Rhincodon typus isolate 14 chromosome 31, 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\nCM038828.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
von Willebrand factor A domain containing 5B1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 5B1
calcium/calmodulin-dependent protein kinase II inhibitor 1-like
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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: 74 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins
peptidylprolyl isomerase H (cyclophilin H)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
TAF10 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 10
solute carrier family 2, facilitated glucose transporter member 1
polyhomeotic-like protein 2, transcript variant X1
polyhomeotic-like protein 2, transcript variant X2
polyhomeotic-like protein 2, transcript variant X4
polyhomeotic-like protein 2, transcript variant X5
polyhomeotic-like protein 2, transcript variant X3
polyhomeotic-like protein 2, transcript variant X6
leucine-rich repeat-containing protein 47-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 2 samples with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit delta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit delta, transcript variant X1
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 4 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit delta isoform X1
gamma-aminobutyric acid receptor subunit delta isoform X2
cilia and flagella associated protein 74
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 74
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X4
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
uncharacterized LOC109912939, 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 1 sample with support for all annotated introns
uncharacterized LOC109912939, transcript variant X3
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
uncharacterized LOC109912939, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109912939, transcript variant X6
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 7 samples with support for all annotated introns
uncharacterized LOC109912939, transcript variant X5
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 10 samples with support for all annotated introns
uncharacterized LOC109912939, 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 4 samples with support for all annotated introns
uncharacterized protein LOC109912939 isoform X2
uncharacterized protein LOC109912939 isoform X1
uncharacterized protein LOC109912939 isoform X3
uncharacterized protein LOC109912939 isoform X5
uncharacterized protein LOC109912939 isoform X4
solute carrier family 35 member E2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 35 member E2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
solute carrier family 35 member E2B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125486650, transcript variant X2
uncharacterized LOC125486650, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative uncharacterized protein DDB_G0271982
uncharacterized LOC109918475, 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
uncharacterized LOC109918475, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125486649, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125486649, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 17 Proteins, and 45% 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 3 samples with support for all annotated introns
castor zinc finger 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
castor zinc finger 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
castor zinc finger 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
castor zinc finger 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein castor homolog 1 isoform X1
zinc finger protein castor homolog 1 isoform X2
zinc finger protein castor homolog 1 isoform X3
peroxisomal biogenesis factor 14, transcript variant X2
peroxisomal biogenesis factor 14, transcript variant X1
peroxisomal membrane protein PEX14 isoform X2
peroxisomal membrane protein PEX14 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 65% 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: 15 long SRA reads, and 42% coverage of the annotated genomic feature by RNAseq alignments
6-phosphogluconate dehydrogenase, decarboxylating
ubiquitination factor E4B, UFD2 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
nicotinamide nucleotide adenylyltransferase 1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
leucine zipper and CTNNBIP1 domain containing
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X7
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X3
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X4
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X6
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X2
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X5
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X8
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X9
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X10
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta, transcript variant X1
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 201, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 201, transcript variant X1
transmembrane protein 201, transcript variant X2
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 4 samples with support for all annotated introns
transmembrane protein 201, transcript variant X5
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
transmembrane protein 201, transcript variant X7
transmembrane protein 201, transcript variant X4
transmembrane protein 201, transcript variant X6
splA/ryanodine receptor domain and SOCS box containing 1, transcript variant X2
splA/ryanodine receptor domain and SOCS box containing 1, transcript variant X1
SPRY domain-containing SOCS box protein 1
hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GDH/6PGL endoplasmic bifunctional protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2, facilitated glucose transporter member 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
enolase 1a, (alpha), transcript variant X1
enolase 1a, (alpha), transcript variant X2
arginine-glutamic acid dipeptide repeats protein-like, transcript variant X2
arginine-glutamic acid dipeptide repeats protein-like, transcript variant X1
arginine-glutamic acid dipeptide repeats protein-like isoform X2
arginine-glutamic acid dipeptide repeats protein-like isoform X1
arginine-glutamic acid dipeptide (RE) repeats a, transcript variant X1
arginine-glutamic acid dipeptide (RE) repeats a, transcript variant X4
arginine-glutamic acid dipeptide (RE) repeats a, transcript variant X2
arginine-glutamic acid dipeptide (RE) repeats a, transcript variant X3
arginine-glutamic acid dipeptide repeats protein
sterile alpha motif domain containing 11, transcript variant X6
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 2 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sterile alpha motif domain-containing protein 11 isoform X1
sterile alpha motif domain-containing protein 11 isoform X2
sterile alpha motif domain-containing protein 11 isoform X3
sterile alpha motif domain-containing protein 11 isoform X4
sterile alpha motif domain-containing protein 11 isoform X5
sterile alpha motif domain-containing protein 11 isoform X6
sterile alpha motif domain containing 11, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sterile alpha motif domain containing 11, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sterile alpha motif domain-containing protein 11 isoform X7
NOC2-like nucleolar associated transcriptional repressor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
kelch-like family member 17, transcript variant X2
kelch-like family member 17, transcript variant X1
kelch-like family member 17, transcript variant X5
kelch-like family member 17, transcript variant X4
kelch-like family member 17, transcript variant X3
uncharacterized LOC109933944, transcript variant X1
uncharacterized LOC109933944, transcript variant X2
uncharacterized LOC109933944, transcript variant X3
uncharacterized protein LOC109933944 isoform X1
uncharacterized protein LOC109933944 isoform X2
uncharacterized protein LOC109933944 isoform X3
rho guanine nucleotide exchange factor 7-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
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
protein tyrosine phosphatase non-receptor type 11b
tyrosine-protein phosphatase non-receptor type 11b
RING finger protein 223, transcript variant X2
RING finger protein 223, transcript variant X1
uncharacterized protein C1orf159 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
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
rho guanine nucleotide exchange factor 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA thioesterase 7, transcript variant X1
cytosolic acyl coenzyme A thioester hydrolase isoform X1
acyl-CoA thioesterase 7, transcript variant X2
cytosolic acyl coenzyme A thioester hydrolase isoform X2
probable G-protein coupled receptor 153, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable G-protein coupled receptor 153, transcript variant X2
probable G-protein coupled receptor 153, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: prostamide/prostaglandin F synthase
membrane metallo-endopeptidase-like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, 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 2 samples with support for all annotated introns
membrane metallo-endopeptidase-like 1, 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 1 sample with support for all annotated introns
membrane metallo-endopeptidase-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane metallo-endopeptidase-like 1 isoform X4
membrane metallo-endopeptidase-like 1 isoform X2
membrane metallo-endopeptidase-like 1 isoform X3
membrane metallo-endopeptidase-like 1 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: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); 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: 857 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins
uncharacterized LOC109920486, transcript variant X4
uncharacterized LOC109920486, transcript variant X2
uncharacterized LOC109920486, transcript variant X1
uncharacterized LOC109920486, transcript variant X3
histone-lysine N-methyltransferase PRDM16-like, transcript variant X1
histone-lysine N-methyltransferase PRDM16-like
histone-lysine N-methyltransferase PRDM16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase PRDM16
Rho guanine nucleotide exchange factor (GEF) 16, transcript variant X2
Rho guanine nucleotide exchange factor (GEF) 16, transcript variant X1
rho guanine nucleotide exchange factor 16
multiple epidermal growth factor-like domains protein 6
tumor protein p63-regulated gene 1-like protein
WD repeat containing, antisense to TP73, transcript variant X2
WD repeat containing, antisense to TP73, transcript variant X1
WD repeat-containing protein WRAP73 isoform X2
WD repeat-containing protein WRAP73 isoform X1
tumor protein p73, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein p73, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein p73, transcript variant X3
tumor protein p73, transcript variant X4
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 1 sample with support for all annotated introns
myo-inositol 2-dehydrogenase-like, transcript variant X2
myo-inositol 2-dehydrogenase-like, transcript variant X1
protein kinase C, zeta, transcript variant X3
protein kinase C, zeta, transcript variant X2
protein kinase C, zeta, transcript variant X1
protein kinase C, zeta, transcript variant X4
FA core complex associated protein 20, transcript variant X3
FA core complex associated protein 20, transcript variant X2
FA core complex associated protein 20, transcript variant X1
uncharacterized protein si:ch73-70k4.1 isoform X3
uncharacterized protein si:ch73-70k4.1 isoform X2
uncharacterized protein si:ch73-70k4.1 isoform X1
v-ski avian sarcoma viral oncogene homolog a
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
retention in endoplasmic reticulum sorting receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
retention in endoplasmic reticulum sorting receptor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retention in endoplasmic reticulum sorting receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2a
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable glutamate receptor, transcript variant X1
probable glutamate receptor, transcript variant X2
pantothenate kinase 4 (inactive), transcript variant X3
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
pantothenate kinase 4 (inactive), transcript variant X5
pantothenate kinase 4 (inactive), transcript variant X4
pantothenate kinase 4 (inactive), transcript variant X2
pantothenate kinase 4 (inactive), transcript variant X1
4'-phosphopantetheine phosphatase isoform X3
4'-phosphopantetheine phosphatase isoform X2
4'-phosphopantetheine phosphatase isoform X1
pantothenate kinase 4 (inactive), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
vesicle-associated membrane protein 3 (cellubrevin)
calmodulin-binding transcription activator 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
DnaJ (Hsp40) homolog, subfamily C, member 11a
THAP domain containing, apoptosis associated protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
THAP domain containing, apoptosis associated protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
THAP domain containing, apoptosis associated protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
THAP domain-containing protein 3 isoform X1
THAP domain-containing protein 3 isoform X2
PHD finger protein 13, transcript variant X2
PHD finger protein 13, transcript variant X1
kelch-like family member 21, transcript variant X1
kelch-like family member 21, transcript variant X3
kelch-like family member 21, transcript variant X2
isoprenylcysteine carboxyl methyltransferase
protein-S-isoprenylcysteine O-methyltransferase
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
telomere zinc finger-associated protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments
chromodomain helicase DNA binding protein 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromodomain helicase DNA binding protein 5, 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 3 samples with support for all annotated introns
chromodomain helicase DNA binding protein 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromodomain-helicase-DNA-binding protein 5
potassium voltage-gated channel subfamily A regulatory beta subunit 2a, transcript variant X2
potassium voltage-gated channel subfamily A regulatory beta subunit 2a, transcript variant X1
potassium voltage-gated channel subfamily A regulatory beta subunit 2a, transcript variant X3
potassium voltage-gated channel subfamily A regulatory beta subunit 2a, transcript variant X4
voltage-gated potassium channel subunit beta-2 isoform X2
voltage-gated potassium channel subunit beta-2 isoform X1
voltage-gated potassium channel subunit beta-2 isoform X3
tumor necrosis factor receptor superfamily member 9-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
coiled-coil domain-containing protein 50-like, transcript variant X1
coiled-coil domain-containing protein 50-like, transcript variant X4
coiled-coil domain-containing protein 50-like, transcript variant X3
coiled-coil domain-containing protein 50-like, transcript variant X2
coiled-coil domain-containing protein 50-like, transcript variant X7
coiled-coil domain-containing protein 50-like, transcript variant X5
coiled-coil domain-containing protein 50-like, transcript variant X9
coiled-coil domain-containing protein 50-like, transcript variant X6
coiled-coil domain-containing protein 50-like, transcript variant X8
coiled-coil domain-containing protein 50-like isoform X1
coiled-coil domain-containing protein 50-like isoform X2
coiled-coil domain-containing protein 50-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
paired box protein Pax-7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
paired box protein Pax-7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
paired box protein Pax-7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
paired box protein Pax-7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
paired box protein Pax-7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
paired box protein Pax-7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sphingosine-1-phosphate phosphatase 2-like, transcript variant X1
sphingosine-1-phosphate phosphatase 2-like, transcript variant X3
sphingosine-1-phosphate phosphatase 2-like, transcript variant X2
sphingosine-1-phosphate phosphatase 2-like isoform X1
sphingosine-1-phosphate phosphatase 2-like isoform X3
sphingosine-1-phosphate phosphatase 2-like isoform X2
28S ribosomal protein S16, mitochondrial
outer dynein arm-docking complex subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC556929 homolog
proton-associated sugar transporter A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125486623, transcript variant X1
uncharacterized LOC125486623, transcript variant X2
ERBB receptor feedback inhibitor 1, transcript variant X1
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 13 samples with support for all annotated introns
ERBB receptor feedback inhibitor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 7% 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
segment polarity protein dishevelled homolog DVL-1, transcript variant X2
segment polarity protein dishevelled homolog DVL-1, transcript variant X1
segment polarity protein dishevelled homolog DVL-1 isoform X2
segment polarity protein dishevelled homolog DVL-1 isoform X1
matrix remodeling-associated protein 8, transcript variant X3
matrix remodeling-associated protein 8, transcript variant X2
matrix remodeling-associated protein 8, transcript variant X1
matrix remodeling-associated protein 8 isoform X3
matrix remodeling-associated protein 8 isoform X2
matrix remodeling-associated protein 8 isoform X1
nucleolar protein 9, transcript variant X1
nucleolar protein 9, transcript variant X5
nucleolar protein 9, transcript variant X4
nucleolar protein 9, transcript variant X3
nucleolar protein 9, transcript variant X2
polynucleotide 5'-hydroxyl-kinase NOL9 isoform X1
polynucleotide 5'-hydroxyl-kinase NOL9 isoform X2
pleckstrin homology domain containing, family G (with RhoGef domain) member 5a
pleckstrin homology domain-containing family G member 5
tumor necrosis factor receptor superfamily member 25-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
migration and invasion inhibitory protein, transcript variant X1
migration and invasion inhibitory protein, transcript variant X2
migration and invasion inhibitory protein, transcript variant X3
migration and invasion inhibitory protein, transcript variant X4
migration and invasion inhibitory protein, transcript variant X5
uncharacterized protein LOC109919458 isoform X2
uncharacterized protein LOC109919458 isoform X3
uncharacterized protein LOC109919458 isoform X4
uncharacterized protein LOC109919458 isoform X1
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a, 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 4 samples with support for all annotated introns
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 isoform X2
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 isoform X3
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 isoform X1
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a, 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 2 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog
C-type natriuretic peptide prohormone-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
chloride channel 6, transcript variant X2
chloride channel 6, transcript variant X1
chloride channel 6, transcript variant X3
H(+)/Cl(-) exchange transporter 6 isoform X1
H(+)/Cl(-) exchange transporter 6 isoform X2
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X1
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X2
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X3
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X4
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X5
methylenetetrahydrofolate reductase (NAD(P)H), transcript variant X6
aldehyde dehydrogenase 4 family, member A1, transcript variant X2
aldehyde dehydrogenase 4 family, member A1, transcript variant X1
aldehyde dehydrogenase 4 family, member A1, transcript variant X3
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial isoform X1
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial isoform X2
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial isoform X3
MRT4 homolog, ribosome maturation factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 19 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: 70 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X1
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X2
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X4
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X5
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X3
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X6
ubiquitin protein ligase E3 component n-recognin 4, transcript variant X7
E3 ubiquitin-protein ligase UBR4 isoform X1
E3 ubiquitin-protein ligase UBR4 isoform X2
E3 ubiquitin-protein ligase UBR4 isoform X4
E3 ubiquitin-protein ligase UBR4 isoform X5
E3 ubiquitin-protein ligase UBR4 isoform X3
E3 ubiquitin-protein ligase UBR4 isoform X6
E3 ubiquitin-protein ligase UBR4 isoform X7
aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase), transcript variant X1
aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase), transcript variant X2
aflatoxin B1 aldehyde reductase member 3 isoform X1
aflatoxin B1 aldehyde reductase member 3 isoform X2
mitotic spindle assembly checkpoint protein MAD2B
dorsal inhibitory axon guidance protein b
angiotensin II receptor-associated protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
angiotensin II receptor-associated protein, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
angiotensin II receptor-associated protein, transcript variant X2
angiotensin II receptor-associated protein, transcript variant X1
angiotensin II receptor-associated protein, transcript variant X6
angiotensin II receptor-associated protein, transcript variant X5
type-1 angiotensin II receptor-associated protein isoform X3
type-1 angiotensin II receptor-associated protein isoform X1
angiotensin II receptor-associated protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
type-1 angiotensin II receptor-associated protein isoform X2
intermediate filament family orphan 2-like
aurora kinase A interacting protein 1, transcript variant X2
aurora kinase A interacting protein 1, transcript variant X1
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3a, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 11, transcript variant X1
integrator complex subunit 11, transcript variant X3
integrator complex subunit 11, transcript variant X2
tumor necrosis factor receptor superfamily member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
C1q and TNF related 12, transcript variant X4
C1q and TNF related 12, transcript variant X3
C1q and TNF related 12, transcript variant X2
C1q and TNF related 12, transcript variant X1
ubiquitin-conjugating enzyme E2, J2 (UBC6 homolog, yeast), transcript variant X3
ubiquitin-conjugating enzyme E2, J2 (UBC6 homolog, yeast), transcript variant X2
ubiquitin-conjugating enzyme E2, J2 (UBC6 homolog, yeast), transcript variant X1
ubiquitin-conjugating enzyme E2 J2 isoform X1
ubiquitin-conjugating enzyme E2 J2 isoform X2
39S ribosomal protein L20, mitochondrial
ankyrin repeat domain-containing protein 65-like
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: 3 Proteins
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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein 65-like
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
von Willebrand factor A domain containing 1
von Willebrand factor A domain-containing protein 1
uncharacterized LOC125486658, transcript variant X2
uncharacterized LOC125486658, transcript variant X1
uncharacterized LOC125486658, transcript variant X3
uncharacterized LOC125486658, 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 3 samples with support for all annotated introns
uncharacterized protein LOC125486658 isoform X2
uncharacterized protein LOC125486658 isoform X1
uncharacterized protein LOC125486658 isoform X3
SSU72 homolog, RNA polymerase II CTD phosphatase
RNA polymerase II subunit A C-terminal domain phosphatase SSU72
fibronectin type III domain containing 10
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
fibronectin type III domain-containing protein 10
Golgi integral membrane protein 4-like, transcript variant X3
Golgi integral membrane protein 4-like, transcript variant X2
Golgi integral membrane protein 4-like, transcript variant X1
Golgi integral membrane protein 4-like isoform X3
Golgi integral membrane protein 4-like isoform X2
Golgi integral membrane protein 4-like isoform X1
olfactory receptor class A-like protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
OTU deubiquitinase 3, transcript variant X1
OTU deubiquitinase 3, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RNF186
transmembrane and coiled-coil domains 4, transcript variant X4
transmembrane and coiled-coil domains 4, transcript variant X8
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 1 sample with support for all annotated introns
transmembrane and coiled-coil domains 4, transcript variant X7
transmembrane and coiled-coil domains 4, transcript variant X5
transmembrane and coiled-coil domains 4, transcript variant X1
transmembrane and coiled-coil domains 4, transcript variant X3
transmembrane and coiled-coil domains 4, transcript variant X2
transmembrane and coiled-coil domain-containing protein 4 isoform X1
transmembrane and coiled-coil domains 4, transcript variant X6
transmembrane and coiled-coil domain-containing protein 4 isoform X2
transmembrane and coiled-coil domain-containing protein 4 isoform X3
5-hydroxytryptamine (serotonin) receptor 6
NBL1, DAN family BMP antagonist, transcript variant X2
NBL1, DAN family BMP antagonist, transcript variant X4
NBL1, DAN family BMP antagonist, transcript variant X1
NBL1, DAN family BMP antagonist, transcript variant X3
neuroblastoma suppressor of tumorigenicity 1
mitochondrial contact site and cristae organizing system subunit 10, transcript variant X1
mitochondrial contact site and cristae organizing system subunit 10, transcript variant X2
DNA-damage inducible protein 2, transcript variant X4
DNA-damage inducible protein 2, transcript variant X2
DNA-damage inducible protein 2, transcript variant X3
DNA-damage inducible protein 2, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit (non-catalytic)
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit
caspase 9, apoptosis-related cysteine peptidase, transcript variant X1
caspase 9, apoptosis-related cysteine peptidase, transcript variant X2
DnaJ (Hsp40) homolog, subfamily C, member 16, transcript variant X3
DnaJ (Hsp40) homolog, subfamily C, member 16, transcript variant X4
DnaJ (Hsp40) homolog, subfamily C, member 16, transcript variant X1
DnaJ (Hsp40) homolog, subfamily C, member 16, transcript variant X2
dnaJ homolog subfamily C member 16 isoform X1
dnaJ homolog subfamily C member 16 isoform X3
dnaJ homolog subfamily C member 16 isoform X2
dnaJ homolog subfamily C member 16 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PTEN induced kinase 1, transcript variant X2
PTEN induced kinase 1, transcript variant X1
serine/threonine-protein kinase PINK1, mitochondrial isoform X2
serine/threonine-protein kinase PINK1, mitochondrial isoform X1
solute carrier family 66 member 1, transcript variant X2
solute carrier family 66 member 1, transcript variant X1
solute carrier family 66 member 1, transcript variant X3
lysosomal amino acid transporter 1 homolog
capping actin protein of muscle Z-line subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 19 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 19-like
ciliogenesis and planar polarity effector 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rho guanine nucleotide exchange factor 19-like, transcript variant X3
rho guanine nucleotide exchange factor 19-like, transcript variant X1
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 3 samples with support for all annotated introns
rho guanine nucleotide exchange factor 19-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rho guanine nucleotide exchange factor 19-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 19-like isoform X1
rho guanine nucleotide exchange factor 19-like isoform X2
rho guanine nucleotide exchange factor 19-like isoform X3
eph receptor A2 b, transcript variant X2
eph receptor A2 b, transcript variant X1
family with sequence similarity 131 member C
chloride channel K, transcript variant X1
chloride channel K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heat shock protein family, member 7 (cardiovascular), transcript variant X2
heat shock protein family, member 7 (cardiovascular), transcript variant X1
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X2
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X4
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X3
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X1
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X5
pleckstrin homology domain containing, family M (with RUN domain) member 2, transcript variant X6
pleckstrin homology domain-containing family M member 2 isoform X1
pleckstrin homology domain-containing family M member 2 isoform X2
pleckstrin homology domain-containing family M member 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 25 member 35, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 25 member 35, 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 4 samples with support for all annotated introns
solute carrier family 25 member 35 isoform X1
solute carrier family 25 member 35 isoform X2
transmembrane protein 82, transcript variant X1
transmembrane protein 82, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
filamin-binding LIM protein 1-like, transcript variant X1
filamin-binding LIM protein 1-like, transcript variant X2
filamin-binding LIM protein 1-like isoform X1
filamin-binding LIM protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger and BTB domain containing 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
adaptin ear-binding coat-associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
something about silencing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger MYND domain-containing protein 12
UTP3 small subunit processome component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
UTP3 small subunit processome component, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
something about silencing protein 10 isoform X2
something about silencing protein 10 isoform X1
coiled-coil domain containing 30, transcript variant X1
coiled-coil domain containing 30, transcript variant X2
coiled-coil domain-containing protein 30 isoform X1
coiled-coil domain-containing protein 30 isoform X2
leucine-rich repeat transmembrane protein FLRT1-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 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
ribosomal modification protein rimK-like family member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 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: 2 long SRA reads, 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
forkhead-associated domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
kazrin, periplakin interacting protein a, transcript variant X1
kazrin, periplakin interacting protein a, transcript variant X2
testis-specific serine/threonine-protein kinase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
PR domain containing 2, with ZNF domain a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 2, with ZNF domain a, transcript variant X4
PR domain containing 2, with ZNF domain a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PR domain zinc finger protein 2 isoform X3
PR domain zinc finger protein 2 isoform X1
PR domain zinc finger protein 2 isoform X2
PR domain zinc finger protein 2 isoform X4
PR domain zinc finger protein 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, and 98% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 38-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cilia and flagella associated protein 107
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
arylacetamide deacetylase-like 4, transcript variant X6
arylacetamide deacetylase-like 4, transcript variant X3
arylacetamide deacetylase-like 4, transcript variant X2
arylacetamide deacetylase-like 4, transcript variant X4
arylacetamide deacetylase-like 4, transcript variant X5
arylacetamide deacetylase-like 4, transcript variant X1
arylacetamide deacetylase-like 4 isoform X5
arylacetamide deacetylase-like 4 isoform X3
arylacetamide deacetylase-like 4 isoform X2
arylacetamide deacetylase-like 4 isoform X4
arylacetamide deacetylase-like 4 isoform X1
vacuolar protein sorting 13 homolog D, transcript variant X2
vacuolar protein sorting 13 homolog D, transcript variant X1
intermembrane lipid transfer protein VPS13D isoform X2
intermembrane lipid transfer protein VPS13D isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 10-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
rho guanine nucleotide exchange factor 10-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
rho guanine nucleotide exchange factor 10-like protein, transcript variant X3
rho guanine nucleotide exchange factor 10-like protein, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 10-like protein, transcript variant X8
rho guanine nucleotide exchange factor 10-like protein, transcript variant X5
rho guanine nucleotide exchange factor 10-like protein, transcript variant X4
rho guanine nucleotide exchange factor 10-like protein, transcript variant X6
rho guanine nucleotide exchange factor 10-like protein isoform X2
rho guanine nucleotide exchange factor 10-like protein isoform X1
rho guanine nucleotide exchange factor 10-like protein isoform X3
rho guanine nucleotide exchange factor 10-like protein isoform X5
rho guanine nucleotide exchange factor 10-like protein isoform X4
rho guanine nucleotide exchange factor 10-like protein isoform X6
chymotrypsin-like elastase family member 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 27 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 362, transcript variant X2
zinc finger protein 362, transcript variant X1
tripartite motif containing 62, tandem duplicate 1
wingless-type MMTV integration site family, member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
wingless-type MMTV integration site family, member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cell division cycle 42, transcript variant X1
cell division cycle 42, transcript variant X2
cell division control protein 42 homolog
adaptor related protein complex 5 subunit beta 1, transcript variant X5
adaptor related protein complex 5 subunit beta 1, transcript variant X2
adaptor related protein complex 5 subunit beta 1, transcript variant X4
adaptor related protein complex 5 subunit beta 1, transcript variant X1
adaptor related protein complex 5 subunit beta 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
CTD nuclear envelope phosphatase 1-like, transcript variant X2
CTD nuclear envelope phosphatase 1-like isoform X2
CTD nuclear envelope phosphatase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
CTD nuclear envelope phosphatase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
CTD nuclear envelope phosphatase 1-like isoform X3
CTD nuclear envelope phosphatase 1-like isoform X1
CTD nuclear envelope phosphatase 1-like, transcript variant X4
CTD nuclear envelope phosphatase 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
F-box only protein 6-like, transcript variant X2
F-box only protein 6-like, transcript variant X5
F-box only protein 6-like, transcript variant X7
F-box only protein 6-like, transcript variant X6
F-box only protein 6-like, transcript variant X4
F-box only protein 6-like, transcript variant X1
F-box only protein 6-like, transcript variant X3
dispatched RND transporter family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
UbiA prenyltransferase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 19 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ubiA prenyltransferase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermidine synthase, transcript variant X1
spermidine synthase, transcript variant X2
spermidine synthase, 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 7 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 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TAR DNA binding protein a, transcript variant X7
TAR DNA binding protein a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
TAR DNA binding protein, like isoform X4
TAR DNA binding protein a, transcript variant X6
TAR DNA binding protein a, transcript variant X5
TAR DNA binding protein, like isoform X3
TAR DNA binding protein a, transcript variant X3
TAR DNA binding protein a, transcript variant X1
TAR DNA binding protein a, transcript variant X2
TAR DNA binding protein, like isoform X2
TAR DNA binding protein, like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
nephronophthisis 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nephronophthisis 4, transcript variant X4
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 5 samples with support for all annotated introns
nephronophthisis 4, transcript variant X2
nephronophthisis 4, transcript variant X3
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 1 sample with support for all annotated introns
nephronophthisis 4, transcript variant X5
chromosome 31 C1orf174 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chromosome 31 C1orf174 homolog, transcript variant X1
chromosome 31 C1orf174 homolog, transcript variant X3
UPF0688 protein C1orf174 homolog isoform X1
UPF0688 protein C1orf174 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: centrosomal protein of 104 kDa
COORDINATES: nucleotide motif:Rfam:12.0:RF01233
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7, like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
SH2 domain containing 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SH2 domain containing 5, transcript variant X2
SH2 domain containing 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SH2 domain containing 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SH2 domain-containing protein 5 isoform X4
SH2 domain-containing protein 5 isoform X2
SH2 domain-containing protein 5 isoform X1
SH2 domain-containing protein 5 isoform X3
heterochromatin protein 1, binding protein 3, transcript variant X1
heterochromatin protein 1, binding protein 3, transcript variant X2
heterochromatin protein 1-binding protein 3
eukaryotic translation initiation factor 4 gamma 3
proproteinase E-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proproteinase E-like, 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
proproteinase E-like, transcript variant X1
proproteinase E-like, transcript variant X4
proproteinase E-like, transcript variant X6
proproteinase E-like, transcript variant X3
basement membrane-specific heparan sulfate proteoglycan core protein
low density lipoprotein receptor class A domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 48, transcript variant X3
ubiquitin specific peptidase 48, transcript variant X1
ubiquitin specific peptidase 48, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 48 isoform X1
ubiquitin carboxyl-terminal hydrolase 48 isoform X2
tyrosine-protein kinase STYK1, transcript variant X5
tyrosine-protein kinase STYK1, transcript variant X1
tyrosine-protein kinase STYK1, transcript variant X3
tyrosine-protein kinase STYK1, 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 4 samples with support for all annotated introns
tyrosine-protein kinase STYK1 isoform X1
tyrosine-protein kinase STYK1 isoform X3
tyrosine-protein kinase STYK1, transcript variant X4
tyrosine-protein kinase STYK1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 40, transcript variant X5
zinc finger and BTB domain containing 40, transcript variant X4
zinc finger and BTB domain containing 40, transcript variant X1
zinc finger and BTB domain containing 40, transcript variant X2
zinc finger and BTB domain containing 40, transcript variant X3
zinc finger and BTB domain-containing protein 40 isoform X2
zinc finger and BTB domain-containing protein 40 isoform X3
zinc finger and BTB domain-containing protein 40 isoform X1
zinc finger and BTB domain containing 40, transcript variant X6
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
zinc finger and BTB domain-containing protein 40 isoform X4
uncharacterized si:dkey-205h13.2, transcript variant X12
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
uncharacterized si:dkey-205h13.2, transcript variant X7
uncharacterized si:dkey-205h13.2, transcript variant X1
uncharacterized si:dkey-205h13.2, transcript variant X5
uncharacterized si:dkey-205h13.2, transcript variant X3
uncharacterized si:dkey-205h13.2, transcript variant X8
uncharacterized si:dkey-205h13.2, transcript variant X2
uncharacterized si:dkey-205h13.2, transcript variant X11
uncharacterized si:dkey-205h13.2, transcript variant X6
uncharacterized si:dkey-205h13.2, transcript variant X4
uncharacterized si:dkey-205h13.2, transcript variant X10
uncharacterized si:dkey-205h13.2, transcript variant X9
uncharacterized protein si:dkey-205h13.2
complement C1q subcomponent subunit B-like
complement C1q subcomponent subunit C-like, transcript variant X2
complement C1q subcomponent subunit C-like, transcript variant X1
complement C1q subcomponent subunit C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins