Rhincodon typus isolate 14 chromosome 47, 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\nCM038844.1.\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.

immunoglobulin superfamily member 1-like, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]

immunoglobulin superfamily member 1-like, transcript variant X2

immunoglobulin superfamily member 1-like isoform X1

immunoglobulin superfamily member 1-like, transcript variant X3

uncharacterized protein LOC125487966 isoform X2

The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon

The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: alpha-2-macroglobulin-like

Fc receptor-like protein 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns

Fc receptor-like protein 5, 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 5 samples with support for all annotated introns

Fc receptor-like protein 5, 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 6 samples with support for all annotated introns

The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 24% 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: myelin-associated glycoprotein-like

deleted in malignant brain tumors 1 protein-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 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 77% coverage of the annotated genomic feature by RNAseq alignments

uncharacterized LOC125487945, 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 2 samples with support for all annotated introns

uncharacterized LOC125487945, 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 3 samples with support for all annotated introns

scavenger receptor cysteine-rich type 1 protein M130-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments

uncharacterized LOC125487964, transcript variant X2

uncharacterized LOC125487964, transcript variant X1

uncharacterized protein LOC125487964 isoform X1

uncharacterized protein LOC125487964 isoform X2

uncharacterized LOC109923294, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments

uncharacterized LOC109923294, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns

uncharacterized LOC125487947, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

uncharacterized LOC125487947, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

uncharacterized protein LOC125487947 isoform X2

uncharacterized protein LOC125487947 isoform X1

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 75% coverage of the annotated genomic feature by RNAseq alignments

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments

Derived by automated computational analysis using gene prediction method: tRNAscan-SE.

transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.

glutamate receptor ionotropic, kainate 5-like
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

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% 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 86% coverage of the annotated genomic feature by RNAseq alignments

death effector domain-containing 1, transcript variant X1

death effector domain-containing 1, transcript variant X3

death effector domain-containing 1, transcript variant X2

death effector domain-containing 1, transcript variant X4

death effector domain-containing 1, transcript variant X5

zinc finger protein 420-like, transcript variant X1

zinc finger protein 420-like, transcript variant X2

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments

multiple epidermal growth factor-like domains protein 8

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns

platelet-activating factor acetylhydrolase, isoform Ib, gamma subunit

platelet-activating factor acetylhydrolase IB subunit gamma

myb-related transcription factor, partner of profilin-like, transcript variant X2

uncharacterized protein LOC109911040 isoform X2

myb-related transcription factor, partner of profilin-like, transcript variant X3

myb-related transcription factor, partner of profilin-like, transcript variant X1

myb-related transcription factor, partner of profilin-like isoform X1

uncharacterized protein LOC109911040 isoform X3

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 8 Proteins

uncharacterized LOC109918549, transcript variant X2

uncharacterized LOC109918549, transcript variant X5

uncharacterized LOC109918549, transcript variant X1

uncharacterized LOC109918549, transcript variant X8

uncharacterized LOC109918549, transcript variant X4

uncharacterized LOC109918549, transcript variant X7

uncharacterized LOC109918549, transcript variant X3

uncharacterized LOC109918549, transcript variant X6

uncharacterized protein LOC109918549 isoform X2

uncharacterized protein LOC109918549 isoform X1

uncharacterized protein LOC109918549 isoform X3

uncharacterized protein LOC109918549 isoform X4

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins

uncharacterized LOC125487965, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns

uncharacterized LOC125487965, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

uncharacterized protein LOC125487965 isoform X2

uncharacterized protein LOC125487965 isoform X1

uncharacterized LOC125487965, transcript variant X3

uncharacterized protein LOC125487965 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

claudin domain-containing protein 1, transcript variant X5

claudin domain-containing protein 1, transcript variant X2

claudin domain-containing protein 1, transcript variant X1

claudin domain-containing protein 1, transcript variant X4

claudin domain-containing protein 1, transcript variant X3

claudin domain-containing protein 1, transcript variant X7

claudin domain-containing protein 1, transcript variant X8

claudin domain-containing protein 1, transcript variant X9

claudin domain-containing protein 1, transcript variant X6

claudin domain-containing protein 1 isoform X2

claudin domain-containing protein 1 isoform X1

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments

carcinoembryonic antigen-related cell adhesion molecule 5-like, transcript variant X2

carcinoembryonic antigen-related cell adhesion molecule 5-like, transcript variant X1

carcinoembryonic antigen-related cell adhesion molecule 5-like isoform X2

carcinoembryonic antigen-related cell adhesion molecule 5-like isoform X1

carcinoembryonic antigen-related cell adhesion molecule 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 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: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns

rho guanine nucleotide exchange factor 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments

The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: rho guanine nucleotide exchange factor 11-like

rho guanine nucleotide exchange factor 1-like, transcript variant X2

rho guanine nucleotide exchange factor 1-like, transcript variant X1

rho guanine nucleotide exchange factor 1-like isoform X1

rho guanine nucleotide exchange factor 1-like, transcript variant X3

rho guanine nucleotide exchange factor 1-like isoform 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 10 samples with support for all annotated introns

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

carcinoembryonic antigen-related cell adhesion molecule 2-like

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns

carcinoembryonic antigen-related cell adhesion molecule 8-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, including 2 samples with support for all annotated introns

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments

muscle M-line assembly protein unc-89-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns

poly(A)-specific ribonuclease PNLDC1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% 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

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 31% 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 94% coverage of the annotated genomic feature by RNAseq alignments

The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: 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.

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments

39S ribosomal protein L50, mitochondrial-like

sodium channel subunit beta-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns

sodium channel subunit beta-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns

sodium channel subunit beta-4-like isoform X2

sodium channel subunit beta-4-like isoform X1

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments

HAUS augmin-like complex, subunit 5, transcript variant X6

HAUS augmin-like complex, subunit 5, transcript variant X3

HAUS augmin-like complex, subunit 5, transcript variant X1

HAUS augmin-like complex, subunit 5, transcript variant X5

HAUS augmin-like complex, subunit 5, transcript variant X2

HAUS augmin-like complex, subunit 5, transcript variant X4

HAUS augmin-like complex, subunit 5, transcript variant X7

HAUS augmin-like complex subunit 5 isoform X1

HAUS augmin-like complex subunit 5 isoform 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 6 samples with support for all annotated introns

immunoglobulin superfamily member 1-like

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments

Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns

uncharacterized LOC125487946, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns

uncharacterized LOC125487946, transcript variant X1

SMG9 nonsense mediated mRNA decay factor

nonsense-mediated mRNA decay factor SMG9

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 19 samples with support for all annotated introns

X-ray repair complementing defective repair in Chinese hamster cells 1
D(2)-like dopamine receptor, transcript variant X1
D(2)-like dopamine receptor, transcript variant X2
interferon-inducible GTPase 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X4
interferon-inducible GTPase 5-like, transcript variant X2
interferon-inducible GTPase 5-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X1
interferon-inducible GTPase 5-like isoform X1
interferon-inducible GTPase 5-like isoform X2
uncharacterized LOC125487956, transcript variant X1
uncharacterized LOC125487956, 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 1 sample with support for all annotated introns
uncharacterized LOC125487956, transcript variant X2
uncharacterized protein LOC125487956 isoform X1
uncharacterized protein LOC125487956 isoform X2
lens fiber membrane intrinsic protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 82% 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 long SRA reads, 21 Proteins, and 100% 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: 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC568891 homolog
serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform-like
histone-lysine N-methyltransferase PRDM9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif-containing 13-like, transcript variant X2
tripartite motif-containing 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitochondrial ribosomal protein L17, transcript variant X2
mitochondrial ribosomal protein L17, transcript variant X1
39S ribosomal protein L17, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
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
mitochondrial import receptor subunit TOM40 homolog
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 19 samples with support for all annotated introns
uncharacterized LOC109911796, transcript variant X6
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 3 samples with support for all annotated introns
uncharacterized LOC109911796, transcript variant X3
uncharacterized LOC109911796, transcript variant X5
uncharacterized LOC109911796, transcript variant X1
uncharacterized LOC109911796, transcript variant X2
uncharacterized LOC109911796, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
dehydrogenase/reductase SDR family member 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 75 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 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: dehydrogenase/reductase SDR family member 4-like
urokinase plasminogen activator surface receptor-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
urokinase plasminogen activator surface receptor, transcript variant X2
urokinase plasminogen activator surface receptor isoform X2
urokinase plasminogen activator surface receptor, 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 5 samples with support for all annotated introns
urokinase plasminogen activator surface receptor isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hepatocyte cell adhesion molecule-like, transcript variant X3
hepatocyte cell adhesion molecule-like, transcript variant X2
hepatocyte cell adhesion molecule-like, transcript variant X1
hepatocyte cell adhesion molecule-like isoform X3
hepatocyte cell adhesion molecule-like isoform X2
hepatocyte cell adhesion molecule-like isoform X1
T-cell immunoreceptor with Ig and ITIM domains-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC109922536, 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 2 samples with support for all annotated introns
uncharacterized LOC109922536, 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 9 samples with support for all annotated introns
uncharacterized protein LOC109922536 isoform X2
uncharacterized protein LOC109922536 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
hepatocyte cell adhesion molecule-like, transcript variant X6
hepatocyte cell adhesion molecule-like, transcript variant X5
hepatocyte cell adhesion molecule-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 35% 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
LOW QUALITY PROTEIN: sialic acid-binding Ig-like lectin 13
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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125487916, transcript variant X1
uncharacterized LOC125487916, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase 2B-like
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
presenilin enhancer, gamma-secretase subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glyceraldehyde-3-phosphate dehydrogenase 2, transcript variant X1
glyceraldehyde-3-phosphate dehydrogenase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
glyceraldehyde-3-phosphate dehydrogenase 2, transcript variant X2
glyceraldehyde-3-phosphate dehydrogenase 2 isoform X1
glyceraldehyde-3-phosphate dehydrogenase 2 isoform X2
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B, transcript variant X1
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 1B isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 1B isoform X2
lin-37 DREAM MuvB core complex component
proline and serine rich 3, 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 15 samples with support for all annotated introns
proline and serine rich 3, transcript variant X3
proline and serine rich 3, transcript variant X4
proline and serine rich 3, transcript variant X2
proline and serine rich 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
proline and serine-rich protein 3 isoform X3
proline and serine-rich protein 3 isoform X4
proline and serine-rich protein 3 isoform X2
proline and serine-rich protein 3 isoform X5
proline and serine-rich protein 3 isoform X1
retroviral integration site protein Fli-1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
lipolysis stimulated lipoprotein receptor, transcript variant X4
lipolysis stimulated lipoprotein receptor, transcript variant X1
lipolysis stimulated lipoprotein receptor, transcript variant X3
lipolysis stimulated lipoprotein receptor, transcript variant X2
lipolysis-stimulated lipoprotein receptor isoform X4
lipolysis-stimulated lipoprotein receptor isoform X3
lipolysis-stimulated lipoprotein receptor isoform X1
lipolysis-stimulated lipoprotein receptor isoform X2