Xiphias gladius isolate SHS-SW01 ecotype Sanya breed wild chromosome 13, ASM1685928v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Carangaria; Istiophoriformes; Xiphiidae; Xiphias.
The genomes of two billfishes provide insights into the evolution of endothermy in teleosts
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM029147.1.\nAssembly name: ASM1685928v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Institute of Deep-Sea Science\nand Engineering, Chinese Academy of Sciences on 2021/02/12. The\noriginal whole-genome shotgun project has the accession\nJADGDB000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Institute of Deep-Sea Science and\n Engineering, Chinese Academy of Sciences\nAssembly Date :: 01-JAN-2020\nAssembly Method :: NextDenovo v. 2.0; wdtbg v. 2.0; 3D-DNA\n v. 180114\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 79x\nSequencing Technology :: Oxford Nanopore GridION; Illumina HiSeq;\n Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Xiphias gladius Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.6\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
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
uncharacterized LOC120797966, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC120797966, transcript variant X2
uncharacterized LOC120797966, transcript variant X3
uncharacterized LOC120797966, 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 3 samples with support for all annotated introns
CD276 antigen homolog, 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
CD276 antigen homolog, 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 8 samples with support for all annotated introns
uncharacterized protein LOC120798276 isoform X1
sentrin-specific protease 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sentrin-specific protease 7-like, transcript variant X1
interphotoreceptor matrix proteoglycan 2-like, 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
interphotoreceptor matrix proteoglycan 2-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 1 sample with support for all annotated introns
interphotoreceptor matrix proteoglycan 2-like
target of Nesh-SH3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
target of Nesh-SH3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
target of Nesh-SH3-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 4 samples with support for all annotated introns
mid1-interacting protein 1-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mid1-interacting protein 1-B-like, transcript variant X3
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
mid1-interacting protein 1-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
xanthine dehydrogenase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
xanthine dehydrogenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
xanthine dehydrogenase/oxidase isoform X2
xanthine dehydrogenase/oxidase isoform X1
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 47% 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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adenylate cyclase type 8-like
DnaJ (Hsp40) homolog, subfamily C, member 27
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
T-cell surface glycoprotein CD3 zeta chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
T-cell surface glycoprotein CD3 zeta chain-like, transcript variant X1
T-cell surface glycoprotein CD3 zeta chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
T-cell surface glycoprotein CD3 zeta chain-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
T-cell surface glycoprotein CD3 zeta chain-like, transcript variant X4
T-cell surface glycoprotein CD3 zeta chain-like isoform X1
T-cell surface glycoprotein CD3 zeta chain-like isoform X2
cellular repressor of E1A-stimulated genes 1
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 8 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB2 isoform X2
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB2 isoform X1
uncharacterized LOC120797956, transcript variant X4
uncharacterized LOC120797956, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC120797956 isoform X3
uncharacterized LOC120797956, transcript variant X2
uncharacterized LOC120797956, transcript variant X1
uncharacterized protein LOC120797956 isoform X1
uncharacterized protein LOC120797956 isoform X2
uncharacterized protein LOC120797956 isoform X4
coagulation factor VII, like, transcript variant X1
coagulation factor VII, like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
venom prothrombin activator notecarin-D1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
T-box transcription factor TBX19-like, transcript variant X3
T-box transcription factor TBX19-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
T-box transcription factor TBX19-like, transcript variant X2
T-box transcription factor TBX19-like isoform X2
T-box transcription factor TBX19-like isoform X1
T-box transcription factor TBX19-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
T-box transcription factor TBX19-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 271-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 8 samples with support for all annotated introns
zinc finger protein 271-like, transcript variant X2
oocyte zinc finger protein XlCOF22-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 125 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X4
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 7 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like isoform X2
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC120798232, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC120798232, transcript variant X3
uncharacterized LOC120798232, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SH3 domain-containing YSC84-like protein 1
solute carrier family 22 member 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 22 member 13, 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 1 sample with support for all annotated introns
solute carrier family 22 member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 22 member 13 isoform X1
organic cation transporter-like protein isoform X2
uncharacterized LOC120798227, 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
uncharacterized protein LOC120798227 isoform X1
uncharacterized LOC120798227, transcript variant X3
uncharacterized LOC120798227, transcript variant X2
uncharacterized protein LOC120798227 isoform X3
uncharacterized protein LOC120798227 isoform 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 7 samples with support for all annotated introns
eukaryotic translation initiation factor 5B
beta-carotene oxygenase 1, like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-carotene oxygenase 1, like, transcript variant X2
beta-carotene oxygenase 1, like isoform X1
beta-carotene oxygenase 1, like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
IQ motif containing B1, 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 3 samples with support for all annotated introns
IQ motif containing B1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ motif containing B1, transcript variant X3
IQ calmodulin-binding motif-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
pro-opiomelanocortin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pro-opiomelanocortin, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pro-opiomelanocortin, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pro-opiomelanocortin, transcript variant X6
pro-opiomelanocortin, transcript variant X4
pro-opiomelanocortin, transcript variant X3
pro-opiomelanocortin, transcript variant X1
gastrulation brain homeobox 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gastrulation brain homeobox 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X2
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related protein ralB-B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related protein ralB-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ras-related protein ralB-B-like, transcript variant X2
ras-related protein ralB-B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
CLIP-associating protein 1-B-like, 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 1 sample with support for all annotated introns
CLIP-associating protein 1-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
CLIP-associating protein 1-B-like isoform X2
CLIP-associating protein 1-B-like isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00618
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
H(+)/Cl(-) exchange transporter 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
H(+)/Cl(-) exchange transporter 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
H(+)/Cl(-) exchange transporter 4 isoform X1
H(+)/Cl(-) exchange transporter 4 isoform X2
NLR family CARD domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 169 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A and acyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase A and acyltransferase 1-like, transcript variant X1
phospholipase A and acyltransferase 1 isoform X2
phospholipase A and acyltransferase 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual specificity phosphatase 27, 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 1 sample with support for all annotated introns
dual specificity phosphatase 27, transcript variant X1
serine/threonine/tyrosine-interacting-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 84% 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: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
nonhomologous end-joining factor 1, transcript variant X2
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
nonhomologous end-joining factor 1, 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 2 samples with support for all annotated introns
non-homologous end-joining factor 1 isoform X2
non-homologous end-joining factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 94% 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: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
myc box-dependent-interacting protein 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 597 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 601 Proteins, and 92% 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: 598 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase-like N
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
aspartyl aminopeptidase, 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 8 samples with support for all annotated introns
aspartyl aminopeptidase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
aspartyl aminopeptidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 96% 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: 25 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein Shroom2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein Shroom2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein Shroom2-like, 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 2 samples with support for all annotated introns
protein Shroom2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein Shroom2-like, transcript variant X5
protein Shroom2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein Shroom2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein Shroom2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal transducer and activator of transcription 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
signal transducer and activator of transcription 1a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
signal transducer and activator of transcription 1a, transcript variant X3
signal transducer and activator of transcription 1a, transcript variant X4
signal transducer and activator of transcription 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
signal transducer and activator of transcription 1a isoform X3
signal transducer and activator of transcription 1a isoform X4
signal transducer and activator of transcription 1a isoform X5
signal transducer and activator of transcription 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
signal transducer and activator of transcription 1a isoform X1
signal transducer and activator of transcription 1a isoform X2
signal transducer and activator of transcription 1a isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NGFI-A binding protein 1b (EGR1 binding protein 1)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-A-like, transcript variant X2
major facilitator superfamily domain-containing protein 6-A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-A-like isoform X1
major facilitator superfamily domain-containing protein 6-A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-A-like isoform X2
leucine-rich repeat-containing protein 4C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 55% coverage of the annotated genomic feature by RNAseq alignments
aryl hydrocarbon receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aryl hydrocarbon receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
aryl hydrocarbon receptor-like isoform X1
aryl hydrocarbon receptor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
S100 calcium binding protein, beta (neural)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
SH3-domain binding protein 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SH3-domain binding protein 4a, transcript variant X3
SH3-domain binding protein 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
aldehyde oxidase 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
aldehyde oxidase 6, transcript variant X4
aldehyde oxidase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
aldehyde oxidase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
aldehyde oxidase 1-like, transcript variant X4
aldehyde oxidase 1-like, transcript variant X6
aldehyde oxidase 1-like, transcript variant X3
aldehyde oxidase 1-like, transcript variant X5
aldehyde oxidase 1-like, transcript variant X2
aldehyde oxidase 1-like, transcript variant X1
aldehyde oxidase 1-like, transcript variant X7
basic leucine zipper and W2 domains 1a, transcript variant X1
basic leucine zipper and W2 domain-containing protein 1-A isoform X1
basic leucine zipper and W2 domains 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
basic leucine zipper and W2 domain-containing protein 1-A isoform X2
basic helix-loop-helix transcription factor scleraxis
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
von Willebrand factor D and EGF domain-containing protein, transcript variant X4
von Willebrand factor D and EGF domain-containing protein, transcript variant X2
von Willebrand factor D and EGF domain-containing protein, transcript variant X3
von Willebrand factor D and EGF domain-containing protein, transcript variant X1
von Willebrand factor D and EGF domain-containing protein isoform X4
von Willebrand factor D and EGF domain-containing protein isoform X2
von Willebrand factor D and EGF domain-containing protein isoform X3
von Willebrand factor D and EGF domain-containing protein isoform X1
uncharacterized LOC120798353, transcript variant X3
uncharacterized LOC120798353, transcript variant X5
uncharacterized LOC120798353, transcript variant X10
uncharacterized LOC120798353, transcript variant X8
uncharacterized LOC120798353, transcript variant X6
uncharacterized LOC120798353, transcript variant X2
uncharacterized LOC120798353, transcript variant X9
uncharacterized LOC120798353, transcript variant X1
uncharacterized LOC120798353, transcript variant X4
uncharacterized LOC120798353, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger E-box binding homeobox 2b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger E-box binding homeobox 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger E-box binding homeobox 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger E-box binding homeobox 2b, transcript variant X1
zinc finger E-box binding homeobox 2b, transcript variant X6
zinc finger E-box-binding homeobox 2b isoform X4
zinc finger E-box-binding homeobox 2b isoform X2
zinc finger E-box-binding homeobox 2b isoform X3
zinc finger E-box-binding homeobox 2b isoform X1
zinc finger E-box-binding homeobox 2b isoform X6
zinc finger E-box binding homeobox 2b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger E-box-binding homeobox 2b isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
origin recognition complex, subunit 4, transcript variant X2
origin recognition complex, subunit 4, transcript variant X3
origin recognition complex, subunit 4, transcript variant X1
methyl-CpG-binding domain protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C7orf57 homolog, transcript variant X3
uncharacterized protein C7orf57 homolog, 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 8 samples with support for all annotated introns
uncharacterized protein C7orf57 homolog, 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 4 samples with support for all annotated introns
uncharacterized protein C7orf57 homolog isoform X1
uncharacterized protein C7orf57 homolog isoform X2
four and a half LIM domains protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
PI-PLC X domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 96% 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NLR family CARD domain-containing protein 3-like
collagen alpha-1(XVIII) chain-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
collagen alpha-1(XVIII) chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
collagen alpha-1(XVIII) chain-like, transcript variant X2
collagen alpha-1(XVIII) chain-like, transcript variant X1
collagen alpha-1(XVIII) chain-like isoform X4
collagen alpha-1(XVIII) chain-like isoform X3
collagen alpha-1(XVIII) chain-like isoform X2
collagen alpha-1(XVIII) chain-like isoform X1
uncharacterized LOC120798047, transcript variant X12
uncharacterized LOC120798047, transcript variant X3
uncharacterized LOC120798047, transcript variant X6
uncharacterized LOC120798047, transcript variant X9
uncharacterized LOC120798047, transcript variant X8
uncharacterized LOC120798047, transcript variant X10
uncharacterized LOC120798047, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC120798047, transcript variant X11
uncharacterized LOC120798047, transcript variant X5
uncharacterized LOC120798047, transcript variant X4
uncharacterized LOC120798047, transcript variant X2
uncharacterized LOC120798047, transcript variant X1
uncharacterized protein LOC120798047 isoform X2
uncharacterized protein LOC120798047 isoform X12
uncharacterized protein LOC120798047 isoform X3
uncharacterized protein LOC120798047 isoform X6
uncharacterized protein LOC120798047 isoform X9
uncharacterized protein LOC120798047 isoform X8
uncharacterized protein LOC120798047 isoform X10
uncharacterized protein LOC120798047 isoform X7
uncharacterized protein LOC120798047 isoform X11
uncharacterized protein LOC120798047 isoform X5
uncharacterized protein LOC120798047 isoform X4
uncharacterized protein LOC120798047 isoform X1
abl interactor 2-like, transcript variant X1
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, including 2 samples with support for all annotated introns
abl interactor 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
abl interactor 2-like, transcript variant X2
abl interactor 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 96% coverage of the annotated genomic feature by RNAseq alignments
alsin Rho guanine nucleotide exchange factor ALS2 b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
inositol polyphosphate-4-phosphatase type I A-like, transcript variant X4
inositol polyphosphate-4-phosphatase type I A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inositol polyphosphate-4-phosphatase type I A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inositol polyphosphate-4-phosphatase type I A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inositol polyphosphate-4-phosphatase type I A-like, transcript variant X2
inositol polyphosphate-4-phosphatase type I A-like isoform X2
inositol polyphosphate-4-phosphatase type I A-like isoform X3
inositol polyphosphate-4-phosphatase type I A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 537 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
glycerol-3-phosphate dehydrogenase 2 (mitochondrial), transcript variant X2
glycerol-3-phosphate dehydrogenase 2 (mitochondrial), transcript variant X1
glycerol-3-phosphate dehydrogenase 2 (mitochondrial), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase, mitochondrial isoform X1
glycerol-3-phosphate dehydrogenase, mitochondrial isoform X2
fibronectin type III domain-containing protein 5-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins
leucine-rich repeat-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATPase copper transporting beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATPase copper transporting beta, transcript variant X2
transfer RNA arginine (anticodon CCU); 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); 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: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
calcitonin gene-related peptide type 1 receptor-like, transcript variant X2
calcitonin gene-related peptide type 1 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcitonin gene-related peptide type 1 receptor-like isoform X1
calcitonin gene-related peptide type 1 receptor-like isoform X2
zinc finger, SWIM-type containing 2, transcript variant X5
zinc finger, SWIM-type containing 2, 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 7 samples with support for all annotated introns
zinc finger, SWIM-type containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase ZSWIM2 isoform X3
E3 ubiquitin-protein ligase ZSWIM2 isoform X1
E3 ubiquitin-protein ligase ZSWIM2 isoform X4
zinc finger, SWIM-type containing 2, transcript variant X3
zinc finger, SWIM-type containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger, SWIM-type containing 2, transcript variant X4
E3 ubiquitin-protein ligase ZSWIM2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
SLAIN motif-containing protein 1-like, transcript variant X3
SLAIN motif-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SLAIN motif-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SLAIN motif-containing protein 1-like, transcript variant X4
SLAIN motif-containing protein 1-like isoform X3
SLAIN motif-containing protein 1-like isoform X2
SLAIN motif-containing protein 1-like isoform X1
SLAIN motif-containing protein 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
POU domain, class 3, transcription factor 3-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ly6/PLAUR domain-containing protein 1-like
nck-associated protein 5-like, transcript variant X3
nck-associated protein 5-like, transcript variant X1
nck-associated protein 5-like, transcript variant X2
nck-associated protein 5-like, transcript variant X4
nck-associated protein 5-like isoform X3
nck-associated protein 5-like isoform X1
nck-associated protein 5-like isoform X2
nck-associated protein 5-like isoform X4
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, 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 8 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like isoform X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like isoform X2
oxysterol binding protein-like 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
oxysterol-binding protein-related protein 11 isoform X2
oxysterol binding protein-like 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
oxysterol-binding protein-related protein 11 isoform X1
uncharacterized LOC120798178, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC120798178, transcript variant X2
uncharacterized LOC120798178, transcript variant X4
uncharacterized LOC120798178, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
microtubule-associated protein tau-like, transcript variant X2
microtubule-associated protein tau-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA dehydrogenase long chain, transcript variant X2
acyl-CoA dehydrogenase long chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
acyl-CoA dehydrogenase long chain, transcript variant X3
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
myosin, light polypeptide 3, skeletal muscle
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 129 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LanC antibiotic synthetase component C-like 1 (bacterial)
receptor tyrosine-protein kinase erbB-4-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
receptor activity-modifying protein 1-like
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
Krueppel-like factor 7, transcript variant X1
Krueppel-like factor 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic AMP-responsive element-binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cyclic AMP-responsive element-binding protein 1, transcript variant X2
cyclic AMP-responsive element-binding protein 1
methyltransferase like 21A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
methyltransferase like 21A, transcript variant X1
protein N-lysine methyltransferase METTL21A isoform X1
protein N-lysine methyltransferase METTL21A isoform X2
insulin-like growth factor binding protein 5a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
insulin-like growth factor-binding protein 5a
insulin-like growth factor binding protein 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
insulin-like growth factor-binding protein 2-A
serine/threonine kinase 11 interacting protein, transcript variant X1
serine/threonine kinase 11 interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
serine/threonine kinase 11 interacting protein, transcript variant X2
serine/threonine kinase 11 interacting protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase 11-interacting protein isoform X1
serine/threonine-protein kinase 11-interacting protein isoform X3
serine/threonine-protein kinase 11-interacting protein isoform X2
serine/threonine-protein kinase 11-interacting protein isoform X4
gap junction gamma-1 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
inhibin subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inhibin subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
striated muscle enriched protein kinase a, transcript variant X1
striated muscle enriched protein kinase a, transcript variant X2
striated muscle preferentially expressed protein kinase isoform X1
striated muscle preferentially expressed protein kinase isoform X2
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
obscurin like cytoskeletal adaptor 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
obscurin like cytoskeletal adaptor 1a, transcript variant X3
obscurin like cytoskeletal adaptor 1a, transcript variant X2
obscurin like cytoskeletal adaptor 1a, transcript variant X1
sodium/potassium-transporting ATPase subunit alpha-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 323 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 332 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
prospero homeobox protein 1-like, transcript variant X1
prospero homeobox protein 1-like, transcript variant X2
prospero homeobox 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 7 samples with support for all annotated introns
coiled-coil domain-containing protein 28A
epithelial cell-transforming sequence 2 oncogene-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
filamin A interacting protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
filamin A-interacting protein 1-like isoform X3
filamin A interacting protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
filamin A interacting protein 1-like, transcript variant X2
filamin A-interacting protein 1-like isoform X1
filamin A-interacting protein 1-like isoform X2
uncharacterized protein LOC570187 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
glycerol kinase-like, transcript variant X1
glycerol kinase-like, transcript variant X2
transfer RNA glutamic acid (anticodon UUC); 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitochondrial translational release factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
peptide chain release factor 1, mitochondrial
coiled-coil domain-containing protein 122-like
uncharacterized protein LOC393546 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X4
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X1
FERM, ARHGEF and pleckstrin domain-containing protein 1-like isoform X1
FERM, ARHGEF and pleckstrin domain-containing protein 1-like isoform X2
gamma-glutamylaminecyclotransferase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
gamma-glutamylaminecyclotransferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gamma-glutamylaminecyclotransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gamma-glutamylaminecyclotransferase-like isoform X1
gamma-glutamylaminecyclotransferase-like isoform X2
ADP-ribosylation factor-like 13b, 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 3 samples with support for all annotated introns
ADP-ribosylation factor-like 13b, transcript variant X3
ADP-ribosylation factor-like 13b, transcript variant X4
ADP-ribosylation factor-like 13b, transcript variant X5
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
ADP-ribosylation factor-like protein 13B isoform X3
ADP-ribosylation factor-like protein 13B isoform X5
ADP-ribosylation factor-like protein 13B isoform X1
ADP-ribosylation factor-like protein 13B isoform X4
ADP-ribosylation factor-like 13b, transcript variant X2
ADP-ribosylation factor-like protein 13B isoform X2
neural cell adhesion molecule 2-like, transcript variant X17
neural cell adhesion molecule 2-like, transcript variant X16
neural cell adhesion molecule 2-like, transcript variant X6
neural cell adhesion molecule 2-like, transcript variant X15
neural cell adhesion molecule 2-like, transcript variant X10
neural cell adhesion molecule 2-like, transcript variant X7
neural cell adhesion molecule 2-like, transcript variant X11
neural cell adhesion molecule 2-like, transcript variant X9
neural cell adhesion molecule 2-like, transcript variant X5
neural cell adhesion molecule 2-like, transcript variant X8
neural cell adhesion molecule 2-like, transcript variant X4
neural cell adhesion molecule 2-like, transcript variant X13
neural cell adhesion molecule 2-like, transcript variant X14
neural cell adhesion molecule 2-like, transcript variant X12
neural cell adhesion molecule 2-like, transcript variant X18
neural cell adhesion molecule 2-like, transcript variant X2
neural cell adhesion molecule 2-like, transcript variant X1
neural cell adhesion molecule 2-like, transcript variant X3
neural cell adhesion molecule 2-like isoform X1
neural cell adhesion molecule 2-like isoform X2
neural cell adhesion molecule 2-like isoform X3
uncharacterized LOC120797912, transcript variant X2
uncharacterized LOC120797912, transcript variant X7
uncharacterized LOC120797912, transcript variant X3
uncharacterized LOC120797912, transcript variant X4
uncharacterized LOC120797912, transcript variant X5
uncharacterized LOC120797912, transcript variant X6
uncharacterized LOC120797912, transcript variant X1
phosphoribosylglycinamide formyltransferase
trifunctional purine biosynthetic protein adenosine-3
N-6 adenine-specific DNA methyltransferase 1
trace amine-associated receptor 13c-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: stomatin-like protein 2, mitochondrial
vascular endothelial growth factor C-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 5 samples with support for all annotated introns
cystathionine beta-synthase a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cystathionine beta-synthase a, transcript variant X2
cystathionine beta-synthase a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cystathionine beta-synthase a, transcript variant X3
B- and T-lymphocyte attenuator-like, transcript variant X1
B- and T-lymphocyte attenuator-like, transcript variant X2
B- and T-lymphocyte attenuator-like isoform X1
B- and T-lymphocyte attenuator-like isoform X2
OX-2 membrane glycoprotein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
OX-2 membrane glycoprotein-like, transcript variant X1
OX-2 membrane glycoprotein-like, transcript variant X2
OX-2 membrane glycoprotein-like isoform X1
OX-2 membrane glycoprotein-like isoform X2
uncharacterized LOC120797922, transcript variant X3
uncharacterized LOC120797922, transcript variant X9
uncharacterized LOC120797922, transcript variant X2
uncharacterized LOC120797922, transcript variant X8
uncharacterized LOC120797922, transcript variant X1
uncharacterized LOC120797922, transcript variant X7
uncharacterized LOC120797922, transcript variant X6
uncharacterized LOC120797922, transcript variant X5
uncharacterized LOC120797922, transcript variant X4
gem (nuclear organelle) associated protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
neuronal membrane glycoprotein M6-b-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
ras-related protein Rab-9A-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 8 samples with support for all annotated introns
ras-related protein Rab-9A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription elongation factor A N-terminal and central domain-containing protein
ribose-phosphate pyrophosphokinase 2, 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 8 samples with support for all annotated introns
ribose-phosphate pyrophosphokinase 2, transcript variant X2
ribose-phosphate pyrophosphokinase 2 isoform X1
ribose-phosphate pyrophosphokinase 2 isoform X2
histone deacetylase 4-like, transcript variant X4
histone deacetylase 4-like, transcript variant X3
histone deacetylase 4-like, transcript variant 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, including 1 sample with support for all annotated introns
histone deacetylase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone deacetylase 4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
angio-associated, migratory cell protein
G-protein coupled bile acid receptor 1-like
keratin, type I cytoskeletal 18-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
keratin, type I cytoskeletal 18-like isoform X1
keratin, type I cytoskeletal 18-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
keratin, type I cytoskeletal 18-like isoform X2
actin related protein 2/3 complex, subunit 2
actin-related protein 2/3 complex subunit 2
C-X-C chemokine receptor type 2-like, transcript variant X2
C-X-C chemokine receptor type 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-X-C chemokine receptor type 2-like isoform X1
C-X-C chemokine receptor type 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC120798328, transcript variant X2
uncharacterized LOC120798328, transcript variant X1
cytochrome P450 4F3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytochrome P450 4F3, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
ETS translocation variant 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ETS translocation variant 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ETS translocation variant 5-like isoform X1
ETS translocation variant 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 182 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 147 Proteins
gamma-crystallin M2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 157 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
gamma-crystallin M2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 181 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, 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: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
prostaglandin F2 receptor negative regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
ATP-dependent RNA helicase DDX3X-like, transcript variant X1
ATP-dependent RNA helicase DDX3X-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ATP-dependent RNA helicase DDX3X-like, transcript variant X3
ATP-dependent RNA helicase DDX3X-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATP-dependent RNA helicase DDX3X-like isoform X1
ATP-dependent RNA helicase DDX3X-like isoform X2
ATP-dependent RNA helicase DDX3X-like isoform X3
ATP-dependent RNA helicase DDX3X-like isoform X4
dTDP-D-glucose 4,6-dehydratase-like, transcript variant X2
dTDP-D-glucose 4,6-dehydratase-like, transcript variant X1
dTDP-D-glucose 4,6-dehydratase-like isoform X1
dTDP-D-glucose 4,6-dehydratase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-4-like
semaphorin-5B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
semaphorin-5B-like, transcript variant X2
semaphorin-5B-like, transcript variant X3
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X2
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X1
harbinger transposase derived 1, transcript variant X1
harbinger transposase derived 1, transcript variant X2
cAMP responsive element binding protein 3-like 1
cyclic AMP-responsive element-binding protein 3-like protein 1
uncharacterized protein LOC325371 homolog, transcript variant X3
uncharacterized protein LOC325371 homolog, transcript variant X4
uncharacterized protein LOC325371 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC325371 homolog, transcript variant X5
uncharacterized protein LOC325371 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor isoform X2
ras-related and estrogen-regulated growth inhibitor isoform X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-like
inosine-uridine preferring nucleoside hydrolase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
inosine-uridine preferring nucleoside hydrolase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
inosine-uridine preferring nucleoside hydrolase-like isoform X1
inosine-uridine preferring nucleoside hydrolase-like isoform X3
inosine-uridine preferring nucleoside hydrolase-like, transcript variant X2
probable uridine nucleosidase 2 isoform X2
inosine-uridine preferring nucleoside hydrolase-like, transcript variant X4
inosine-uridine preferring nucleoside hydrolase-like, transcript variant X5
probable uridine nucleosidase 2 isoform X4
inosine-uridine preferring nucleoside hydrolase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 7b, transcript variant X4
Rho guanine nucleotide exchange factor (GEF) 7b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7b isoform X4
rho guanine nucleotide exchange factor 7b isoform X1
Rho guanine nucleotide exchange factor (GEF) 7b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 7b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7b isoform X2
rho guanine nucleotide exchange factor 7b isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins
ATPase phospholipid transporting 11A, transcript variant X4
ATPase phospholipid transporting 11A, transcript variant X2
ATPase phospholipid transporting 11A, transcript variant X5
ATPase phospholipid transporting 11A, transcript variant X1
ATPase phospholipid transporting 11A, transcript variant X3
probable phospholipid-transporting ATPase IH isoform X5
probable phospholipid-transporting ATPase IH isoform X4
probable phospholipid-transporting ATPase IH isoform X2
probable phospholipid-transporting ATPase IH isoform X1
probable phospholipid-transporting ATPase IH isoform X3
ATPase phospholipid transporting 11A, transcript variant X7
ATPase phospholipid transporting 11A, transcript variant X6
probable phospholipid-transporting ATPase IH isoform X7
probable phospholipid-transporting ATPase IH isoform X6
tubulin, gamma complex associated protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tubulin, gamma complex associated protein 3, 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 5 samples with support for all annotated introns
tubulin, gamma complex associated protein 3, transcript variant X2
gamma-tubulin complex component 3 isoform X3
gamma-tubulin complex component 3 isoform X1
gamma-tubulin complex component 3 isoform X2
fibroblast growth factor 14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 12-like isoform X1
fibroblast growth factor 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14-like isoform X2
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X1
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RCC1 and BTB domain-containing protein 1 isoform X1
RCC1 and BTB domain-containing protein 1 isoform X2
RCC1 and BTB domain-containing protein 1 isoform X4
RCC1 and BTB domain-containing protein 1 isoform X3
cytidine and dCMP deaminase domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cytidine and dCMP deaminase domain containing 1, transcript variant X1
cytidine and dCMP deaminase domain containing 1, transcript variant X2
cytidine and dCMP deaminase domain-containing protein 1 isoform X1
cytidine and dCMP deaminase domain-containing protein 1 isoform X2
calcium binding protein 39-like, transcript variant X1
calcium binding protein 39-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mcf.2 cell line derived transforming sequence-like a, transcript variant X6
mcf.2 cell line derived transforming sequence-like a, transcript variant X2
mcf.2 cell line derived transforming sequence-like a, transcript variant X3
mcf.2 cell line derived transforming sequence-like a, transcript variant X5
mcf.2 cell line derived transforming sequence-like a, transcript variant X4
mcf.2 cell line derived transforming sequence-like a, transcript variant X7
mcf.2 cell line derived transforming sequence-like a, transcript variant X1
mcf.2 cell line derived transforming sequence-like a, transcript variant X9
mcf.2 cell line derived transforming sequence-like a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanine nucleotide exchange factor DBS isoform X2
guanine nucleotide exchange factor DBS isoform X1
guanine nucleotide exchange factor DBS isoform X4
guanine nucleotide exchange factor DBS isoform X6
mcf.2 cell line derived transforming sequence-like a, transcript variant X8
mcf.2 cell line derived transforming sequence-like a, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide exchange factor DBS isoform X3
guanine nucleotide exchange factor DBS isoform X7
mcf.2 cell line derived transforming sequence-like a, transcript variant X10
guanine nucleotide exchange factor DBS isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 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: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable ribonuclease ZC3H12C, transcript variant X6
probable ribonuclease ZC3H12C, 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 3 samples with support for all annotated introns
probable ribonuclease ZC3H12C, transcript variant X3
probable ribonuclease ZC3H12C, transcript variant X5
probable ribonuclease ZC3H12C, transcript variant X4
probable ribonuclease ZC3H12C, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X8
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X11
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X7
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X6
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X9
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X8
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X11
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X7
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X4
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X10
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X6
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X3
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X2
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X5
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X9
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X1
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X13
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X12
carbohydrate sulfotransferase 10, transcript variant X1
carbohydrate sulfotransferase 10, transcript variant X2
ribosomal protein L31, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ribosomal protein L31, transcript variant X1
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: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger CCCH domain-containing protein 13
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
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 7 samples with support for all annotated introns
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1b, transcript variant X1
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-associated and pleckstrin homology domains-containing protein 1b
uncharacterized si:dkey-1h24.6, transcript variant X2
uncharacterized protein si:dkey-1h24.6 isoform X2
uncharacterized si:dkey-1h24.6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein si:dkey-1h24.6 isoform X1
FAST kinase domain-containing protein 2, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 20% 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 3 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative malate dehydrogenase 1B
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X6
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X1
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X4
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X5
5'-AMP-activated protein kinase subunit gamma-2 isoform X5
protein kinase, AMP-activated, gamma 3a non-catalytic subunit, transcript variant X2
5'-AMP-activated protein kinase subunit gamma-1 isoform X2
5'-AMP-activated protein kinase subunit gamma-1 isoform X1
5'-AMP-activated protein kinase subunit gamma-1 isoform X3
5'-AMP-activated protein kinase subunit gamma-1 isoform X4
ATP-binding cassette, sub-family B (MDR/TAP), member 6a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
par-3 family cell polarity regulator beta a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
par-3 family cell polarity regulator beta a, transcript variant X1
par-3 family cell polarity regulator beta a isoform X2
par-3 family cell polarity regulator beta a isoform X1
par-3 family cell polarity regulator beta a, transcript variant X3
par-3 family cell polarity regulator beta a isoform X3
par-3 family cell polarity regulator beta a, transcript variant X4
par-3 family cell polarity regulator beta a isoform X4
par-3 family cell polarity regulator beta a, transcript variant X5
par-3 family cell polarity regulator beta a isoform X5
zona pellucida sperm-binding protein 3-like
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
muscleblind-like splicing regulator 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like splicing regulator 2, transcript variant X5
muscleblind-like splicing regulator 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like splicing regulator 2, transcript variant X3
muscleblind-like splicing regulator 2, transcript variant X4
muscleblind-like splicing regulator 2, transcript variant X8
muscleblind-like splicing regulator 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like splicing regulator 2, transcript variant X10
muscleblind-like splicing regulator 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like splicing regulator 2, transcript variant X11
muscleblind-like splicing regulator 2, transcript variant X12
muscleblind-like splicing regulator 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
39S ribosomal protein L39, mitochondrial
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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: junctional adhesion molecule 2A
ATP synthase peripheral stalk subunit F6, transcript variant X1
ATP synthase peripheral stalk subunit F6, transcript variant X2
ATP synthase-coupling factor 6, mitochondrial isoform X1
ATP synthase-coupling factor 6, mitochondrial isoform X2
amyloid beta (A4) precursor protein a, transcript variant X2
amyloid beta (A4) precursor protein a, transcript variant X1
amyloid beta (A4) precursor protein a isoform X2
amyloid beta (A4) precursor protein a isoform X1
ADAM metallopeptidase with thrombospondin type 1 motif, 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 1
A disintegrin and metalloproteinase with thrombospondin motifs 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X4
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 2-like isoform X3
sodium- and chloride-dependent GABA transporter 2-like isoform X1
sodium- and chloride-dependent GABA transporter 2-like isoform X2
lysine-specific demethylase 6A-like, transcript variant X2
lysine-specific demethylase 6A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
lysine-specific demethylase 6A-like isoform X2
lysine-specific demethylase 6A-like isoform X1
FUN14 domain-containing protein 1, 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 7 samples with support for all annotated introns
FUN14 domain-containing protein 1 isoform X5
FUN14 domain-containing protein 1, transcript variant X2
FUN14 domain-containing protein 1 isoform X2
FUN14 domain-containing protein 1, transcript variant X1
FUN14 domain-containing protein 1, transcript variant X4
FUN14 domain-containing protein 1, transcript variant X3
FUN14 domain-containing protein 1 isoform X1
FUN14 domain-containing protein 1 isoform X4
FUN14 domain-containing protein 1 isoform X3
centromere protein L, transcript variant X3
centromere protein L, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
centromere protein L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peripheral plasma membrane protein CASK-like, transcript variant X1
peripheral plasma membrane protein CASK-like, transcript variant X2
peripheral plasma membrane protein CASK-like, transcript variant X3
peripheral plasma membrane protein CASK-like isoform X1
peripheral plasma membrane protein CASK-like isoform X2
peripheral plasma membrane protein CASK-like isoform X3
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: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 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.
LOW QUALITY PROTEIN: probable G-protein coupled receptor 34
nuclear receptor subfamily 0 group B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
interleukin-1 receptor accessory protein-like 1, transcript variant X1
interleukin-1 receptor accessory protein-like 1, transcript variant X2
interleukin-1 receptor accessory protein-like 1, transcript variant X3
interleukin-1 receptor accessory protein-like 1, transcript variant X4
interleukin-1 receptor accessory protein-like 1, transcript variant X5
interleukin-1 receptor accessory protein-like 1, transcript variant X6
interleukin-1 receptor accessory protein-like 1, transcript variant X7
interleukin-1 receptor accessory protein-like 1, transcript variant X8
interleukin-1 receptor accessory protein-like 1
uncharacterized LOC120797926, transcript variant X1
uncharacterized LOC120797926, transcript variant X3
uncharacterized protein LOC120797926 isoform X1
uncharacterized LOC120797926, transcript variant X2
uncharacterized protein LOC120797926 isoform X2
FERM and PDZ domain-containing protein 4-like, transcript variant X1
FERM and PDZ domain-containing protein 4-like, transcript variant X2
FERM and PDZ domain-containing protein 4-like isoform X1
FERM and PDZ domain-containing protein 4-like isoform X2
male-specific lethal 3 homolog, transcript variant X2
male-specific lethal 3 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
male-specific lethal 3 homolog, transcript variant X3
male-specific lethal 3 homolog isoform X2
male-specific lethal 3 homolog isoform X1
male-specific lethal 3 homolog isoform X3
rho GTPase-activating protein 6-like, transcript variant X1
rho GTPase-activating protein 6-like isoform X1
rho GTPase-activating protein 6-like, transcript variant X2
rho GTPase-activating protein 6-like isoform X2
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X1
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase Midline-1-like isoform X1
E3 ubiquitin-protein ligase Midline-1-like isoform X2
transfer RNA glycine (anticodon GCC); 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: 47 Proteins
SLIT and NTRK-like family, member 6, transcript variant X1
SLIT and NTRK-like family, member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-3-like isoform X1
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-3-like isoform X3
gamma-aminobutyric acid receptor subunit beta-3-like isoform X2
gamma-aminobutyric acid receptor subunit alpha-5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit gamma-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia and flagella associated protein 221
cilia- and flagella-associated protein 221
acyl-CoA-binding protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-CoA-binding protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acyl-CoA-binding protein-like isoform X1
acyl-CoA-binding protein-like isoform X2
metalloreductase STEAP3-like, transcript variant X9
metalloreductase STEAP3-like, transcript variant X2
metalloreductase STEAP3-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
metalloreductase STEAP3-like, transcript variant X4
metalloreductase STEAP3-like, transcript variant X1
metalloreductase STEAP3-like, transcript variant X3
metalloreductase STEAP3-like, transcript variant X6
metalloreductase STEAP3-like, transcript variant X5
metalloreductase STEAP3-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
homeobox protein engrailed-1-B-like, transcript variant X2
homeobox protein engrailed-1-B-like, transcript variant X1
homeobox protein engrailed-1-B-like isoform X1
homeobox protein engrailed-1-B-like isoform X2
L-threonine 3-dehydrogenase, mitochondrial-like, transcript variant X2
L-threonine 3-dehydrogenase, mitochondrial-like, transcript variant X1
L-threonine 3-dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
ectonucleotide pyrophosphatase/phosphodiesterase 4
chloride intracellular channel 5a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chloride intracellular channel 5a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chloride intracellular channel 5a, transcript variant X3
chloride intracellular channel protein 5a isoform X1
chloride intracellular channel 5a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chloride intracellular channel protein 5a isoform X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X3
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A
zinc finger, RAN-binding domain containing 3, transcript variant X3
zinc finger, RAN-binding domain containing 3, transcript variant X4
zinc finger, RAN-binding domain containing 3, transcript variant X1
zinc finger, RAN-binding domain containing 3, transcript variant X2
DNA annealing helicase and endonuclease ZRANB3 isoform X1
DNA annealing helicase and endonuclease ZRANB3 isoform X2
R3H domain-containing protein 1, transcript variant X2
R3H domain-containing protein 1, transcript variant X3
R3H domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
R3H domain-containing protein 1, transcript variant X6
R3H domain-containing protein 1, transcript variant X8
R3H domain-containing protein 1, transcript variant X7
R3H domain-containing protein 1, transcript variant X4
R3H domain-containing protein 1, transcript variant X5
R3H domain-containing protein 1 isoform X1
R3H domain-containing protein 1 isoform X2
R3H domain-containing protein 1 isoform X4
R3H domain-containing protein 1 isoform X3
R3H domain-containing protein 1 isoform X5
R3H domain-containing protein 1 isoform X6
uncharacterized LOC120797899, transcript variant X1
uncharacterized LOC120797899, transcript variant X2
uncharacterized protein LOC120797899 isoform X1
uncharacterized protein LOC120797899 isoform X2
uncharacterized LOC120797899, transcript variant X3
uncharacterized protein LOC120797899 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cobalamin trafficking protein CblD-like, transcript variant X1
cobalamin trafficking protein CblD-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X4
paraspeckle component 1, transcript variant X1
paraspeckle component 1, transcript variant X3
paraspeckle component 1, transcript variant X2
ly6/PLAUR domain-containing protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ly6/PLAUR domain-containing protein 6-like, transcript variant X1
ly6/PLAUR domain-containing protein 6-like
STE20 related adaptor beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
STE20 related adaptor beta, transcript variant X1
STE20 related adaptor beta, transcript variant X3
STE20-related kinase adapter protein beta isoform X2
STE20-related kinase adapter protein beta isoform X1
STE20-related kinase adapter protein beta isoform X3
trafficking protein, kinesin binding 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
trafficking protein, kinesin binding 2, transcript variant X1
trafficking protein, kinesin binding 2, transcript variant X3
trafficking kinesin-binding protein 2 isoform X1
trafficking kinesin-binding protein 2 isoform X2
trafficking protein, kinesin binding 2, transcript variant X4
trafficking kinesin-binding protein 2 isoform X3
trafficking protein, kinesin binding 2, transcript variant X5
trafficking kinesin-binding protein 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X2
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X3
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X1
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X4
nucleotide triphosphate diphosphatase NUDT15 isoform X1
nucleotide triphosphate diphosphatase NUDT15 isoform X2
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X7
nucleotide triphosphate diphosphatase NUDT15 isoform X4
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X6
nudix (nucleoside diphosphate linked moiety X)-type motif 15, transcript variant X5
nucleotide triphosphate diphosphatase NUDT15 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cholecystokinin B receptor a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cholecystokinin B receptor a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cholecystokinin B receptor a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cholecystokinin B receptor a, transcript variant X2
transmembrane protein FAM155A-like, transcript variant X2
transmembrane protein FAM155A-like, transcript variant X1
transmembrane protein FAM155A-like isoform X2
transmembrane protein FAM155A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
thioredoxin domain-containing protein 16
prostaglandin E receptor 2a (subtype EP2), transcript variant X3
prostaglandin E receptor 2a (subtype EP2), transcript variant X2
prostaglandin E receptor 2a (subtype EP2), transcript variant X1
prostaglandin E receptor 2a (subtype EP2)
nidogen 2a (osteonidogen), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nidogen 2a (osteonidogen), transcript variant X2
nidogen 2a (osteonidogen), transcript variant X8
nidogen 2a (osteonidogen), transcript variant X4
nidogen 2a (osteonidogen), transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nidogen 2a (osteonidogen), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nidogen 2a (osteonidogen), transcript variant X3
nidogen 2a (osteonidogen), transcript variant X6
RNA transcription, translation and transport factor
RNA transcription, translation and transport factor protein
Sin3A-associated protein, transcript variant X4
Sin3A-associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Sin3A-associated protein, transcript variant X2
Sin3A-associated protein, transcript variant X3
Sin3A-associated protein, transcript variant X5
histone deacetylase complex subunit SAP18 isoform X1
histone deacetylase complex subunit SAP18 isoform X2
gap junction beta-6 protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction beta-6 protein-like, transcript variant X1
gap junction beta-6 protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
gap junction beta-6 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction beta-6 protein-like, transcript variant X3
gap junction beta-2 protein-like isoform X2
gap junction beta-6 protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
helix-loop-helix protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
helix-loop-helix protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
helix-loop-helix protein 2-like, transcript variant X6
helix-loop-helix protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
helix-loop-helix protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
helix-loop-helix protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
vang-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vang-like protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vang-like protein 1, transcript variant X4
vang-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vang-like protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
protein O-glucosyltransferase 1, transcript variant X1
protein O-glucosyltransferase 1, transcript variant X2
translocase of inner mitochondrial membrane domain containing 1, transcript variant X3
translocase of inner mitochondrial membrane domain containing 1, transcript variant X1
translocase of inner mitochondrial membrane domain containing 1, transcript variant X2
translocase of inner mitochondrial membrane domain containing 1, transcript variant X5
translocase of inner mitochondrial membrane domain containing 1, transcript variant X4
translocase of inner mitochondrial membrane domain containing 1, transcript variant X6
complex I assembly factor TIMMDC1, mitochondrial
multidrug resistance-associated protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
multidrug resistance-associated protein 4-like, transcript variant X1
multidrug resistance-associated protein 4-like, transcript variant X3
multidrug resistance-associated protein 4-like isoform X1
multidrug resistance-associated protein 4-like isoform X2
ATP-binding cassette, sub-family C (CFTR/MRP), member 4
multidrug resistance-associated protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
DAZ interacting zinc finger protein 1, transcript variant X5
DAZ interacting zinc finger protein 1, transcript variant X4
DAZ interacting zinc finger protein 1, transcript variant X3
DAZ interacting zinc finger protein 1, transcript variant X1
DAZ interacting zinc finger protein 1, transcript variant X2
heparan-sulfate 6-O-sulfotransferase 3-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 17% 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: 22 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen alpha-1(XXVIII) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen alpha-1(XXVIII) chain-like, transcript variant X3
collagen alpha-1(XXVIII) chain-like, transcript variant X2
collagen alpha-1(XXVIII) chain-like, transcript variant X4
collagen alpha-1(XXVIII) chain-like isoform X1
collagen alpha-1(XXVIII) chain-like isoform X2
ATP synthase subunit beta, mitochondrial
retinol dehydrogenase 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
retinol dehydrogenase 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
retinol dehydrogenase 7-like, transcript variant X5
retinol dehydrogenase 7-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinol dehydrogenase 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
bile salt export pump-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bile salt export pump-like, transcript variant X2
bile salt export pump-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bile salt export pump-like, transcript variant X5
bile salt export pump-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bile salt export pump-like, transcript variant X6
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 1 sample with support for all annotated introns
beta-1,3-galactosyltransferase 1-like, transcript variant X4
beta-1,3-galactosyltransferase 1-like, transcript variant X3
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 1 sample with support for all annotated introns
beta-1,3-galactosyltransferase 1-like, transcript variant X6
beta-1,3-galactosyltransferase 1-like, transcript variant X2
beta-1,3-galactosyltransferase 1-like, transcript variant X5
beta-1,3-galactosyltransferase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,3-galactosyltransferase 1-like, transcript variant X8
beta-1,3-galactosyltransferase 1-like, transcript variant X7
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
xin actin-binding repeat-containing protein 2
cysteine/serine-rich nuclear protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
sodium channel, voltage-gated, type I like, alpha b, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X3
sodium channel, voltage-gated, type I like, alpha b, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X1
sodium channel, voltage-gated, type I like, alpha b, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type I like, alpha b isoform X10
sodium channel, voltage-gated, type I like, alpha b isoform X7
sodium channel, voltage-gated, type I like, alpha b isoform X4
sodium channel, voltage-gated, type I like, alpha b isoform X6
sodium channel, voltage-gated, type I like, alpha b isoform X3
sodium channel, voltage-gated, type I like, alpha b isoform X8
sodium channel, voltage-gated, type I like, alpha b isoform X1
sodium channel, voltage-gated, type I like, alpha b isoform X11
sodium channel, voltage-gated, type I like, alpha b isoform X5
sodium channel, voltage-gated, type I like, alpha b isoform X9
sodium channel, voltage-gated, type I like, alpha b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X6
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X1
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X3
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X2
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X5
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X7
potassium channel, voltage gated eag related subfamily H, member 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 7 isoform X1
potassium voltage-gated channel subfamily H member 7 isoform X3
potassium voltage-gated channel subfamily H member 7 isoform X2
potassium voltage-gated channel subfamily H member 7 isoform X4
potassium voltage-gated channel subfamily H member 7 isoform X5
potassium voltage-gated channel subfamily H member 7 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dipeptidyl peptidase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dipeptidyl peptidase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase 24b (STE20 homolog, yeast)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 15 member 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 15 member 1b, transcript variant X1
solute carrier family 15 member 1b isoform X2
solute carrier family 15 member 1b isoform X1
dedicator of cytokinesis 9b, transcript variant X2
dedicator of cytokinesis 9b, transcript variant X3
dedicator of cytokinesis 9b, transcript variant X4
dedicator of cytokinesis 9b, transcript variant X1
dedicator of cytokinesis protein 9 isoform X2
dedicator of cytokinesis protein 9 isoform X3
dedicator of cytokinesis protein 9 isoform X1
dedicator of cytokinesis protein 9 isoform X4
bone morphogenetic protein receptor type-2-like
family with sequence similarity 117 member Ba
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
islet cell autoantigen 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
islet cell autoantigen 1-like, transcript variant X2
islet cell autoantigen 1-like, transcript variant X3
islet cell autoantigen 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
islet cell autoantigen 1-like isoform X4
islet cell autoantigen 1-like isoform X2
islet cell autoantigen 1-like isoform X3
islet cell autoantigen 1-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01192
COORDINATES: nucleotide motif:Rfam:12.0:RF00575
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
nuclear fragile X mental retardation-interacting protein 1
cilia- and flagella-associated protein 47-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA aspartic acid (anticodon GUC); 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 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: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
general transcription factor IIIC, polypeptide 3, transcript variant X1
general transcription factor IIIC, polypeptide 3, transcript variant X2
general transcription factor 3C polypeptide 3 isoform X1
general transcription factor 3C polypeptide 3 isoform X2
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2b, transcript variant X1
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2b, transcript variant X2
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2b, transcript variant X3
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2b, transcript variant X4
E3 ubiquitin-protein ligase HECW2 isoform X1
E3 ubiquitin-protein ligase HECW2 isoform X2
E3 ubiquitin-protein ligase HECW2 isoform X3
E3 ubiquitin-protein ligase HECW2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
diacylglycerol kinase zeta-like, transcript variant X5
diacylglycerol kinase zeta-like, transcript variant X4
diacylglycerol kinase zeta-like, transcript variant X3
diacylglycerol kinase zeta-like, transcript variant X2
diacylglycerol kinase zeta-like, transcript variant X1
diacylglycerol kinase zeta-like isoform X5
diacylglycerol kinase zeta-like isoform X4
diacylglycerol kinase zeta-like isoform X3
diacylglycerol kinase zeta-like isoform X2
diacylglycerol kinase zeta-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heat shock transcription factor 2 binding protein, transcript variant X4
heat shock transcription factor 2 binding protein, transcript variant X6
heat shock transcription factor 2 binding protein, transcript variant X3
heat shock transcription factor 2 binding protein, transcript variant X5
heat shock transcription factor 2 binding protein, transcript variant X2
heat shock transcription factor 2 binding protein, transcript variant X1
heat shock factor 2-binding protein isoform X5
heat shock factor 2-binding protein isoform X3
heat shock factor 2-binding protein isoform X2
heat shock factor 2-binding protein isoform X1
heat shock factor 2-binding protein isoform X4
ankyrin repeat domain-containing protein 10a
coiled-coil domain containing 14, transcript variant X2
coiled-coil domain-containing protein 14 isoform X2
coiled-coil domain containing 14, transcript variant X6
coiled-coil domain containing 14, transcript variant X1
coiled-coil domain-containing protein 14 isoform X5
coiled-coil domain-containing protein 14 isoform X1
coiled-coil domain containing 14, transcript variant X4
coiled-coil domain containing 14, transcript variant X5
coiled-coil domain-containing protein 14 isoform X4
coiled-coil domain containing 14, transcript variant X3
coiled-coil domain-containing protein 14 isoform X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X4
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 4, transcript variant X6
probable ATP-dependent RNA helicase DDX4 isoform X3
probable ATP-dependent RNA helicase DDX4 isoform X1
probable ATP-dependent RNA helicase DDX4 isoform X2
cyclic nucleotide-gated channel cone photoreceptor subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ATPase Na+/K+ transporting subunit beta 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1b
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X4
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X3
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X2
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X1
cysteine--tRNA ligase, mitochondrial isoform X4
cysteine--tRNA ligase, mitochondrial isoform X3
cysteine--tRNA ligase, mitochondrial isoform X2
cysteine--tRNA ligase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ADP-ribosylation factor-like 6 interacting protein 6
ADP-ribosylation factor-like protein 6-interacting protein 6
uncharacterized LOC120797997, transcript variant X2
uncharacterized LOC120797997, transcript variant X1
calcipressin-1-like, transcript variant X1
calcipressin-1-like, 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 6 samples with support for all annotated introns
chloride intracellular channel protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX family transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
runt-related transcription factor 1 isoform X1
RUNX family transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
runt-related transcription factor 1 isoform X2
protein downstream neighbor of son homolog
uncharacterized LOC120798201, transcript variant X1
uncharacterized LOC120798201, transcript variant X3
uncharacterized LOC120798201, transcript variant X2
uncharacterized LOC120798201, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
steroid sulfatase (microsomal), isozyme S
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
patatin-like phospholipase domain containing 4, transcript variant X2
patatin-like phospholipase domain containing 4, transcript variant X1
patatin-like phospholipase domain-containing protein 4 isoform X1
patatin-like phospholipase domain-containing protein 4 isoform X2
pseudouridine 5'-phosphatase, transcript variant X1
pseudouridine 5'-phosphatase, transcript variant X2
neuroligin 4 X-linked a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
neuroligin 4 X-linked a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
neuroligin 4 X-linked a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
neuroligin 4 X-linked a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
LOW QUALITY PROTEIN: uncharacterized protein LOC120798390