Stegostoma fasciatum isolate 6-17 chromosome 26, sSteFas1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Stegostomatidae; Stegostoma.
REFSEQ INFORMATION: The reference sequence is identical to\nCM039252.1.\nAssembly name: sSteFas1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/17. The\noriginal whole-genome shotgun project has the accession\nJAFIRC000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Platanus v. 1.2.4; P_RNA_scaffolder v.\n commit 7941e0f on May 30, at github;\n 3D-DNA v. 180922\nAssembly Name :: sSteFas1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 95.8x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Stegostoma fasciatum Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform-like, 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 14 samples with support for all annotated introns
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform-like, 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 17 samples with support for all annotated introns
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform-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 7 samples with support for all annotated introns
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform-like isoform X1
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform-like isoform X2
sulfatase modifying factor 2, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
sulfatase modifying factor 2, transcript variant X2
inactive C-alpha-formylglycine-generating enzyme 2 isoform X1
inactive C-alpha-formylglycine-generating enzyme 2 isoform X2
chaperonin containing TCP1, subunit 6A (zeta 1)
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00398
DEAH (Asp-Glu-Ala-His) box polypeptide 33, transcript variant X1
ATP-dependent RNA helicase DHX33 isoform X1
DEAH (Asp-Glu-Ala-His) box polypeptide 33, transcript variant X2
ATP-dependent RNA helicase DHX33 isoform X2
carbohydrate-responsive element-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate-responsive element-binding protein-like
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 11 samples with support for all annotated introns
RCC1-like G exchanging factor-like protein isoform X2
RCC1-like G exchanging factor-like protein isoform 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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
myosin regulatory light chain 2, ventricular/cardiac muscle isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein CASP-like, transcript variant X5
protein CASP-like, transcript variant X1
protein CASP-like, transcript variant X4
protein CASP-like, transcript variant X3
protein CASP-like, transcript variant X2
protein CASP-like, transcript variant X6
SH2B adapter protein 2-like, transcript variant X1
SH2B adapter protein 2-like, transcript variant X4
SH2B adapter protein 2-like, transcript variant X5
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
SH2B adapter protein 2-like, transcript variant X2
SH2B adapter protein 2-like, 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 24 samples with support for all annotated introns
neutrophil cytosolic factor 1, 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 4 samples with support for all annotated introns
neutrophil cytosolic factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
rabaptin, RAB GTPase binding effector protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
aurora kinase C-like, transcript variant X3
aurora kinase C-like, transcript variant X1
aurora kinase C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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, including 24 samples with support for all annotated introns
complement component 1, q subcomponent binding protein
complement component 1 Q subcomponent-binding protein, mitochondrial
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, 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 1 sample with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X1
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X8
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X7
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
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, 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
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X3
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 1, alpha a, transcript variant X5
calcium/calmodulin-dependent protein kinase kinase 1 isoform X1
calcium/calmodulin-dependent protein kinase kinase 1 isoform X3
calcium/calmodulin-dependent protein kinase kinase 1 isoform X2
purinergic receptor P2X, ligand-gated ion channel, 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3, transcript variant X1
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X1
zinc finger, ZZ-type with EF hand domain 1, transcript variant X2
zinc finger, ZZ-type with EF hand domain 1, transcript variant X3
zinc finger, ZZ-type with EF hand domain 1, transcript variant X1
zinc finger ZZ-type and EF-hand domain-containing protein 1 isoform X2
zinc finger ZZ-type and EF-hand domain-containing protein 1 isoform X3
zinc finger ZZ-type and EF-hand domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
ankyrin repeat and FYVE domain containing 1
ubiquitin-conjugating enzyme E2G 1a (UBC7 homolog, yeast)
protein arginine N-methyltransferase 6-like
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 13 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sphingosine-1-phosphate transporter SPNS2-like
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 13 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00407
eukaryotic translation initiation factor 4h
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
linker for activation of T-cells family member 2-like, transcript variant X2
linker for activation of T-cells family member 2-like, transcript variant X3
linker for activation of T-cells family member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
linker for activation of T-cells family member 2-like isoform X1
linker for activation of T-cells family member 2-like isoform X2
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 24 samples with support for all annotated introns
ring finger and FYVE-like domain containing E3 ubiquitin protein ligase, 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 2 samples with support for all annotated introns
ring finger and FYVE-like domain containing E3 ubiquitin protein ligase, transcript variant X1
schlafen family member 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
schlafen family member 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
schlafen family member 11-like isoform X2
schlafen family member 11-like isoform X1
serine/threonine/tyrosine interacting-like 1, 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 1 sample with support for all annotated introns
serine/threonine/tyrosine interacting-like 1, transcript variant X3
serine/threonine/tyrosine interacting-like 1, 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
serine/threonine/tyrosine-interacting-like protein 1 isoform X1
serine/threonine/tyrosine-interacting-like protein 1 isoform X2
serine/threonine/tyrosine-interacting-like protein 1 isoform X3
malate dehydrogenase 2, NAD (mitochondrial)
serine/arginine repetitive matrix protein 3-like, transcript variant X3
serine/arginine repetitive matrix protein 3-like, transcript variant X2
serine/arginine repetitive matrix protein 3-like, transcript variant X4
serine/arginine repetitive matrix protein 3-like, transcript variant X10
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
serine/arginine repetitive matrix protein 3-like, transcript variant X11
serine/arginine repetitive matrix protein 3-like, transcript variant X12
serine/arginine repetitive matrix protein 3-like, transcript variant X1
serine/arginine repetitive matrix protein 3-like, transcript variant X8
serine/arginine repetitive matrix protein 3-like, transcript variant X9
serine/arginine repetitive matrix protein 3-like, transcript variant X6
serine/arginine repetitive matrix protein 3-like, transcript variant X7
serine/arginine repetitive matrix protein 3-like, transcript variant X5
serine/arginine repetitive matrix protein 3-like isoform X1
serine/arginine repetitive matrix protein 3-like isoform X2
serine/arginine repetitive matrix protein 3-like isoform X3
serine/arginine repetitive matrix protein 3-like isoform X4
serine/arginine repetitive matrix protein 3-like, transcript variant X13
serine/arginine repetitive matrix protein 3-like, transcript variant X14
serine/arginine repetitive matrix protein 3-like isoform X5
serine/arginine repetitive matrix protein 3-like isoform X6
heat shock protein, alpha-crystallin-related, 1
scavenger receptor cysteine-rich domain-containing group B protein, transcript variant X4
scavenger receptor cysteine-rich domain-containing group B protein, transcript variant X3
scavenger receptor cysteine-rich domain-containing group B protein, transcript variant X2
scavenger receptor cysteine-rich domain-containing group B protein, transcript variant X1
scavenger receptor cysteine-rich domain-containing group B protein isoform X2
scavenger receptor cysteine-rich domain-containing group B protein isoform X1
peroxisomal biogenesis factor 12, 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 22 samples with support for all annotated introns
peroxisomal biogenesis factor 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peroxisome assembly protein 12 isoform X1
peroxisome assembly protein 12 isoform X2
adaptor related protein complex 2 subunit beta 1, 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 22 samples with support for all annotated introns
adaptor related protein complex 2 subunit beta 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GAS2-like protein 2A, transcript variant X2
GAS2-like protein 2A, 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
GAS2-like protein 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, including 5 samples with support for all annotated introns
TATA-binding protein-associated factor 2N-like, transcript variant X2
TATA-binding protein-associated factor 2N-like, transcript variant X1
TATA-binding protein-associated factor 2N-like isoform X1
TATA-binding protein-associated factor 2N-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
TATA-binding protein-associated factor 2N-like isoform X3
rhomboid domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
rhomboid domain containing 2, 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 4 samples with support for all annotated introns
rhomboid domain containing 2, transcript variant X2
uncharacterized protein rhbdd2 isoform X1
uncharacterized protein rhbdd2 isoform X2
microtubule-associated protein RP/EB family member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein RP/EB family member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein RP/EB family member 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein RP/EB family member 1-like isoform X2
microtubule-associated protein RP/EB family member 1-like isoform X1
microtubule-associated protein RP/EB family member 1-like isoform X3
cytochrome P450 2D3-like, transcript variant X1
cytochrome P450 2D3-like, transcript variant X2
transmembrane protein 120Aa, transcript variant X2
transmembrane protein 120Aa, transcript variant X1
ORAI calcium release-activated calcium modulator 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ORAI calcium release-activated calcium modulator 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ORAI calcium release-activated calcium modulator 2, transcript variant X1
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 21 samples with support for all annotated introns
branched chain ketoacid dehydrogenase kinase
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial
leucine-rich repeats and WD repeat domain containing 1, 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 8 samples with support for all annotated introns
leucine-rich repeats and WD repeat domain containing 1, transcript variant X2
leucine-rich repeats and WD repeat domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeat and WD repeat-containing protein 1 isoform X1
leucine-rich repeat and WD repeat-containing protein 1 isoform 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 19 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4
deltex 2, E3 ubiquitin ligase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
deltex 2, E3 ubiquitin ligase, 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 21 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase DTX2 isoform X1
probable E3 ubiquitin-protein ligase DTX2 isoform X2
deltex 2, E3 ubiquitin ligase, transcript variant X3
probable E3 ubiquitin-protein ligase DTX2 isoform X3
RAS p21 protein activator 4, transcript variant X1
RAS p21 protein activator 4, transcript variant X2
ras GTPase-activating protein 4 isoform X2
ras GTPase-activating protein 4 isoform X1
general transcription factor II-I-like, transcript variant X7
general transcription factor II-I-like isoform X3
RNA polymerase II subunit J, transcript variant X1
DNA-directed RNA polymerase II subunit RPB11-a isoform X1
RNA polymerase II subunit J, transcript variant X2
DNA-directed RNA polymerase II subunit RPB11-a isoform X2
general transcription factor II-I-like, transcript variant X9
general transcription factor II-I-like, transcript variant X8
general transcription factor II-I-like, transcript variant X10
general transcription factor II-I-like, transcript variant X11
general transcription factor II-I-like, transcript variant X1
general transcription factor II-I-like, transcript variant X6
general transcription factor II-I-like, transcript variant X5
general transcription factor II-I-like, transcript variant X2
general transcription factor II-I-like, transcript variant X3
general transcription factor II-I-like, transcript variant X4
general transcription factor II-I-like isoform X5
general transcription factor II-I-like isoform X4
general transcription factor II-I-like isoform X6
general transcription factor II-I-like isoform X7
general transcription factor II-I-like isoform X1
general transcription factor II-I-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
GTF2I repeat domain containing 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X7
GTF2I repeat domain containing 1, 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 10 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X10
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 9 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X5
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
GTF2I repeat domain containing 1, transcript variant X6
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 9 samples with support for all annotated introns
GTF2I repeat domain containing 1, 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 13 samples with support for all annotated introns
GTF2I repeat domain containing 1, transcript variant X2
GTF2I repeat domain containing 1, transcript variant X9
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 14 samples with support for all annotated introns
general transcription factor II-I repeat domain-containing protein 1 isoform X6
general transcription factor II-I repeat domain-containing protein 1 isoform X2
general transcription factor II-I repeat domain-containing protein 1 isoform X5
general transcription factor II-I repeat domain-containing protein 1 isoform X8
general transcription factor II-I repeat domain-containing protein 1 isoform X7
general transcription factor II-I repeat domain-containing protein 1 isoform X3
general transcription factor II-I repeat domain-containing protein 1 isoform X4
general transcription factor II-I repeat domain-containing protein 1 isoform X1
general transcription factor II-I repeat domain-containing protein 1 isoform X9
GTF2I repeat domain containing 1, transcript variant X12
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 9 samples with support for all annotated introns
general transcription factor II-I repeat domain-containing protein 1 isoform X10
CAP-GLY domain containing linker protein 2, 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 8 samples with support for all annotated introns
CAP-GLY domain containing linker protein 2, transcript variant X3
CAP-Gly domain-containing linker protein 2 isoform X4
CAP-Gly domain-containing linker protein 2 isoform X3
CAP-GLY domain containing linker protein 2, 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
CAP-GLY domain containing linker protein 2, 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 3 samples with support for all annotated introns
CAP-Gly domain-containing linker protein 2 isoform X2
CAP-Gly domain-containing linker protein 2 isoform 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 15 samples with support for all annotated introns
DNA repair protein RAD51 homolog 4 isoform X1
DNA repair protein RAD51 homolog 4 isoform X2
complement factor B-like, transcript variant X1
complement factor B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable 28S rRNA (cytosine-C(5))-methyltransferase
nuclear envelope pore membrane protein POM 121
huntingtin interacting protein 1, transcript variant X1
huntingtin-interacting protein 1 isoform X1
huntingtin interacting protein 1, transcript variant X2
huntingtin-interacting protein 1 isoform X2
transmembrane protein 132E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 132E, 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 7 samples with support for all annotated introns
uncharacterized LOC125464690, transcript variant X2
uncharacterized LOC125464690, transcript variant X1
uncharacterized LOC125464690, transcript variant X3
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
inactive peptidyl-prolyl cis-trans isomerase FKBP6
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
bromodomain adjacent to zinc finger domain, 1B, 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 5 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain, 1B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain, 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
tyrosine-protein kinase BAZ1B isoform X2
tyrosine-protein kinase BAZ1B isoform X1
tyrosine-protein kinase BAZ1B isoform X3
MKS transition zone complex subunit 1, transcript variant X2
MKS transition zone complex subunit 1, transcript variant X1
Meckel syndrome type 1 protein isoform X2
Meckel syndrome type 1 protein isoform X1
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X6
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X4
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X3
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X2
B-cell CLL/lymphoma 7 protein family member B-like isoform X4
B-cell CLL/lymphoma 7 protein family member B-like isoform X2
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X5
B-cell CLL/lymphoma 7 protein family member B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
B-cell CLL/lymphoma 7 protein family member B-like isoform X3
B-cell CLL/lymphoma 7 protein family member B-like isoform 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
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
vacuolar protein sorting-associated protein 37D
uncharacterized LOC125464479, transcript variant X2
uncharacterized LOC125464479, 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 6 samples with support for all annotated introns
uncharacterized LOC125464479, transcript variant X3
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 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: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LIM domain kinase 1a, transcript variant X1
LIM domain kinase 1a, transcript variant X3
LIM domain kinase 1a, transcript variant X5
LIM domain kinase 1a, transcript variant X2
LIM domain kinase 1a, transcript variant X4
methyltransferase like 27, 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 1 sample with support for all annotated introns
methyltransferase like 27, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methyltransferase like 27, transcript variant X2
methyltransferase-like protein 27 isoform X1
methyltransferase like 27, 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 1 sample with support for all annotated introns
methyltransferase-like protein 27 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
BICD family-like cargo adapter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
BICD family-like cargo adapter 1, transcript variant X2
BICD family-like cargo adapter 1 isoform X1
BICD family-like cargo adapter 1 isoform X2
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 9 samples with support for all annotated introns
cytochrome b-c1 complex subunit 6, mitochondrial-like
fibrinogen-like protein 1-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fibrinogen-like protein 1-like protein, transcript variant X2
myotubularin related protein 4, transcript variant X2
myotubularin related protein 4, transcript variant X3
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 20 samples with support for all annotated introns
myotubularin related protein 4, 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 1 sample with support for all annotated introns
myotubularin related protein 4, 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 15 samples with support for all annotated introns
myotubularin related protein 4, transcript variant X7
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 10 samples with support for all annotated introns
myotubularin related protein 4, transcript variant X6
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 6 samples with support for all annotated introns
myotubularin related protein 4, 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 5 samples with support for all annotated introns
myotubularin-related protein 4 isoform X2
myotubularin-related protein 4 isoform X4
myotubularin-related protein 4 isoform X3
myotubularin-related protein 4 isoform X1
4-hydroxyphenylpyruvate dioxygenase a, transcript variant X2
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 4 samples with support for all annotated introns
4-hydroxyphenylpyruvate dioxygenase a, 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
4-hydroxyphenylpyruvate dioxygenase a, transcript variant X1
E3 ubiquitin-protein ligase RNF43, 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
E3 ubiquitin-protein ligase RNF43, transcript variant X1
E3 ubiquitin-protein ligase RNF43 isoform X2
E3 ubiquitin-protein ligase RNF43 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
heat shock transcription factor family member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
SPT4 homolog, DSIF elongation factor subunit
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
myeloperoxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myeloperoxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myeloperoxidase-like, transcript variant X3
eosinophil peroxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
eosinophil peroxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
eosinophil peroxidase-like, transcript variant X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
RIMS-binding protein 2, 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 3 samples with support for all annotated introns
RIMS-binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RIMS-binding protein 2, transcript variant X8
RIMS-binding protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RIMS-binding protein 2, transcript variant X1
RIMS-binding protein 2, transcript variant X2
peripheral-type benzodiazepine receptor-associated protein 1 isoform X7
peripheral-type benzodiazepine receptor-associated protein 1 isoform X1
RIMS-binding protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RIMS-binding protein 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transducin beta like 2, transcript variant X1
transducin beta like 2, transcript variant X3
transducin beta like 2, transcript variant X2
transducin beta-like protein 2 isoform X1
transducin beta-like protein 2 isoform X3
transducin beta-like protein 2 isoform X2
sodium/glucose cotransporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/glucose cotransporter 2-like, transcript variant X3
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
sodium/glucose cotransporter 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/glucose cotransporter 2-like isoform X1
sodium/glucose cotransporter 2-like isoform X3
sodium/glucose cotransporter 2-like, 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
sodium/glucose cotransporter 2-like isoform X2
phosphoserine phosphatase, 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 8 samples with support for all annotated introns
phosphoserine phosphatase, transcript variant X3
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 24 samples with support for all annotated introns
phosphoserine phosphatase, transcript variant X2
phosphoserine phosphatase, transcript variant X4
28S ribosomal protein S17, mitochondrial
NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
tRNA-yW synthesizing protein 1 homolog (S. cerevisiae), transcript variant X1
tRNA-yW synthesizing protein 1 homolog (S. cerevisiae), transcript variant X2
tRNA-yW synthesizing protein 1 homolog (S. cerevisiae), 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 3 samples with support for all annotated introns
S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 isoform X1
S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 isoform X2
S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polypeptide N-acetylgalactosaminyltransferase 17, transcript variant 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 4 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 17, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 17, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 17, 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 8 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 17 isoform X4
polypeptide N-acetylgalactosaminyltransferase 17 isoform X2
polypeptide N-acetylgalactosaminyltransferase 17 isoform X3
polypeptide N-acetylgalactosaminyltransferase 17 isoform X1
activator of transcription and developmental regulator AUTS2 a, transcript variant X2
activator of transcription and developmental regulator AUTS2 a, transcript variant X3
activator of transcription and developmental regulator AUTS2 a, transcript variant X6
activator of transcription and developmental regulator AUTS2 a, transcript variant X4
activator of transcription and developmental regulator AUTS2 a, transcript variant X5
activator of transcription and developmental regulator AUTS2 a, transcript variant X8
activator of transcription and developmental regulator AUTS2 a, transcript variant X7
activator of transcription and developmental regulator AUTS2 a, transcript variant X1
activator of transcription and developmental regulator AUTS2 a, transcript variant X9
activator of transcription and developmental regulator AUTS2 a, transcript variant X10
autism susceptibility gene 2 protein isoform X2
autism susceptibility gene 2 protein isoform X5
autism susceptibility gene 2 protein isoform X3
autism susceptibility gene 2 protein isoform X4
autism susceptibility gene 2 protein isoform X7
autism susceptibility gene 2 protein isoform X6
autism susceptibility gene 2 protein isoform X1
autism susceptibility gene 2 protein isoform X8
autism susceptibility gene 2 protein isoform X9
chromosome 26 C11orf54 homolog, transcript variant X2
chromosome 26 C11orf54 homolog, transcript variant X4
chromosome 26 C11orf54 homolog, transcript variant X3
chromosome 26 C11orf54 homolog, transcript variant X1
chromosome 26 C11orf54 homolog, transcript variant X5
chromosome 26 C11orf54 homolog, transcript variant X6
ester hydrolase C11orf54 homolog isoform X3
ester hydrolase C11orf54 homolog isoform X2
ester hydrolase C11orf54 homolog isoform X4
ester hydrolase C11orf54 homolog isoform X1
ester hydrolase C11orf54 homolog isoform X5
ester hydrolase C11orf54 homolog isoform X6
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X1
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X10
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
TATA box-binding protein-associated factor RNA polymerase I subunit D-like isoform X1
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X4
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X5
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 11 samples with support for all annotated introns
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X8
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X9
TATA box-binding protein-associated factor RNA polymerase I subunit D-like, transcript variant X2
TATA box-binding protein-associated factor RNA polymerase I subunit D-like isoform X2
TATA box-binding protein-associated factor RNA polymerase I subunit D-like isoform X3
TATA box-binding protein-associated factor RNA polymerase I subunit D-like isoform X4
uncharacterized LOC125464561, 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 24 samples with support for all annotated introns
uncharacterized LOC125464561, transcript variant X2
uncharacterized LOC125464561, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00425
COORDINATES: nucleotide motif:Rfam:12.0:RF00393
cytosolic arginine sensor for mTORC1 subunit 2
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 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
vitamin K epoxide reductase complex, subunit 1-like 1
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 19 samples with support for all annotated introns
vitamin K epoxide reductase complex subunit 1-like protein 1
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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger, HIT-type containing 3, transcript variant X2
zinc finger, HIT-type containing 3, transcript variant X1
zinc finger HIT domain-containing protein 3 isoform X1
zinc finger HIT domain-containing protein 3 isoform X2
zinc finger, HIT-type containing 3, transcript variant X3
zinc finger HIT domain-containing protein 3 isoform X3
unconventional myosin-XIX, 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 1 sample with support for all annotated introns
unconventional myosin-XIX, 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 6 samples with support for all annotated introns
unconventional myosin-XIX, transcript variant X2
unconventional myosin-XIX, transcript variant X5
unconventional myosin-XIX, 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 5 samples with support for all annotated introns
unconventional myosin-XIX, 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 2 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis, class W
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
phosphatidylinositol-glycan biosynthesis class W protein
gametogenetin binding protein 2, 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 20 samples with support for all annotated introns
gametogenetin binding protein 2, transcript variant X1
gametogenetin-binding protein 2 isoform X1
gametogenetin-binding protein 2 isoform X2
dehydrogenase/reductase SDR family member 11a
sodium- and chloride-dependent GABA transporter ine, 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 1 sample with support for all annotated introns
sodium- and chloride-dependent GABA transporter ine, 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 1 sample with support for all annotated introns
sodium- and chloride-dependent glycine transporter 2 isoform X2
sodium- and chloride-dependent GABA transporter ine isoform X1
double C2-like domain-containing protein beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
double C2-like domain-containing protein beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
double C2-like domain-containing protein beta isoform X2
double C2-like domain-containing protein beta isoform X1
rab effector Noc2-like, transcript variant X2
rab effector Noc2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
rab effector Noc2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transmembrane protein 248, transcript variant X1
transmembrane protein 248, transcript variant X2
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X2
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X7
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X6
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X1
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X3
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X4
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X5
potassium channel tetramerization domain containing 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tyrosylprotein sulfotransferase 1, transcript variant X1
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 18 samples with support for all annotated introns
tyrosylprotein sulfotransferase 1, transcript variant X4
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 5 samples with support for all annotated introns
tyrosylprotein sulfotransferase 1, transcript variant X2
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 4 samples with support for all annotated introns
tyrosylprotein sulfotransferase 1, transcript variant X8
tyrosylprotein sulfotransferase 1, 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 2 samples with support for all annotated introns
tyrosylprotein sulfotransferase 1, transcript variant X6
tyrosylprotein sulfotransferase 1, transcript variant X7
tyrosylprotein sulfotransferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calcitonin gene-related peptide-receptor component protein
DNA-directed RNA polymerase III subunit RPC9
ubiquitin specific peptidase 32, transcript variant X3
ubiquitin specific peptidase 32, transcript variant X2
ubiquitin specific peptidase 32, 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 14 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 32 isoform X3
ubiquitin carboxyl-terminal hydrolase 32 isoform X2
ubiquitin carboxyl-terminal hydrolase 32 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
uncharacterized si:ch1073-145m9.1, transcript variant X6
uncharacterized si:ch1073-145m9.1, transcript variant X5
uncharacterized si:ch1073-145m9.1, transcript variant X2
uncharacterized si:ch1073-145m9.1, transcript variant X1
uncharacterized si:ch1073-145m9.1, transcript variant X3
uncharacterized protein si:ch1073-145m9.1 isoform X1
uncharacterized protein si:ch1073-145m9.1 isoform X3
uncharacterized protein si:ch1073-145m9.1 isoform X4
uncharacterized si:ch1073-145m9.1, transcript variant X4
uncharacterized protein si:ch1073-145m9.1 isoform X2
amyloid beta precursor protein (cytoplasmic tail) binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
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 21 samples with support for all annotated introns
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Rab interacting lysosomal protein, 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 24 samples with support for all annotated introns
Rab interacting lysosomal protein, 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 16 samples with support for all annotated introns
thioredoxin domain-containing protein 17
KIAA0753 ortholog, transcript variant X2
KIAA0753 ortholog, transcript variant X1
KIAA0753 ortholog, transcript variant X3
PITPNM family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
membrane-associated phosphatidylinositol transfer protein 3 isoform X2
PITPNM family member 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane-associated phosphatidylinositol transfer protein 3 isoform X4
PITPNM family member 3, transcript variant X1
membrane-associated phosphatidylinositol transfer protein 3 isoform X1
PITPNM family member 3, transcript variant X5
PITPNM family member 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PITPNM family member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PITPNM family member 3, transcript variant X7
membrane-associated phosphatidylinositol transfer protein 3 isoform X3
PITPNM family member 3, transcript variant X8
membrane-associated phosphatidylinositol transfer protein 3 isoform X5
protein PIMREG-like, transcript variant X1
protein PIMREG-like, transcript variant X2
uncharacterized LOC125464714, transcript variant X2
uncharacterized LOC125464714, transcript variant X1
uncharacterized LOC125464714, transcript variant X4
uncharacterized LOC125464714, transcript variant X3
uncharacterized protein LOC125464714 isoform X1
uncharacterized protein LOC125464714 isoform X4
uncharacterized protein LOC125464714 isoform X2
uncharacterized protein LOC125464714 isoform X3
aryl hydrocarbon receptor interacting protein-like 1, transcript variant X3
aryl hydrocarbon receptor interacting protein-like 1, transcript variant X1
aryl hydrocarbon receptor interacting protein-like 1, transcript variant X2
aryl-hydrocarbon-interacting protein-like 1 isoform X1
aryl-hydrocarbon-interacting protein-like 1 isoform X2
WSC domain containing 1a, transcript variant X3
WSC domain containing 1a, 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 1 sample with support for all annotated introns
WSC domain containing 1a, 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
WSC domain-containing protein 1 isoform X1
WSC domain-containing protein 1 isoform X2
SPT6 homolog, histone chaperone and transcription elongation factor
uncharacterized protein LOC100126024 homolog, transcript variant X1
uncharacterized protein LOC100126024 homolog, transcript variant X2
ras-related protein Rab-34-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ras-related protein Rab-34-like, 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
ras-related protein Rab-34-like, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00266
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X4
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
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
rRNA methyltransferase 1, mitochondrial isoform X1
rRNA methyltransferase 1, mitochondrial isoform X2
uncharacterized LOC125464613, transcript variant X1
uncharacterized LOC125464613, 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 1 sample with support for all annotated introns
apoptosis antagonizing transcription factor
acetyl-CoA carboxylase alpha, transcript variant X1
acetyl-CoA carboxylase alpha, transcript variant X2
zinc finger and BTB domain-containing protein 11-like, transcript variant X2
zinc finger and BTB domain-containing protein 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 11-like, 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 12 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 11-like isoform X2
zinc finger and BTB domain-containing protein 11-like isoform X1
zinc finger and BTB domain-containing protein 11-like, transcript variant X3
dehydrogenase/reductase SDR family member 13-like, transcript variant X2
dehydrogenase/reductase SDR family member 13-like, transcript variant X1
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 23 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13-like isoform X1
dehydrogenase/reductase SDR family member 13-like isoform 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 21 samples with support for all annotated introns
pipecolic acid oxidase, 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 1 sample with support for all annotated introns
pipecolic acid oxidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
unconventional myosin-XVIIIa isoform X15
unconventional myosin-XVIIIa isoform X14
unconventional myosin-XVIIIa isoform X13
unconventional myosin-XVIIIa isoform X12
unconventional myosin-XVIIIa isoform X11
unconventional myosin-XVIIIa isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
crystallin, beta B1, like 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
crystallin, beta B1, like 3, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transmembrane and immunoglobulin domain-containing protein 1-like
solute carrier family 6 member 4a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 6 member 4a, transcript variant X4
solute carrier family 6 member 4a, transcript variant X1
solute carrier family 6 member 4a, transcript variant X2
nuclear speckle splicing regulatory protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
EF-hand calcium-binding domain-containing protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
slingshot protein phosphatase 2a, transcript variant X3
slingshot protein phosphatase 2a, transcript variant X4
protein phosphatase Slingshot homolog 2 isoform X3
protein phosphatase Slingshot homolog 2 isoform X4
slingshot protein phosphatase 2a, transcript variant X1
slingshot protein phosphatase 2a, transcript variant X2
protein phosphatase Slingshot homolog 2 isoform X1
protein phosphatase Slingshot homolog 2 isoform X2
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 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: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ankyrin repeat domain 13B, transcript variant X1
ankyrin repeat domain 13B, transcript variant X2
ankyrin repeat domain-containing protein 13B isoform X2
ankyrin repeat domain-containing protein 13B isoform X1
ankyrin repeat domain 13B, transcript variant X3
ankyrin repeat domain-containing protein 13B isoform X3
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X8
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X1
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X7
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X2
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X4
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X5
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X3
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X6
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X9
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X11
G protein-coupled receptor kinase interacting ArfGAP 1, transcript variant X10
ARF GTPase-activating protein GIT1 isoform X1
ARF GTPase-activating protein GIT1 isoform X3
ARF GTPase-activating protein GIT1 isoform X6
ARF GTPase-activating protein GIT1 isoform X7
ARF GTPase-activating protein GIT1 isoform X2
ARF GTPase-activating protein GIT1 isoform X9
ARF GTPase-activating protein GIT1 isoform X4
ARF GTPase-activating protein GIT1 isoform X11
ARF GTPase-activating protein GIT1 isoform X5
ARF GTPase-activating protein GIT1 isoform X10
ARF GTPase-activating protein GIT1 isoform X8
armadillo repeat-containing protein 10-like
protein ABHD15-like, transcript variant X1
protein ABHD15-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125464711, transcript variant X3
uncharacterized LOC125464711, transcript variant X1
uncharacterized LOC125464711, transcript variant X2
nuclear fragile X mental retardation-interacting protein 2
class A basic helix-loop-helix protein 9
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
class A basic helix-loop-helix protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
golgi SNAP receptor complex member 1, transcript variant X2
golgi SNAP receptor complex member 1, transcript variant X1
Golgi SNAP receptor complex member 1 isoform X2
Golgi SNAP receptor complex member 1 isoform X1
carboxypeptidase D-like, transcript variant X2
carboxypeptidase D-like, transcript variant X1
carboxypeptidase D-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125464482, transcript variant X2
uncharacterized LOC125464482, transcript variant X1
TNF receptor-associated factor 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TNF receptor-associated factor 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
TNF receptor-associated factor 4-like, 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 8 samples with support for all annotated introns
TNF receptor-associated factor 4-like, transcript variant X4
TNF receptor-associated factor 4-like, transcript variant X5
TNF receptor-associated factor 4-like isoform X1
TNF receptor-associated factor 4-like isoform X2
TNF receptor-associated factor 4-like isoform X3
NIMA-related kinase 8, transcript variant X2
NIMA-related kinase 8, transcript variant X1
serine/threonine-protein kinase Nek8 isoform X2
serine/threonine-protein kinase Nek8 isoform X1
nuclear pore membrane glycoprotein 210-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
transcriptional adaptor 2A, 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 17 samples with support for all annotated introns
transcriptional adaptor 2A, 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 23 samples with support for all annotated introns
transcriptional adaptor 2A, transcript variant X3
transcriptional adapter 2-alpha isoform X1
transcriptional adapter 2-alpha isoform X2
transcriptional adapter 2-alpha isoform X3
dual specificity phosphatase 14, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
dual specificity phosphatase 14, transcript variant X1
dual specificity phosphatase 14, transcript variant X3
dual specificity phosphatase 14, 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 52, 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 15 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 52, 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 23 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 52, transcript variant X3
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 10 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX52 isoform X2
probable ATP-dependent RNA helicase DDX52 isoform X1
probable ATP-dependent RNA helicase DDX52 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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
hepatocyte nuclear factor 1-beta-A isoform X2
hepatocyte nuclear factor 1-beta-A isoform X6
hepatocyte nuclear factor 1-beta-A isoform X3
hepatocyte nuclear factor 1-beta-A isoform X5
hepatocyte nuclear factor 1-beta-A isoform X4
hepatocyte nuclear factor 1-beta-A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
dynein light chain 2, cytoplasmic, transcript variant X1
dynein light chain 2, cytoplasmic, transcript variant X2
dynein light chain 2, cytoplasmic, transcript variant X3
dynein light chain 2, cytoplasmic isoform X1
dynein light chain 2, cytoplasmic isoform X2
serine and arginine rich splicing factor 1b, transcript variant X2
serine and arginine rich splicing factor 1b, transcript variant X1
vascular endothelial zinc finger 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
vascular endothelial zinc finger 1-like, 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 8 samples with support for all annotated introns
vascular endothelial zinc finger 1-like, transcript variant X6
vascular endothelial zinc finger 1-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 11 samples with support for all annotated introns
vascular endothelial zinc finger 1-like, transcript variant X4
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
vascular endothelial zinc finger 1-like, transcript variant X2
vascular endothelial zinc finger 1-like, transcript variant X7
vascular endothelial zinc finger 1-like isoform X5
vascular endothelial zinc finger 1-like isoform X2
vascular endothelial zinc finger 1-like isoform X4
vascular endothelial zinc finger 1-like isoform X1
vascular endothelial zinc finger 1-like isoform X3
vascular endothelial zinc finger 1-like isoform X6
CUE domain containing 1b, transcript variant X1
CUE domain containing 1b, transcript variant X2
CUE domain containing 1b, transcript variant X3
CUE domain containing 1b, transcript variant X4
gem (nuclear organelle) associated protein 4
vacuolar protein sorting-associated protein 53 homolog
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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 11 samples with support for all annotated introns
RAP1 GTPase activating protein 2a, transcript variant X5
RAP1 GTPase activating protein 2a, transcript variant X4
RAP1 GTPase activating protein 2a, transcript variant X6
RAP1 GTPase activating protein 2a, transcript variant X3
RAP1 GTPase activating protein 2a, transcript variant X2
RAP1 GTPase activating protein 2a, transcript variant X1
RAP1 GTPase activating protein 2a, transcript variant X7
rap1 GTPase-activating protein 2a isoform X3
rap1 GTPase-activating protein 2a isoform X4
rap1 GTPase-activating protein 2a isoform X2
rap1 GTPase-activating protein 2a isoform X1
rap1 GTPase-activating protein 2a isoform X5
rap1 GTPase-activating protein 2a isoform X6
coiled-coil domain-containing protein 92
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
A kinase (PRKA) anchor protein 10, transcript variant X1
A kinase (PRKA) anchor protein 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
A-kinase anchor protein 10, mitochondrial isoform X2
A-kinase anchor protein 10, mitochondrial isoform X1
LHFPL tetraspan subfamily member 7 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
RNA N6-adenosine-methyltransferase mettl16
small G protein signaling modulator 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small G protein signaling modulator 2, 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
small G protein signaling modulator 2 isoform X2
small G protein signaling modulator 2 isoform X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2, transcript variant X4
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2, transcript variant X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2, transcript variant X2
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2, transcript variant X3
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 isoform X2
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 isoform X1
intraflagellar transport 20 homolog (Chlamydomonas)
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 24 samples with support for all annotated introns
intraflagellar transport protein 20 homolog
nemo-like kinase, type 2, transcript variant X1
serine/threonine-protein kinase NLK isoform X1
nemo-like kinase, type 2, 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 6 samples with support for all annotated introns
serine/threonine-protein kinase NLK isoform X2
nemo-like kinase, type 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine/threonine-protein kinase NLK isoform X3
clustered mitochondria (cluA/CLU1) homolog a, transcript variant X1
clustered mitochondria (cluA/CLU1) homolog a, transcript variant X2
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog isoform X2
platelet-activating factor acetylhydrolase IB subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis-associated protein 22, transcript variant X3
spermatogenesis-associated protein 22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spermatogenesis-associated protein 22, transcript variant X4
spermatogenesis-associated protein 22, transcript variant X5
spermatogenesis-associated protein 22 isoform X3
spermatogenesis-associated protein 22 isoform X1
spermatogenesis-associated protein 22 isoform X4
spermatogenesis-associated protein 22, transcript variant X2
spermatogenesis-associated protein 22 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
WD repeat and SOCS box containing 1, transcript variant X1
WD repeat and SOCS box containing 1, transcript variant X2
WD repeat and SOCS box-containing protein 1 isoform X1
WD repeat and SOCS box-containing protein 1 isoform X2
kinase suppressor of Ras 1-like, transcript variant X4
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 7 samples with support for all annotated introns
kinase suppressor of Ras 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kinase suppressor of Ras 1-like, transcript variant X7
kinase suppressor of Ras 1-like, transcript variant X2
kinase suppressor of Ras 1-like, transcript variant X6
kinase suppressor of Ras 1-like, transcript variant X8
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
kinase suppressor of Ras 1-like, transcript variant X3
kinase suppressor of Ras 1-like, transcript variant X1
kinase suppressor of Ras 1-like isoform X2
kinase suppressor of Ras 1-like isoform X5
kinase suppressor of Ras 1-like isoform X4
kinase suppressor of Ras 1-like isoform X1
kinase suppressor of Ras 1-like isoform X3
kinase suppressor of Ras 1-like isoform X6
kinase suppressor of Ras 1-like, transcript variant X9
kinase suppressor of Ras 1-like isoform X7
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 2 samples with support for all annotated introns
LYR motif containing 9, transcript variant X1
LYR motif-containing protein 9 isoform X1
LYR motif containing 9, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LYR motif containing 9, transcript variant X6
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 16 samples with support for all annotated introns
LYR motif containing 9, transcript variant X4
LYR motif containing 9, 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 4 samples with support for all annotated introns
LYR motif-containing protein 9 isoform X3
LYR motif containing 9, transcript variant X2
LYR motif-containing protein 9 isoform X2
musashi RNA-binding protein 2b, transcript variant X18
musashi RNA-binding protein 2b, transcript variant X17
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 13 samples with support for all annotated introns
musashi RNA-binding protein 2b, transcript variant X14
musashi RNA-binding protein 2b, transcript variant X12
musashi RNA-binding protein 2b, transcript variant X10
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 6 samples with support for all annotated introns
musashi RNA-binding protein 2b, transcript variant X4
musashi RNA-binding protein 2b, transcript variant X16
musashi RNA-binding protein 2b, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
musashi RNA-binding protein 2b, transcript variant X13
musashi RNA-binding protein 2b, transcript variant X11
musashi RNA-binding protein 2b, transcript variant X9
musashi RNA-binding protein 2b, transcript variant X8
musashi RNA-binding protein 2b, transcript variant X7
musashi RNA-binding protein 2b, transcript variant X6
musashi RNA-binding protein 2b, 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 4 samples with support for all annotated introns
musashi RNA-binding protein 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
musashi RNA-binding protein 2b, transcript variant X2
musashi RNA-binding protein 2b, transcript variant X1
RNA-binding protein Musashi homolog 2b isoform X2
RNA-binding protein Musashi homolog 2b isoform X18
RNA-binding protein Musashi homolog 2b isoform X17
RNA-binding protein Musashi homolog 2b isoform X14
RNA-binding protein Musashi homolog 2b isoform X12
RNA-binding protein Musashi homolog 2b isoform X10
RNA-binding protein Musashi homolog 2b isoform X4
RNA-binding protein Musashi homolog 2b isoform X16
RNA-binding protein Musashi homolog 2b isoform X15
RNA-binding protein Musashi homolog 2b isoform X13
RNA-binding protein Musashi homolog 2b isoform X11
RNA-binding protein Musashi homolog 2b isoform X9
RNA-binding protein Musashi homolog 2b isoform X8
RNA-binding protein Musashi homolog 2b isoform X7
RNA-binding protein Musashi homolog 2b isoform X6
RNA-binding protein Musashi homolog 2b isoform X5
RNA-binding protein Musashi homolog 2b isoform X3
RNA-binding protein Musashi homolog 2b isoform X1
musashi RNA-binding protein 2b, transcript variant X19
RNA-binding protein Musashi homolog 2b isoform X19
A kinase (PRKA) anchor protein 1b, 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 24 samples with support for all annotated introns
A kinase (PRKA) anchor protein 1b, transcript variant X2
uncharacterized LOC125464491, transcript variant X2
uncharacterized LOC125464491, transcript variant X1
uncharacterized protein LOC125464491 isoform X1
uncharacterized protein LOC125464491 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
28S ribosomal protein S23, mitochondrial
glyoxalase domain containing 4, transcript variant X1
glyoxalase domain containing 4, transcript variant X2
glyoxalase domain-containing protein 4 isoform X1
glyoxalase domain-containing protein 4 isoform 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 20 samples with support for all annotated introns
rRNA methyltransferase 3A, mitochondrial
multidrug and toxin extrusion protein 1-like, transcript variant X2
multidrug and toxin extrusion protein 1-like, transcript variant X4
multidrug and toxin extrusion protein 1-like isoform X2
multidrug and toxin extrusion protein 1-like isoform X3
multidrug and toxin extrusion protein 1-like, transcript variant X3
multidrug and toxin extrusion protein 1-like, transcript variant X1
multidrug and toxin extrusion protein 1-like isoform X1
multidrug and toxin extrusion protein 1-like isoform X4
multidrug and toxin extrusion protein 1-like
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
multidrug and toxin extrusion protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, 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 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
replication protein A1, transcript variant X1
replication protein A1, transcript variant X2
replication protein A 70 kDa DNA-binding subunit isoform X1
replication protein A 70 kDa DNA-binding subunit isoform X2
aldehyde dehydrogenase family 3 member A2-like, transcript variant X1
aldehyde dehydrogenase family 3 member A2-like, transcript variant X2
aldehyde dehydrogenase, dimeric NADP-preferring-like isoform X1
aldehyde dehydrogenase family 3 member A2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
unc-51 like autophagy activating kinase 2, transcript variant X2
unc-51 like autophagy activating kinase 2, transcript variant X1
unc-51 like autophagy activating kinase 2, transcript variant X3
serine/threonine-protein kinase ULK2 isoform X1
serine/threonine-protein kinase ULK2 isoform X2
unc-51 like autophagy activating kinase 2, transcript variant X4
serine/threonine-protein kinase ULK2 isoform X3
aldehyde dehydrogenase family 3 member A2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
multidrug and toxin extrusion protein 2-like isoform X1
multidrug and toxin extrusion protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
2-(3-amino-3-carboxypropyl)histidine synthase subunit 1
OVCA2 serine hydrolase domain containing
tripartite motif containing 37, transcript variant X1
tripartite motif containing 37, transcript variant X2
tripartite motif containing 37, transcript variant X3
tripartite motif containing 37, transcript variant X7
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 11 samples with support for all annotated introns
tripartite motif containing 37, transcript variant X9
tripartite motif containing 37, transcript variant X8
tripartite motif containing 37, transcript variant X4
E3 ubiquitin-protein ligase TRIM37 isoform X1
E3 ubiquitin-protein ligase TRIM37 isoform X2
E3 ubiquitin-protein ligase TRIM37 isoform X3
E3 ubiquitin-protein ligase TRIM37 isoform X4
tripartite motif containing 37, transcript variant X5
tripartite motif containing 37, transcript variant X6
E3 ubiquitin-protein ligase TRIM37 isoform X5
protein phosphatase, Mg2+/Mn2+ dependent, 1E
DNA repair protein RAD51 homolog 3 isoform X1
DNA repair protein RAD51 homolog 3 isoform X2
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
spindle and kinetochore associated complex subunit 2, transcript variant X2
spindle and kinetochore associated complex subunit 2, transcript variant X4
spindle and kinetochore associated complex subunit 2, transcript variant X3
spindle and kinetochore associated complex subunit 2, transcript variant X1
spindle and kinetochore-associated protein 2 isoform X2
spindle and kinetochore-associated protein 2 isoform X3
spindle and kinetochore-associated protein 2 isoform X1
spindle and kinetochore-associated protein 2 isoform X4
SMG8 nonsense mediated mRNA decay factor
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 20 samples with support for all annotated introns
nonsense-mediated mRNA decay factor SMG8
glycerophosphodiester phosphodiesterase domain containing 1, 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 14 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase domain containing 1, transcript variant X1
glycerophosphodiester phosphodiesterase domain containing 1, transcript variant X4
glycerophosphodiester phosphodiesterase domain containing 1, transcript variant X2
uncharacterized protein ypel2a isoform X2
DEAH (Asp-Glu-Ala-His) box polypeptide 40, transcript variant X3
DEAH (Asp-Glu-Ala-His) box polypeptide 40, transcript variant X1
DEAH (Asp-Glu-Ala-His) box polypeptide 40, transcript variant X2
probable ATP-dependent RNA helicase DHX40 isoform X1
probable ATP-dependent RNA helicase DHX40 isoform X2
probable ATP-dependent RNA helicase DHX40 isoform X3
clathrin, heavy chain b (Hc), transcript variant X1
clathrin, heavy chain b (Hc), transcript variant X3
clathrin, heavy chain b (Hc), transcript variant X2
clathrin, heavy chain b (Hc), transcript variant X4
peptidyl-tRNA hydrolase 2, transcript variant X2
peptidyl-tRNA hydrolase 2, 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 22 samples with support for all annotated introns
peptidyl-tRNA hydrolase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
peptidyl-tRNA hydrolase 2, mitochondrial isoform X1
peptidyl-tRNA hydrolase 2, mitochondrial isoform X2
vacuole membrane protein 1, transcript variant X4
vacuole membrane protein 1, transcript variant X3
vacuole membrane protein 1, transcript variant X1
vacuole membrane protein 1, transcript variant X9
vacuole membrane protein 1, transcript variant X7
vacuole membrane protein 1, transcript variant X5
vacuole membrane protein 1, transcript variant X6
vacuole membrane protein 1, transcript variant X2
vacuole membrane protein 1, transcript variant X8
ribosomal protein S6 kinase b, polypeptide 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ribosomal protein S6 kinase beta-1 isoform X1
ribosomal protein S6 kinase b, polypeptide 1b, transcript variant X2
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 3 samples with support for all annotated introns
ribosomal protein S6 kinase beta-1 isoform X2
uncharacterized LOC125464605, transcript variant X1
uncharacterized LOC125464605, transcript variant X3
uncharacterized LOC125464605, transcript variant X6
uncharacterized LOC125464605, transcript variant X5
uncharacterized LOC125464605, transcript variant X2
uncharacterized LOC125464605, transcript variant X4
uncharacterized LOC125464605, transcript variant X7
uncharacterized LOC125464605, transcript variant X10
uncharacterized LOC125464605, transcript variant X9
uncharacterized protein LOC125464605 isoform X1
uncharacterized protein LOC125464605 isoform X3
uncharacterized protein LOC125464605 isoform X6
uncharacterized protein LOC125464605 isoform X5
uncharacterized protein LOC125464605 isoform X2
uncharacterized protein LOC125464605 isoform X4
uncharacterized protein LOC125464605 isoform X7
uncharacterized protein LOC125464605 isoform X9
uncharacterized LOC125464605, transcript variant X11
uncharacterized LOC125464605, transcript variant X8
uncharacterized protein LOC125464605 isoform X8
uncharacterized protein LOC125464605 isoform X10
mediator complex subunit 13a, transcript variant X1
mediator complex subunit 13a, 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 10 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 13a isoform X1
mediator of RNA polymerase II transcription subunit 13a isoform X2
integrator complex subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
integrator complex subunit 2, 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
T-box transcription factor 4, transcript variant X2
T-box transcription factor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
T-box transcription factor TBX4 isoform X2
T-box transcription factor TBX4 isoform X1
T-box transcription factor 2b, transcript variant X1
T-box transcription factor 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
T-box transcription factor 2b, transcript variant X3
T-box transcription factor TBX2b isoform X2
T-box transcription factor TBX2b isoform X1
T-box transcription factor TBX2b isoform X3
uncharacterized LOC125464550, transcript variant X2
uncharacterized LOC125464550, transcript variant X1
BCAS3 microtubule associated cell migration factor
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
protein phosphatase, Mg2+/Mn2+ dependent, 1Da
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 22 samples with support for all annotated introns
protein KIAA0100-like, transcript variant X1
protein KIAA0100-like, transcript variant X2
ER membrane protein complex subunit 6, transcript variant X2
ER membrane protein complex subunit 6, transcript variant X1
sedoheptulokinase, transcript variant X2
sedoheptulokinase, 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 12 samples with support for all annotated introns
transient receptor potential cation channel, subfamily V, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily V member 1
transient receptor potential cation channel subfamily V member 3-like
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 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily V member 3-like, transcript variant X4
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
transient receptor potential cation channel subfamily V member 3-like, transcript variant X1
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 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily V member 3-like, transcript variant X2
transient receptor potential cation channel subfamily V member 3-like, transcript variant X3
transient receptor potential cation channel subfamily V member 3-like isoform X1
transient receptor potential cation channel subfamily V member 3-like isoform X2
family with sequence similarity 222 member Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
family with sequence similarity 222 member Ba, transcript variant X2
Era-like 12S mitochondrial rRNA chaperone 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 204 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase-related protein-like, 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 7 samples with support for all annotated introns
ribosomal protein S6 kinase-related protein-like, transcript variant X2
ribosomal protein S6 kinase-related protein-like isoform X1
ribosomal protein S6 kinase-related protein-like isoform X2
sterile alpha and TIR motif containing 1
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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mediator complex subunit 31, transcript variant X2
mediator complex subunit 31, transcript variant X1
mediator complex subunit 31, transcript variant X5
mediator complex subunit 31, transcript variant X4
mediator complex subunit 31, transcript variant X3
mediator of RNA polymerase II transcription subunit 31 isoform X1
mediator of RNA polymerase II transcription subunit 31 isoform X4
mediator of RNA polymerase II transcription subunit 31 isoform X3
mediator of RNA polymerase II transcription subunit 31 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% 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: 14 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol transfer protein, alpha a
inositol polyphosphate 5-phosphatase K-like, transcript variant X3
inositol polyphosphate 5-phosphatase K-like, transcript variant X2
inositol polyphosphate 5-phosphatase K-like, transcript variant X4
inositol polyphosphate 5-phosphatase K-like, transcript variant X1
inositol polyphosphate 5-phosphatase K-like isoform X2
inositol polyphosphate 5-phosphatase K-like isoform X3
inositol polyphosphate 5-phosphatase K-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
nuclear cap binding subunit 3, transcript variant X1
nuclear cap binding subunit 3, transcript variant X2
nuclear cap-binding protein subunit 3 isoform X1
nuclear cap-binding protein subunit 3 isoform X2
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide 1
v-crk avian sarcoma virus CT10 oncogene homolog
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 21 samples with support for all annotated introns
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 17 samples with support for all annotated introns
leucine-rich repeat-containing protein 75A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
fructose-bisphosphate aldolase C-like, transcript variant X1
fructose-bisphosphate aldolase C-like, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis, class S
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
unc-119 homolog a (C. elegans), transcript variant X2
unc-119 homolog a (C. elegans), transcript variant X3
unc-119 homolog a (C. elegans), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
unconventional myosin-Ic-like, transcript variant X4
unconventional myosin-Ic-like, transcript variant X2
unconventional myosin-Ic-like isoform X2
unconventional myosin-Ic-like, transcript variant X1
unconventional myosin-Ic-like isoform X1
unconventional myosin-Ic-like, transcript variant X3
unconventional myosin-Ic-like isoform X3
unconventional myosin-Ic-like isoform X4
serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
pre-rRNA-processing protein TSR1 homolog
SMG6 nonsense mediated mRNA decay factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
polymerase (DNA-directed), delta interacting protein 2, transcript variant X3
polymerase delta-interacting protein 2 isoform X2
polymerase (DNA-directed), delta interacting protein 2, transcript variant X2
polymerase (DNA-directed), delta interacting protein 2, transcript variant X1
polymerase delta-interacting protein 2 isoform X1
transmembrane protein 199, transcript variant X2
transmembrane protein 199, transcript variant X3
transmembrane protein 199, transcript variant X1
transmembrane protein 199, transcript variant X5
transmembrane protein 199, transcript variant X4
transmembrane protein 199, transcript variant X6
SET and MYND domain containing 4, transcript variant X2
SET and MYND domain containing 4, transcript variant X1
SET and MYND domain-containing protein 4 isoform X2
SET and MYND domain-containing protein 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
active breakpoint cluster region-related protein
translocase of inner mitochondrial membrane 22 homolog (yeast)
mitochondrial import inner membrane translocase subunit Tim22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
zinc finger SWIM domain-containing protein 7
nuclear receptor corepressor 1-like, transcript variant X6
nuclear receptor corepressor 1-like, transcript variant X8
nuclear receptor corepressor 1-like, transcript variant X2
nuclear receptor corepressor 1-like, transcript variant X3
nuclear receptor corepressor 1-like, transcript variant X5
nuclear receptor corepressor 1-like, transcript variant X4
nuclear receptor corepressor 1-like, transcript variant X1
nuclear receptor corepressor 1-like isoform X6
nuclear receptor corepressor 1-like isoform X8
nuclear receptor corepressor 1-like isoform X2
nuclear receptor corepressor 1-like isoform X3
nuclear receptor corepressor 1-like isoform X5
nuclear receptor corepressor 1-like isoform X4
nuclear receptor corepressor 1-like isoform X1
nuclear receptor corepressor 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nuclear receptor corepressor 1-like isoform X7
phosphatidylinositol glycan anchor biosynthesis, class L, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis, class L, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis, class L, transcript variant X1
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X1
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X2
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase isoform X3
centromere protein V, transcript variant X2
centromere protein V, 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 17 samples with support for all annotated introns