Rhincodon typus isolate 14 chromosome 39, 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\nCM038836.1.\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.
latent-transforming growth factor beta-binding protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
latent-transforming growth factor beta-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
SH3KBP1 binding protein 1, transcript variant X4
COORDINATES: polyA evidence [ECO:0006239]
SH3KBP1 binding protein 1, transcript variant X1
SH3KBP1 binding protein 1, transcript variant X2
SH3KBP1 binding protein 1, transcript variant X3
excision repair cross-complementation group 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
general transcription and DNA repair factor IIH helicase subunit XPD
trafficking protein particle complex subunit 6b-like
leucine-rich repeat and fibronectin type III domain-containing protein 1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat and fibronectin type-III domain-containing protein 5-like
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, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 541-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 541-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BRD4 interacting chromatin remodeling complex associated protein, transcript variant X1
BRD4 interacting chromatin remodeling complex associated protein, transcript variant X2
BRD4 interacting chromatin remodeling complex associated protein, transcript variant X3
BRD4 interacting chromatin remodeling complex associated protein, transcript variant X4
BRD4 interacting chromatin remodeling complex associated protein, transcript variant X5
28S ribosomal protein S12, mitochondrial-like
suppressor of cytokine signaling 9, transcript variant X1
suppressor of cytokine signaling 9, 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 3 samples with support for all annotated introns
BRD4-interacting chromatin-remodeling complex-associated protein isoform X1
BRD4-interacting chromatin-remodeling complex-associated protein isoform X2
BRD4-interacting chromatin-remodeling complex-associated protein isoform X4
BRD4-interacting chromatin-remodeling complex-associated protein isoform X5
BRD4-interacting chromatin-remodeling complex-associated protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 997 long SRA reads, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
endothelial PAS domain-containing protein 1-like
protein phosphatase 1 regulatory subunit 14A-like, transcript variant X3
protein phosphatase 1 regulatory subunit 14A-like, transcript variant X2
protein phosphatase 1 regulatory subunit 14A-like, transcript variant X4
protein phosphatase 1 regulatory subunit 14A-like, transcript variant X1
protein phosphatase 1 regulatory subunit 14A-like
pleckstrin homology domain-containing family G member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
nascent polypeptide-associated complex subunit alpha, muscle-specific form-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125487278, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125487278, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125487279, 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 2 samples with support for all annotated introns
uncharacterized protein LOC125487279 isoform X1
uncharacterized LOC125487279, transcript variant X2
uncharacterized LOC125487279, transcript variant X3
uncharacterized protein LOC125487279 isoform X2
coiled-coil domain containing 9, transcript variant X1
coiled-coil domain containing 9, transcript variant X2
coiled-coil domain-containing protein 9 isoform X1
coiled-coil domain-containing protein 9 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
p21 protein (Cdc42/Rac)-activated kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 17 Proteins, and 99% 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: 3 long SRA reads, 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: 3 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: 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
eukaryotic translation initiation factor 3, subunit K
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1067 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit K
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
CAP-GLY domain containing linker protein 3, transcript variant X1
CAP-GLY domain containing linker protein 3, transcript variant X2
CAP-Gly domain-containing linker protein 3 isoform X1
CAP-Gly domain-containing linker protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6 isoform X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
SPARC-related modular calcium-binding protein 1-like, transcript variant X2
SPARC-related modular calcium-binding protein 1-like, transcript variant X1
SPARC-related modular calcium-binding protein 1-like isoform X2
SPARC-related modular calcium-binding protein 1-like isoform X1
dynein axonemal assembly factor 10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal assembly factor 10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynein axonemal assembly factor 10-like, transcript variant X3
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 3 samples with support for all annotated introns
dynein axonemal assembly factor 10-like, 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 3 samples with support for all annotated introns
dynein axonemal assembly factor 10-like isoform X1
dynein axonemal assembly factor 10-like isoform X2
dynein axonemal assembly factor 10-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
serine/arginine-rich splicing factor 5-like, transcript variant X1
serine/arginine-rich splicing factor 5-like, transcript variant X2
serine/arginine-rich splicing factor 5-like, transcript variant X3
serine/arginine-rich splicing factor 5-like
coiled-coil domain-containing protein 97
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
tetratricopeptide repeat protein 9A-like
mitogen-activated protein kinase kinase kinase 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
atypical kinase COQ8B, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger FYVE domain-containing protein 1
atypical kinase COQ8B, mitochondrial-like, transcript variant X1
atypical kinase COQ8B, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
H3 histone, family 3C, transcript variant X1
H3 histone, family 3C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 380 long SRA reads, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NAD-dependent protein deacetylase sirtuin-2 isoform X4
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NAD-dependent protein deacetylase sirtuin-2 isoform X3
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 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
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X5
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X12
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X1
NAD-dependent protein deacetylase sirtuin-2 isoform X1
sirtuin 2 (silent mating type information regulation 2, homolog) 2 (S. cerevisiae), transcript variant X2
NAD-dependent protein deacetylase sirtuin-2 isoform X2
NAD-dependent protein deacetylase sirtuin-2 isoform X5
Ras and Rab interactor-like, transcript variant X1
Ras and Rab interactor-like, transcript variant X2
chromogranin-A-like, transcript variant X1
chromogranin-A-like, transcript variant X2
inositol-tetrakisphosphate 1-kinase-like, transcript variant X1
inositol-tetrakisphosphate 1-kinase-like isoform X1
inositol-tetrakisphosphate 1-kinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
inositol-tetrakisphosphate 1-kinase-like isoform X2
BTB/POZ domain-containing protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
proteasome subunit alpha type-6-like, transcript variant X2
proteasome subunit alpha type-6-like isoform X2
proteasome subunit alpha type-6-like, transcript variant X1
proteasome subunit alpha type-6-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 61, transcript variant X2
coiled-coil domain containing 61, 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 5 samples with support for all annotated introns
outer mitochondrial membrane lipid metabolism regulator OPA3
mitochondrial ribosomal protein L28, transcript variant X2
mitochondrial ribosomal protein L28, transcript variant X3
mitochondrial ribosomal protein L28, transcript variant X4
mitochondrial ribosomal protein L28, transcript variant X1
39S ribosomal protein L28, mitochondrial isoform X1
39S ribosomal protein L28, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
B-cell lymphoma/leukemia 11A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
B-cell lymphoma/leukemia 11A-like isoform X1
B-cell lymphoma/leukemia 11A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
B-cell lymphoma/leukemia 11A-like isoform X2
CLK4-associating serine/arginine rich protein, transcript variant X1
CLK4-associating serine/arginine rich protein, transcript variant X2
CLK4-associating serine/arginine rich protein, transcript variant X3
CLK4-associating serine/arginine rich protein
CLK4-associating serine/arginine rich protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 37-like
uncharacterized LOC125487282, transcript variant X3
uncharacterized LOC125487282, transcript variant X2
uncharacterized LOC125487282, transcript variant X1
uncharacterized LOC125487282, transcript variant X4
protein phosphatase 1, regulatory subunit 13 like
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
protein phosphatase 5, catalytic subunit
potassium channel, subfamily K, member 6
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 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 10 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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
kinesin light chain 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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
kinesin light chain 1-like, transcript variant 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
insulin-like growth factor-binding protein complex acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
MAP/microtubule affinity-regulating kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
MAP/microtubule affinity-regulating kinase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
exocyst complex component 3, transcript variant X2
exocyst complex component 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
echinoderm microtubule-associated protein-like 2
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
vasodilator-stimulated phosphoprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sphingolipid delta(4)-desaturase/C4-monooxygenase DES2-like
DNA-directed RNA polymerase II subunit RPB9
uncharacterized protein LOC100124596 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
putative transcription factor Ovo-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 79% 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 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
G-protein coupled receptor 4, transcript variant X2
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
G-protein coupled receptor 4, transcript variant X1
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 5 samples with support for all annotated introns
CD3e molecule, epsilon associated protein
zinc finger and BTB domain-containing protein 1-like, transcript variant X1
zinc finger and BTB domain-containing protein 1-like
zinc finger and BTB domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
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: F-box only protein 46
small nuclear ribonucleoprotein D2 polypeptide
fukutin related protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fukutin related protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fukutin related protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adaptor related protein complex 2 subunit sigma 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 24 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: 2 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
neuronal PAS domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 128 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
7 transmembrane receptor domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins
RNA-binding protein Nova-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding protein Nova-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA-binding protein Nova-1-like isoform X2
RNA-binding protein Nova-1-like isoform X1
interferon regulatory factor 2-binding protein 1-like
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
prostaglandin I2 receptor, transcript variant X1
prostaglandin I2 receptor, transcript variant X3
prostaglandin I2 receptor, 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 4 samples with support for all annotated introns
prostaglandin I2 receptor, 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 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium channel subfamily K member 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CLPTM1 regulator of GABA type A receptor forward trafficking
cleft lip and palate transmembrane protein 1 homolog
succinate dehydrogenase complex assembly factor 1, transcript variant X1
succinate dehydrogenase complex assembly factor 1, transcript variant X2
succinate dehydrogenase complex assembly factor 1, transcript variant X4
succinate dehydrogenase complex assembly factor 1, transcript variant X5
succinate dehydrogenase complex assembly factor 1, transcript variant X3
succinate dehydrogenase assembly factor 1, mitochondrial
WD repeat-containing protein 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
WD repeat-containing protein 20-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
WD repeat-containing protein 20-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WD repeat-containing protein 20-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WD repeat-containing protein 20-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WD repeat-containing protein 20-like isoform X3
WD repeat-containing protein 20-like isoform X5
WD repeat-containing protein 20-like isoform X1
WD repeat-containing protein 20-like isoform X4
WD repeat-containing protein 20-like isoform X2
WD repeat-containing protein 20-like, 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 3 samples with support for all annotated introns
WD repeat-containing protein 20-like isoform X6
forkhead box protein A2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
forkhead box protein A2-like, transcript variant X1
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 11 samples with support for all annotated introns
gem (nuclear organelle) associated protein 7, transcript variant X1
gem (nuclear organelle) associated protein 7, transcript variant X2
Yip1 interacting factor homolog B (S. cerevisiae), transcript variant X1
Yip1 interacting factor homolog B (S. cerevisiae), transcript variant X2
small nuclear ribonucleoprotein polypeptide A
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 13 samples with support for all annotated introns
melanoma-derived growth regulatory protein
vascular endothelial growth factor A-like, transcript variant X2
vascular endothelial growth factor A-like, transcript variant X1
vascular endothelial growth factor A-like isoform X2
vascular endothelial growth factor A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
reticulon-1-A-like, transcript variant 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
reticulon-1-A-like, transcript variant X4
reticulon-1-A-like, transcript variant X1
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 2 samples with support for all annotated introns
reticulon-1-A-like, transcript variant X3
reticulon-1-A-like, transcript variant X5
RAC-beta serine/threonine-protein kinase, transcript variant X8
RAC-beta serine/threonine-protein kinase, transcript variant X3
RAC-beta serine/threonine-protein kinase, transcript variant X2
RAC-beta serine/threonine-protein kinase, transcript variant X6
RAC-beta serine/threonine-protein kinase, transcript variant X4
RAC-beta serine/threonine-protein kinase, transcript variant X1
RAC-beta serine/threonine-protein kinase, transcript variant X7
RAC-beta serine/threonine-protein kinase, transcript variant X5
RAC-beta serine/threonine-protein kinase isoform X1
RAC-beta serine/threonine-protein kinase isoform X2
transforming growth factor beta-3 proprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
synapse differentiation-inducing gene protein 1
branched chain keto acid dehydrogenase E1 subunit alpha
2-oxoisovalerate dehydrogenase subunit alpha, mitochondrial
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like
distal membrane arm assembly component 2
distal membrane-arm assembly complex protein 2
serine protease 16, transcript variant X1
serine protease 16, transcript variant X2
thymus-specific serine protease isoform X1
thymus-specific serine protease isoform X2
uncharacterized LOC109926914, transcript variant X2
uncharacterized LOC109926914, transcript variant X1
uncharacterized LOC109926914, transcript variant X3
uncharacterized LOC109926914, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
SERTA domain-containing protein 1-like, transcript variant X1
SERTA domain-containing protein 1-like, transcript variant X2
SERTA domain-containing protein 1-like, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 5-like isoform X1
mitogen-activated protein kinase kinase kinase kinase 5-like isoform X2
uncharacterized LOC125487317, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125487317, transcript variant X1
uncharacterized LOC125487317, 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 3 samples with support for all annotated introns
serine and arginine rich splicing factor 7a, transcript variant X1
serine and arginine rich splicing factor 7a, transcript variant X5
serine and arginine rich splicing factor 7a, transcript variant X4
serine and arginine rich splicing factor 7a, transcript variant X7
serine and arginine rich splicing factor 7a, transcript variant X6
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 20 samples with support for all annotated introns
serine and arginine rich splicing factor 7a, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
serine and arginine rich splicing factor 7a, transcript variant X8
serine and arginine rich splicing factor 7a, transcript variant X2
serine and arginine rich splicing factor 7a, transcript variant X3
serine and arginine rich splicing factor 7a isoform X1
serine and arginine rich splicing factor 7a isoform X3
serine and arginine rich splicing factor 7a isoform X2
serine and arginine rich splicing factor 7a isoform X5
serine and arginine rich splicing factor 7a isoform X4
serine and arginine rich splicing factor 7a isoform X6
heterogeneous nuclear ribonucleoprotein L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial
heterogeneous nuclear ribonucleoprotein U-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein L
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 55 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cation channel sperm-associated auxiliary subunit gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 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: 75% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 33 Proteins, and 89% 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: 31 long SRA reads, 33 Proteins, and 89% 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, 33 Proteins, and 89% 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: 31 long SRA reads, 33 Proteins, and 89% 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
Myb/SANT-like DNA-binding domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myb/SANT-like DNA-binding domain-containing 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 8% 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactomedin-4-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: 8 Proteins, and 36% 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.
spectrin beta chain, non-erythrocytic 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 229B-like, transcript variant X1
transmembrane protein 229B-like, transcript variant X2
PAF1 homolog, Paf1/RNA polymerase II complex component
RNA polymerase II-associated factor 1 homolog
mRNA decay activator protein ZFP36L1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 29
metastasis-associated protein MTA1-like, transcript variant X2
metastasis-associated protein MTA1-like, transcript variant X1
metastasis-associated protein MTA1-like, transcript variant X3
metastasis-associated protein MTA1-like isoform X2
metastasis-associated protein MTA1-like isoform X1
metastasis-associated protein MTA1-like isoform X3
elongation factor 1-gamma-like, transcript variant X1
elongation factor 1-gamma-like isoform X1
elongation factor 1-gamma-like, transcript variant X2
elongation factor 1-gamma-like isoform X2
neuroblast differentiation-associated protein AHNAK-like, transcript variant X5
neuroblast differentiation-associated protein AHNAK-like, transcript variant X1
neuroblast differentiation-associated protein AHNAK-like, transcript variant X2
neuroblast differentiation-associated protein AHNAK-like, transcript variant X4
neuroblast differentiation-associated protein AHNAK-like, transcript variant X3
neuroblast differentiation-associated protein AHNAK-like, transcript variant X6
neuroblast differentiation-associated protein AHNAK-like
homeodomain-interacting protein kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
phospholipase D family, member 3, transcript variant X5
phospholipase D family, member 3, transcript variant X3
phospholipase D family, member 3, transcript variant X6
phospholipase D family, member 3, transcript variant X4
phospholipase D family, member 3, transcript variant X2
phospholipase D family, member 3, transcript variant X7
phospholipase D family, member 3, transcript variant X1
uncharacterized protein LOC777623 homolog, transcript variant X1
uncharacterized protein LOC777623 homolog, transcript variant X2
regulator of microtubule dynamics protein 3-like, 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 6 samples with support for all annotated introns
regulator of microtubule dynamics protein 3-like, 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 8 samples with support for all annotated introns
regulator of microtubule dynamics protein 3-like isoform X2
regulator of microtubule dynamics protein 3-like isoform X1
zinc finger CCCH-type containing 4, transcript variant X1
zinc finger CCCH domain-containing protein 4 isoform X1
zinc finger CCCH-type containing 4, transcript variant X2
zinc finger CCCH domain-containing protein 4 isoform X2
SPT5 homolog, DSIF elongation factor subunit, transcript variant X1
SPT5 homolog, DSIF elongation factor subunit, transcript variant X2
transcription elongation factor SPT5 isoform X1
transcription elongation factor SPT5 isoform X2
translocase of inner mitochondrial membrane 50 homolog (S. cerevisiae)
mitochondrial import inner membrane translocase subunit TIM50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adenosine deaminase domain-containing protein 1-like
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 2 samples with support for all annotated introns
ribonuclease T2, like, transcript variant X2
ribonuclease T2, like, transcript variant X1
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 4 samples with support for all annotated introns
synaptosomal-associated protein 25-like, transcript variant X2
synaptosomal-associated protein 25-like, transcript variant X1
synaptosomal-associated protein 25-like isoform X2
synaptosomal-associated protein 25-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
calpain, small subunit 1 b, transcript variant X3
calpain, small subunit 1 b, transcript variant X2
calpain, small subunit 1 b, transcript variant X1
calpain, small subunit 1 b, transcript variant X4
calpain, small subunit 1 b, transcript variant X5
transmembrane protein 87A-like, 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 15 samples with support for all annotated introns
transmembrane protein 87A-like, transcript variant X3
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 5 samples with support for all annotated introns
transmembrane protein 87A-like, transcript variant X5
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 2 samples with support for all annotated introns
transmembrane protein 87A-like, transcript variant X4
transmembrane protein 87A-like, transcript variant X1
transmembrane protein 87A-like isoform X1
transmembrane protein 87B-like isoform X2
transmembrane protein 87B-like isoform X3
transmembrane protein 87B-like isoform X4
nuclear localization sequence-binding protein-like
uncharacterized protein DDB_G0280579-like, transcript variant X1
uncharacterized protein DDB_G0280579-like isoform X1
uncharacterized protein DDB_G0280579-like, transcript variant X2
uncharacterized protein DDB_G0280579-like isoform X2
mitogen-activated protein kinase-binding protein 1-like
THAP domain-containing protein 5-like, transcript variant X2
THAP domain-containing protein 5-like, transcript variant X1
THAP domain-containing protein 5-like, transcript variant X3
THAP domain-containing protein 5-like, transcript variant X4
THAP domain-containing protein 5-like isoform X2
THAP domain-containing protein 5-like isoform X1
THAP domain-containing protein 5-like isoform X3
THAP domain-containing protein 5-like isoform X4
uncharacterized LOC125487302, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125487302, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125487302, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 239-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X3
zinc finger protein 664-like, transcript variant X3
zinc finger protein 664-like, transcript variant X1
zinc finger protein 664-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
M1-specific T cell receptor beta chain-like
tigger transposable element-derived protein 1-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC109914350, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109914350, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 53% coverage of the annotated genomic feature by RNAseq alignments
NTPase, KAP family P-loop domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NTPase KAP family P-loop domain-containing protein 1
biogenesis of lysosomal organelles complex-1, subunit 3
biogenesis of lysosome-related organelles complex 1 subunit 3