Dermochelys coriacea isolate rDerCor1 chromosome 28, rDerCor1.pri.v4, whole genome shotgun sequence.
Dermochelys coriacea (leatherback sea turtle)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Americhelydia; Chelonioidea; Dermochelyidae; Dermochelys.
REFSEQ INFORMATION: The reference sequence is identical to\nCM019962.2.\nAssembly name: rDerCor1.pri.v4\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the G10K on 2021/08/25. The\noriginal whole-genome shotgun project has the accession\nWSPL00000000.4.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: G10K\nAssembly Date :: 24-MAY-2021\nAssembly Method :: FALCON DNANexus v. 1.9.0; FALCON-Unzip\n DNANexus v. 1.0.6; purge_dups v. v1;\n scaff10x v. 4.1.0; Bionano Solve DLS v.\n 3.2.1; Salsa HiC v. 2.2.2; Arrow\n smrtanalysis Pacbio polishing & gap\n filling v. 6.0.0.47841; longranger align\n v. 2.2.2; freebayes Illumina polishing v.\n 1.3.1; gEVAL manual curation v.\n 2021-05-24; VGP assembly pipeline\n individual v. 1.6\nAssembly Name :: rDerCor1.pri.v4\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 63.68x\nSequencing Technology :: PacBio Sequel I CLR; llumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Dermochelys coriacea Annotation\n Release 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: 20 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
stromal antigen 3, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X9
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 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X11
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
stromal antigen 3, transcript variant X12
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
stromal antigen 3, transcript variant X10
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
stromal antigen 3, transcript variant X15
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 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X17
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 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X19
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 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X14
stromal antigen 3, transcript variant X16
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
stromal antigen 3, transcript variant X20
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
stromal antigen 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X1
stromal antigen 3, transcript variant X2
stromal antigen 3, transcript variant X4
stromal antigen 3, transcript variant X5
stromal antigen 3, 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 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X7
stromal antigen 3, transcript variant X3
adaptor related protein complex 4 subunit mu 1, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
adaptor related protein complex 4 subunit mu 1, transcript variant X3
adaptor related protein complex 4 subunit mu 1, transcript variant X1
adaptor related protein complex 4 subunit mu 1, transcript variant X4
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 32 samples with support for all annotated introns
minichromosome maintenance complex component 7
beta-galactoside alpha-2,6-sialyltransferase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta-galactoside alpha-2,6-sialyltransferase 1-like
lysophosphatidic acid receptor 6-like, transcript variant X3
lysophosphatidic acid receptor 6-like, transcript variant X1
lysophosphatidic acid receptor 6-like, transcript variant X2
lysophosphatidic acid receptor 6-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lysophosphatidic acid receptor 6-like, transcript variant X4
flavin-containing monooxygenase FMO GS-OX4-like, transcript variant X3
flavin-containing monooxygenase FMO GS-OX4-like, transcript variant X1
flavin-containing monooxygenase FMO GS-OX4-like, transcript variant X2
flavin-containing monooxygenase FMO GS-OX4-like, transcript variant X4
flavin-containing monooxygenase FMO GS-OX4-like, transcript variant X5
flavin-containing monooxygenase FMO GS-OX-like 4 isoform X1
flavin-containing monooxygenase FMO GS-OX4-like isoform X2
flavin-containing monooxygenase FMO GS-OX4-like isoform X3
zinc finger protein 3, transcript variant X5
zinc finger protein 3, transcript variant X8
zinc finger protein 3, transcript variant X4
zinc finger protein 3, transcript variant X13
zinc finger protein 3, transcript variant X11
zinc finger protein 3, transcript variant X12
zinc finger protein 3, transcript variant X9
zinc finger protein 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
zinc finger protein 3, transcript variant X1
zinc finger protein 3, transcript variant X7
zinc finger protein 3, transcript variant X2
zinc finger protein 3, transcript variant X6
zinc finger protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
VGF nerve growth factor inducible, 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
VGF nerve growth factor inducible, transcript variant X1
adaptor related protein complex 1 subunit sigma 1
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 45 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
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
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: 5 Proteins
cell wall integrity and stress response component 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholinesterase (Cartwright blood group), transcript variant X3
acetylcholinesterase (Cartwright blood group), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
acetylcholinesterase (Cartwright blood group), transcript variant X1
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: chromatin complexes subunit BAP18
proline, glutamate and leucine rich protein 1, transcript variant X1
proline, glutamate and leucine rich protein 1, transcript variant X2
proline-, glutamic acid- and leucine-rich protein 1 isoform X1
proline-, glutamic acid- and leucine-rich protein 1 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger MYND domain-containing protein 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vitelline membrane outer layer protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
immunoglobulin lambda-1 light chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
immunoglobulin lambda-1 light chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
immunoglobulin lambda-1 light chain-like isoform X2
immunoglobulin lambda-1 light chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
immunoglobulin lambda-1 light chain-like isoform X1
glycolipid transfer protein domain containing 2, transcript variant X1
glycolipid transfer protein domain-containing protein 2 isoform X1
glycolipid transfer protein domain containing 2, transcript variant X3
glycolipid transfer protein domain containing 2, transcript variant X2
glycolipid transfer protein domain-containing protein 2 isoform X2
glycolipid transfer protein domain-containing protein 2 isoform X3
misshapen like kinase 1, transcript variant X1
misshapen like kinase 1, transcript variant X10
misshapen like kinase 1, transcript variant X7
misshapen like kinase 1, transcript variant X3
misshapen like kinase 1, transcript variant X11
misshapen like kinase 1, transcript variant X8
misshapen like kinase 1, transcript variant X12
misshapen like kinase 1, transcript variant X4
misshapen like kinase 1, transcript variant X15
misshapen like kinase 1, transcript variant X13
misshapen like kinase 1, transcript variant X16
misshapen like kinase 1, transcript variant X14
misshapen like kinase 1, transcript variant X17
misshapen like kinase 1, transcript variant X9
misshapen like kinase 1, transcript variant X18
misshapen like kinase 1, transcript variant X2
misshapen like kinase 1, transcript variant X5
misshapen like kinase 1, transcript variant X6
cholinergic receptor nicotinic epsilon subunit
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
solute carrier family 25 member 11, transcript variant X2
solute carrier family 25 member 11, transcript variant X1
mitochondrial 2-oxoglutarate/malate carrier protein isoform X2
mitochondrial 2-oxoglutarate/malate carrier protein isoform X1
ring finger protein 167, transcript variant X1
ring finger protein 167, transcript variant X2
LOW QUALITY PROTEIN: sperm-associated antigen 7
calmodulin binding transcription activator 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: calmodulin-binding transcription activator 2
inhibitor of CDK, cyclin A1 interacting protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: kinesin-like protein KIF1C
procollagen C-endopeptidase enhancer, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
procollagen C-endopeptidase enhancer, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
procollagen C-endopeptidase enhancer 1 isoform X1
procollagen C-endopeptidase enhancer 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeats and calponin homology domain containing 4, transcript variant X2
leucine rich repeats and calponin homology domain containing 4, transcript variant X4
leucine rich repeats and calponin homology domain containing 4, transcript variant X1
leucine rich repeats and calponin homology domain containing 4, transcript variant X3
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X2
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X4
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X3
leucine rich repeats and calponin homology domain containing 4, transcript variant X5
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
rhomboid-related protein 4-like, transcript variant X1
rhomboid-related protein 4-like, transcript variant X2
rhomboid-related protein 4-like isoform X1
rhomboid-related protein 4-like isoform X2
ArfGAP with FG repeats 2, transcript variant X5
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 39 samples with support for all annotated introns
ArfGAP with FG repeats 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
ArfGAP with FG repeats 2, transcript variant X3
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 34 samples with support for all annotated introns
ArfGAP with FG repeats 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
ArfGAP with FG repeats 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
arf-GAP domain and FG repeat-containing protein 2 isoform X4
arf-GAP domain and FG repeat-containing protein 2 isoform X3
arf-GAP domain and FG repeat-containing protein 2 isoform X2
arf-GAP domain and FG repeat-containing protein 2 isoform X1
arf-GAP domain and FG repeat-containing protein 2 isoform X5
uncharacterized LOC122457723, transcript variant X1
uncharacterized LOC122457723, transcript variant X2
neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1, transcript variant X4
neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1, 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
neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1, transcript variant X3
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X2
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X1
TSC22 domain family member 4, transcript variant X1
TSC22 domain family member 4, 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 31 samples with support for all annotated introns
TSC22 domain family member 4, transcript variant X2
TSC22 domain family protein 4 isoform X3
TSC22 domain family protein 4 isoform X1
TSC22 domain family protein 4 isoform X2
protein phosphatase 1 regulatory subunit 35, transcript variant X2
protein phosphatase 1 regulatory subunit 35, transcript variant X1
protein phosphatase 1 regulatory subunit 35, transcript variant X4
protein phosphatase 1 regulatory subunit 35, transcript variant X3
protein phosphatase 1 regulatory subunit 35 isoform X2
protein phosphatase 1 regulatory subunit 35 isoform X1
protein phosphatase 1 regulatory subunit 35 isoform X4
protein phosphatase 1 regulatory subunit 35 isoform X3
protein phosphatase 1 regulatory subunit 35, transcript variant X5
protein phosphatase 1 regulatory subunit 35 isoform X5
protein phosphatase 1 regulatory subunit 35, transcript variant X6
protein phosphatase 1 regulatory subunit 35 isoform X6
methylphosphate capping enzyme, transcript variant X2
methylphosphate capping enzyme, transcript variant X1
7SK snRNA methylphosphate capping enzyme isoform X2
7SK snRNA methylphosphate capping enzyme isoform X1
zinc finger CW-type and PWWP domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CW-type PWWP domain protein 1
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like, transcript variant X1
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like, transcript variant X2
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like
transferrin receptor 2, transcript variant X3
transferrin receptor 2, transcript variant X2
transferrin receptor 2, transcript variant X1
transferrin receptor 2, transcript variant X4
transferrin receptor protein 2 isoform X2
transferrin receptor protein 2 isoform X1
transferrin receptor protein 2 isoform X3
chloride channel protein ClC-Kb-like, transcript variant X7
chloride channel protein ClC-Kb-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
POP7 homolog, ribonuclease P/MRP subunit, transcript variant X2
POP7 homolog, ribonuclease P/MRP subunit, transcript variant X1
chloride channel protein ClC-Kb-like, transcript variant X1
chloride channel protein ClC-Kb-like, transcript variant X2
chloride channel protein ClC-Kb-like, transcript variant X3
chloride channel protein ClC-Kb-like, transcript variant X4
chloride channel protein ClC-Kb-like, transcript variant X6
chloride channel protein ClC-Kb-like, transcript variant X5
chloride channel protein ClC-Kb-like isoform X1
chloride channel protein ClC-Kb-like isoform X2
chloride channel protein ClC-Kb-like isoform X3
chloride channel protein ClC-Kb-like isoform X4
chloride channel protein ClC-Kb-like isoform X6
chloride channel protein ClC-Kb-like isoform X5
chloride channel protein ClC-Kb-like isoform X7
chloride channel protein ClC-Kb-like isoform X8
GRB10 interacting GYF protein 1, transcript variant X1
GRB10 interacting GYF protein 1, transcript variant X2
GRB10-interacting GYF protein 1 isoform X1
GRB10-interacting GYF protein 1 isoform X2
G protein subunit beta 2, transcript variant X2
G protein subunit beta 2, transcript variant X1
G protein subunit beta 2, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2 isoform X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 74% 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: deleted 2 bases in 1 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: 10 long SRA reads, 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
stress-associated endoplasmic reticulum protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1, 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 21 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1, transcript variant X1
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 51 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1 protein isoform X1
mannose-P-dolichol utilization defect 1 protein isoform X3
mannose-P-dolichol utilization defect 1 protein isoform X2
mannose-P-dolichol utilization defect 1 protein isoform X4
fragile X mental retardation syndrome-related protein 2
thialysine N-epsilon-acetyltransferase-like
thialysine N-epsilon-acetyltransferase-like, transcript variant X1
uncharacterized protein LOC119849226 isoform X1
thialysine N-epsilon-acetyltransferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase-like, transcript variant X3
thialysine N-epsilon-acetyltransferase-like isoform X3
thialysine N-epsilon-acetyltransferase-like isoform X2
cholinergic receptor nicotinic beta 1 subunit
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: fibroblast growth factor 11
WAS/WASL-interacting protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
segment polarity protein dishevelled homolog DVL-2
very long-chain specific acyl-CoA dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
very long-chain specific acyl-CoA dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 6 bases in 6 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 6 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
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: 38 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LOW QUALITY PROTEIN: solute carrier family 2, facilitated glucose transporter member 4
eukaryotic translation initiation factor 5A, transcript variant X1
eukaryotic translation initiation factor 5A, transcript variant X2
eukaryotic translation initiation factor 5A-1
G protein pathway suppressor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
G protein pathway suppressor 2, 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
G protein pathway suppressor 2, transcript variant X3
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 32 samples with support for all annotated introns
G protein pathway suppressor 2 isoform X2
G protein pathway suppressor 2 isoform X3
G protein pathway suppressor 2 isoform X1
neuralized E3 ubiquitin protein ligase 4
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
LOW QUALITY PROTEIN: neuralized-like protein 4
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1, transcript variant X1
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
monocarboxylate transporter 13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
monocarboxylate transporter 13-like, transcript variant X1
monocarboxylate transporter 13-like, transcript variant X3
monocarboxylate transporter 13-like, transcript variant X4
monocarboxylate transporter 13-like isoform X2
monocarboxylate transporter 13-like isoform X3
monocarboxylate transporter 13-like, transcript variant X5
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 4 samples with support for all annotated introns
monocarboxylate transporter 13-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 10 bases in 7 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 83% 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: inserted 10 bases in 7 codons; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: B-cell CLL/lymphoma 6 member B protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
ATPase Na+/K+ transporting subunit beta 2
sodium/potassium-transporting ATPase subunit beta-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
zinc finger and BTB domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
zinc finger and BTB domain containing 4, 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 13 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II subunit A, transcript variant X1
RNA polymerase II subunit A, transcript variant X3
RNA polymerase II subunit A, transcript variant X2
DNA-directed RNA polymerase II subunit RPB1 isoform X1
DNA-directed RNA polymerase II subunit RPB1 isoform X3
DNA-directed RNA polymerase II subunit RPB1 isoform X2
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
dynein axonemal heavy chain 2, 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 2 samples with support for all annotated introns
dynein axonemal heavy chain 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 2 isoform X1
dynein axonemal heavy chain 2 isoform X2
dynein axonemal heavy chain 2, transcript variant X3
dynein axonemal heavy chain 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 17 Proteins, 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
N-alpha-acetyltransferase 38, NatC auxiliary subunit
cytochrome b5 domain-containing protein 1, transcript variant X1
cytochrome b5 domain-containing protein 1, transcript variant X3
cytochrome b5 domain-containing protein 1, transcript variant X2
cytochrome b5 domain-containing protein 1
chromodomain helicase DNA binding protein 3, transcript variant X15
chromodomain helicase DNA binding protein 3, transcript variant X7
chromodomain helicase DNA binding protein 3, transcript variant X13
chromodomain helicase DNA binding protein 3, transcript variant X17
chromodomain helicase DNA binding protein 3, transcript variant X12
chromodomain helicase DNA binding protein 3, transcript variant X16
chromodomain helicase DNA binding protein 3, transcript variant X9
chromodomain helicase DNA binding protein 3, transcript variant X5
chromodomain helicase DNA binding protein 3, transcript variant X6
chromodomain helicase DNA binding protein 3, transcript variant X11
chromodomain helicase DNA binding protein 3, transcript variant X10
chromodomain helicase DNA binding protein 3, transcript variant X20
chromodomain helicase DNA binding protein 3, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
chromodomain helicase DNA binding protein 3, transcript variant X2
chromodomain helicase DNA binding protein 3, transcript variant X1
chromodomain helicase DNA binding protein 3, transcript variant X3
chromodomain helicase DNA binding protein 3, transcript variant X4
chromodomain helicase DNA binding protein 3, transcript variant X8
chromodomain helicase DNA binding protein 3, transcript variant X14
chromodomain helicase DNA binding protein 3, transcript variant X21
chromodomain-helicase-DNA-binding protein 3 isoform X1
chromodomain-helicase-DNA-binding protein 3 isoform X2
chromodomain-helicase-DNA-binding protein 3 isoform X3
chromodomain-helicase-DNA-binding protein 3 isoform X4
chromodomain-helicase-DNA-binding protein 3 isoform X5
chromodomain-helicase-DNA-binding protein 3 isoform X7
chromodomain-helicase-DNA-binding protein 3 isoform X6
chromodomain-helicase-DNA-binding protein 3 isoform X9
chromodomain-helicase-DNA-binding protein 3 isoform X11
chromodomain-helicase-DNA-binding protein 3 isoform X10
chromodomain-helicase-DNA-binding protein 3 isoform X8
chromodomain-helicase-DNA-binding protein 3 isoform X13
chromodomain-helicase-DNA-binding protein 3 isoform X15
chromodomain-helicase-DNA-binding protein 3 isoform X17
chromodomain-helicase-DNA-binding protein 3 isoform X14
chromodomain-helicase-DNA-binding protein 3 isoform X12
chromodomain-helicase-DNA-binding protein 3 isoform X16
chromodomain-helicase-DNA-binding protein 3 isoform X20
chromodomain-helicase-DNA-binding protein 3 isoform X21
chromodomain-helicase-DNA-binding protein 3 isoform X24
chromodomain helicase DNA binding protein 3, transcript variant X19
chromodomain helicase DNA binding protein 3, transcript variant X22
chromodomain helicase DNA binding protein 3, transcript variant X18
chromodomain helicase DNA binding protein 3, transcript variant X23
chromodomain-helicase-DNA-binding protein 3 isoform X18
chromodomain-helicase-DNA-binding protein 3 isoform X19
chromodomain-helicase-DNA-binding protein 3 isoform X22
chromodomain-helicase-DNA-binding protein 3 isoform X23
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X2
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X7
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X6
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X4
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X5
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X8
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X1
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X3
protein mono-ADP-ribosyltransferase TIPARP-like isoform X2
protein mono-ADP-ribosyltransferase TIPARP-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
potassium voltage-gated channel subfamily A regulatory beta subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
potassium voltage-gated channel subfamily A regulatory beta subunit 3, transcript variant X2
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 11 samples with support for all annotated introns
potassium voltage-gated channel subfamily A regulatory beta subunit 3, 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 4 samples with support for all annotated introns
voltage-gated potassium channel subunit beta-3 isoform X2
voltage-gated potassium channel subunit beta-3 isoform X1
voltage-gated potassium channel subunit beta-3 isoform X3
trafficking protein particle complex subunit 1
centrobin, centriole duplication and spindle assembly protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: hydroperoxide isomerase ALOXE3-like
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transmembrane protein 107, transcript variant X1
transmembrane protein 107, transcript variant X4
transmembrane protein 107, transcript variant X3
transmembrane protein 107, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 31 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: period circadian protein homolog 1-like
period circadian protein homolog 1-like, transcript variant X3
period circadian protein homolog 1-like, transcript variant X1
period circadian protein homolog 1-like, transcript variant X2
period circadian protein homolog 1-like isoform X1
period circadian protein homolog 1-like isoform X2
period circadian protein homolog 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor HES-7.1-like, transcript variant X2
transcription factor HES-7.1-like, transcript variant X1
transcription factor HES-7.1-like isoform X2
transcription factor HES-7.1-like isoform X1
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X9
zinc finger protein OZF-like, transcript variant X4
zinc finger protein OZF-like, transcript variant X6
zinc finger protein OZF-like, transcript variant X7
zinc finger protein OZF-like, transcript variant X5
zinc finger protein OZF-like, transcript variant X8
zinc finger protein OZF-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
hydroperoxide isomerase ALOXE3-like, transcript variant X2
hydroperoxide isomerase ALOXE3-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 13 samples with support for all annotated introns
hydroperoxide isomerase ALOXE3-like isoform X1
hydroperoxide isomerase ALOXE3-like isoform X2
cytosolic Fe-S cluster assembly factor nubp1-like, transcript variant X1
cytosolic Fe-S cluster assembly factor nubp1-like isoform X1
cytosolic Fe-S cluster assembly factor nubp1-like, transcript variant X2
cytosolic Fe-S cluster assembly factor nubp1-like isoform X2
zinc finger protein 420-like, transcript variant X50
zinc finger protein 585A-like isoform X45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 436-like, transcript variant X1
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein OZF-like, transcript variant X2
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon AAA); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 34-like, transcript variant X2
zinc finger protein 34-like, transcript variant X1
zinc finger protein 34-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X10
zinc finger protein 883-like, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X16
zinc finger protein 883-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X18
zinc finger protein 883-like, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X4
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 13 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X3
zinc finger protein 883-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 236 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
zinc finger protein 383-like isoform X16
zinc finger protein 883-like isoform X15
zinc finger protein 383-like isoform X20
zinc finger protein 383-like isoform X18
zinc finger protein 883-like isoform X13
zinc finger protein 883-like isoform X14
zinc finger protein 883-like isoform X12
zinc finger protein 883-like isoform X11
zinc finger protein 883-like isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 420-like isoform X24
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 420-like, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 420-like isoform X23
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 49 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 288 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X26
zinc finger protein 420-like, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 288 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 420-like isoform X26
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gastrula zinc finger protein XlCGF7.1-like
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 420-like, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 420-like isoform X25
transfer RNA valine (anticodon CAC); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X32
zinc finger protein 420-like, transcript variant X44
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 420-like, transcript variant X45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 226 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X46
zinc finger protein 420-like, transcript variant X35
zinc finger protein 420-like, transcript variant X39
zinc finger protein 420-like, transcript variant X43
zinc finger protein 420-like, transcript variant X38
zinc finger protein 420-like, transcript variant X36
zinc finger protein 420-like, transcript variant X37
zinc finger protein 420-like, transcript variant X4
zinc finger protein 420-like, transcript variant X10
zinc finger protein 420-like, transcript variant X19
zinc finger protein 420-like, transcript variant X22
zinc finger protein 420-like, transcript variant X21
zinc finger protein 420-like, transcript variant X20
zinc finger protein 420-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X7
zinc finger protein 420-like, transcript variant X14
zinc finger protein 420-like, transcript variant X13
zinc finger protein 420-like, transcript variant X9
zinc finger protein 420-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 288 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X1
zinc finger protein 420-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 420-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X12
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 3 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X33
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X16
zinc finger protein 420-like, transcript variant X15
zinc finger protein 420-like, transcript variant X17
zinc finger protein 420-like, transcript variant X3
zinc finger protein 420-like, transcript variant X18
zinc finger protein 420-like, transcript variant X41
zinc finger protein 420-like, transcript variant X42
zinc finger protein 420-like, transcript variant X40
zinc finger protein 420-like, transcript variant X47
zinc finger protein 436-like isoform X42
zinc finger protein 436-like isoform X34
zinc finger protein 436-like isoform X35
zinc finger protein 436-like isoform X32
zinc finger protein 436-like isoform X33
zinc finger protein 436-like isoform X36
zinc finger protein 436-like isoform X40
zinc finger protein 271-like isoform X11
zinc finger protein 271-like isoform X12
zinc finger protein 436-like isoform X30
zinc finger protein 271-like isoform X14
zinc finger protein 271-like isoform X10
zinc finger protein 271-like isoform X13
zinc finger protein 271-like isoform X16
zinc finger protein 271-like isoform X15
zinc finger protein 271-like isoform X18
zinc finger protein 271-like isoform X17
zinc finger protein 271-like isoform X19
zinc finger protein 271-like isoform X22
zinc finger protein 271-like isoform X21
zinc finger protein 271-like isoform X20
zinc finger protein 436-like isoform X41
zinc finger protein 2 homolog isoform X37
zinc finger protein 436-like isoform X38
zinc finger protein 436-like isoform X39
zinc finger protein 883-like isoform X43
zinc finger protein 420-like isoform X31
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
zinc finger protein 420-like, transcript variant X31
zinc finger protein 420-like, transcript variant X29
zinc finger protein 420-like, transcript variant X30
zinc finger protein 420-like isoform X28
zinc finger protein 420-like isoform X27
zinc finger protein 420-like isoform X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 501-like, transcript variant X4
zinc finger protein 501-like, transcript variant X3
zinc finger protein 501-like, transcript variant X5
zinc finger protein 501-like, transcript variant X21
zinc finger protein 501-like, transcript variant X20
zinc finger protein 501-like, transcript variant X24
zinc finger protein 501-like, transcript variant X25
zinc finger protein 501-like, transcript variant X12
zinc finger protein 501-like, transcript variant X11
zinc finger protein 501-like, transcript variant X17
zinc finger protein 501-like, transcript variant X16
zinc finger protein 501-like, transcript variant X19
zinc finger protein 501-like, transcript variant X18
zinc finger protein 501-like isoform X11
zinc finger protein 154-like isoform X10
zinc finger protein 501-like isoform X19
zinc finger protein 501-like isoform X16
zinc finger protein 501-like isoform X15
zinc finger protein 501-like isoform X18
zinc finger protein 501-like isoform X17
zinc finger protein 501-like isoform X21
zinc finger protein 420-like, transcript variant X49
zinc finger protein 420-like, transcript variant X48
zinc finger protein 436-like isoform X44
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
probable inactive tRNA-specific adenosine deaminase-like protein 3
LOW QUALITY PROTEIN: dnaJ homolog subfamily C member 3-like
fission, mitochondrial 1, transcript variant X1
mitochondrial fission 1 protein isoform X1
fission, mitochondrial 1, transcript variant X2
mitochondrial fission 1 protein isoform X2
alpha-2,8-sialyltransferase 8E-like, transcript variant X3
alpha-2,8-sialyltransferase 8E-like, transcript variant X5
alpha-2,8-sialyltransferase 8E-like, transcript variant X1
alpha-2,8-sialyltransferase 8E-like, transcript variant X6
alpha-2,8-sialyltransferase 8E-like, transcript variant X4
alpha-2,8-sialyltransferase 8E-like, transcript variant X2
alpha-2,8-sialyltransferase 8E-like isoform X5
alpha-2,8-sialyltransferase 8E-like isoform X4
alpha-2,8-sialyltransferase 8E-like isoform X2
alpha-2,8-sialyltransferase 8F-like isoform X3
alpha-2,8-sialyltransferase 8E-like isoform X1
uncharacterized LOC119849434, transcript variant X1
uncharacterized LOC119849434, 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
zinc finger HIT-type containing 1, transcript variant X2
zinc finger HIT-type containing 1, transcript variant X1
zinc finger HIT domain-containing protein 1 isoform X2
zinc finger HIT domain-containing protein 1 isoform X1
procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3
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 47 samples with support for all annotated introns
phosphoribosylformylglycinamidine synthase, transcript variant X6
phosphoribosylformylglycinamidine synthase, transcript variant X5
phosphoribosylformylglycinamidine synthase, transcript variant X2
phosphoribosylformylglycinamidine synthase, transcript variant X4
phosphoribosylformylglycinamidine synthase, transcript variant X3
phosphoribosylformylglycinamidine synthase, transcript variant X1
phosphoribosylformylglycinamidine synthase isoform X3
phosphoribosylformylglycinamidine synthase isoform X2
phosphoribosylformylglycinamidine synthase isoform X1
zinc finger protein 418-like, transcript variant X3
zinc finger protein 418-like, transcript variant X2
zinc finger protein 418-like, transcript variant X1
zinc finger protein 501-like, transcript variant X7
zinc finger protein 501-like, transcript variant X9
zinc finger protein 501-like, transcript variant X15
zinc finger protein 501-like, transcript variant X14
zinc finger protein 501-like, transcript variant X8
zinc finger protein 501-like, transcript variant X10
zinc finger protein OZF-like isoform X14
zinc finger protein OZF-like isoform X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
zinc finger protein 3-like, transcript variant X1
zinc finger protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 138 Proteins, and 96% 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, 102 Proteins, and 96% 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: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 501-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 501-like, transcript variant X22
zinc finger protein 501-like, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 154-like isoform X12
zinc finger protein 501-like isoform X20
zinc finger protein 501-like, transcript variant X6
zinc finger protein 501-like, transcript variant X1
zinc finger protein 501-like, transcript variant X2
uncharacterized LOC122457741, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC122457741, transcript variant X1
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 9 samples with support for all annotated introns
uncharacterized protein LOC122457741 isoform X2
uncharacterized protein LOC122457741 isoform X1
zinc finger protein 260-like, transcript variant X2
zinc finger protein 260-like, transcript variant X1
zinc finger protein 260-like, transcript variant X4
zinc finger protein 260-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 34-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X4
zinc finger protein 251-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 251-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif-containing protein 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 300-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 300-like, transcript variant X3
zinc finger protein 300-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 300-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 300-like, transcript variant X4
zinc finger protein 3-like, transcript variant X3
zinc finger protein 3-like, transcript variant X4