Stegostoma fasciatum isolate 6-17 chromosome 30, 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\nCM039256.1.\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.
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
COORDINATES: polyA evidence [ECO:0006239]
bifunctional coenzyme A synthase isoform X2
bifunctional coenzyme A synthase isoform X1
bifunctional coenzyme A synthase isoform X3
bifunctional coenzyme A synthase isoform X4
PSMC3 interacting 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 2 samples with support for all annotated introns
homologous-pairing protein 2 homolog isoform X2
PSMC3 interacting protein, transcript variant X1
homologous-pairing protein 2 homolog isoform X1
reticulophagy regulator family member 3, transcript variant X3
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 4 samples with support for all annotated introns
reticulophagy regulator family member 3, transcript variant X2
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 9 samples with support for all annotated introns
reticulophagy regulator family member 3, 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 24 samples with support for all annotated introns
pleckstrin homology, MyTH4 and FERM domain containing H3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
pleckstrin homology, MyTH4 and FERM domain containing H3, 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 2 samples with support for all annotated introns
pleckstrin homology domain-containing family H member 3 isoform X2
pleckstrin homology domain-containing family H member 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
enhancer of zeste 1 polycomb repressive complex 2 subunit
receptor (G protein-coupled) activity modifying protein 2
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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
StAR-related lipid transfer (START) domain containing 3, transcript variant X1
StAR-related lipid transfer (START) domain containing 3, transcript variant X6
StAR-related lipid transfer (START) domain containing 3, transcript variant X3
StAR-related lipid transfer (START) domain containing 3, transcript variant X5
StAR-related lipid transfer (START) domain containing 3, transcript variant X4
StAR-related lipid transfer (START) domain containing 3, transcript variant X2
stAR-related lipid transfer protein 3 isoform X1
stAR-related lipid transfer protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins phospholipase 3, 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 9 samples with support for all annotated introns
post-GPI attachment to proteins phospholipase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
post-GPI attachment to proteins phospholipase 3, transcript variant X1
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 21 samples with support for all annotated introns
post-GPI attachment to proteins factor 3 isoform X1
post-GPI attachment to proteins factor 3 isoform X2
post-GPI attachment to proteins phospholipase 3, 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 10 samples with support for all annotated introns
post-GPI attachment to proteins factor 3 isoform X3
erb-b2 receptor tyrosine kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
erb-b2 receptor tyrosine kinase 2, transcript variant X1
erb-b2 receptor tyrosine kinase 2, transcript variant X3
receptor tyrosine-protein kinase erbB-2 isoform X1
receptor tyrosine-protein kinase erbB-2 isoform X2
von Willebrand factor C domain-containing protein 2-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 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 67% coverage of the annotated genomic feature by RNAseq alignments
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
growth factor receptor-bound protein 7-like
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 5 samples with support for all annotated introns
insulin-like growth factor-binding protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 8 samples with support for all annotated introns
eukaryotic translation initiation factor 1b-like
trafficking kinesin-binding protein 1-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
junction plakoglobin-like, transcript variant X1
junction plakoglobin-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
insulin-like growth factor 2 mRNA binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin-like growth factor 2 mRNA-binding protein 1
transformer-2 protein homolog alpha-like, transcript variant X3
transformer-2 protein homolog alpha-like, transcript variant X2
transformer-2 protein homolog alpha-like, transcript variant X1
transformer-2 protein homolog alpha-like isoform X3
transformer-2 protein homolog alpha-like isoform X2
transformer-2 protein homolog alpha-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
ATP synthase membrane subunit c locus 1, transcript variant X3
ATP synthase membrane subunit c locus 1, transcript variant X2
ATP synthase membrane subunit c locus 1, transcript variant X1
ATP synthase F(0) complex subunit C1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 11, transcript variant X2
kelch-like family member 11, transcript variant X1
ATP-citrate synthase, transcript variant X3
ATP-citrate synthase, transcript variant X1
ATP-citrate synthase, transcript variant X2
outer dynein arm docking complex subunit 4, 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
outer dynein arm docking complex subunit 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X2
outer dynein arm docking complex subunit 4, transcript variant X3
outer dynein arm docking complex subunit 4, transcript variant X4
outer dynein arm docking complex subunit 4, transcript variant X7
outer dynein arm docking complex subunit 4, transcript variant X9
outer dynein arm docking complex subunit 4, transcript variant X6
outer dynein arm docking complex subunit 4, transcript variant X8
outer dynein arm docking complex subunit 4, transcript variant X11
outer dynein arm docking complex subunit 4, transcript variant X14
outer dynein arm docking complex subunit 4, transcript variant X10
outer dynein arm docking complex subunit 4, transcript variant X12
outer dynein arm docking complex subunit 4, transcript variant X16
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 2 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X13
outer dynein arm docking complex subunit 4, transcript variant X15
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 3 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X18
outer dynein arm docking complex subunit 4, transcript variant X17
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 6 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X20
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
outer dynein arm docking complex subunit 4, transcript variant X21
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 5 samples with support for all annotated introns
outer dynein arm-docking complex subunit 4 isoform X1
outer dynein arm-docking complex subunit 4 isoform X5
outer dynein arm-docking complex subunit 4 isoform X2
outer dynein arm-docking complex subunit 4 isoform X3
outer dynein arm-docking complex subunit 4 isoform X4
outer dynein arm-docking complex subunit 4 isoform X7
outer dynein arm-docking complex subunit 4 isoform X9
outer dynein arm-docking complex subunit 4 isoform X6
outer dynein arm-docking complex subunit 4 isoform X8
outer dynein arm-docking complex subunit 4 isoform X11
outer dynein arm-docking complex subunit 4 isoform X14
outer dynein arm-docking complex subunit 4 isoform X10
outer dynein arm-docking complex subunit 4 isoform X12
outer dynein arm-docking complex subunit 4 isoform X16
outer dynein arm-docking complex subunit 4 isoform X13
outer dynein arm-docking complex subunit 4 isoform X15
outer dynein arm-docking complex subunit 4 isoform X18
outer dynein arm-docking complex subunit 4 isoform X17
outer dynein arm-docking complex subunit 4 isoform X19
outer dynein arm-docking complex subunit 4 isoform X20
outer dynein arm-docking complex subunit 4 isoform X21
sp2 transcription factor, transcript variant X2
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 19 samples with support for all annotated introns
sp2 transcription factor, transcript variant X3
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 9 samples with support for all annotated introns
sp2 transcription factor, transcript variant X1
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 6 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 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
CDK5 regulatory subunit associated protein 3
CDK5 regulatory subunit-associated protein 3
coatomer subunit zeta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nfe2 like bZIP transcription factor 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
nfe2 like bZIP transcription factor 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
endoplasmic reticulum membrane sensor NFE2L1b isoform X1
endoplasmic reticulum membrane sensor NFE2L1b isoform X2
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X2
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X4
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X1
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X3
sorting nexin-11-like, transcript variant X1
sorting nexin-11-like, transcript variant X5
sorting nexin-11-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sorting nexin-11-like, transcript variant X7
sorting nexin-11-like, transcript variant X3
sorting nexin-11-like, transcript variant X4
sorting nexin-11-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
homeobox protein Hox-A2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
homeobox protein Hox-A2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 5 samples with support for all annotated introns
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 11 samples with support for all annotated introns
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125466256, 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 6 samples with support for all annotated introns
uncharacterized LOC125466256, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125466256, 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
homeobox protein Hox-B8a-like, transcript variant X3
homeobox protein Hox-B8a-like, transcript variant X2
homeobox protein Hox-B8a-like, transcript variant X1
homeobox protein Hox-B8a-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
homeobox protein Hox-A10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
homeobox protein Hox-A10-like, 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, including 5 samples with support for all annotated introns
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 5 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 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 51% coverage of the annotated genomic feature by RNAseq alignments
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X1
calcium-binding and coiled-coil domain-containing protein 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 15 samples with support for all annotated introns
calcium-binding and coiled-coil domain-containing protein 2-like isoform X1
calcium-binding and coiled-coil domain-containing protein 2-like isoform X2
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 24 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
39S ribosomal protein L45, mitochondrial
probable G-protein coupled receptor 158, transcript variant X2
probable G-protein coupled receptor 158, transcript variant X1
probable G-protein coupled receptor 158 isoform X2
probable G-protein coupled receptor 158 isoform X1
suppressor of cytokine signaling 7, transcript variant X1
suppressor of cytokine signaling 7, transcript variant X2
suppressor of cytokine signaling 7, transcript variant X3
suppressor of cytokine signaling 7 isoform X1
suppressor of cytokine signaling 7 isoform X2
rho GTPase-activating protein 23-like, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 23-like isoform X3
rho GTPase-activating protein 23-like, transcript variant X4
rho GTPase-activating protein 23-like isoform X4
rho GTPase-activating protein 23-like, transcript variant X1
rho GTPase-activating protein 23-like, transcript variant X2
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 4 samples with support for all annotated introns
rho GTPase-activating protein 23-like isoform X1
rho GTPase-activating protein 23-like isoform X2
rho GTPase-activating protein 23-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 2 samples with support for all annotated introns
rho GTPase-activating protein 23-like isoform X5
SRC kinase signaling inhibitor 1-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 3 samples with support for all annotated introns
SRC kinase signaling inhibitor 1-like, transcript variant X4
SRC kinase signaling inhibitor 1-like, transcript variant X3
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
SRC kinase signaling inhibitor 1-like, 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
SRC kinase signaling inhibitor 1-like, transcript variant X2
SRC kinase signaling inhibitor 1-like isoform X5
SRC kinase signaling inhibitor 1-like isoform X4
SRC kinase signaling inhibitor 1-like isoform X3
SRC kinase signaling inhibitor 1-like isoform X1
SRC kinase signaling inhibitor 1-like isoform X2
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.
SKI/DACH domain-containing protein 1-like
protein AF-10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein AF-10-like, transcript variant X2
protein AF-10-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein AF-10-like, transcript variant X3
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like
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 14 samples with support for all annotated introns
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 20 samples with support for all annotated introns
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X4
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X3
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X1
CWC25 spliceosome associated protein homolog, 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 22 samples with support for all annotated introns
CWC25 spliceosome associated protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
CWC25 spliceosome associated protein homolog, 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 7 samples with support for all annotated introns
pre-mRNA-splicing factor CWC25 homolog isoform X2
pre-mRNA-splicing factor CWC25 homolog isoform X1
pre-mRNA-splicing factor CWC25 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 2 samples with support for all annotated introns
plexin domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
plexin domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
plexin domain-containing protein 1-like isoform X2
plexin domain-containing protein 1-like isoform X1
SWI5 homologous recombination repair protein
ADP-ribosylation factor-like protein 5B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ADP-ribosylation factor-like protein 5B, 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 19 samples with support for all annotated introns
ADP-ribosylation factor-like protein 5B isoform X1
ADP-ribosylation factor-like protein 5B isoform X2
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X5
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 8 samples with support for all annotated introns
calcium channel, voltage-dependent, beta 1 subunit, 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 7 samples with support for all annotated introns
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X3
calcium channel, voltage-dependent, beta 1 subunit, 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
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-1 isoform X5
voltage-dependent L-type calcium channel subunit beta-1 isoform X4
voltage-dependent L-type calcium channel subunit beta-1 isoform X3
voltage-dependent L-type calcium channel subunit beta-1 isoform X1
voltage-dependent L-type calcium channel subunit beta-1 isoform X2
alpha-2,8-sialyltransferase 8F-like, transcript variant X1
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
alpha-2,8-sialyltransferase 8F-like, 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 13 samples with support for all annotated introns
PR domain zinc finger protein 5-like isoform X1
alpha-2,8-sialyltransferase 8F-like isoform X2
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X4
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X5
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X2
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X1
SH3 and cysteine-rich domain-containing protein 2-like, 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 5 samples with support for all annotated introns
SH3 and cysteine-rich domain-containing protein 2-like isoform X5
SH3 and cysteine-rich domain-containing protein 2-like isoform X4
SH3 and cysteine-rich domain-containing protein 2-like isoform X2
SH3 and cysteine-rich domain-containing protein 2-like isoform X1
SH3 and cysteine-rich domain-containing protein 2-like isoform X3
transcription factor CP2-like protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription factor CP2-like protein 1, transcript variant X4
transcription factor CP2-like protein 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 3 samples with support for all annotated introns
transcription factor CP2-like protein 1, transcript variant X2
transcription factor CP2-like protein 1, 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 2 samples with support for all annotated introns
transcription factor CP2-like protein 1, transcript variant X5
transcription factor CP2-like protein 1 isoform X5
transcription factor CP2-like protein 1 isoform X1
transcription factor CP2-like protein 1 isoform X2
transcription factor CP2-like isoform X3
transcription factor CP2-like protein 1 isoform X4
F-box/LRR-repeat protein 20, transcript variant X3
F-box/LRR-repeat protein 20, transcript variant X5
F-box/LRR-repeat protein 20, transcript variant X1
F-box/LRR-repeat protein 20, transcript variant X2
F-box/LRR-repeat protein 20, transcript variant X4
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 10 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 1
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 5 samples with support for all annotated introns
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 46-like
WAS/WASL interacting protein family, member 2b, transcript variant X1
WAS/WASL interacting protein family, member 2b, transcript variant X3
WAS/WASL interacting protein family, member 2b, transcript variant X2
WAS/WASL-interacting protein family member 2b isoform X1
WAS/WASL-interacting protein family member 2b isoform X2
TBK1 binding protein 1, transcript variant X3
TBK1 binding protein 1, transcript variant X1
TBK1 binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBK1 binding protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TBK1 binding protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oxysterol binding protein-like 7, transcript variant X2
oxysterol binding protein-like 7, transcript variant X4
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 6 samples with support for all annotated introns
oxysterol binding protein-like 7, transcript variant X3
oxysterol binding protein-like 7, transcript variant X1
oxysterol-binding protein-related protein 7 isoform X2
oxysterol-binding protein-related protein 7 isoform X3
oxysterol-binding protein-related protein 7 isoform X1
39S ribosomal protein L10, mitochondrial
interleukin-6-like, transcript variant X2
interleukin-6-like, transcript variant X1
uncharacterized protein LOC125466128 isoform 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 13 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 24
Rap guanine nucleotide exchange factor (GEF)-like 1, 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 3 samples with support for all annotated introns
Rap guanine nucleotide exchange factor (GEF)-like 1, 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 2 samples with support for all annotated introns
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X2
rap guanine nucleotide exchange factor-like 1
gasdermin-A2-like, transcript variant X2
gasdermin-A2-like, transcript variant X4
gasdermin-A2-like, transcript variant X3
gasdermin-A2-like, transcript variant X1
leucine rich repeat containing 3Ca, transcript variant X1
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 8 samples with support for all annotated introns
leucine rich repeat containing 3Ca, 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 7 samples with support for all annotated introns
leucine-rich repeat-containing protein 3B
DNA topoisomerase II alpha, transcript variant X1
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 14 samples with support for all annotated introns
DNA topoisomerase II alpha, transcript variant X2
gap junction delta-3 protein-like, transcript variant X5
gap junction delta-3 protein-like, 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
gap junction delta-3 protein-like, transcript variant X4
gap junction delta-3 protein-like, transcript variant X2
gap junction delta-3 protein-like, transcript variant X6
gap junction delta-3 protein-like, transcript variant X3
retinoic acid receptor, alpha a, transcript variant X2
retinoic acid receptor, alpha a, transcript variant X1
retinoic acid receptor, alpha a, transcript variant X3
retinoic acid receptor, alpha a, transcript variant X9
retinoic acid receptor, alpha a, transcript variant X4
retinoic acid receptor, alpha a, transcript variant X5
retinoic acid receptor, alpha a, transcript variant X7
retinoic acid receptor, alpha a, transcript variant X8
retinoic acid receptor, alpha a, transcript variant X11
retinoic acid receptor, alpha a, transcript variant X6
retinoic acid receptor, alpha a, transcript variant X12
retinoic acid receptor, alpha a, transcript variant X10
retinoic acid receptor, alpha a, transcript variant X13
retinoic acid receptor alpha-A isoform X3
retinoic acid receptor alpha-A isoform X1
retinoic acid receptor alpha-A isoform X4
retinoic acid receptor alpha-A isoform X2
retinoic acid receptor alpha-A isoform X5
cell division cycle 6 homolog (S. cerevisiae)
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 163 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 1, group d, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
nuclear receptor subfamily 1 group D member 1
MSL complex subunit 1a, transcript variant X1
MSL complex subunit 1a, transcript variant X2
male-specific lethal 1-like 1 isoform X1
male-specific lethal 1-like 1 isoform X2
casc3 exon junction complex subunit, 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 7 samples with support for all annotated introns
casc3 exon junction complex subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
casc3 exon junction complex subunit, 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 14 samples with support for all annotated introns
casc3 exon junction complex subunit, transcript variant X2
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 4 samples with support for all annotated introns
ORM1-like protein 3, transcript variant X1
ORM1-like protein 3, transcript variant X3
ORM1-like protein 3, transcript variant X4
ORM1-like protein 3, transcript variant X2
26S proteasome non-ATPase regulatory subunit 3
NGFI-A-binding protein 1-like, transcript variant X1
NGFI-A-binding protein 1-like, transcript variant X2
NGFI-A-binding protein 1-like, transcript variant X3
NGFI-A-binding protein 1-like, transcript variant X4
NGFI-A-binding protein 1-like isoform X1
NGFI-A-binding protein 1-like isoform X2
NGFI-A-binding protein 1-like isoform X3
NGFI-A-binding protein 1-like isoform X4
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X2
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X4
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X1
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X1
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X3
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X3
DnaJ (Hsp40) homolog, subfamily C, member 7
NF-kappa-B inhibitor-interacting Ras-like protein 2
zinc finger protein 385C, 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
zinc finger protein 385C, transcript variant X1
zinc finger protein 385C, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 385C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 385C, transcript variant X6
zinc finger protein 385C, transcript variant X2
zinc finger protein 385C, transcript variant X5
zinc finger protein 385C, transcript variant X10
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 4 samples with support for all annotated introns
zinc finger protein 385C, transcript variant X7
zinc finger protein 385C, transcript variant X11
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
zinc finger protein 385C, transcript variant X13
zinc finger protein 385C, transcript variant X9
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 10 samples with support for all annotated introns
zinc finger protein 385C, transcript variant X12
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X4
probable ATP-dependent RNA helicase DHX58 isoform X1
probable ATP-dependent RNA helicase DHX58 isoform 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
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
ras-related protein Rab-5C, transcript variant X1
ras-related protein Rab-5C, transcript variant X2
potassium voltage-gated channel, subfamily H (eag-related), member 4b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 4 isoform X1
potassium voltage-gated channel, subfamily H (eag-related), member 4b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 8 isoform X2
hypocretin (orexin) neuropeptide precursor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 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: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
signal transducer and activator of transcription 5a, transcript variant X2
signal transducer and activator of transcription 5a, transcript variant X1
signal transducer and activator of transcription 5a, transcript variant X3
signal transducer and activator of transcription 5A
signal transducer and activator of transcription 3 (acute-phase response factor), transcript variant X3
signal transducer and activator of transcription 3 (acute-phase response factor), transcript variant X2
signal transducer and activator of transcription 3 (acute-phase response factor), transcript variant X1
signal transducer and activator of transcription 3
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 23 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 1, transcript variant X1
V-type proton ATPase 116 kDa subunit a 1, transcript variant X5
V-type proton ATPase 116 kDa subunit a 1, transcript variant X6
V-type proton ATPase 116 kDa subunit a 1, transcript variant X7
V-type proton ATPase 116 kDa subunit a 1, transcript variant X8
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 11 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 1, transcript variant X2
V-type proton ATPase 116 kDa subunit a 1, transcript variant X3
V-type proton ATPase 116 kDa subunit a 1, transcript variant X4
V-type proton ATPase 116 kDa subunit a 1 isoform X1
V-type proton ATPase 116 kDa subunit a 1 isoform X2
V-type proton ATPase 116 kDa subunit a 1 isoform X3
V-type proton ATPase 116 kDa subunit a 1 isoform X4
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 24 samples with support for all annotated introns
vacuolar protein-sorting-associated protein 25
WNK lysine deficient protein kinase 4a, transcript variant X1
WNK lysine deficient protein kinase 4a, transcript variant X2
serine/threonine-protein kinase WNK4 isoform X1
serine/threonine-protein kinase WNK4 isoform X2
cytochrome c oxidase assembly factor 3 homolog, mitochondrial
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
cyclin N-terminal domain-containing protein 1
beclin 1, autophagy related, transcript variant X3
beclin 1, autophagy related, transcript variant X1
beclin 1, autophagy related, transcript variant X2
proteasome activator subunit 3, transcript variant X1
proteasome activator subunit 3, transcript variant X2
proteasome activator complex subunit 3 isoform X1
proteasome activator complex subunit 3 isoform X2
membrane primary amine oxidase-like, transcript variant X1
membrane primary amine oxidase-like, transcript variant X2
membrane primary amine oxidase-like isoform X1
membrane primary amine oxidase-like isoform X2
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X1
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 1 sample with support for all annotated introns
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glucose-6-phosphatase catalytic subunit 1-like isoform X2
glucose-6-phosphatase catalytic subunit 1-like isoform X1
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X3
glucose-6-phosphatase catalytic subunit 1-like isoform X3
glucose-6-phosphatase catalytic subunit 1-like
alanyl-tRNA synthetase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
interferon-induced protein 35, transcript variant X1
interferon-induced protein 35, transcript variant X2
uncharacterized si:busm1-163l24.3, 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
uncharacterized si:busm1-163l24.3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein si:busm1-163l24.3 isoform X2
uncharacterized protein si:busm1-163l24.3 isoform X1
uncharacterized si:busm1-163l24.3, transcript variant X4
uncharacterized si:busm1-163l24.3, transcript variant X3
uncharacterized protein si:busm1-163l24.3 isoform X3
synaptic vesicle membrane protein VAT-1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
breast cancer type 1 susceptibility protein homolog, transcript variant X3
breast cancer type 1 susceptibility protein homolog, transcript variant X1
breast cancer type 1 susceptibility protein homolog, transcript variant X2
breast cancer type 1 susceptibility protein homolog isoform X2
breast cancer type 1 susceptibility protein homolog isoform X1
breast cancer type 1 susceptibility protein homolog, transcript variant X4
NBR1 autophagy cargo receptor a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
NBR1 autophagy cargo receptor a, 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 11 samples with support for all annotated introns
NBR1 autophagy cargo receptor a, transcript variant X4
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 17 samples with support for all annotated introns
NBR1 autophagy cargo receptor a, transcript variant X1
NBR1 autophagy cargo receptor a, transcript variant X5
NBR1 autophagy cargo receptor a isoform X1
NBR1 autophagy cargo receptor a isoform X2
NBR1 autophagy cargo receptor a isoform X3
NBR1 autophagy cargo receptor a isoform X4
NBR1 autophagy cargo receptor a isoform X5
transmembrane protein 106A, 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 22 samples with support for all annotated introns
transmembrane protein 106A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DEAH (Asp-Glu-Ala-His) box polypeptide 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
DEAH (Asp-Glu-Ala-His) box polypeptide 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
ATP-dependent RNA helicase DHX8 isoform X1
ATP-dependent RNA helicase DHX8 isoform X2
ETS variant transcription factor 4, transcript variant X3
ETS variant transcription factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ETS variant transcription factor 4, transcript variant X1
ETS variant transcription factor 4, transcript variant X4
ETS variant transcription factor 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ETS variant transcription factor 4, transcript variant X6
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
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 21 samples with support for all annotated introns
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 15 samples with support for all annotated introns
ras-related protein Rab-18-like, transcript variant X1
ras-related protein Rab-18-like, transcript variant X2
ras-related protein Rab-18-like isoform X1
ras-related protein Rab-18-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
10 kDa heat shock protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
MAGUK p55 subfamily member 3-like, transcript variant X5
MAGUK p55 subfamily member 3-like isoform X5
MAGUK p55 subfamily member 3-like, transcript variant X3
MAGUK p55 subfamily member 3-like isoform X3
MAGUK p55 subfamily member 3-like, transcript variant X6
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 6 samples with support for all annotated introns
MAGUK p55 subfamily member 3-like, transcript variant X2
MAGUK p55 subfamily member 3-like, transcript variant X4
MAGUK p55 subfamily member 3-like, transcript variant X1
MAGUK p55 subfamily member 3-like isoform X6
MAGUK p55 subfamily member 3-like isoform X2
MAGUK p55 subfamily member 3-like isoform X4
MAGUK p55 subfamily member 3-like isoform X1
G protein-activated inward rectifier potassium channel 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 1-like, transcript variant X4
G protein-activated inward rectifier potassium channel 1-like, transcript variant X3
G protein-activated inward rectifier potassium channel 1-like, transcript variant X2
G protein-activated inward rectifier potassium channel 1-like isoform X1
G protein-activated inward rectifier potassium channel 1-like isoform X4
G protein-activated inward rectifier potassium channel 1-like isoform X3
G protein-activated inward rectifier potassium channel 1-like isoform X2
mucin 13b, cell surface associated, transcript variant X1
mucin 13b, cell surface associated, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA binding domain containing 4, transcript variant X6
acyl-CoA binding domain containing 4, 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
acyl-CoA binding domain containing 4, transcript variant X3
acyl-CoA binding domain containing 4, transcript variant X5
acyl-CoA binding domain containing 4, transcript variant X4
acyl-CoA binding domain containing 4, transcript variant X1
acyl-CoA binding domain containing 4, transcript variant X7
acyl-CoA-binding domain-containing protein 4 isoform X1
acyl-CoA-binding domain-containing protein 4 isoform X2
abl interactor 1-like, transcript variant X1
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
abl interactor 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
abl interactor 1-like, transcript variant X2
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 2 samples with support for all annotated introns
abl interactor 1-like, transcript variant X3
abl interactor 1-like, transcript variant X4
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 2 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
MAGUK p55 scaffold protein 2b, transcript variant X3
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
MAGUK p55 scaffold protein 2b, transcript variant X2
MAGUK p55 scaffold protein 2b, transcript variant X4
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 2 samples with support for all annotated introns
MAGUK p55 scaffold protein 2b, transcript variant X1
MAGUK p55 scaffold protein 2b, transcript variant X5
MAGUK p55 subfamily member 2b isoform X2
MAGUK p55 subfamily member 2b isoform X1
MAGUK p55 subfamily member 2b isoform X3
uncharacterized LOC125466336, transcript variant X4
uncharacterized LOC125466336, transcript variant X1
uncharacterized LOC125466336, transcript variant X2
uncharacterized LOC125466336, transcript variant X3
N-acetylglutamate synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
N-acetylglutamate synthase, transcript variant X2
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 6 samples with support for all annotated introns
N-acetylglutamate synthase, transcript variant X3
N-acetylglutamate synthase, mitochondrial isoform X1
N-acetylglutamate synthase, mitochondrial isoform X2
transmembrane protein 101, 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 10 samples with support for all annotated introns
transmembrane protein 101, transcript variant X4
transmembrane protein 101, transcript variant X3
transmembrane protein 101, transcript variant X1
transmembrane protein 101, transcript variant X2
insulin-like growth factor-binding protein complex acid labile subunit, transcript variant X3
insulin-like growth factor-binding protein complex acid labile subunit, transcript variant X1
insulin-like growth factor-binding protein complex acid labile subunit, transcript variant X2
insulin-like growth factor-binding protein complex acid labile subunit
glucose-6-phosphatase catalytic subunit 3
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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125466182, transcript variant X2
uncharacterized LOC125466182, transcript variant X3
uncharacterized LOC125466182, transcript variant X1
uncharacterized LOC125466182, transcript variant X4
terminal uridylyl transferase 1, U6 snRNA-specific
speckle targeted PIP5K1A-regulated poly(A) polymerase
beta-1,4 N-acetylgalactosaminyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X2
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X3
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X4
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X1
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X2
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X1
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X5
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
collagen alpha-1(I) chain-like, transcript variant X1
collagen alpha-1(I) chain-like, transcript variant X2
collagen alpha-1(I) chain-like isoform X1
collagen alpha-1(I) chain-like isoform X2
sterile alpha motif domain containing 14
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
sterile alpha motif domain-containing protein 14
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like
integrin, alpha 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrin, alpha 3b, transcript variant X2
integrin, alpha 3b, 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 18 samples with support for all annotated introns
distal-less homeobox 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
distal-less homeobox 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125466334, transcript variant X6
uncharacterized LOC125466334, transcript variant X4
uncharacterized LOC125466334, transcript variant X3
uncharacterized LOC125466334, transcript variant X2
uncharacterized LOC125466334, transcript variant X5
uncharacterized LOC125466334, transcript variant X1
homeobox protein DLX-6-like, transcript variant X2
homeobox protein DLX-6-like, transcript variant X1
uncharacterized protein si:ch211-131k2.2
K(lysine) acetyltransferase 7b, 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 23 samples with support for all annotated introns
K(lysine) acetyltransferase 7b, transcript variant X3
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
K(lysine) acetyltransferase 7b, transcript variant X1
histone acetyltransferase KAT7 isoform X2
histone acetyltransferase KAT7 isoform X3
histone acetyltransferase KAT7 isoform X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X1
glucocorticoid-induced transcript 1 protein-like
proteasome 26S subunit, ATPase 5, transcript variant X1
26S proteasome regulatory subunit 8 isoform X1
proteasome 26S subunit, ATPase 5, transcript variant X2
26S proteasome regulatory subunit 8 isoform X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 isoform X1
acid-sensing ion channel 2-like, transcript variant X5
acid-sensing ion channel 2-like, transcript variant X2
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 4 samples with support for all annotated introns
acid-sensing ion channel 2-like isoform X2
acid-sensing ion channel 2-like, transcript variant X3
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 7 samples with support for all annotated introns
acid-sensing ion channel 2-like, transcript variant X1
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 8 samples with support for all annotated introns
acid-sensing ion channel 2-like isoform X3
acid-sensing ion channel 2-like isoform X1
acid-sensing ion channel 2-like, transcript variant X4
acid-sensing ion channel 2-like, transcript variant X6
acid-sensing ion channel 2-like isoform X4
acid-sensing ion channel 2-like isoform X5
acid-sensing ion channel 2-like, transcript variant X7
acid-sensing ion channel 2-like isoform X6
homologous recombination factor with OB-fold, transcript variant X1
homologous recombination factor with OB-fold, transcript variant X4
homologous recombination factor with OB-fold, transcript variant X3
homologous recombination factor with OB-fold, transcript variant X2
ankyrin repeat and SOCS box containing 16
transmembrane and ubiquitin-like domain containing 2
transmembrane and ubiquitin-like domain-containing protein 2
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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
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 21 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 12 samples with support for all annotated introns
upstream binding transcription factor, transcript variant X2
upstream binding transcription factor, transcript variant X5
upstream binding transcription factor, transcript variant X3
upstream binding transcription factor, transcript variant X4
upstream binding transcription factor, transcript variant X6
upstream binding transcription factor, transcript variant X12
upstream binding transcription factor, transcript variant X11
upstream binding transcription factor, transcript variant X8
upstream binding transcription factor, transcript variant X10
upstream binding transcription factor, transcript variant X9
upstream binding transcription factor, transcript variant X7
upstream binding transcription factor, transcript variant X1
nucleolar transcription factor 1 isoform X7
nucleolar transcription factor 1 isoform X6
nucleolar transcription factor 1 isoform X3
nucleolar transcription factor 1 isoform X5
nucleolar transcription factor 1 isoform X4
nucleolar transcription factor 1 isoform X2
nucleolar transcription factor 1 isoform X1
anion exchange protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
anion exchange protein 2-like, transcript variant X2
anion exchange protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
anion exchange protein 2-like, transcript variant X3
anion exchange protein 2-like isoform X4
anion exchange protein 2-like isoform X3
anion exchange protein 2-like isoform X2
band 3 anion transport protein-like isoform X1
cytochrome c oxidase subunit NDUFA4-like
speckle type BTB/POZ protein, transcript variant X1
speckle type BTB/POZ protein, transcript variant X2
neurexophilin-1-like, transcript variant X2
neurexophilin-1-like, transcript variant X1
BMP and activin membrane-bound inhibitor homolog
tumor necrosis factor receptor superfamily member 16-like, transcript variant X2
tumor necrosis factor receptor superfamily member 16-like, transcript variant X1
tumor necrosis factor receptor superfamily member 16-like isoform X2
tumor necrosis factor receptor superfamily member 16-like isoform X1
zinc finger protein 652-like, transcript variant X4
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 2 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X3
zinc finger protein 652-like, 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 19 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X2
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 12 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X5
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
phosphoethanolamine/phosphocholine phosphatase-like, transcript variant X1
phosphoethanolamine/phosphocholine phosphatase-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 24 samples with support for all annotated introns
phosphoethanolamine/phosphocholine phosphatase-like
elongation factor Tu GTP binding domain containing 2
116 kDa U5 small nuclear ribonucleoprotein component
HIG1 domain family member 1A, mitochondrial-like, transcript variant X4
HIG1 domain family member 1A, mitochondrial-like, transcript variant X3
HIG1 domain family member 1A, mitochondrial-like, transcript variant X2
HIG1 domain family member 1A, mitochondrial-like, transcript variant X5
HIG1 domain family member 1A, mitochondrial-like, transcript variant X1
HIG1 domain family member 1A, mitochondrial-like
gap junction gamma-1 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gap junction gamma-1 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X4
gap junction gamma-1 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X7
gap junction gamma-1 protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADAM metallopeptidase domain 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADAM metallopeptidase domain 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADAM metallopeptidase domain 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 11 isoform X2
disintegrin and metalloproteinase domain-containing protein 11 isoform X1
uncharacterized LOC125466312, transcript variant X1
uncharacterized LOC125466312, transcript variant X2
coiled-coil domain containing 43, transcript variant X4
coiled-coil domain containing 43, 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 12 samples with support for all annotated introns
coiled-coil domain containing 43, transcript variant X3
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 20 samples with support for all annotated introns
coiled-coil domain containing 43, transcript variant X6
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 11 samples with support for all annotated introns
coiled-coil domain containing 43, transcript variant X5
coiled-coil domain containing 43, transcript variant X1
coiled-coil domain-containing protein 43
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
meiosis-specific coiled-coil domain-containing protein MEIOC
small ubiquitin like modifier 1, transcript variant X1
small ubiquitin like modifier 1, transcript variant X2
small ubiquitin-related modifier 1 isoform X1
small ubiquitin-related modifier 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
G patch domain containing 8, 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 23 samples with support for all annotated introns
G patch domain-containing protein 8 isoform X1
G patch domain containing 8, transcript variant X2
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 14 samples with support for all annotated introns
G patch domain containing 8, 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 7 samples with support for all annotated introns
G patch domain containing 8, transcript variant X4
G patch domain-containing protein 8 isoform X2
G patch domain-containing protein 8 isoform X3
G patch domain containing 8, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
G patch domain-containing protein 8 isoform X4
integrin alpha-8-like, transcript variant X1
integrin alpha-8-like, transcript variant X2
family with sequence similarity 171 member A2a
sodium channel protein type 4 subunit alpha-like, transcript variant X2
sodium channel protein type 4 subunit alpha-like, transcript variant X3
sodium channel protein type 4 subunit alpha-like, transcript variant X6
sodium channel protein type 4 subunit alpha-like, transcript variant X7
sodium channel protein type 4 subunit alpha-like, transcript variant X1
sodium channel protein type 4 subunit alpha-like, transcript variant X5
sodium channel protein type 4 subunit alpha-like, transcript variant X4
sodium channel protein type 4 subunit alpha-like isoform X2
sodium channel protein type 4 subunit alpha-like isoform X1
B-cell antigen receptor complex-associated protein beta chain-like
RAD52 motif containing 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 9 samples with support for all annotated introns
RAD52 motif containing 1, 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 23 samples with support for all annotated introns
RAD52 motif-containing protein 1 isoform X1
RAD52 motif-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% 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: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X1
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X2
pleckstrin homology domain-containing family M member 1
Rho GTPase activating protein 27, like, transcript variant X1
Rho GTPase activating protein 27, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 12 isoform X1
rho GTPase-activating protein 12 isoform X2
Rho GTPase activating protein 27, like, transcript variant X3
rho GTPase-activating protein 15 isoform X3
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.
LOW QUALITY PROTEIN: transmembrane protein 98
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 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: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like, transcript variant X4
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
myosin light chain kinase, smooth muscle-like, transcript variant X2
myosin light chain kinase, smooth muscle-like, transcript variant X3
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 7 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like, transcript variant X1
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 11 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like isoform X4
myosin light chain kinase, smooth muscle-like isoform X3
myosin light chain kinase, smooth muscle-like isoform X2
myosin light chain kinase, smooth muscle-like isoform X1
mitogen-activated protein kinase kinase kinase 14a, transcript variant X2
mitogen-activated protein kinase kinase kinase 14a, transcript variant X1
mitogen-activated protein kinase kinase kinase 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 2 Proteins
cyclin-dependent kinase 5 activator 1-like
26S proteasome non-ATPase regulatory subunit 11
ADP-ribosylation factor-like, transcript variant X2
ADP-ribosylation factor-like, transcript variant X1
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 4 samples with support for all annotated introns
golgi SNAP receptor complex member 2, transcript variant X3
golgi SNAP receptor complex member 2, transcript variant X2
golgi SNAP receptor complex member 2, transcript variant X1
Golgi SNAP receptor complex member 2 isoform X1
Golgi SNAP receptor complex member 2 isoform X3
Golgi SNAP receptor complex member 2 isoform X2
reprimo-like protein, transcript variant X3
reprimo-like protein, transcript variant X1
reprimo-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL2
tousled-like kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tousled-like kinase 2, transcript variant X3
tousled-like kinase 2, transcript variant X4
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 1 sample with support for all annotated introns
tousled-like kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X2
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X6
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X1
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, 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 2 samples with support for all annotated introns
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X3
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, 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 1 sample with support for all annotated introns
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X7
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X5
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X9
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X8
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X10
vasoactive intestinal polypeptide receptor-like, transcript variant X3
vasoactive intestinal polypeptide receptor-like, transcript variant X2
vasoactive intestinal polypeptide receptor-like isoform X2
vasoactive intestinal polypeptide receptor-like, transcript variant X4
vasoactive intestinal polypeptide receptor-like, transcript variant X1
vasoactive intestinal polypeptide receptor-like isoform X1
vasoactive intestinal polypeptide receptor-like isoform X3
uncharacterized LOC125466328, transcript variant X2
uncharacterized protein LOC125466328 isoform X2
uncharacterized LOC125466328, transcript variant X1
uncharacterized LOC125466328, transcript variant X3
uncharacterized protein LOC125466328 isoform X1
uncharacterized protein LOC125466328 isoform X3
proline-rich protein 29-like, transcript variant X2
proline-rich protein 29-like, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
transmembrane ascorbate-dependent reductase CYB561, transcript variant X2
transmembrane ascorbate-dependent reductase CYB561, 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 17 samples with support for all annotated introns
transmembrane ascorbate-dependent reductase CYB561
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 103
Ig-like V-type domain-containing protein FAM187A
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: 9 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 3, transcript variant X2
mitogen-activated protein kinase kinase kinase 3, 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 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 3
coiled-coil domain containing 47, transcript variant X1
coiled-coil domain containing 47, transcript variant X2
translational activator of cytochrome c oxidase 1-like
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 11 samples with support for all annotated introns
potassium voltage-gated channel, subfamily H (eag-related), member 6a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
potassium voltage-gated channel, subfamily H (eag-related), member 6a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
potassium voltage-gated channel, subfamily H (eag-related), member 6a, transcript variant X2
potassium voltage-gated channel subfamily H member 6a isoform X3
potassium voltage-gated channel subfamily H member 6a isoform X2
potassium voltage-gated channel subfamily H member 6a isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 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: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X3
dephospho-CoA kinase domain containing, transcript variant X1
dephospho-CoA kinase domain containing, transcript variant X2
dephospho-CoA kinase domain-containing protein
glycylpeptide N-tetradecanoyltransferase 1-like, transcript variant X1
glycylpeptide N-tetradecanoyltransferase 1-like, transcript variant X2
glycylpeptide N-tetradecanoyltransferase 1-like isoform X1
glycylpeptide N-tetradecanoyltransferase 2-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, 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 12 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X2
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 12 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X3
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
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X4
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 6 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
parathyroid hormone/parathyroid hormone-related peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
STE20 related adaptor alpha, transcript variant X1
STE20 related adaptor alpha, transcript variant X6
STE20 related adaptor alpha, transcript variant X4
STE20 related adaptor alpha, transcript variant X5
STE20 related adaptor alpha, transcript variant X2
STE20 related adaptor alpha, transcript variant X7
STE20 related adaptor alpha, transcript variant X8
STE20-related kinase adapter protein alpha isoform X1
STE20-related kinase adapter protein alpha isoform X5
STE20-related kinase adapter protein alpha isoform X4
STE20-related kinase adapter protein alpha isoform X3
STE20 related adaptor alpha, transcript variant X3
STE20-related kinase adapter protein alpha isoform X2
STE20-related kinase adapter protein alpha isoform X6
myosin, light chain 4, alkali; atrial, embryonic
microtubule-associated protein tau b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
microtubule-associated protein tau b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
microtubule-associated protein tau b, transcript variant X3
microtubule-associated protein tau b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microtubule-associated protein tau b, transcript variant X4
microtubule-associated protein tau b, transcript variant X6
microtubule-associated protein tau isoform X1
microtubule-associated protein tau isoform X2
microtubule-associated protein tau isoform X4
microtubule-associated protein tau isoform X5
microtubule-associated protein tau isoform X3
KAT8 regulatory NSL complex subunit 1-like, transcript variant X4
KAT8 regulatory NSL complex subunit 1-like isoform X2
KAT8 regulatory NSL complex subunit 1-like, transcript variant X3
KAT8 regulatory NSL complex subunit 1-like, transcript variant X2
KAT8 regulatory NSL complex subunit 1-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 5 samples with support for all annotated introns
KAT8 regulatory NSL complex subunit 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
corticotropin-releasing factor receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125466435, transcript variant X1
uncharacterized LOC125466435, transcript variant X2
uncharacterized LOC125466435, transcript variant X3