Oncorhynchus tshawytscha isolate Ot180627B linkage group LG32, Otsh_v2.0, whole genome shotgun sequence.
Oncorhynchus tshawytscha (Chinook salmon)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Protacanthopterygii; Salmoniformes; Salmonidae; Salmoninae; Oncorhynchus.
Chinook salmon (Oncorhynchus tshawytscha) genome and transcriptome
REFSEQ INFORMATION: The reference sequence is identical to\nCM031230.1.\nAssembly name: Otsh_v2.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Fisheries and Oceans Canada\non 2021/05/07. The original whole-genome shotgun project has the\naccession JAEPEU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Fisheries and Oceans Canada\nAssembly Date :: NOV-2020\nAssembly Method :: Flye v. 2.6-g6f887ae; Racon v. 1.4.16;\n Pilon v. 1.22; Pilon v. 1.22; Chromonomer\n v. 1.10; Ragtag v. 1.0.1; Custom v. 1.0\nAssembly Name :: Otsh_v2.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 130.0x\nSequencing Technology :: Oxford Nanopore MinION; PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Oncorhynchus tshawytscha Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Canada: British Columbia, Capilano River
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon.
spectrin beta chain, non-erythrocytic 1, transcript variant X4
COORDINATES: polyA evidence [ECO:0006239]
spectrin beta chain, non-erythrocytic 1, transcript variant X1
spectrin beta chain, non-erythrocytic 1 isoform X4
spectrin beta chain, non-erythrocytic 1 isoform X1
spectrin beta chain, non-erythrocytic 1, transcript variant X3
spectrin beta chain, non-erythrocytic 1, transcript variant X2
spectrin beta chain, non-erythrocytic 1 isoform X2
spectrin beta chain, non-erythrocytic 1 isoform X3
protein jagged-1b, transcript variant X3
protein jagged-1b, transcript variant X2
protein jagged-1b, transcript variant X1
zinc finger protein 501-like, transcript variant X2
zinc finger protein 501-like, transcript variant X1
zinc finger protein 2 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
gastrula zinc finger protein XlCGF17.1-like
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 53 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
induced myeloid leukemia cell differentiation protein Mcl-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
zinc finger protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger protein 2-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 58 samples with support for all annotated introns
uncharacterized protein LOC112239676 isoform X2
zinc finger protein 501, 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
zinc finger protein 501, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 771-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 39 samples with support for all annotated introns
zinc finger protein 771-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 44 samples with support for all annotated introns
zinc finger protein 771-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 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cilia- and flagella-associated protein 251-like isoform X2
zinc finger protein 501-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 32 samples with support for all annotated introns
cilia- and flagella-associated protein 251-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
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 49 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 219 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
oocyte zinc finger protein XlCOF22-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 14 samples with support for all annotated introns
oocyte zinc finger protein XlCOF22-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 218 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
oocyte zinc finger protein XlCOF22-like isoform X1
zinc finger protein 2 homolog, transcript variant X1
zinc finger protein 2 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
gastrula zinc finger protein XlCGF49.1-like
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
endothelial zinc finger protein induced by tumor necrosis factor alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC112245074, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC112245074, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 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: 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
zinc finger protein 239-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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 198 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC121841607, transcript variant X2
uncharacterized LOC121841607, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 261 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and SCAN domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glutamic acid-rich protein-like isoform X2
uncharacterized LOC121841597, transcript variant X1
uncharacterized LOC121841597, 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 3 samples with support for all annotated introns
uncharacterized LOC121841597, transcript variant X2
uncharacterized protein LOC121841597 isoform X1
uncharacterized protein LOC121841597 isoform 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 53 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized protein LOC112245066 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 436-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121841610, transcript variant X3
uncharacterized LOC121841610, transcript variant X4
uncharacterized LOC121841610, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC121841610, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 154 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 45 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 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 201 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
zinc finger protein 2 homolog, transcript variant X4
zinc finger protein 2 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X5
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 54 samples with support for all annotated introns
translation initiation factor IF-2-like isoform X5
zinc finger protein 354C-like isoform X2
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X4
glutamic acid-rich protein-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 42 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 32 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 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
egl nine homolog 1, transcript variant X1
egl nine homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 2, transcript variant X7
signal-induced proliferation-associated 1-like protein 2, transcript variant X5
signal-induced proliferation-associated 1-like protein 2, transcript variant X6
signal-induced proliferation-associated 1-like protein 2, transcript variant X4
signal-induced proliferation-associated 1-like protein 2, transcript variant X3
signal-induced proliferation-associated 1-like protein 2, transcript variant X2
signal-induced proliferation-associated 1-like protein 2, transcript variant X1
signal-induced proliferation-associated 1-like protein 2 isoform X7
signal-induced proliferation-associated 1-like protein 2 isoform X5
signal-induced proliferation-associated 1-like protein 2 isoform X6
signal-induced proliferation-associated 1-like protein 2 isoform X4
signal-induced proliferation-associated 1-like protein 2 isoform X3
signal-induced proliferation-associated 1-like protein 2 isoform X2
signal-induced proliferation-associated 1-like protein 2 isoform X1
uncharacterized LOC112230439, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC112230439, transcript variant X1
uncharacterized protein LOC112230439 isoform X2
uncharacterized protein LOC112230439 isoform X1
ribosomal RNA processing protein 36 homolog
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
phosphofurin acidic cluster sorting protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: phosphofurin acidic cluster sorting protein 2
kinesin light chain 1, transcript variant X2
kinesin light chain 1, transcript variant X1
kinesin light chain 1, 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 61 samples with support for all annotated introns
serine/threonine-protein kinase MARK1, transcript variant X1
serine/threonine-protein kinase MARK1, transcript variant X3
serine/threonine-protein kinase MARK1, transcript variant X2
serine/threonine-protein kinase MARK1, transcript variant X4
serine/threonine-protein kinase MARK1 isoform X1
serine/threonine-protein kinase MARK1 isoform X3
serine/threonine-protein kinase MARK1 isoform X2
serine/threonine-protein kinase MARK1 isoform 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 11 samples with support for all annotated introns
Tnf receptor-associated factor 5, transcript variant X1
Tnf receptor-associated factor 5, transcript variant X2
Tnf receptor-associated factor 5, transcript variant X3
TNF receptor-associated factor 5 isoform X1
TNF receptor-associated factor 5 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
potassium voltage-gated channel subfamily H member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 1 isoform X1
potassium voltage-gated channel subfamily H member 1 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 17% coverage of the annotated genomic feature by RNAseq alignments
sodium/calcium exchanger 1, transcript variant X1
sodium/calcium exchanger 1, 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 8 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 3, 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 2 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X7
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 3, 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
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X6
mitogen-activated protein kinase kinase kinase kinase 3 isoform X3
mitogen-activated protein kinase kinase kinase kinase 3 isoform X2
mitogen-activated protein kinase kinase kinase kinase 3 isoform X1
mitogen-activated protein kinase kinase kinase kinase 3 isoform X4
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X9
mitogen-activated protein kinase kinase kinase kinase 3 isoform X5
mitogen-activated protein kinase kinase kinase kinase 3-like
son of sevenless homolog 1, transcript variant X5
son of sevenless homolog 1, transcript variant X1
son of sevenless homolog 1, transcript variant X2
son of sevenless homolog 1, transcript variant X3
son of sevenless homolog 1, transcript variant X4
serine/arginine-rich splicing factor 7, transcript variant X1
serine/arginine-rich splicing factor 7, transcript variant X2
serine/arginine-rich splicing factor 7, transcript variant X3
serine/arginine-rich splicing factor 7 isoform X2
serine/arginine-rich splicing factor 7 isoform X3
serine/arginine-rich splicing factor 7 isoform X1
heterogeneous nuclear ribonucleoprotein L-like
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00430
serum response factor, transcript variant X1
serum response factor, transcript variant X2
EGF-containing fibulin-like extracellular matrix protein 1, transcript variant X2
EGF-containing fibulin-like extracellular matrix protein 1, transcript variant X1
EGF-containing fibulin-like extracellular matrix protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC121841618, transcript variant X2
uncharacterized LOC121841618, transcript variant X1
cysteine-rich protein 2-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 178 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
CSC1-like protein 2, transcript variant X2
CSC1-like protein 2, transcript variant X3
CSC1-like protein 2, transcript variant X1
microtubule-associated proteins 1A/1B light chain 3C
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
interferon regulatory factor 2-binding protein 2-B
mitochondrial import receptor subunit TOM20 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RNA-binding protein 34-like
glycine-rich cell wall structural protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
ERO1-like protein beta, transcript variant X1
ERO1-like protein beta, transcript variant X2
BTB/POZ domain-containing protein 3, transcript variant X1
BTB/POZ domain-containing protein 3 isoform X1
BTB/POZ domain-containing protein 3, transcript variant X2
BTB/POZ domain-containing protein 3 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
NADH:ubiquinone oxidoreductase complex assembly factor 5
arginine-hydroxylase NDUFAF5, mitochondrial
kinesin-like protein KIF16B, transcript variant X7
kinesin-like protein KIF16B, transcript variant X6
kinesin-like protein KIF16B, transcript variant X5
kinesin-like protein KIF16B, transcript variant X11
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
kinesin-like protein KIF16B, transcript variant X2
kinesin-like protein KIF16B, transcript variant X3
kinesin-like protein KIF16B, transcript variant X1
kinesin-like protein KIF16B, transcript variant X4
kinesin-like protein KIF16B, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
kinesin-like protein KIF16B, transcript variant X10
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 18 samples with support for all annotated introns
kinesin-like protein KIF16B, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
U2 small nuclear ribonucleoprotein B'', transcript variant X1
U2 small nuclear ribonucleoprotein B'', transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC112230386, transcript variant X2
uncharacterized LOC112230386, transcript variant X3
uncharacterized LOC112230386, transcript variant X1
F-box only protein 48, 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 60 samples with support for all annotated introns
F-box only protein 48, transcript variant X2
CB1 cannabinoid receptor-interacting protein 1
ewing's tumor-associated antigen 1 homolog, transcript variant X2
ewing's tumor-associated antigen 1 homolog, transcript variant X1
ewing's tumor-associated antigen 1 homolog isoform X1
ewing's tumor-associated antigen 1 isoform X2
homeobox protein Meis1, transcript variant X3
homeobox protein Meis1, transcript variant X1
homeobox protein Meis1, transcript variant X2
sprouty-related, EVH1 domain-containing protein 2, transcript variant X1
sprouty-related, EVH1 domain-containing protein 2, transcript variant X2
sprouty-related, EVH1 domain-containing protein 2, transcript variant X3
sprouty-related, EVH1 domain-containing protein 2, transcript variant X4
sprouty-related, EVH1 domain-containing protein 2 isoform X1
sprouty-related, EVH1 domain-containing protein 2 isoform X2
sprouty-related, EVH1 domain-containing protein 2 isoform X3
sprouty-related, EVH1 domain-containing protein 2 isoform X4
E3 ubiquitin-protein ligase pellino homolog 1
vacuolar protein sorting-associated protein 54, transcript variant X1
vacuolar protein sorting-associated protein 54, transcript variant X5
vacuolar protein sorting-associated protein 54, transcript variant X3
vacuolar protein sorting-associated protein 54, transcript variant X4
vacuolar protein sorting-associated protein 54, transcript variant X2
vacuolar protein sorting-associated protein 54 isoform X1
vacuolar protein sorting-associated protein 54 isoform X2
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X2
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X1
UTP--glucose-1-phosphate uridylyltransferase isoform X1
UTP--glucose-1-phosphate uridylyltransferase isoform X2
malate dehydrogenase 1Aa, NAD (soluble), transcript variant X1
malate dehydrogenase 1Aa, NAD (soluble), transcript variant X2
malate dehydrogenase, cytoplasmic isoform X1
malate dehydrogenase, cytoplasmic isoform X2
homeobox protein OTX1 B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
homeobox protein OTX1 B-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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2, transcript variant X1
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2, transcript variant X2
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2, transcript variant X3
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 34, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 34 isoform X6
ubiquitin carboxyl-terminal hydrolase 34 isoform X5
ubiquitin carboxyl-terminal hydrolase 34 isoform X3
ubiquitin carboxyl-terminal hydrolase 34 isoform X4
ubiquitin carboxyl-terminal hydrolase 34 isoform X2
ubiquitin carboxyl-terminal hydrolase 34 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00405
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
COORDINATES: nucleotide motif:Rfam:12.0:RF00392
COORDINATES: nucleotide motif:Rfam:12.0:RF00560
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
tRNA pseudouridine synthase Pus10, transcript variant X2
tRNA pseudouridine synthase Pus10, transcript variant X1
RAC-gamma serine/threonine-protein kinase, transcript variant X1
RAC-gamma serine/threonine-protein kinase, transcript variant X2
RAC-gamma serine/threonine-protein kinase
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleoplasmin-like protein ANO39
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
COORDINATES: nucleotide motif:Rfam:12.0:RF00056
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF, 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 34 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF, transcript variant X1
nucleosome-remodeling factor subunit BPTF, 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 53 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF isoform X3
nucleosome-remodeling factor subunit BPTF isoform X2
nucleosome-remodeling factor subunit BPTF isoform X1
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytoplasmic phosphatidylinositol transfer protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
LOW QUALITY PROTEIN: cytoplasmic phosphatidylinositol transfer protein 1
26S proteasome non-ATPase regulatory subunit 12
probable helicase with zinc finger domain
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
LOW QUALITY PROTEIN: probable helicase with zinc finger domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel gamma-1 subunit
voltage-dependent calcium channel gamma-4 subunit-like
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
voltage-dependent calcium channel gamma-5 subunit-like
myeloid-associated differentiation marker
testis-expressed protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
testis-expressed protein 2-like, transcript variant X1
testis-expressed protein 2-like, transcript variant X2
testis-expressed protein 2-like isoform X1
testis-expressed protein 2-like isoform X2
coiled-coil domain containing 40, transcript variant X6
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
coiled-coil domain containing 40, 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 6 samples with support for all annotated introns
coiled-coil domain containing 40, transcript variant X1
coiled-coil domain containing 40, 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 9 samples with support for all annotated introns
coiled-coil domain containing 40, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
coiled-coil domain containing 40, transcript variant X2
coiled-coil domain-containing protein 40 isoform X1
coiled-coil domain containing 40, 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 4 samples with support for all annotated introns
coiled-coil domain-containing protein 40 isoform X2
caspase recruitment domain-containing protein 14, 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 38 samples with support for all annotated introns
caspase recruitment domain-containing protein 14, 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 20 samples with support for all annotated introns
caspase recruitment domain-containing protein 14 isoform X1
caspase recruitment domain-containing protein 14 isoform X2
uncharacterized protein C17orf67 homolog
diacylglycerol kinase epsilon, transcript variant X1
diacylglycerol kinase epsilon, transcript variant X2
diacylglycerol kinase epsilon isoform X1
diacylglycerol kinase epsilon isoform X2
E3 ubiquitin/ISG15 ligase TRIM25, transcript variant X2
E3 ubiquitin/ISG15 ligase TRIM25, transcript variant X1
E3 ubiquitin/ISG15 ligase TRIM25 isoform X2
E3 ubiquitin/ISG15 ligase TRIM25 isoform X1
ras GTPase-activating protein nGAP, transcript variant X2
ras GTPase-activating protein nGAP, transcript variant X1
ras GTPase-activating protein nGAP, transcript variant X4
ras GTPase-activating protein nGAP, transcript variant X3
ras GTPase-activating protein nGAP isoform X4
ras GTPase-activating protein nGAP isoform X3
trafficking protein particle complex subunit 5
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 40 samples with support for all annotated introns
zinc finger protein 32, 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 46 samples with support for all annotated introns
zinc finger protein 32, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
E3 ubiquitin-protein ligase SMURF2-like, transcript variant X1
E3 ubiquitin-protein ligase SMURF2-like, transcript variant X2
E3 ubiquitin-protein ligase SMURF2-like, transcript variant X3
E3 ubiquitin-protein ligase SMURF2-like, transcript variant X5
E3 ubiquitin-protein ligase SMURF2-like, transcript variant X4
E3 ubiquitin-protein ligase SMURF2-like isoform X1
E3 ubiquitin-protein ligase SMURF2-like isoform X2
E3 ubiquitin-protein ligase SMURF2-like isoform X3
E3 ubiquitin-protein ligase SMURF2-like isoform X4
E3 ubiquitin-protein ligase SMURF2-like isoform X5
centrosomal protein of 95 kDa, transcript variant X6
centrosomal protein of 95 kDa, transcript variant X2
centrosomal protein of 95 kDa, transcript variant X1
centrosomal protein of 95 kDa, transcript variant X5
centrosomal protein of 95 kDa, transcript variant X4
centrosomal protein of 95 kDa isoform X6
centrosomal protein of 95 kDa isoform X2
centrosomal protein of 95 kDa isoform X1
centrosomal protein of 95 kDa isoform X5
centrosomal protein of 95 kDa isoform X4
centrosomal protein of 95 kDa, transcript variant X3
centrosomal protein of 95 kDa isoform X3
probable ATP-dependent RNA helicase DDX5
signal recognition particle subunit SRP68
acyl-CoA oxidase 1, palmitoyl, transcript variant X1
acyl-CoA oxidase 1, palmitoyl, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 1 isoform X1
peroxisomal acyl-coenzyme A oxidase 1 isoform X2
inactive rhomboid protein 2-like, transcript variant X2
inactive rhomboid protein 2-like, transcript variant X1
inactive rhomboid protein 2-like, transcript variant X6
inactive rhomboid protein 2-like, transcript variant X3
inactive rhomboid protein 2-like, transcript variant X4
inactive rhomboid protein 2-like, transcript variant X5
inactive rhomboid protein 2-like isoform X1
inactive rhomboid protein 2-like isoform 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 4 samples with support for all annotated introns
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like, transcript variant X1
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like, transcript variant X2
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like isoform X1
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like 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 42 samples with support for all annotated introns
uncharacterized LOC112230320, transcript variant X2
uncharacterized LOC112230320, 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
phosphoribosyl pyrophosphate synthase-associated protein 1, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 1, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 1, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X2
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC112230315, transcript variant X2
uncharacterized LOC112230315, transcript variant X1
uncharacterized protein LOC112230315 isoform X2
uncharacterized protein LOC112230315 isoform X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-like, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-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 4 samples with support for all annotated introns
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-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 3 samples with support for all annotated introns
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-like isoform X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-like isoform X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B-like isoform X3
SEC14-like protein 1, transcript variant X1
SEC14-like protein 1, transcript variant X2
SEC14-like protein 1, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: regulatory-associated protein of mTOR
platelet and endothelial cell adhesion molecule 1b
platelet endothelial cell adhesion molecule
protein phosphatase 1 regulatory subunit 27-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 65 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12C, transcript variant X1
protein phosphatase 1 regulatory subunit 12C, transcript variant X2
protein phosphatase 1 regulatory subunit 12C isoform X2
protein phosphatase 1 regulatory subunit 12C isoform X1
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like, transcript variant X1
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like isoform X1
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like, transcript variant X2
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like isoform X2
uncharacterized LOC112245642, transcript variant X4
uncharacterized LOC112245642, transcript variant X3
uncharacterized LOC112245642, transcript variant X2
uncharacterized LOC112245642, transcript variant X1
uncharacterized protein LOC112245642 isoform X2
uncharacterized protein LOC112245642 isoform X1
uncharacterized protein LOC112245642 isoform X3
group XIIB secretory phospholipase A2-like protein, transcript variant X2
group XIIB secretory phospholipase A2-like protein, transcript variant X1
group XIIB secretory phospholipase A2-like protein isoform X1
group XIIB secretory phospholipase A2-like protein isoform X2
uncharacterized LOC112245720, 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 64 samples with support for all annotated introns
uncharacterized LOC112245720, 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 63 samples with support for all annotated introns
G patch domain-containing protein 8, transcript variant X1
G patch domain-containing protein 8, transcript variant X3
G patch domain-containing protein 8, transcript variant X2
G patch domain-containing protein 8 isoform X2
G patch domain-containing protein 8 isoform X1
uncharacterized protein LOC112245517 isoform X3
zinc finger protein 318-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 11 samples with support for all annotated introns
zinc finger protein 318-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 9 samples with support for all annotated introns
uncharacterized protein LOC121841580 isoform X1
zinc finger CCCH domain-containing protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta-like
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 47 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial
zinc finger protein Aiolos-like, transcript variant X3
zinc finger protein Aiolos-like, transcript variant X2
zinc finger protein Aiolos-like, transcript variant X1
zinc finger protein Aiolos-like isoform X2
zinc finger protein Aiolos-like isoform X1
insulin-like growth factor-binding protein 4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X3
C-C chemokine receptor type 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
C-C chemokine receptor type 7, 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 39 samples with support for all annotated introns
C-C chemokine receptor type 7 isoform X1
C-C chemokine receptor type 7 isoform X2
keratin, type I cytoskeletal 18-A, 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 46 samples with support for all annotated introns
keratin, type I cytoskeletal 18-A, 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 47 samples with support for all annotated introns
keratin, type I cytoskeletal 13, transcript variant X6
keratin, type I cytoskeletal 13, transcript variant X8
keratin, type I cytoskeletal 13 isoform X6
keratin, type I cytoskeletal 13 isoform X8
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
keratin, type I cytoskeletal 13, transcript variant X2
keratin, type I cytoskeletal 13, transcript variant X5
keratin, type I cytoskeletal 13, transcript variant X4
keratin, type I cytoskeletal 13, transcript variant X1
keratin, type I cytoskeletal 13, transcript variant X7
keratin, type I cytoskeletal 13 isoform X2
keratin, type I cytoskeletal 13 isoform X5
keratin, type I cytoskeletal 13 isoform X7
keratin, type I cytoskeletal 13 isoform X4
keratin, type I cytoskeletal 13 isoform X1
keratin, type I cytoskeletal 13, transcript variant X3
keratin, type I cytoskeletal 13 isoform X3
keratin, type I cytoskeletal 13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
keratin, type I cytoskeletal 13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
keratin, type I cytoskeletal 19-like isoform X2
keratin, type I cytoskeletal 42-like, 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 19 samples with support for all annotated introns
keratin, type I cytoskeletal 42-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
keratin, type I cytoskeletal 42-like isoform X1
keratin, type I cytoskeletal 42-like isoform X2
keratin, type I cytoskeletal 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
keratin, type I cytoskeletal 13-like isoform X1
cholecystokinin-like, transcript variant X3
cholecystokinin-like, transcript variant X2
cholecystokinin-like, transcript variant X1
trafficking kinesin-binding protein 1, transcript variant X1
trafficking kinesin-binding protein 1, transcript variant X3
trafficking kinesin-binding protein 1, transcript variant X2
trafficking kinesin-binding protein 1, transcript variant X4
trafficking kinesin-binding protein 1 isoform X1
trafficking kinesin-binding protein 1 isoform X2
trafficking kinesin-binding protein 1, transcript variant X8
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
trafficking kinesin-binding protein 1, 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 13 samples with support for all annotated introns
trafficking kinesin-binding protein 1 isoform X5
trafficking kinesin-binding protein 1 isoform X3
trafficking kinesin-binding protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
trafficking kinesin-binding protein 1, 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 15 samples with support for all annotated introns
trafficking kinesin-binding protein 1 isoform X4
WAS/WASL-interacting protein family member 2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: WAS/WASL-interacting protein family member 2
puromycin-sensitive aminopeptidase, transcript variant X4
puromycin-sensitive aminopeptidase, transcript variant X3
puromycin-sensitive aminopeptidase, transcript variant X2
puromycin-sensitive aminopeptidase, transcript variant X1
puromycin-sensitive aminopeptidase isoform X4
puromycin-sensitive aminopeptidase isoform X2
puromycin-sensitive aminopeptidase isoform X3
puromycin-sensitive aminopeptidase isoform X1
39S ribosomal protein L45, mitochondrial
suppressor of cytokine signaling 7, 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 28 samples with support for all annotated introns
suppressor of cytokine signaling 7, 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 26 samples with support for all annotated introns
suppressor of cytokine signaling 7, 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 16 samples with support for all annotated introns
suppressor of cytokine signaling 7 isoform X1
suppressor of cytokine signaling 7 isoform X2
suppressor of cytokine signaling 7 isoform X3
transcription factor Sp2, transcript variant X1
transcription factor Sp2, transcript variant X2
ATP-binding cassette sub-family C member 10, transcript variant X2
ATP-binding cassette sub-family C member 10, transcript variant X1
ATP-binding cassette sub-family C member 10 isoform X2
ATP-binding cassette sub-family C member 10 isoform X1
neuroblast differentiation-associated protein AHNAK-like, transcript variant X1
neuroblast differentiation-associated protein AHNAK-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 42 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK-like isoform X1
neuroblast differentiation-associated protein AHNAK-like isoform X2
neuroblast differentiation-associated protein AHNAK-like
39S ribosomal protein L4, mitochondrial-like, transcript variant X1
39S ribosomal protein L4, mitochondrial-like, transcript variant X2
39S ribosomal protein L4, mitochondrial-like, transcript variant X3
39S ribosomal protein L4, mitochondrial-like isoform X3
hydrolethalus syndrome protein 1 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 57 samples with support for all annotated introns
protein tyrosine phosphatase type IVA 1, transcript variant X2
protein tyrosine phosphatase type IVA 1, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGDU01482491.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1180 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1045 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
rho-related GTP-binding protein RhoU-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 10 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGDU01694776.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1405 bases not found in genome assembly; 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 59 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1278 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L
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 59 samples with support for all annotated introns
protein LTV1 homolog, transcript variant X2
protein LTV1 homolog, transcript variant X1
small integral membrane protein 28-like, transcript variant X1
uncharacterized protein LOC112245820 isoform X1
small integral membrane protein 28-like, transcript variant X2
small integral membrane protein 28-like isoform X2
UPF0575 protein C19orf67 homolog, transcript variant X2
UPF0575 protein C19orf67 homolog, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 7-like, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 7-like, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 7-like isoform X1
dual specificity mitogen-activated protein kinase kinase 7-like isoform X2
dual specificity mitogen-activated protein kinase kinase 7-like, transcript variant X3
dual specificity mitogen-activated protein kinase kinase 7-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 35% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein Gfi-1b, transcript variant X2
zinc finger protein Gfi-1b, transcript variant X1
EVI5-like protein, 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
EVI5-like protein, 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 5 samples with support for all annotated introns
EVI5-like protein, 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 8 samples with support for all annotated introns
EVI5-like protein, 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 9 samples with support for all annotated introns
EVI5-like protein, transcript variant X4
uncharacterized LOC121841576, transcript variant X1
uncharacterized LOC121841576, transcript variant X5
uncharacterized LOC121841576, transcript variant X4
uncharacterized LOC121841576, transcript variant X2
uncharacterized LOC121841576, transcript variant X3
uncharacterized protein LOC121841576 isoform X4
uncharacterized protein LOC121841576 isoform X3
uncharacterized protein LOC121841576 isoform X1
uncharacterized protein LOC121841576 isoform X2
uncharacterized LOC112245818, transcript variant X1
uncharacterized LOC112245818, transcript variant X2
uncharacterized protein LOC112245818 isoform X2
uncharacterized protein LOC112245818 isoform X1
LOW QUALITY PROTEIN: ATP-dependent RNA helicase DDX39A
CCN family member 1, transcript variant X1
CCN family member 1, transcript variant X2
RAB11 family interacting protein 4 (class II) a, transcript variant X1
RAB11 family interacting protein 4 (class II) a, transcript variant X2
rab11 family-interacting protein 4A isoform X1
rab11 family-interacting protein 4A isoform X2
RAB11 family interacting protein 4 (class II) a, transcript variant X3
rab11 family-interacting protein 4A isoform X3
polycomb protein suz12-B, transcript variant X2
polycomb protein suz12-B, transcript variant X1
arf-GAP with dual PH domain-containing protein 2
tripartite motif-containing protein 65, transcript variant X1
tripartite motif-containing protein 65, transcript variant X2
tripartite motif-containing protein 65, transcript variant X4
tripartite motif-containing protein 65 isoform X1
tripartite motif-containing protein 65 isoform X2
tripartite motif-containing protein 65, transcript variant X3
tripartite motif-containing protein 65 isoform X3
fibronectin type III and SPRY domain-containing protein 2 isoform X4
mitochondrial Rho GTPase 1-A, transcript variant X2
mitochondrial Rho GTPase 1-A, transcript variant X1
mitochondrial Rho GTPase 1-A, transcript variant X3
rhomboid-related protein 3-like, transcript variant X1
rhomboid-related protein 3-like, transcript variant X2
rhomboid-related protein 3-like, transcript variant X3
rhomboid-related protein 3-like isoform X1
rhomboid-related protein 3-like isoform X2
rhomboid-related protein 3-like isoform X3
BUB3-interacting and GLEBS motif-containing protein ZNF207, transcript variant X1
BUB3-interacting and GLEBS motif-containing protein ZNF207, transcript variant X2
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X1
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00562
uncharacterized LOC112230292, transcript variant X1
uncharacterized LOC112230292, transcript variant X2
uncharacterized protein LOC112230292 isoform X1
uncharacterized protein LOC112230292 isoform X2
trinucleotide repeat-containing gene 6C protein-like
LOW QUALITY PROTEIN: trinucleotide repeat-containing gene 6C protein-like
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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
neuronal-specific septin-3-like isoform X2
neuronal-specific septin-3-like isoform X3
neuronal-specific septin-3-like isoform 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 21 samples with support for all annotated introns
jupiter microtubule associated homolog 1
ADP-ribosylation factor-binding protein GGA3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
ubiquitin carboxyl-terminal hydrolase 43-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 43-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 43-like isoform X2
ubiquitin carboxyl-terminal hydrolase 43-like isoform X1
cilia- and flagella-associated protein 52-like
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 28 samples with support for all annotated introns
phosphoinositide 3-kinase regulatory subunit 5, transcript variant X3
phosphoinositide 3-kinase regulatory subunit 5, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 5, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 5
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X3
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X4
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 6 isoform X1
phosphoinositide 3-kinase regulatory subunit 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
40S ribosomal protein SA, transcript variant X2
40S ribosomal protein SA, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00568
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
mitochondrial glycine transporter B, transcript variant X4
mitochondrial glycine transporter B, transcript variant X5
mitochondrial glycine transporter B, transcript variant X3
mitochondrial glycine transporter B, transcript variant X1
mitochondrial glycine transporter B, transcript variant X2
mitochondrial glycine transporter B, transcript variant X6
mitochondrial glycine transporter B, transcript variant X7
mitochondrial glycine transporter B isoform X2
mitochondrial glycine transporter B isoform X1
patatin-like phospholipase domain-containing protein 6, transcript variant X5
patatin-like phospholipase domain-containing protein 6, transcript variant X4
patatin-like phospholipase domain-containing protein 6, transcript variant X1
patatin-like phospholipase domain-containing protein 6, transcript variant X3
patatin-like phospholipase domain-containing protein 6, transcript variant X2
patatin-like phospholipase domain-containing protein 6 isoform X4
patatin-like phospholipase domain-containing protein 6 isoform X2
patatin-like phospholipase domain-containing protein 6 isoform X3
patatin-like phospholipase domain-containing protein 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
neuronal vesicle trafficking-associated protein 1
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 16 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
VPS10 domain-containing receptor SorCS1-like, transcript variant X2
VPS10 domain-containing receptor SorCS1-like, transcript variant X3
VPS10 domain-containing receptor SorCS1-like, transcript variant X1
VPS10 domain-containing receptor SorCS1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
sortilin related VPS10 domain containing receptor 3
SH3 and PX domain-containing protein 2A, transcript variant X3
SH3 and PX domain-containing protein 2A, transcript variant X2
SH3 and PX domain-containing protein 2A, transcript variant X1
SH3 and PX domain-containing protein 2A, transcript variant X4
SH3 and PX domain-containing protein 2A isoform X2
SH3 and PX domain-containing protein 2A isoform X3
SH3 and PX domain-containing protein 2A isoform X1
SH3 and PX domain-containing protein 2A isoform X4
STE20-like serine/threonine-protein kinase, transcript variant X1
STE20-like serine/threonine-protein kinase, transcript variant X2
STE20-like serine/threonine-protein kinase, transcript variant X3
STE20-like serine/threonine-protein kinase, transcript variant X4
STE20-like serine/threonine-protein kinase isoform X1
STE20-like serine/threonine-protein kinase isoform X2
STE20-like serine/threonine-protein kinase isoform X4
STE20-like serine/threonine-protein kinase isoform 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 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: ras and Rab interactor 2-like
ribonuclease inhibitor-like, transcript variant X2
ribonuclease inhibitor-like, transcript variant X1
ribonuclease inhibitor-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12, transcript variant X2
NACHT, LRR and PYD domains-containing protein 12, transcript variant X1
NACHT, LRR and PYD domains-containing protein 12, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily KQT member 5, transcript variant X3
potassium voltage-gated channel subfamily KQT member 5, transcript variant X1
potassium voltage-gated channel subfamily KQT member 5, transcript variant X2
potassium voltage-gated channel subfamily KQT member 5 isoform X2
potassium voltage-gated channel subfamily KQT member 5 isoform X1
potassium voltage-gated channel subfamily KQT member 4 isoform X3
regulating synaptic membrane exocytosis protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like, 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, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like, transcript variant X7
regulating synaptic membrane exocytosis protein 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like, transcript variant X2
regulating synaptic membrane exocytosis protein 1-like, transcript variant X8
regulating synaptic membrane exocytosis protein 1-like, transcript variant X4
regulating synaptic membrane exocytosis protein 1-like, transcript variant X9
regulating synaptic membrane exocytosis protein 1-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like, transcript variant X10
regulating synaptic membrane exocytosis protein 1-like, transcript variant X11
regulating synaptic membrane exocytosis protein 1-like, transcript variant X1
regulating synaptic membrane exocytosis protein 1-like, transcript variant X13
regulating synaptic membrane exocytosis protein 1-like, transcript variant X14
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
regulating synaptic membrane exocytosis protein 1-like, transcript variant X15
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 7 samples with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like isoform X5
regulating synaptic membrane exocytosis protein 1-like isoform X16
regulating synaptic membrane exocytosis protein 1-like isoform X3
regulating synaptic membrane exocytosis protein 1-like isoform X7
regulating synaptic membrane exocytosis protein 1-like isoform X6
regulating synaptic membrane exocytosis protein 1-like isoform X2
regulating synaptic membrane exocytosis protein 1-like isoform X8
regulating synaptic membrane exocytosis protein 1-like isoform X4
regulating synaptic membrane exocytosis protein 1-like isoform X9
regulating synaptic membrane exocytosis protein 1-like isoform X13
regulating synaptic membrane exocytosis protein 1-like isoform X12
regulating synaptic membrane exocytosis protein 1-like isoform X10
regulating synaptic membrane exocytosis protein 1-like isoform X11
regulating synaptic membrane exocytosis protein 1-like isoform X1
regulating synaptic membrane exocytosis protein 1-like isoform X14
regulating synaptic membrane exocytosis protein 1-like isoform X15
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
solute carrier family 2, facilitated glucose transporter member 9-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 4 samples with support for all annotated introns
deleted in primary ciliary dyskinesia homolog (mouse)
WW domain binding protein 1-like b, transcript variant X1
WW domain binding protein 1-like isoform X1
WW domain binding protein 1-like b, transcript variant X2
WW domain binding protein 1-like isoform X2
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
LOW QUALITY PROTEIN: metal transporter CNNM2
cytosolic purine 5'-nucleotidase-like, transcript variant X1
cytosolic purine 5'-nucleotidase-like, transcript variant X2
cytosolic purine 5'-nucleotidase-like, transcript variant X6
cytosolic purine 5'-nucleotidase-like, transcript variant X3
cytosolic purine 5'-nucleotidase-like, transcript variant X5
cytosolic purine 5'-nucleotidase-like, transcript variant X4
cytosolic purine 5'-nucleotidase-like, transcript variant X7
cytosolic purine 5'-nucleotidase-like isoform X1
cytosolic purine 5'-nucleotidase-like isoform X2
cytosolic purine 5'-nucleotidase-like isoform X3
cytosolic purine 5'-nucleotidase-like isoform X4
cytosolic purine 5'-nucleotidase-like isoform X5
TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 5
ATP synthase membrane subunit K, mitochondrial
protein RRP5 homolog, transcript variant X2
protein RRP5 homolog, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00067
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
RING finger protein 122, transcript variant X1
RING finger protein 122, transcript variant X2
calcium homeostasis modulator protein 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 7 samples with support for all annotated introns
calcium homeostasis modulator protein 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, including 23 samples with support for all annotated introns
inositol 1,4,5-trisphosphate receptor-interacting protein-like
zona pellucida sperm-binding protein 3-like
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
inactive phospholipase D5-like, transcript variant X1
inactive phospholipase D5-like, transcript variant X2
inactive phospholipase D5-like isoform X1
inactive phospholipase D5-like isoform X2
centrosomal protein of 170 kDa-like, transcript variant X1
centrosomal protein of 170 kDa-like, transcript variant X2
centrosomal protein of 170 kDa-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5-demethoxyubiquinone hydroxylase, mitochondrial-like
multidrug resistance-associated protein 1, transcript variant X2
multidrug resistance-associated protein 1, transcript variant X3
multidrug resistance-associated protein 1 isoform X2
multidrug resistance-associated protein 1, transcript variant X1
multidrug resistance-associated protein 1 isoform X1
nuclear distribution protein nudE homolog 1, transcript variant X1
nuclear distribution protein nudE homolog 1, transcript variant X2
nuclear distribution protein nudE homolog 1 isoform X1
nuclear distribution protein nudE homolog 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
nuclear distribution protein nudE homolog 1 isoform X2
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1, transcript variant X3
meiosis regulator and mRNA stability factor 1, transcript variant X4
meiosis regulator and mRNA stability factor 1, transcript variant X5
meiosis regulator and mRNA stability factor 1, transcript variant X6
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X2
meiosis regulator and mRNA stability factor 1 isoform X5
meiosis regulator and mRNA stability factor 1 isoform X3
meiosis regulator and mRNA stability factor 1 isoform X6
meiosis regulator and mRNA stability factor 1 isoform 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
uncharacterized LOC112230134, transcript variant X2
uncharacterized LOC112230134, transcript variant X1
target of Myb protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
target of Myb protein 1, transcript variant X1
target of Myb protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X3
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X4
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X6
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X5
mediator of RNA polymerase II transcription subunit 15-like, transcript variant X7
mediator of RNA polymerase II transcription subunit 15-like isoform X1
chromatin modification-related protein eaf-1-like isoform X3
mediator of RNA polymerase II transcription subunit 15-like isoform X2
mediator of RNA polymerase II transcription subunit 15-like isoform X4
mediator of RNA polymerase II transcription subunit 15-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum resident protein 27-like
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like
RNA binding protein fox-1 homolog 2, transcript variant X2
RNA binding protein fox-1 homolog 2, transcript variant X7
RNA binding protein fox-1 homolog 2, transcript variant X3
RNA binding protein fox-1 homolog 2, transcript variant X1
RNA binding protein fox-1 homolog 2, transcript variant X4
RNA binding protein fox-1 homolog 2, transcript variant X8
RNA binding protein fox-1 homolog 2 isoform X2
RNA binding protein fox-1 homolog 2 isoform X4
RNA binding protein fox-1 homolog 2 isoform X3
RNA binding protein fox-1 homolog 2 isoform X1
RNA binding protein fox-1 homolog 2 isoform X6
RNA binding protein fox-1 homolog 2, transcript variant X5
RNA binding protein fox-1 homolog 2, transcript variant X6
RNA binding protein fox-1 homolog 2 isoform X5
zona pellucida sperm-binding protein 1-like
ras-associated and pleckstrin homology domains-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
40-kDa huntingtin-associated protein, transcript variant X1
40-kDa huntingtin-associated protein, transcript variant X2
40-kDa huntingtin-associated protein isoform X1
40-kDa huntingtin-associated protein isoform X2
uncharacterized si:ch211-243a20.4, transcript variant X2
uncharacterized si:ch211-243a20.4, transcript variant X1
uncharacterized protein si:ch211-243a20.4 isoform X2
uncharacterized protein si:ch211-243a20.4 isoform X1
uncharacterized LOC121841621, transcript variant X2
uncharacterized LOC121841621, transcript variant X1
glutamate receptor, ionotropic, N-methyl D-aspartate 2B, genome duplicate b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glutamate receptor, ionotropic, N-methyl D-aspartate 2B, genome duplicate b
activating transcription factor 7-interacting protein 1
serine hydrolase-like protein, transcript variant X2
serine hydrolase-like protein, transcript variant X4
serine hydrolase-like protein, transcript variant X3
serine hydrolase-like protein, transcript variant X1
serine hydrolase-like protein, transcript variant X5
serine hydrolase-like protein isoform X3
serine hydrolase-like protein isoform X2
serine hydrolase-like protein isoform X1
serine hydrolase-like protein isoform X4
centromere protein M, transcript variant X2
centromere protein M, transcript variant X1
putative RNA-binding protein Luc7-like 2
TRIO and F-actin-binding protein, transcript variant X2
TRIO and F-actin-binding protein, transcript variant X1
TRIO and F-actin-binding protein isoform X2
TRIO and F-actin-binding protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
guided entry of tail-anchored proteins factor 3, ATPase
protein N-terminal asparagine amidohydrolase-like
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X1
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X2
ADP-ribosylation factor-binding protein GGA1 isoform X1
ADP-ribosylation factor-binding protein GGA1 isoform X2
linkage group 32 C22orf23 homolog, transcript variant X1
linkage group 32 C22orf23 homolog, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcription factor SOX-10
ATP-sensitive inward rectifier potassium channel 12-like
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 7 samples with support for all annotated introns