Stegostoma fasciatum isolate 6-17 chromosome 42, sSteFas1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Stegostomatidae; Stegostoma.
REFSEQ INFORMATION: The reference sequence is identical to\nCM039268.1.\nAssembly name: sSteFas1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/17. The\noriginal whole-genome shotgun project has the accession\nJAFIRC000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Platanus v. 1.2.4; P_RNA_scaffolder v.\n commit 7941e0f on May 30, at github;\n 3D-DNA v. 180922\nAssembly Name :: sSteFas1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 95.8x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Stegostoma fasciatum Annotation\n Release 100\nAnnotation Version :: 100\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]
lipolysis stimulated lipoprotein receptor
lipolysis-stimulated lipoprotein receptor
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: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Friend leukemia integration 1 transcription factor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
amyloid beta precursor like protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
suppressor of tumorigenicity 14 protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 97% coverage of the annotated genomic feature by RNAseq alignments
proline and serine rich 3, 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
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 4 samples with support for all annotated introns
proline and serine-rich protein 3 isoform X2
proline and serine-rich protein 3 isoform X1
uncharacterized LOC125448589, 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 22 samples with support for all annotated introns
uncharacterized LOC125448589, transcript variant X3
uncharacterized LOC125448589, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
rRNA 2'-O-methyltransferase fibrillarin-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
potassium-transporting ATPase alpha chain 1-like
glyceraldehyde-3-phosphate dehydrogenase, spermatogenic, transcript variant X2
glyceraldehyde-3-phosphate dehydrogenase, spermatogenic, transcript variant X1
glyceraldehyde-3-phosphate dehydrogenase 2
lysine (K)-specific methyltransferase 2Bb
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
beta-1,4-galactosyltransferase 3, transcript variant X2
beta-1,4-galactosyltransferase 3, transcript variant X1
beta-1,4-galactosyltransferase 3 isoform X2
beta-1,4-galactosyltransferase 3 isoform X1
presenilin enhancer, gamma-secretase subunit, transcript variant X4
presenilin enhancer, gamma-secretase subunit, transcript variant X3
presenilin enhancer, gamma-secretase subunit, transcript variant X2
presenilin enhancer, gamma-secretase subunit, transcript variant X5
presenilin enhancer, gamma-secretase subunit, transcript variant X1
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
von Willebrand factor A domain containing 11, 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 14 samples with support for all annotated introns
von Willebrand factor A domain containing 11, 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 3 samples with support for all annotated introns
von Willebrand factor A domain containing 11, 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 4 samples with support for all annotated introns
von Willebrand factor A domain containing 11, transcript variant X1
von Willebrand factor A domain-containing protein 7
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sialic acid-binding Ig-like lectin 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sialic acid-binding Ig-like lectin 11, 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 2 samples with support for all annotated introns
sialic acid-binding Ig-like lectin 11, transcript variant X2
sialic acid-binding Ig-like lectin 11 isoform X1
sialic acid-binding Ig-like lectin 11 isoform X2
sialic acid-binding Ig-like lectin 11, transcript variant X4
Schwann cell myelin protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
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 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: 95% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
carcinoembryonic antigen-related cell adhesion molecule 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
carcinoembryonic antigen-related cell adhesion molecule 2-like, transcript variant X1
carcinoembryonic antigen-related cell adhesion molecule 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
carcinoembryonic antigen-related cell adhesion molecule 2-like isoform X2
carcinoembryonic antigen-related cell adhesion molecule 6-like isoform X1
hepatocyte cell adhesion molecule-like, transcript variant X5
hepatocyte cell adhesion molecule-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
hepatocyte cell adhesion molecule-like, transcript variant X4
hepatocyte cell adhesion molecule-like, transcript variant X2
hepatocyte cell adhesion molecule-like, transcript variant X6
hepatocyte cell adhesion molecule-like, transcript variant X8
hepatocyte cell adhesion molecule-like, transcript variant X1
hepatocyte cell adhesion molecule-like, transcript variant X11
hepatocyte cell adhesion molecule-like, transcript variant X9
hepatocyte cell adhesion molecule-like, transcript variant X7
hepatocyte cell adhesion molecule-like, transcript variant X10
hepatocyte cell adhesion molecule-like isoform X1
uncharacterized protein LOC125448410 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC125448416 isoform X4
hepatocyte cell adhesion molecule-like isoform X2
hepatocyte cell adhesion molecule-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
basal cell adhesion molecule-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
basal cell adhesion molecule-like, 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 7 samples with support for all annotated introns
basal cell adhesion molecule-like isoform X2
basal cell adhesion molecule-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125448590, 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
uncharacterized LOC125448590, 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 17 samples with support for all annotated introns
uncharacterized LOC125448590, transcript variant X2
uncharacterized protein LOC125448590 isoform X1
uncharacterized protein LOC125448590 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 3 samples with support for all annotated introns
urokinase plasminogen activator surface receptor-like, 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 2 samples with support for all annotated introns
urokinase plasminogen activator surface receptor-like isoform X1
urokinase plasminogen activator surface receptor-like, transcript variant X3
urokinase plasminogen activator surface receptor-like, transcript variant X2
urokinase plasminogen activator surface receptor-like isoform X3
phospholipase A2 inhibitor and Ly6/PLAUR domain-containing protein-like isoform X2
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
uncharacterized LOC125448548, transcript variant X3
uncharacterized LOC125448548, 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 18 samples with support for all annotated introns
uncharacterized LOC125448548, transcript variant X1
uncharacterized protein LOC125448548 isoform X3
uncharacterized protein LOC125448548 isoform X2
uncharacterized protein LOC125448548 isoform X1
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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
dehydrogenase/reductase (SDR family) member 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 33% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dehydrogenase/reductase SDR family member 4
uncharacterized LOC125448559, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC125448559, 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 19 samples with support for all annotated introns
uncharacterized LOC125448559, transcript variant X1
uncharacterized protein LOC125448559 isoform X1
uncharacterized protein LOC125448559 isoform X2
mitochondrial import receptor subunit TOM40 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
cationic trypsin-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cationic trypsin-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 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: 20 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L17, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
doublesex- and mab-3-related transcription factor C2-like, transcript variant X1
doublesex- and mab-3-related transcription factor C2-like, transcript variant X2
doublesex- and mab-3-related transcription factor C2-like isoform X1
doublesex- and mab-3-related transcription factor C2-like isoform X2
coiled-coil domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 10% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase PRDM9
serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC568891 homolog
advanced glycosylation end product-specific receptor
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
fish-egg lectin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fish-egg lectin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X5
interferon-inducible GTPase 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
interferon-inducible GTPase 5-like, transcript variant X6
interferon-inducible GTPase 5-like, transcript variant X11
interferon-inducible GTPase 5-like, transcript variant X8
interferon-inducible GTPase 5-like, transcript variant X7
interferon-inducible GTPase 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
X-ray repair complementing defective repair in Chinese hamster cells 1, transcript variant X2
X-ray repair complementing defective repair in Chinese hamster cells 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125448544, transcript variant X1
uncharacterized protein LOC125448544 isoform X1
uncharacterized LOC125448544, 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 16 samples with support for all annotated introns
uncharacterized protein LOC125448544 isoform X2
pleckstrin homology-like domain family B member 1
SMG9 nonsense mediated mRNA decay factor
nonsense-mediated mRNA decay factor SMG9
intermediate conductance calcium-activated potassium channel protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
intermediate conductance calcium-activated potassium channel protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
intermediate conductance calcium-activated potassium channel protein 4-like isoform X2
intermediate conductance calcium-activated potassium channel protein 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125448582, transcript variant X7
uncharacterized LOC125448582, transcript variant X4
uncharacterized LOC125448582, transcript variant X6
uncharacterized LOC125448582, transcript variant X3
uncharacterized LOC125448582, transcript variant X2
uncharacterized LOC125448582, transcript variant X1
uncharacterized protein LOC125448582 isoform X2
uncharacterized protein LOC125448582 isoform X3
uncharacterized protein LOC125448582 isoform X1
uncharacterized protein LOC125448582 isoform X4
uncharacterized protein LOC125448582 isoform X6
uncharacterized LOC125448582, transcript variant X5
uncharacterized protein LOC125448582 isoform X5
uncharacterized LOC125448413, 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 9 samples with support for all annotated introns
uncharacterized LOC125448413, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon-inducible GTPase 5-like isoform X1
interferon-inducible GTPase 5-like isoform X2
lens fiber membrane intrinsic protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
electron transfer flavoprotein subunit beta, transcript variant X2
electron transfer flavoprotein subunit beta, transcript variant X1
electron transfer flavoprotein subunit beta
V-set and immunoglobulin domain containing 10 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
V-set and immunoglobulin domain-containing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
free fatty acid receptor 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
free fatty acid receptor 2-like, transcript variant X2
free fatty acid receptor 2-like, transcript variant X5
free fatty acid receptor 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
free fatty acid receptor 2-like, transcript variant X3
free fatty acid receptor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
free fatty acid receptor 2-like, transcript variant X6
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sialic acid-binding Ig-like lectin 10, transcript variant X2
sialic acid-binding Ig-like lectin 10, transcript variant X6
sialic acid-binding Ig-like lectin 10, transcript variant X3
sialic acid-binding Ig-like lectin 10, transcript variant X7
sialic acid-binding Ig-like lectin 10, transcript variant X1
sialic acid-binding Ig-like lectin 10, transcript variant X4
sialic acid-binding Ig-like lectin 10, transcript variant X5
sialic acid-binding Ig-like lectin 10, transcript variant X8
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
sialic acid-binding Ig-like lectin 10 isoform X2
Schwann cell myelin protein-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
poly(A)-specific ribonuclease PNLDC1-like
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
fructose-bisphosphate aldolase B-like, transcript variant X1
fructose-bisphosphate aldolase B-like, transcript variant X2
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, and 22% 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: mucosal pentraxin-like
carcinoembryonic antigen-related cell adhesion molecule 21, transcript variant X1
carcinoembryonic antigen-related cell adhesion molecule 21, transcript variant X2
carcinoembryonic antigen-related cell adhesion molecule 21 isoform X1
uncharacterized protein LOC125448563 isoform X2
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 X1
carcinoembryonic antigen-related cell adhesion molecule 5-like isoform X2
carcinoembryonic antigen-related cell adhesion molecule 15-like, transcript variant X2
carcinoembryonic antigen-related cell adhesion molecule 15-like, transcript variant X1
carcinoembryonic antigen-related cell adhesion molecule 15-like isoform X1
carcinoembryonic antigen-related cell adhesion molecule 15-like isoform X2
uncharacterized LOC125448540, transcript variant X1
uncharacterized LOC125448540, transcript variant X3
uncharacterized LOC125448540, transcript variant X2
mucosal pentraxin-like, transcript variant X1
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 4 samples with support for all annotated introns
mucosal pentraxin-like, transcript variant X2
mucosal pentraxin-like, transcript variant X4
mucosal pentraxin-like, transcript variant X5
mucosal pentraxin-like, transcript variant X3
uncharacterized LOC125448405, transcript variant X2
uncharacterized LOC125448405, transcript variant X1
uncharacterized protein LOC125448405 isoform X2
uncharacterized protein LOC125448405 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
CD79a molecule, immunoglobulin-associated alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
B-cell antigen receptor complex-associated protein alpha chain
uncharacterized LOC125448593, transcript variant X1
uncharacterized LOC125448593, transcript variant X2
rho guanine nucleotide exchange factor 11-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
cyclin-dependent kinase 11B-like, transcript variant X1
cyclin-dependent kinase 11B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cyclin-dependent kinase 11B-like isoform X1
ETS domain-containing transcription factor ERF-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lipase, hormone-sensitive b, transcript variant X3
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 3 samples with support for all annotated introns
lipase, hormone-sensitive b, transcript variant X4
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 4 samples with support for all annotated introns
lipase, hormone-sensitive b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lipase, hormone-sensitive b, transcript variant X1
lipase, hormone-sensitive b, transcript variant X5
guanylate-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
guanylate-binding protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
guanylate-binding protein 1-like isoform X1
guanylate-binding protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carcinoembryonic antigen-related cell adhesion molecule 5-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
claudin domain-containing protein 1-like, transcript variant X5
claudin domain-containing protein 1-like, transcript variant X4
claudin domain-containing protein 1-like, transcript variant X1
claudin domain-containing protein 1-like, transcript variant X7
claudin domain-containing protein 1-like, transcript variant X2
claudin domain-containing protein 1-like, transcript variant X6
claudin domain-containing protein 1-like, transcript variant X3
claudin domain-containing protein 1-like isoform X1
claudin domain-containing protein 1-like isoform X2
probable G-protein coupled receptor 139, transcript variant X3
probable G-protein coupled receptor 139, transcript variant X2
uncharacterized protein LOC125448552 isoform X3
probable G-protein coupled receptor 139 isoform X2
probable G-protein coupled receptor 139, transcript variant X1
probable G-protein coupled receptor 139 isoform X1
neuropeptides capa receptor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40% 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: 90% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myb-related transcription factor, partner of profilin-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 24 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
platelet-activating factor acetylhydrolase IB subunit alpha2-like, transcript variant X2
platelet-activating factor acetylhydrolase IB subunit alpha2-like, transcript variant X1
platelet-activating factor acetylhydrolase IB subunit alpha2-like isoform X1
platelet-activating factor acetylhydrolase IB subunit alpha2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 8
zinc finger protein 420-like, transcript variant X2
zinc finger protein 420-like, transcript variant X1
zinc finger protein 420-like, transcript variant X3
phospholipase A2 inhibitor CNF-like, transcript variant X1
phospholipase A2 inhibitor CNF-like isoform X1
phospholipase A2 inhibitor CNF-like, transcript variant X2
uncharacterized protein LOC125448412 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glycogen synthase kinase-3 beta-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
glycogen synthase kinase-3 beta-like isoform X1
POU domain, class 2, transcription factor 2
glycogen synthase kinase-3 beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glycogen synthase kinase-3 beta-like isoform X2
glutamate receptor, ionotropic, kainate 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 5
sodium/potassium-transporting ATPase subunit alpha-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 271 Proteins, and 99% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
myelin-associated glycoprotein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
myelin-associated glycoprotein-like, 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 1 sample with support for all annotated introns
platelet endothelial cell adhesion molecule-like, transcript variant X4
platelet endothelial cell adhesion molecule-like, transcript variant X7
platelet endothelial cell adhesion molecule-like, transcript variant X5
platelet endothelial cell adhesion molecule-like, transcript variant X6
platelet endothelial cell adhesion molecule-like, transcript variant X1
platelet endothelial cell adhesion molecule-like, transcript variant X3
platelet endothelial cell adhesion molecule-like, transcript variant X2
platelet endothelial cell adhesion molecule-like isoform X4
platelet endothelial cell adhesion molecule-like isoform X2
platelet endothelial cell adhesion molecule-like isoform X3
platelet endothelial cell adhesion molecule-like isoform X1
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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% 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: 3 Proteins, 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: 82% coverage of the annotated genomic feature by RNAseq alignments
deleted in malignant brain tumors 1 protein-like, transcript variant X1
deleted in malignant brain tumors 1 protein-like, transcript variant X2
deleted in malignant brain tumors 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
uncharacterized LOC125448547, transcript variant X1
uncharacterized LOC125448547, transcript variant X2
immunoglobulin superfamily member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns