform X3
C-terminal-binding protein 2, transcript variant X7
zinc finger, RAN-binding domain containing 1a, transcript variant X1
zinc finger, RAN-binding domain containing 1a, transcript variant X2
zinc finger, RAN-binding domain containing 1a, transcript variant X3
zinc finger, RAN-binding domain containing 1a, transcript variant X4
ubiquitin thioesterase ZRANB1 isoform X2
ubiquitin thioesterase ZRANB1 isoform X1
4-hydroxyphenylpyruvate dioxygenase-like, transcript variant X3
4-hydroxyphenylpyruvate dioxygenase-like, transcript variant X1
4-hydroxyphenylpyruvate dioxygenase-like, transcript variant X2
4-hydroxyphenylpyruvate dioxygenase-like protein isoform X1
4-hydroxyphenylpyruvate dioxygenase-like protein isoform X2
4-hydroxyphenylpyruvate dioxygenase-like protein isoform X3
family with sequence similarity 53 member B, 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 1 sample with support for all annotated introns
family with sequence similarity 53 member B, transcript variant X7
family with sequence similarity 53 member B, 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 9 samples with support for all annotated introns
family with sequence similarity 53 member B, 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 8 samples with support for all annotated introns
family with sequence similarity 53 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
family with sequence similarity 53 member B, transcript variant X8
family with sequence similarity 53 member B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
family with sequence similarity 53 member B, transcript variant X5
phospholysine phosphohistidine inorganic pyrophosphate phosphatase, transcript variant X2
phospholysine phosphohistidine inorganic pyrophosphate phosphatase, transcript variant X1
phospholysine phosphohistidine inorganic pyrophosphate phosphatase, 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 5 samples with support for all annotated introns
phospholysine phosphohistidine inorganic pyrophosphate phosphatase, 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 6 samples with support for all annotated introns
phospholysine phosphohistidine inorganic pyrophosphate phosphatase isoform X1
phospholysine phosphohistidine inorganic pyrophosphate phosphatase isoform X2
phospholysine phosphohistidine inorganic pyrophosphate phosphatase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholysine phosphohistidine inorganic pyrophosphate phosphatase isoform X3
NK1 transcription factor related 2-like,a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ornithine aminotransferase, transcript variant X1
ornithine aminotransferase, transcript variant X2
ornithine aminotransferase, transcript variant X3
ornithine aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
carbohydrate (N-acetylgalactosamine 4-sulfate 6-O) sulfotransferase 15
inactive carboxypeptidase-like protein X2
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 17 Proteins, and 86% 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: 42 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-CoA dehydrogenase short/branched chain
short/branched chain specific acyl-CoA dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 9-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 1 sample with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 9-like, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 9-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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 9-like isoform X2
disintegrin and metalloproteinase domain-containing protein 9-like isoform X1
disintegrin and metalloproteinase domain-containing protein 9-like isoform X3
chromosome 20 C10orf88 homolog, transcript variant X1
chromosome 20 C10orf88 homolog, transcript variant X2
deleted in malignant brain tumors 1 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein 16-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
transforming acidic coiled-coil-containing protein 1-like
transforming acidic coiled-coil-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1b, transcript variant X1
pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1b, transcript variant X3
pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1b, transcript variant X2
pleckstrin homology domain-containing family A member 1 isoform X1
pleckstrin homology domain-containing family A member 1 isoform X3
pleckstrin homology domain-containing family A member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 81% coverage of the annotated genomic feature by RNAseq alignments
NSE4 homolog A, SMC5-SMC6 complex component, transcript variant X2
NSE4 homolog A, SMC5-SMC6 complex component, transcript variant X1
non-structural maintenance of chromosomes element 4 homolog A
arginyl-tRNA--protein transferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
arginyl-tRNA--protein transferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
arginyl-tRNA--protein transferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
arginyl-tRNA--protein transferase 1, transcript variant X1
arginyl-tRNA--protein transferase 1, transcript variant X3
arginyl-tRNA--protein transferase 1, transcript variant X6
arginyl-tRNA--protein transferase 1, transcript variant X7
arginyl-tRNA--protein transferase 1 isoform X3
arginyl-tRNA--protein transferase 1 isoform X4
arginyl-tRNA--protein transferase 1 isoform X1
arginyl-tRNA--protein transferase 1 isoform X2
fibroblast growth factor receptor 2, transcript variant X7
fibroblast growth factor receptor 2, transcript variant X6
fibroblast growth factor receptor 2, transcript variant X1
fibroblast growth factor receptor 2 isoform X1
fibroblast growth factor receptor 2, transcript variant X9
fibroblast growth factor receptor 2, transcript variant X8
fibroblast growth factor receptor 2, transcript variant X2
fibroblast growth factor receptor 2 isoform X2
fibroblast growth factor receptor 2, transcript variant X5
fibroblast growth factor receptor 2, transcript variant X3
fibroblast growth factor receptor 2, transcript variant X4
fibroblast growth factor receptor 2 isoform X3
fibroblast growth factor receptor 2 isoform X4
phospholipid phosphatase 4, 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 1 sample with support for all annotated introns
phospholipid phosphatase 4, transcript variant X4
phospholipid phosphatase 4, transcript variant X2
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 2 samples with support for all annotated introns
phospholipid phosphatase 4, transcript variant X3
minichromosome maintenance complex binding protein
mini-chromosome maintenance complex-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
BAG family molecular chaperone regulator 3
TIA1 cytotoxic granule-associated RNA binding protein-like 1, transcript variant X1
TIA1 cytotoxic granule-associated RNA binding protein-like 1, transcript variant X2
TIA1 cytotoxic granule-associated RNA binding protein-like 1, transcript variant X3
G protein-coupled receptor kinase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
G protein-coupled receptor kinase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-coupled receptor kinase 5 isoform X1
G protein-coupled receptor kinase 5 isoform X2
U6 snRNA-associated Sm-like protein LSm1, transcript variant X2
U6 snRNA-associated Sm-like protein LSm1, transcript variant X1
U6 snRNA-associated Sm-like protein LSm1 isoform X2
U6 snRNA-associated Sm-like protein LSm1 isoform X1
thioredoxin-dependent peroxide reductase, mitochondrial
EF-hand calcium-binding domain-containing protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
LOW QUALITY PROTEIN: guanylate cyclase 2G
acyl-CoA synthetase long chain family member 5, transcript variant X1
acyl-CoA synthetase long chain family member 5, transcript variant X2
long-chain-fatty-acid--CoA ligase 5 isoform X1
acyl-CoA synthetase long chain family member 5, transcript variant X3
long-chain-fatty-acid--CoA ligase 5 isoform X2
zinc finger DHHC-type palmitoyltransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs 1A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs 1A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs 1A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1A isoform X1
vesicle transport through interaction with t-SNAREs homolog 1A isoform X2
vesicle transport through interaction with t-SNAREs homolog 1A isoform X3
transcription factor 7 like 2, transcript variant X14
transcription factor 7 like 2, transcript variant X28
transcription factor 7 like 2, transcript variant X16
transcription factor 7 like 2, transcript variant X17
transcription factor 7 like 2, transcript variant X1
transcription factor 7 like 2, transcript variant X7
transcription factor 7 like 2, transcript variant X2
transcription factor 7 like 2, transcript variant X6
transcription factor 7 like 2, transcript variant X11
transcription factor 7 like 2, transcript variant X22
transcription factor 7 like 2, transcript variant X18
transcription factor 7 like 2, transcript variant X4
transcription factor 7 like 2, transcript variant X8
transcription factor 7 like 2, transcript variant X9
transcription factor 7 like 2, transcript variant X13
transcription factor 7 like 2, transcript variant X25
transcription factor 7 like 2, transcript variant X3
transcription factor 7 like 2, transcript variant X5
transcription factor 7 like 2, transcript variant X26
transcription factor 7 like 2, transcript variant X10
transcription factor 7 like 2, transcript variant X12
transcription factor 7 like 2, transcript variant X27
transcription factor 7 like 2, transcript variant X15
transcription factor 7 like 2, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor 7 like 2, transcript variant X20
transcription factor 7 like 2, transcript variant X24
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 8 samples with support for all annotated introns
transcription factor 7 like 2, transcript variant X23
transcription factor 7 like 2, transcript variant X21
transcription factor 7-like 2 isoform X14
transcription factor 7-like 2 isoform X28
transcription factor 7-like 2 isoform X1
transcription factor 7-like 2 isoform X7
transcription factor 7-like 2 isoform X2
transcription factor 7-like 2 isoform X6
transcription factor 7-like 2 isoform X11
transcription factor 7-like 2 isoform X4
transcription factor 7-like 2 isoform X8
transcription factor 7-like 2 isoform X9
transcription factor 7-like 2 isoform X13
transcription factor 7-like 2 isoform X3
transcription factor 7-like 2 isoform X5
transcription factor 7-like 2 isoform X10
transcription factor 7-like 2 isoform X12
transcription factor 7-like 2 isoform X15
transcription factor 7-like 2 isoform X16
transcription factor 7-like 2 isoform X22
transcription factor 7-like 2 isoform X25
transcription factor 7-like 2 isoform X26
transcription factor 7-like 2 isoform X27
transcription factor 7-like 2 isoform X17
transcription factor 7-like 2 isoform X19
transcription factor 7-like 2 isoform X20
transcription factor 7-like 2 isoform X18
transcription factor 7-like 2 isoform X23
transcription factor 7-like 2 isoform X24
transcription factor 7-like 2 isoform X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
caspase 7, apoptosis-related cysteine peptidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 108 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
pleckstrin homology domain-containing family S member 1
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
DNA cross-link repair 1A (PSO2 homolog, S. cerevisiae), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA cross-link repair 1A (PSO2 homolog, S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DNA cross-link repair 1A protein isoform X2
DNA cross-link repair 1A protein isoform X1
DNA cross-link repair 1A (PSO2 homolog, S. cerevisiae), transcript variant X3
NHL repeat containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NHL repeat-containing protein 2 isoform X1
NHL repeat containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NHL repeat-containing protein 2 isoform X2
coiled-coil domain-containing protein 186, transcript variant X3
coiled-coil domain-containing protein 186, transcript variant X1
coiled-coil domain-containing protein 186, transcript variant X4
coiled-coil domain-containing protein 186, transcript variant X2
coiled-coil domain-containing protein 186 isoform X2
coiled-coil domain-containing protein 186 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 2
actin filament associated protein 1-like 2, transcript variant X2
actin filament associated protein 1-like 2, transcript variant X1
actin filament-associated protein 1-like 2 isoform X2
actin filament-associated protein 1-like 2 isoform X1
FHF complex subunit HOOK interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
TruB pseudouridine (psi) synthase family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); 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: 96% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 172, transcript variant X2
coiled-coil domain containing 172, transcript variant X4
coiled-coil domain containing 172, transcript variant X3
coiled-coil domain containing 172, transcript variant X1
coiled-coil domain containing 172, transcript variant X5
coiled-coil domain-containing protein 172 isoform X2
coiled-coil domain-containing protein 172 isoform X1
coiled-coil domain-containing protein 172 isoform X3
coiled-coil domain-containing protein 172 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 1 sample with support for all annotated introns
pancreatic lipase-related protein 2-like
heat shock protein 12A, transcript variant X4
heat shock protein 12A, transcript variant X3
heat shock protein 12A, transcript variant X2
heat shock protein 12A, transcript variant X5
heat shock protein 12A, transcript variant X1
heat shock protein 12A, transcript variant X6
heat shock 70 kDa protein 12A isoform X4
heat shock 70 kDa protein 12A isoform X3
heat shock 70 kDa protein 12A isoform X2
heat shock 70 kDa protein 12A isoform X5
heat shock 70 kDa protein 12A isoform X1
heat shock 70 kDa protein 12A isoform X6
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
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
potassium channel, subfamily K, member 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
solute carrier family 18 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 18 member 2, transcript variant X2
synaptic vesicular amine transporter isoform X1
solute carrier family 18 member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptic vesicular amine transporter isoform X2
uncharacterized LOC125485585, transcript variant X3
uncharacterized LOC125485585, transcript variant X1
uncharacterized LOC125485585, transcript variant X2
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 8 samples with support for all annotated introns
family with sequence similarity 204 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
family with sequence similarity 204 member A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
family with sequence similarity 204 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
CDK2-associated and cullin domain-containing protein 1
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
eukaryotic translation initiation factor 3, subunit 10 (theta)
eukaryotic translation initiation factor 3 subunit A
COORDINATES: nucleotide motif:Rfam:12.0:RF00413
DENN domain containing 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DENN domain containing 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DENN domain containing 10, transcript variant X1
glycerol-3-phosphate acyltransferase 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
SH3 and PX domains 2Aa, transcript variant X2
SH3 and PX domains 2Aa, transcript variant X1
SH3 and PX domains 2Aa, transcript variant X3
SH3 and PX domain-containing protein 2A isoform X2
SH3 and PX domain-containing protein 2A isoform X1
SH3 and PX domain-containing protein 2A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
peroxisome proliferator-activated receptor gamma coactivator-related protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ectonucleoside triphosphate diphosphohydrolase 1, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 1, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 1, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 1, transcript variant X4
ectonucleoside triphosphate diphosphohydrolase 1 isoform X2
ectonucleoside triphosphate diphosphohydrolase 1 isoform X1
ectonucleoside triphosphate diphosphohydrolase 1 isoform X3
aldehyde dehydrogenase 18 family, member A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
aldehyde dehydrogenase 18 family, member A1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aldehyde dehydrogenase 18 family, member A1, transcript variant X4
aldehyde dehydrogenase 18 family, member A1, 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 11 samples with support for all annotated introns
aldehyde dehydrogenase 18 family, member A1, transcript variant X6
aldehyde dehydrogenase 18 family, member A1, transcript variant X8
aldehyde dehydrogenase 18 family, member A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
aldehyde dehydrogenase 18 family, member A1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate synthase isoform X1
delta-1-pyrroline-5-carboxylate synthase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
polycomb group ring finger 6, transcript variant X2
polycomb group ring finger 6, transcript variant X1
polycomb group RING finger protein 6 isoform X2
polycomb group RING finger protein 6 isoform X1
polycomb group ring finger 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
STE20-like kinase a, transcript variant X3
STE20-like kinase a, transcript variant X2
STE20-like kinase a, transcript variant X1
STE20-like serine/threonine-protein kinase isoform X3
STE20-like serine/threonine-protein kinase isoform X2
STE20-like serine/threonine-protein kinase isoform X1
STN1 subunit of CST complex, transcript variant X1
STN1 subunit of CST complex, transcript variant X2
collagen, type XVII, alpha 1a, transcript variant X2
collagen, type XVII, alpha 1a, transcript variant X1
collagen, type XVII, alpha 1a isoform X2
collagen, type XVII, alpha 1a isoform X1
SWI5-dependent homologous recombination repair protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 8 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
swi5-dependent recombination DNA repair protein 1 homolog isoform X1
SWI5-dependent homologous recombination repair protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
swi5-dependent recombination DNA repair protein 1 homolog isoform X2
SWI5-dependent homologous recombination repair protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 8 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
swi5-dependent recombination DNA repair protein 1 homolog isoform X3
cilia and flagella associated protein 43, transcript variant X1
cilia and flagella associated protein 43, 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 3 samples with support for all annotated introns
cilia and flagella associated protein 43, transcript variant X2
cilia and flagella associated protein 43, 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 2 samples with support for all annotated introns
cilia- and flagella-associated protein 43 isoform X4
cilia- and flagella-associated protein 43 isoform X1
cilia- and flagella-associated protein 43 isoform X2
cilia- and flagella-associated protein 43 isoform X3
inositol 1,4,5-trisphosphate receptor-interacting protein, transcript variant X1
inositol 1,4,5-trisphosphate receptor-interacting protein, transcript variant X3
inositol 1,4,5-trisphosphate receptor-interacting protein, transcript variant X4
inositol 1,4,5-trisphosphate receptor-interacting protein, transcript variant X2
inositol 1,4,5-trisphosphate receptor-interacting protein isoform X2
inositol 1,4,5-trisphosphate receptor-interacting protein isoform X1
inositol 1,4,5-trisphosphate receptor-interacting protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
calcium homeostasis modulator protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium homeostasis modulator protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
programmed cell death 11, transcript variant X2
programmed cell death 11, transcript variant X1
programmed cell death 11, transcript variant X3
programmed cell death 11, transcript variant X4
ATP synthase membrane subunit k, transcript variant X1
ATP synthase membrane subunit k, transcript variant X2
ATP synthase membrane subunit DAPIT, mitochondrial
TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
kazal-type serine protease inhibitor domain-containing protein 1
uncharacterized LOC109928498, transcript variant X2
uncharacterized LOC109928498, transcript variant X1
uncharacterized protein LOC109928498 isoform X2
uncharacterized protein LOC109928498 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
F-box and WD repeat domain containing 4, transcript variant X1
F-box and WD repeat domain containing 4, transcript variant X2
F-box/WD repeat-containing protein 4 isoform X1
F-box/WD repeat-containing protein 4 isoform X2
deleted in primary ciliary dyskinesia homolog (mouse)
LIM domain binding 1a, transcript variant X1
LIM domain binding 1a, transcript variant X2
LIM domain binding 1a, transcript variant X3
LIM domain-binding protein 1-A isoform X1
LIM domain-binding protein 1-A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
HPS6 biogenesis of lysosomal organelles complex 2 subunit 3
Hermansky-Pudlak syndrome 6 protein homolog
armadillo like helical domain containing 3, transcript variant X1
armadillo-like helical domain-containing protein 3 isoform X1
armadillo like helical domain containing 3, transcript variant X2
armadillo-like helical domain-containing protein 3 isoform X2
Kv channel-interacting protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 55 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Kv channel-interacting protein 2-like isoform X2
Kv channel-interacting protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 56 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Kv channel-interacting protein 2-like isoform X3
Kv channel-interacting protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 55 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Kv channel-interacting protein 2-like isoform X1
dynamin binding protein, transcript variant X1
dynamin binding protein, transcript variant X5
dynamin binding protein, transcript variant X2
dynamin binding protein, transcript variant X3
dynamin binding protein, transcript variant X4
ATP-binding cassette, sub-family C (CFTR/MRP), member 2, transcript variant X1
ATP-binding cassette, sub-family C (CFTR/MRP), member 2, transcript variant X2
canalicular multispecific organic anion transporter 1 isoform X1
canalicular multispecific organic anion transporter 1 isoform X2
cutC copper transporter homolog (E. coli), transcript variant X1
cutC copper transporter homolog (E. coli), transcript variant X2
copper homeostasis protein cutC homolog isoform X1
copper homeostasis protein cutC homolog isoform X2
cytochrome c oxidase assembly protein COX15 homolog
ST3 beta-galactoside alpha-2,3-sialyltransferase 7, transcript variant X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 7, transcript variant X2
ST3 beta-galactoside alpha-2,3-sialyltransferase 7 isoform X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 7 isoform X2
HPS1 biogenesis of lysosomal organelles complex 3 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 16 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-kinase type 2 alpha
phosphatidylinositol 4-kinase type 2-alpha
exosome component 1, transcript variant X2
exosome component 1, transcript variant X1
exosome complex component CSL4 isoform X2
exosome complex component CSL4 isoform X1
ligand dependent nuclear receptor corepressor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X3
ligand dependent nuclear receptor corepressor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ligand dependent nuclear receptor corepressor, transcript variant X6
MMS19 nucleotide excision repair protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 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: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
4-hydroxy-2-oxoglutarate aldolase, mitochondrial
ankyrin repeat domain 2 (stretch responsive muscle)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
zinc finger, FYVE domain containing 27, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger, FYVE domain containing 27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger, FYVE domain containing 27, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
secreted frizzled-related protein 1-like
secreted frizzled-related protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
R3H domain and coiled-coil containing 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
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 11 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 57% 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 76% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
UPF0329 protein ECU05_1680/ECU11_0050-like, transcript variant X2
UPF0329 protein ECU05_1680/ECU11_0050-like isoform X2
UPF0329 protein ECU05_1680/ECU11_0050-like, transcript variant X3
UPF0329 protein ECU05_1680/ECU11_0050-like, transcript variant X1
uncharacterized protein LOC125485550 isoform X3
uncharacterized protein LOC125485550 isoform X1
pyridine nucleotide-disulphide oxidoreductase domain 2
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 2
ATPase H+ transporting V0 subunit e2, transcript variant X2
ATPase H+ transporting V0 subunit e2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
V-type proton ATPase subunit e 2 isoform X2
V-type proton ATPase subunit e 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 25 member 28, transcript variant X1
solute carrier family 25 member 28, transcript variant X12
solute carrier family 25 member 28, transcript variant X7
solute carrier family 25 member 28, transcript variant X2
solute carrier family 25 member 28, transcript variant X3
solute carrier family 25 member 28, transcript variant X5
solute carrier family 25 member 28, transcript variant X9
solute carrier family 25 member 28, transcript variant X6
solute carrier family 25 member 28, transcript variant X4
solute carrier family 25 member 28, transcript variant X11
solute carrier family 25 member 28, transcript variant X10
solute carrier family 25 member 28, transcript variant X8
uncharacterized LOC125485552, transcript variant X2
uncharacterized LOC125485552, 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 7 samples with support for all annotated introns
glutamic-oxaloacetic transaminase 1, soluble
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
metal transporter CNNM2-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 2 samples with support for all annotated introns
metal transporter CNNM2-like, transcript variant X1
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 4 samples with support for all annotated introns
metal transporter CNNM2-like, transcript variant X3
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
arsenite methyltransferase, transcript variant X1
arsenite methyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC109925326, transcript variant X2
uncharacterized LOC109925326, transcript variant X1
steroid 17-alpha-hydroxylase/17,20 lyase
sideroflexin-2-like, transcript variant X4
sideroflexin-2-like, transcript variant X2
sideroflexin-2-like, transcript variant X3
sideroflexin-2-like, transcript variant X6
sideroflexin-2-like, transcript variant X5
sideroflexin-2-like, transcript variant X1
major facilitator superfamily domain containing 13A, transcript variant X2
major facilitator superfamily domain containing 13A, transcript variant X1
ADP ribosylation factor like GTPase 3b, transcript variant X1
ADP ribosylation factor like GTPase 3b, transcript variant X2
ADP-ribosylation factor-like protein 3 isoform X2
ADP-ribosylation factor-like protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 23 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: 1 long SRA read, 23 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: 8 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
suppressor of fused homolog (Drosophila)
uncharacterized LOC125485547, transcript variant X1
uncharacterized LOC125485547, transcript variant X2
E3 ubiquitin-protein ligase TRIM8-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM8-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM8-like, transcript variant X2
SMC5-SMC6 complex localization factor protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L43, mitochondrial
twinkle mtDNA helicase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
twinkle mtDNA helicase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
twinkle protein, mitochondrial isoform X1
twinkle protein, mitochondrial isoform X2
leucine zipper, putative tumor suppressor 2a, transcript variant X1
leucine zipper, putative tumor suppressor 2a, transcript variant X2
leucine zipper, putative tumor suppressor 2a, transcript variant X3
leucine zipper, putative tumor suppressor 2a, transcript variant X4
leucine zipper putative tumor suppressor 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sideroflexin-1-like, transcript variant X4
sideroflexin-1-like, transcript variant X3
sideroflexin-1-like, transcript variant X1
sideroflexin-1-like, transcript variant X2
cilia and flagella associated protein 58
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia- and flagella-associated protein 58
VPS10 domain-containing receptor SorCS1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
SHOC2 leucine rich repeat scaffold protein, transcript variant X2
SHOC2 leucine rich repeat scaffold protein, transcript variant X1
leucine-rich repeat protein SHOC-2 isoform X2
leucine-rich repeat protein SHOC-2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 3
survival motor neuron domain containing 1
survival of motor neuron-related-splicing factor 30
uncharacterized LOC125485596, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125485596, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485597, transcript variant X1
uncharacterized LOC125485597, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
X-prolyl aminopeptidase (aminopeptidase P) 1, soluble