Carcharodon carcharias isolate sCarCar2 chromosome 23, sCarCar2.pri, whole genome shotgun sequence.
Carcharodon carcharias (great white shark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Lamniformes; Alopiidae; Carcharodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM029987.1.\nAssembly name: sCarCar2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/03/30. The original whole-genome shotgun project has the\naccession JAGDEE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 05-FEB-2021\nAssembly Method :: FALCON v. DX 2.0.1; FALCON-Unzip v. DX\n 1.2.1; purge_dups v. DX 19-08-10;\n scaff10X v. DX 2.0.3; bionano Solve v. DX\n 3.4.0; Salsa2 HiC v. DX 2.2.0; Arrow\n polishing and gap filling v. DX 7.0.1.1;\n Longranger Align DX v. 2.2.2.1; freebayes\n DX v. 19-07-11; gEVAL manual curation v.\n 2021-02-05; VGP assembly pipeline v. 1.6\nAssembly Name :: sCarCar2.pri\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 66.84x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Carcharodon carcharias Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.6\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.
contactin associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
contactin associated protein 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 1 sample with support for all annotated introns
contactin associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
contactin associated protein 1, 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 1 sample with support for all annotated introns
contactin associated protein 1, 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 1 sample with support for all annotated introns
contactin-associated protein 1 isoform X1
contactin-associated protein 1 isoform X3
contactin-associated protein 1 isoform X4
contactin-associated protein 1 isoform X5
contactin-associated protein 1 isoform X2
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pleckstrin homology, MyTH4 and FERM domain containing H3, 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
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pleckstrin homology domain-containing family H member 3 isoform X1
pleckstrin homology domain-containing family H member 3 isoform X3
pleckstrin homology, MyTH4 and FERM domain containing H3, 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 4 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 X4
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 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
reticulophagy regulator family member 3, transcript variant X4
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
reticulophagy regulator family member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PSMC3 interacting protein, 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
homologous-pairing protein 2 homolog isoform X1
PSMC3 interacting protein, 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 1 sample with support for all annotated introns
homologous-pairing protein 2 homolog isoform X2
MAX dimerization protein MLX, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
MAX dimerization protein MLX, transcript variant X3
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 4 samples with support for all annotated introns
MAX dimerization protein MLX, 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 4 samples with support for all annotated introns
bifunctional coenzyme A synthase isoform X1
bifunctional coenzyme A synthase isoform 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 4 samples with support for all annotated introns
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X7
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X6
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
enhancer of zeste 1 polycomb repressive complex 2 subunit, 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 4 samples with support for all annotated introns
enhancer of zeste 1 polycomb repressive complex 2 subunit, 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 4 samples with support for all annotated introns
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X5
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 3 samples with support for all annotated introns
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X8
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X3
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone-lysine N-methyltransferase EZH1 isoform X7
histone-lysine N-methyltransferase EZH1 isoform X6
histone-lysine N-methyltransferase EZH1 isoform X4
histone-lysine N-methyltransferase EZH1 isoform X2
histone-lysine N-methyltransferase EZH1 isoform X5
histone-lysine N-methyltransferase EZH1 isoform X3
histone-lysine N-methyltransferase EZH1 isoform X1
enhancer of zeste 1 polycomb repressive complex 2 subunit, transcript variant X9
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 3 samples with support for all annotated introns
receptor (G protein-coupled) activity modifying protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
protein phosphatase 1 regulatory subunit 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
StAR-related lipid transfer (START) domain containing 3, 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 4 samples with support for all annotated introns
StAR-related lipid transfer (START) domain containing 3, transcript variant X5
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
StAR-related lipid transfer (START) domain containing 3, transcript variant X2
StAR-related lipid transfer (START) domain containing 3, transcript variant X4
StAR-related lipid transfer (START) domain containing 3, transcript variant X3
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: 5 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: 19 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phenylethanolamine N-methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins factor 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
post-GPI attachment to proteins factor 3-like, transcript variant X2
post-GPI attachment to proteins factor 3-like, 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 2 samples with support for all annotated introns
post-GPI attachment to proteins factor 3-like isoform X4
post-GPI attachment to proteins factor 3-like isoform X1
post-GPI attachment to proteins factor 3-like isoform X2
post-GPI attachment to proteins factor 3-like, transcript variant X5
post-GPI attachment to proteins factor 3-like isoform X5
post-GPI attachment to proteins factor 3-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 1 sample with support for all annotated introns
post-GPI attachment to proteins factor 3-like isoform X3
receptor tyrosine-protein kinase erbB-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
receptor tyrosine-protein kinase erbB-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
receptor tyrosine-protein kinase erbB-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
receptor tyrosine-protein kinase erbB-2-like isoform X1
receptor tyrosine-protein kinase erbB-2-like isoform X2
von Willebrand factor C domain-containing protein 2-like, 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
von Willebrand factor C domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
von Willebrand factor C domain-containing protein 2-like, transcript variant X3
von Willebrand factor C domain-containing protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
growth factor receptor-bound protein 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
growth factor receptor-bound protein 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
growth factor receptor-bound protein 7-like, transcript variant X2
growth factor receptor-bound protein 7-like, transcript variant X4
growth factor receptor-bound protein 7-like isoform X1
growth factor receptor-bound protein 7-like isoform X3
growth factor receptor-bound protein 7-like isoform X2
growth factor receptor-bound protein 7-like isoform X4
insulin-like growth factor-binding protein 4
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 4 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
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
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 147 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: 79 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: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 1b-like
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
trafficking kinesin-binding protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
junction plakoglobin-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
junction plakoglobin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
junction plakoglobin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase FKBP10-like
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 2 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 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP-citrate synthase, transcript variant X5
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
ATP-citrate synthase, transcript variant X4
ATP-citrate synthase, transcript variant X1
ATP-citrate synthase, transcript variant X3
ATP-citrate synthase, transcript variant X2
outer dynein arm docking complex subunit 4, transcript variant X10
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: 12 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 X4
outer dynein arm docking complex subunit 4, 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 1 sample with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X7
outer dynein arm docking complex subunit 4, transcript variant X6
outer dynein arm docking complex subunit 4, transcript variant X5
outer dynein arm docking complex subunit 4, transcript variant X9
outer dynein arm docking complex subunit 4, transcript variant X2
outer dynein arm docking complex subunit 4, transcript variant X8
outer dynein arm docking complex subunit 4, transcript variant X13
outer dynein arm docking complex subunit 4, transcript variant X14
outer dynein arm docking complex subunit 4, transcript variant X11
outer dynein arm docking complex subunit 4, transcript variant X12
outer dynein arm docking complex subunit 4, transcript variant X15
outer dynein arm-docking complex subunit 4 isoform X1
outer dynein arm-docking complex subunit 4 isoform X4
outer dynein arm-docking complex subunit 4 isoform X3
outer dynein arm-docking complex subunit 4 isoform X7
outer dynein arm-docking complex subunit 4 isoform X6
outer dynein arm-docking complex subunit 4 isoform X5
outer dynein arm-docking complex subunit 4 isoform X9
outer dynein arm-docking complex subunit 4 isoform X2
outer dynein arm-docking complex subunit 4 isoform X8
outer dynein arm-docking complex subunit 4 isoform X13
outer dynein arm-docking complex subunit 4 isoform X14
outer dynein arm-docking complex subunit 4 isoform X11
outer dynein arm-docking complex subunit 4 isoform X12
outer dynein arm-docking complex subunit 4 isoform X15
outer dynein arm-docking complex subunit 4 isoform X10
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 3 samples with support for all annotated introns
uncharacterized LOC121269214, transcript variant X2
uncharacterized LOC121269214, 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
uncharacterized protein LOC121269214 isoform X2
uncharacterized protein LOC121269214 isoform 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
CDK5 regulatory subunit associated protein 3, transcript variant X1
CDK5 regulatory subunit associated protein 3, transcript variant X3
CDK5 regulatory subunit associated protein 3, transcript variant X2
CDK5 regulatory subunit-associated protein 3 isoform X1
CDK5 regulatory subunit-associated protein 3 isoform X3
CDK5 regulatory subunit-associated protein 3 isoform X2
coatomer subunit zeta-1-like, transcript variant X4
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
coatomer subunit zeta-1-like, transcript variant X1
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 3 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X2
coatomer subunit zeta-1-like, transcript variant X3
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear factor, erythroid 2-like 1b, transcript variant X1
nuclear factor, erythroid 2-like 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear factor, erythroid 2-like 1b, transcript variant X3
nuclear factor, erythroid 2-like 1b, transcript variant X4
endoplasmic reticulum membrane sensor NFE2L1b isoform X1
endoplasmic reticulum membrane sensor NFE2L1b isoform X2
endoplasmic reticulum membrane sensor NFE2L1b isoform X3
endoplasmic reticulum membrane sensor NFE2L1b isoform X4
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X2
chromobox homolog 1b (HP1 beta homolog Drosophila), 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 4 samples with support for all annotated introns
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sorting nexin-11-like, 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 3 samples with support for all annotated introns
sorting nexin-11-like, transcript variant X3
sorting nexin-11-like, transcript variant X5
sorting nexin-11-like, transcript variant X2
sorting nexin-11-like, transcript variant X4
src kinase-associated phosphoprotein 1-like, transcript variant X2
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
src kinase-associated phosphoprotein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
src kinase-associated phosphoprotein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
src kinase-associated phosphoprotein 1-like isoform X2
src kinase-associated phosphoprotein 1-like isoform X1
src kinase-associated phosphoprotein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins
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 3 samples with support for all annotated introns
homeobox protein Hox-B3a-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeobox protein Hox-B3a-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 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: 49 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: 29 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: 28 Proteins, and 74% 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: 31 Proteins, and 81% 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: 27 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: 34 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 77% 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: 41 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
tax1-binding protein 1 homolog B-like, transcript variant X2
tax1-binding protein 1 homolog B-like, transcript variant X3
tax1-binding protein 1 homolog B-like, transcript variant X4
tax1-binding protein 1 homolog B-like, transcript variant X1
calcium-binding and coiled-coil domain-containing protein 2-like isoform X1
calcium-binding and coiled-coil domain-containing protein 2-like isoform X2
tax1-binding protein 1 homolog B-like isoform X3
ATP synthase membrane subunit c locus 1, 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 4 samples with support for all annotated introns
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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SNF8 subunit of ESCRT-II, transcript variant X1
SNF8 subunit of ESCRT-II, 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 4 samples with support for all annotated introns
vacuolar-sorting protein SNF8 isoform X2
vacuolar-sorting protein SNF8 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
transformer-2 protein homolog alpha-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transformer-2 protein homolog alpha-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transformer-2 protein homolog alpha-like, transcript variant X1
transformer-2 protein homolog alpha-like, transcript variant X2
transformer-2 protein homolog alpha-like, transcript variant X7
transformer-2 protein homolog alpha-like isoform X1
transformer-2 protein homolog alpha-like isoform X2
transformer-2 protein homolog alpha-like isoform X5
transformer-2 protein homolog alpha-like, transcript variant X5
transformer-2 protein homolog alpha-like, transcript variant X4
transformer-2 protein homolog alpha-like isoform X3
transformer-2 protein homolog alpha-like isoform X4
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin-like growth factor 2 mRNA-binding protein 1 isoform X1
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X2
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X9
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X4
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X7
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X5
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X6
insulin-like growth factor 2 mRNA binding protein 1, transcript variant X8
insulin-like growth factor 2 mRNA-binding protein 1 isoform X3
insulin-like growth factor 2 mRNA-binding protein 1 isoform X2
aminopeptidase puromycin sensitive, 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 4 samples with support for all annotated introns
aminopeptidase puromycin sensitive, 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 3 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 11% 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
39S ribosomal protein L45, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
suppressor of cytokine signaling 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
suppressor of cytokine signaling 7, transcript variant X2
suppressor of cytokine signaling 7 isoform X1
suppressor of cytokine signaling 7 isoform X2
rho GTPase-activating protein 23-like, transcript variant X4
rho GTPase-activating protein 23-like, transcript variant X3
rho GTPase-activating protein 21-like isoform X3
rho GTPase-activating protein 23-like, transcript variant X5
rho GTPase-activating protein 23-like isoform X4
rho GTPase-activating protein 23-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, including 2 samples with support for all annotated introns
rho GTPase-activating protein 23-like, transcript variant X2
rho GTPase-activating protein 21-like isoform X1
rho GTPase-activating protein 23-like isoform X2
rho GTPase-activating protein 23-like, transcript variant X6
rho GTPase-activating protein 21-like isoform X5
SRC kinase signaling inhibitor 1-like, transcript variant X3
SRC kinase signaling inhibitor 1-like, transcript variant X2
SRC kinase signaling inhibitor 1-like, transcript variant X1
SRC kinase signaling inhibitor 1-like isoform X2
SRC kinase signaling inhibitor 1-like isoform X3
SRC kinase signaling inhibitor 1-like isoform X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
protein AF-10-like, transcript variant X1
protein AF-10-like, transcript variant X6
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
protein AF-10-like, transcript variant X5
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
protein AF-10-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 3 samples with support for all annotated introns
protein AF-10-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein AF-10-like, transcript variant X3
protein AF-10-like, transcript variant X4
protein AF-10-like, transcript variant X7
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 2 samples with support for all annotated introns
protein AF-10-like, transcript variant X9
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
protein AF-10-like, transcript variant X8
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X3
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 3 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
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 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00412
LIM and SH3 protein 1, 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 4 samples with support for all annotated introns
LIM and SH3 protein 1, transcript variant X2
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 3 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
SWI5 homologous recombination repair protein, transcript variant X2
SWI5 homologous recombination repair protein, transcript variant X1
DNA repair protein SWI5 homolog isoform X1
SWI5 homologous recombination repair protein, transcript variant X3
DNA repair protein SWI5 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 38% 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 4 samples with support for all annotated introns
alpha-2,8-sialyltransferase 8F-like, transcript variant X1
alpha-2,8-sialyltransferase 8F-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 1 sample with support for all annotated introns
alpha-2,8-sialyltransferase 8F-like, transcript variant X2
alpha-2,8-sialyltransferase 8F-like isoform X1
alpha-2,8-sialyltransferase 8F-like isoform X3
alpha-2,8-sialyltransferase 8F-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X1
SH3 and cysteine-rich domain-containing protein 2-like isoform X2
SH3 and cysteine-rich domain-containing protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
F-box/LRR-repeat protein 20, transcript variant X3
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 3 samples with support for all annotated introns
F-box/LRR-repeat protein 20, 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 1 sample with support for all annotated introns
F-box/LRR-repeat protein 20, transcript variant X1
F-box/LRR-repeat protein 20, transcript variant X4
mediator complex subunit 1, transcript variant X2
mediator complex subunit 1, transcript variant X1
mediator of RNA polymerase II transcription subunit 1 isoform X2
mediator of RNA polymerase II transcription subunit 1 isoform X1
transcription factor Sp6-like, transcript variant X1
transcription factor Sp6-like, 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
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
leucine-rich repeat-containing protein 46-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50% coverage of the annotated genomic feature by RNAseq alignments
WAS/WASL interacting protein family, member 2b, transcript variant X2
WAS/WASL interacting protein family, member 2b, 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 2 samples with support for all annotated introns
WAS/WASL interacting protein family, member 2b, transcript variant X3
WAS/WASL interacting protein family, member 2b, transcript variant X4
WAS/WASL-interacting protein family member 2b
TBK1 binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TBK1 binding protein 1, transcript variant X3
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 2 samples with support for all annotated introns
TANK-binding kinase 1-binding protein 1 isoform X1
TANK-binding kinase 1-binding protein 1 isoform X2
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
oxysterol binding protein-like 7, transcript variant X3
oxysterol binding protein-like 7, transcript variant X2
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 2 samples with support for all annotated introns
oxysterol binding protein-like 7, transcript variant X4
oxysterol binding protein-like 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
mediator complex subunit 24, 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
mediator complex subunit 24, transcript variant X1
mediator of RNA polymerase II transcription subunit 24
COORDINATES: nucleotide motif:Rfam:12.0:RF01211
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X5
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 2 samples with support for all annotated introns
Rap guanine nucleotide exchange factor (GEF)-like 1, 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 3 samples with support for all annotated introns
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X4
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X1
rap guanine nucleotide exchange factor-like 1 isoform X1
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X6
Rap guanine nucleotide exchange factor (GEF)-like 1, transcript variant X3
rap guanine nucleotide exchange factor-like 1 isoform X2
gasdermin-A2-like, transcript variant X2
gasdermin-A2-like, transcript variant X3
gasdermin-A2-like, transcript variant X5
gasdermin-A2-like, transcript variant X4
gasdermin-A2-like, transcript variant X6
gasdermin-A2-like, transcript variant X1
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 1 sample with support for all annotated introns
leucine rich repeat containing 3Ca, transcript variant X1
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: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA topoisomerase II alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 30% coverage of the annotated genomic feature by RNAseq alignments
retinoic acid receptor, alpha a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinoic acid receptor, alpha a, transcript variant X6
retinoic acid receptor, alpha a, transcript variant X13
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 1 sample with support for all annotated introns
retinoic acid receptor, alpha a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
retinoic acid receptor, alpha a, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinoic acid receptor, alpha a, transcript variant X10
retinoic acid receptor, alpha a, transcript variant X9
retinoic acid receptor, alpha a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinoic acid receptor, alpha a, transcript variant X12
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 X3
cell division cycle 6 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 167 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 1 group D member 1-like, transcript variant X2
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 4 samples with support for all annotated introns
nuclear receptor subfamily 1 group D member 1-like, transcript variant X1
nuclear receptor subfamily 1 group D member 1-like isoform X2
nuclear receptor subfamily 1 group D member 1-like isoform X1
male-specific lethal 1 homolog, transcript variant X1
male-specific lethal 1 homolog, transcript variant X2
male-specific lethal 1 homolog, transcript variant X4
male-specific lethal 1 homolog, transcript variant X5
male-specific lethal 1 homolog, transcript variant X3
male-specific lethal 1 homolog isoform X2
male-specific lethal 1 homolog isoform X1
male-specific lethal 1 homolog isoform X5
male-specific lethal 1 homolog isoform X3
male-specific lethal 1 homolog isoform X4
casc3 exon junction complex subunit, transcript variant X1
casc3 exon junction complex subunit, transcript variant X2
casc3 exon junction complex subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49% coverage of the annotated genomic feature by RNAseq alignments
ORM1-like protein 3, transcript variant X6
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 4 samples with support for all annotated introns
ORM1-like protein 3, transcript variant X1
ORM1-like protein 3, transcript variant X4
ORM1-like protein 3, transcript variant X5
ORM1-like protein 3, transcript variant X2
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
ORM1-like protein 3, transcript variant X3
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 1 sample with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 3
NGFI-A-binding protein 1-like, transcript variant X4
NGFI-A-binding protein 1-like, transcript variant X3
NGFI-A-binding protein 1-like, transcript variant X1
NGFI-A-binding protein 1-like, transcript variant X6
NGFI-A-binding protein 1-like, transcript variant X5
NGFI-A-binding protein 1-like, transcript variant X2
NGFI-A-binding protein 1-like isoform X1
NGFI-A-binding protein 1-like isoform X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X5
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
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X3
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X1
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X4
2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform X3
DnaJ (Hsp40) homolog, subfamily C, member 7, transcript variant X2
DnaJ (Hsp40) homolog, subfamily C, member 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DnaJ (Hsp40) homolog, subfamily C, member 7, transcript variant X3
dnaJ homolog subfamily C member 7 isoform X2
dnaJ homolog subfamily C member 7 isoform X1
dnaJ homolog subfamily C member 7 isoform X3
NFKB inhibitor interacting Ras-like 2, transcript variant X1
NFKB inhibitor interacting Ras-like 2, transcript variant X2
NF-kappa-B inhibitor-interacting Ras-like protein 2 isoform X1
NF-kappa-B inhibitor-interacting Ras-like protein 2 isoform X2
zinc finger protein 385C, transcript variant X1
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
zinc finger protein 385C, transcript variant X3
zinc finger protein 385C, transcript variant X2
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: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X2
DEXH (Asp-Glu-X-His) box polypeptide 58, transcript variant X4
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 3 samples with support for all annotated introns
probable ATP-dependent RNA helicase DHX58 isoform X1
probable ATP-dependent RNA helicase DHX58 isoform X2
K(lysine) acetyltransferase 2A, transcript variant X1
K(lysine) acetyltransferase 2A, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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
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: 7 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
ras-related protein Rab-5C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related protein Rab-5C, transcript variant X2
potassium voltage-gated channel, subfamily H (eag-related), member 4b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
potassium voltage-gated channel subfamily H member 4
inactive phospholipase C-like protein 2, transcript variant X2
inactive phospholipase C-like protein 2, 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 3 samples with support for all annotated introns
inactive phospholipase C-like protein 2, transcript variant X3
inactive phospholipase C-like protein 2 isoform X2
inactive phospholipase C-like protein 2 isoform X1
inactive phospholipase C-like protein 2 isoform X3
inactive phospholipase C-like protein 2, transcript variant X4
signal transducer and activator of transcription 5B-like, transcript variant X7
signal transducer and activator of transcription 5B-like, transcript variant X9
signal transducer and activator of transcription 5B-like, transcript variant X1
signal transducer and activator of transcription 5B-like, transcript variant X2
signal transducer and activator of transcription 5B-like, transcript variant X3
signal transducer and activator of transcription 5B-like, transcript variant X5
signal transducer and activator of transcription 5B-like, transcript variant X4
signal transducer and activator of transcription 5B-like, transcript variant X6
signal transducer and activator of transcription 5B-like, transcript variant X8
signal transducer and activator of transcription 5B-like isoform X1
signal transducer and activator of transcription 5B-like isoform X2
uncharacterized LOC121294062, transcript variant X1
uncharacterized LOC121294062, transcript variant X2
signal transducer and activator of transcription 3 (acute-phase response factor), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 3 (acute-phase response factor), transcript variant X2
signal transducer and activator of transcription 3
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
V-type proton ATPase 116 kDa subunit a1, transcript variant X1
V-type proton ATPase 116 kDa subunit a1, transcript variant X3
V-type proton ATPase 116 kDa subunit a1, transcript variant X4
V-type proton ATPase 116 kDa subunit a1, transcript variant X2
V-type proton ATPase 116 kDa subunit a1, transcript variant X5
V-type proton ATPase 116 kDa subunit a1 isoform X1
V-type proton ATPase 116 kDa subunit a1 isoform X2
V-type proton ATPase 116 kDa subunit a1 isoform X3
V-type proton ATPase 116 kDa subunit a1 isoform X4
V-type proton ATPase 116 kDa subunit a1, transcript variant X6
V-type proton ATPase 116 kDa subunit a1 isoform X5
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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
beclin 1, autophagy related, transcript variant X2
cytochrome c oxidase assembly factor 3 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
cyclin N-terminal domain-containing protein 1
beclin 1, autophagy related, transcript variant X1
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
glucose-6-phosphatase catalytic subunit 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
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: 18 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
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: 37 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphatase catalytic subunit 1-like isoform X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alanyl-tRNA synthetase domain containing 1
prostaglandin E synthase 3 like, transcript variant X1
prostaglandin E synthase 3 like, transcript variant X2
ceramide synthase 5-like, transcript variant X1
ceramide synthase 5-like, transcript variant X2
RUN domain containing 1, transcript variant X1
RUN domain containing 1, 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 4 samples with support for all annotated introns
interferon-induced protein 35, transcript variant X3
interferon-induced protein 35, transcript variant X1
interferon-induced protein 35, transcript variant X2
uncharacterized si:busm1-163l24.3, transcript variant X1
uncharacterized si:busm1-163l24.3, transcript variant X2
uncharacterized protein si:busm1-163l24.3
vesicle amine transport 1, transcript variant X2
vesicle amine transport 1, transcript variant X1
synaptic vesicle membrane protein VAT-1 homolog isoform X2
synaptic vesicle membrane protein VAT-1 homolog isoform 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 3 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
NBR1 autophagy cargo receptor a, transcript variant X1
NBR1 autophagy cargo receptor a, transcript variant X2
NBR1 autophagy cargo receptor a, transcript variant X4
NBR1 autophagy cargo receptor a, transcript variant X3
NBR1 autophagy cargo receptor a isoform X1
NBR1 autophagy cargo receptor a isoform X2
NBR1 autophagy cargo receptor a isoform X4
NBR1 autophagy cargo receptor a isoform X3
DEAH (Asp-Glu-Ala-His) box polypeptide 8, transcript variant X2
DEAH (Asp-Glu-Ala-His) box polypeptide 8, transcript variant X3
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
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 3 samples with support for all annotated introns
ras-related protein Rab-18-like, 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 4 samples with support for all annotated introns
ras-related protein Rab-18-like isoform X1
ras-related protein Rab-18-like, transcript variant X2
ras-related protein Rab-18-like isoform X2
HAUS augmin-like complex, subunit 7, transcript variant X1
HAUS augmin-like complex subunit 7 isoform X1
HAUS augmin-like complex, subunit 7, transcript variant X2
HAUS augmin-like complex subunit 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
membrane palmitoylated protein 3a, transcript variant X3
membrane palmitoylated protein 3a, transcript variant X2
membrane palmitoylated protein 3a, transcript variant X8
membrane palmitoylated protein 3a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane palmitoylated protein 3a, transcript variant X6
membrane palmitoylated protein 3a, transcript variant X1
membrane palmitoylated protein 3a, transcript variant X7
membrane palmitoylated protein 3a, transcript variant X4
membrane palmitoylated protein 3a, transcript variant X9
membrane palmitoylated protein 3a, transcript variant X10
G protein-activated inward rectifier potassium channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins
zinc finger protein 281b, transcript variant X2
zinc finger protein 281b, transcript variant X3
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 3 samples with support for all annotated introns
zinc finger protein 281b, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
acyl-CoA-binding domain-containing protein 5-like, transcript variant X5
acyl-CoA-binding domain-containing protein 5-like, transcript variant X4
acyl-CoA-binding domain-containing protein 5-like, transcript variant X2
acyl-CoA-binding domain-containing protein 5-like, transcript variant X1
acyl-CoA-binding domain-containing protein 5-like, transcript variant X3
acyl-CoA-binding domain-containing protein 5-like, transcript variant X6
acyl-CoA-binding domain-containing protein 5-like isoform X1
acyl-CoA-binding domain-containing protein 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
galactoside alpha-(1,2)-fucosyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X1
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X3
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X2
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X1
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121294012, transcript variant X1
uncharacterized LOC121294012, transcript variant X2
N-acetylglutamate synthase, transcript variant X2
N-acetylglutamate synthase, transcript variant X1
N-acetylglutamate synthase, transcript variant X3
N-acetylglutamate synthase, mitochondrial isoform X2
N-acetylglutamate synthase, mitochondrial isoform X1
transmembrane protein 101, transcript variant X3
transmembrane protein 101, transcript variant X2
transmembrane protein 101, transcript variant X1
glucose-6-phosphatase catalytic subunit 3
histone deacetylase 5, transcript variant X3
histone deacetylase 5, transcript variant X8
histone deacetylase 5, transcript variant X6
histone deacetylase 5, transcript variant X5
histone deacetylase 5, transcript variant X4
histone deacetylase 5, transcript variant X7
histone deacetylase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 5, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 5, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histone deacetylase 5, transcript variant X10
histone deacetylase 5, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
terminal uridylyl transferase 1, U6 snRNA-specific, transcript variant X1
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X1
terminal uridylyl transferase 1, U6 snRNA-specific, transcript variant X2
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X2
beta-1,4 N-acetylgalactosaminyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
collagen, type I, alpha 1b, transcript variant X2
collagen, type I, alpha 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain containing 14
sterile alpha motif domain-containing protein 14
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like, transcript variant X2
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-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 4 samples with support for all annotated introns
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like, transcript variant X3
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like, transcript variant X4
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like isoform X2
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like isoform X1
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like isoform X3
uncharacterized LOC121269189, transcript variant X2
uncharacterized LOC121269189, transcript variant X1
K(lysine) acetyltransferase 7b, transcript variant X2
K(lysine) acetyltransferase 7b, transcript variant X4
K(lysine) acetyltransferase 7b, transcript variant X3
K(lysine) acetyltransferase 7b, transcript variant X5
K(lysine) acetyltransferase 7b, transcript variant X6
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 X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like
glucocorticoid-induced transcript 1 protein-like, transcript variant X3
glucocorticoid-induced transcript 1 protein-like, transcript variant X2
glucocorticoid-induced transcript 1 protein-like, transcript variant X1
glucocorticoid-induced transcript 1 protein-like isoform X1
glucocorticoid-induced transcript 1 protein-like isoform X3
glucocorticoid-induced transcript 1 protein-like isoform X2
proteasome 26S subunit, ATPase 5, transcript variant X1
proteasome 26S subunit, ATPase 5, transcript variant X2
proteasome 26S subunit, ATPase 5, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2, 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 2 samples with support for all annotated introns
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
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
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins
acid-sensing (proton-gated) ion channel 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
homologous recombination factor with OB-fold, transcript variant X1
homologous recombination factor with OB-fold, transcript variant X2
homologous recombination factor with OB-fold, transcript variant X3
homologous recombination OB-fold protein isoform X1
homologous recombination OB-fold protein isoform X2
ankyrin repeat and SOCS box containing 16, transcript variant X2
ankyrin repeat and SOCS box containing 16, 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
ankyrin repeat and SOCS box protein 16 isoform X1
ankyrin repeat and SOCS box protein 16 isoform X2
transmembrane and ubiquitin-like domain containing 2, transcript variant X2
transmembrane and ubiquitin-like domain containing 2, transcript variant X1
transmembrane and ubiquitin-like domain-containing protein 2
upstream binding transcription factor, transcript variant X6
upstream binding transcription factor, transcript variant X5
upstream binding transcription factor, transcript variant X4
upstream binding transcription factor, transcript variant X3
upstream binding transcription factor, transcript variant X1
upstream binding transcription factor, transcript variant X7
upstream binding transcription factor, transcript variant X2
nucleolar transcription factor 1 isoform X6
nucleolar transcription factor 1 isoform X5
nucleolar transcription factor 1 isoform X4
nucleolar transcription factor 1 isoform X3
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: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
anion exchange protein 2-like, transcript variant X2
anion exchange protein 2-like isoform X2
anion exchange protein 2-like isoform 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 4 samples with support for all annotated introns
cytochrome c oxidase subunit NDUFA4-like
speckle type BTB/POZ protein, transcript variant X2
speckle type BTB/POZ protein, transcript variant X1
speckle type BTB/POZ protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
BMP and activin membrane-bound inhibitor homolog, transcript variant X1
BMP and activin membrane-bound inhibitor homolog, transcript variant X2
BMP and activin membrane-bound inhibitor homolog isoform X2
BMP and activin membrane-bound inhibitor homolog isoform X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 652
uncharacterized LOC121294059, transcript variant X1
uncharacterized LOC121294059, transcript variant X2
phosphoethanolamine/phosphocholine phosphatase-like, transcript variant X1
phosphoethanolamine/phosphocholine phosphatase-like, transcript variant X2
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 X2
HIG1 domain family member 1A, mitochondrial-like, transcript variant X3
HIG1 domain family member 1A, mitochondrial-like, transcript variant X1
HIG1 domain family member 1A, mitochondrial-like isoform X1
HIG1 domain family member 1A, mitochondrial-like isoform X2
gap junction gamma-1 protein-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 2 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X4
gap junction gamma-1 protein-like, transcript variant X3
gap junction gamma-1 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 11
uncharacterized LOC121268998, transcript variant X3
uncharacterized LOC121268998, transcript variant X4
uncharacterized LOC121268998, transcript variant X1
uncharacterized LOC121268998, transcript variant X2
uncharacterized LOC121268998, transcript variant X5
uncharacterized protein LOC121268998 isoform X2
uncharacterized protein LOC121268998 isoform X1
uncharacterized protein LOC121268998 isoform X3
coiled-coil domain-containing protein 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific coiled-coil domain-containing protein MEIOC
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 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
G patch domain containing 8, transcript variant X1
G patch domain containing 8, transcript variant X5
G patch domain containing 8, transcript variant X3
G patch domain containing 8, transcript variant X2
G patch domain-containing protein 8 isoform X1
G patch domain containing 8, transcript variant X4
G patch domain-containing protein 8 isoform X2
G patch domain-containing protein 8 isoform X3
integrin alpha-8-like, transcript variant X1
integrin alpha-8-like, transcript variant X2
family with sequence similarity 171 member A2a
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
sodium channel protein type 4 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
CD79b molecule, immunoglobulin-associated beta
B-cell antigen receptor complex-associated protein beta chain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins
interferon alpha-1-like, transcript variant X1
interferon alpha-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X2
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 X4
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X3
pleckstrin homology domain-containing family M member 1 isoform X1
pleckstrin homology domain-containing family M member 1 isoform X2
rho GTPase-activating protein 27-like, transcript variant X2
rho GTPase-activating protein 27-like, transcript variant X1
rho GTPase-activating protein 27-like, transcript variant X3
rho GTPase-activating protein 27-like isoform X1
rho GTPase-activating protein 27-like isoform X2
rho GTPase-activating protein 27-like, transcript variant X5
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 1 sample with support for all annotated introns
rho GTPase-activating protein 27-like, transcript variant X4
rho GTPase-activating protein 15-like isoform X3
rho GTPase-activating protein 27-like, transcript variant X6
rho GTPase-activating protein 27-like isoform X4
transmembrane protein 98, transcript variant X1
transmembrane protein 98, transcript variant X2
transmembrane protein 98, transcript variant X4
transmembrane protein 98, transcript variant X5
transmembrane protein 98, transcript variant X3
transmembrane protein 98, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 99% 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: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myosin light chain kinase, smooth muscle-like, transcript variant X1
myosin light chain kinase, smooth muscle-like isoform X1
myosin light chain kinase, smooth muscle-like, transcript variant X2
myosin light chain kinase, smooth muscle-like isoform X2
mitogen-activated protein kinase kinase kinase 14a
mitogen-activated protein kinase kinase kinase 14
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
cyclin-dependent kinase 5 activator 1-like
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
26S proteasome non-ATPase regulatory subunit 11, transcript variant X1
26S proteasome non-ATPase regulatory subunit 11, transcript variant X2
26S proteasome non-ATPase regulatory subunit 11
ADP-ribosylation factor 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ADP-ribosylation factor 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADP-ribosylation factor 2-like, transcript variant X1
ADP-ribosylation factor 2-like, transcript variant X4
ADP-ribosylation factor 2-like, transcript variant X2
ADP-ribosylation factor 2-like isoform X1
ADP-ribosylation factor 2-like isoform X2
ADP-ribosylation factor 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins
vesicle-fusing ATPase, transcript variant X5
vesicle-fusing ATPase, transcript variant X3
vesicle-fusing ATPase, transcript variant X6
vesicle-fusing ATPase, 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 1 sample with support for all annotated introns
vesicle-fusing ATPase, transcript variant X1
vesicle-fusing ATPase, transcript variant X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 X2
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: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
tousled-like kinase 2, transcript variant X1
tousled-like kinase 2, transcript variant X3
tousled-like kinase 2, transcript variant X4
tousled-like kinase 2, transcript variant X2
tousled-like kinase 2, transcript variant X5
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X3
mannose receptor, C type 2, transcript variant X1
mannose receptor, C type 2, transcript variant X2
mannose receptor, C type 2, transcript variant X3
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X2
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, 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
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X1
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X4
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X5
vasoactive intestinal polypeptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
transmembrane ascorbate-dependent reductase CYB561, transcript variant X2
transmembrane ascorbate-dependent reductase CYB561, transcript variant X1
transmembrane ascorbate-dependent reductase CYB561
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1, transcript variant X1
angiotensin-converting enzyme isoform X1
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1, transcript variant X2
angiotensin-converting enzyme isoform X2
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1, transcript variant X3
angiotensin-converting enzyme isoform X3
solute carrier family 15 member 2-like, transcript variant X2
solute carrier family 15 member 2-like, transcript variant X3
solute carrier family 15 member 2-like, transcript variant X1
solute carrier family 15 member 2-like isoform X1
solute carrier family 15 member 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 253 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Ig-like V-type domain-containing protein FAM187A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
coiled-coil domain containing 103, transcript variant X1
coiled-coil domain containing 103, transcript variant X2
coiled-coil domain-containing protein 103
LIM domain containing 2, transcript variant X1
LIM domain containing 2, transcript variant X2
LIM domain containing 2, transcript variant X3
LIM domain containing 2, transcript variant X4
mitogen-activated protein kinase kinase kinase 3, transcript variant X1
mitogen-activated protein kinase kinase kinase 3, transcript variant X2
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, transcript variant X2
translational activator of cytochrome c oxidase 1-like, transcript variant X1
translational activator of cytochrome c oxidase 1-like
potassium voltage-gated channel, subfamily H (eag-related), member 6a
potassium voltage-gated channel subfamily H member 6a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycylpeptide N-tetradecanoyltransferase 1
dephospho-CoA kinase domain containing, transcript variant X2
dephospho-CoA kinase domain containing, transcript variant X3
dephospho-CoA kinase domain containing, transcript variant X1
dephospho-CoA kinase domain containing, transcript variant X5
dephospho-CoA kinase domain containing, transcript variant X4
dephospho-CoA kinase domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: 16 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like
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 1 sample with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
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
ring finger protein 113A, transcript variant X1
ring finger protein 113A, transcript variant X2
E3 ubiquitin-protein ligase RNF113A isoform X2
E3 ubiquitin-protein ligase RNF113A isoform X1
parathyroid hormone/parathyroid hormone-related peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
DEAD (Asp-Glu-Ala-Asp) box helicase 42, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box helicase 42, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box helicase 42, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box helicase 42, transcript variant X4
ATP-dependent RNA helicase DDX42 isoform X1
ATP-dependent RNA helicase DDX42 isoform X2
STE20 related adaptor alpha, transcript variant X1
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 4 samples with support for all annotated introns
STE20 related adaptor alpha, transcript variant X2
STE20 related adaptor alpha, transcript variant X4
STE20-related kinase adapter protein alpha isoform X1
STE20-related kinase adapter protein alpha isoform X4
STE20-related kinase adapter protein alpha isoform X2
STE20 related adaptor alpha, transcript variant X3
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 2 samples with support for all annotated introns
STE20-related kinase adapter protein alpha isoform X3
myosin, light chain 4, alkali; atrial, embryonic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle 27, transcript variant X1
cell division cycle 27, transcript variant X3
cell division cycle 27, transcript variant X2
cell division cycle 27, transcript variant X5
cell division cycle 27, transcript variant X4
cell division cycle protein 27 homolog isoform X1
cell division cycle protein 27 homolog isoform X2
uncharacterized LOC121268942, transcript variant X1
uncharacterized LOC121268942, transcript variant X2
KAT8 regulatory NSL complex subunit 1b, transcript variant X1
KAT8 regulatory NSL complex subunit 1b, transcript variant X2
uncharacterized LOC121294030, transcript variant X2
uncharacterized LOC121294030, transcript variant X1
KAT8 regulatory NSL complex subunit 1b, transcript variant X3