Osmia bicornis bicornis chromosome 7, iOsmBic2.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Apoidea; Megachilidae; Megachilinae; Osmia.
REFSEQ INFORMATION: The reference sequence is identical to\nOU015510.1.\nAssembly name: iOsmBic2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/05/17. The original whole-genome shotgun project has the\naccession CAJRAL000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Osmia bicornis bicornis Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
inositol hexakisphosphate kinase 1, transcript variant X6
COORDINATES: polyA evidence [ECO:0006239]
inositol hexakisphosphate kinase 1, transcript variant X5
inositol hexakisphosphate kinase 1, transcript variant X4
inositol hexakisphosphate kinase 1, transcript variant X3
inositol hexakisphosphate kinase 1, transcript variant X2
inositol hexakisphosphate kinase 1, transcript variant X7
inositol hexakisphosphate kinase 1, transcript variant X1
inositol hexakisphosphate kinase 1, transcript variant X10
inositol hexakisphosphate kinase 1, transcript variant X9
inositol hexakisphosphate kinase 1, transcript variant X8
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 19 samples with support for all annotated introns
inositol hexakisphosphate kinase 2 isoform X2
inositol hexakisphosphate kinase 2 isoform X1
uncharacterized protein LOC114880744 isoform X4
uncharacterized protein LOC114880744 isoform X5
inositol hexakisphosphate kinase 1 isoform X3
protein kinase C-binding protein 1, transcript variant X2
protein kinase C-binding protein 1, transcript variant X1
protein kinase C-binding protein 1, transcript variant X5
protein kinase C-binding protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein kinase C-binding protein 1, transcript variant X3
protein kinase C-binding protein 1, transcript variant X4
protein kinase C-binding protein 1 isoform X1
protein kinase C-binding protein 1 isoform X2
protein kinase C-binding protein 1 isoform X3
N-alpha-acetyltransferase 30-like, transcript variant X2
N-alpha-acetyltransferase 30-like, transcript variant X3
N-alpha-acetyltransferase 30-like isoform X2
N-alpha-acetyltransferase 30-like, transcript variant X1
N-alpha-acetyltransferase 30-like isoform X1
prolactin-releasing peptide receptor-like, transcript variant X5
prolactin-releasing peptide receptor-like isoform X2
prolactin-releasing peptide receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
prolactin-releasing peptide receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
prolactin-releasing peptide receptor-like, 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 11 samples with support for all annotated introns
prolactin-releasing peptide receptor-like, transcript variant X4
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
prolactin-releasing peptide receptor-like isoform X1
autophagy-related protein 101, transcript variant X4
autophagy-related protein 101, transcript variant X3
autophagy-related protein 101, transcript variant X2
autophagy-related protein 101, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
epimerase family protein SDR39U1, transcript variant X4
epimerase family protein SDR39U1, transcript variant X2
epimerase family protein SDR39U1, transcript variant X3
epimerase family protein SDR39U1, transcript variant X1
epimerase family protein SDR39U1 isoform X1
epimerase family protein SDR39U1 isoform X2
histone-lysine N-methyltransferase E(z), transcript variant X1
histone-lysine N-methyltransferase E(z), transcript variant X4
histone-lysine N-methyltransferase E(z), transcript variant X2
histone-lysine N-methyltransferase E(z), transcript variant X3
histone-lysine N-methyltransferase E(z), transcript variant X5
histone-lysine N-methyltransferase E(z) isoform X1
histone-lysine N-methyltransferase E(z) isoform X4
histone-lysine N-methyltransferase E(z) isoform X2
histone-lysine N-methyltransferase E(z) isoform X3
histone-lysine N-methyltransferase E(z) isoform X5
histone-lysine N-methyltransferase E(z), transcript variant X6
histone-lysine N-methyltransferase E(z) isoform X6
adenylate cyclase type 2, transcript variant X1
adenylate cyclase type 2, transcript variant X5
adenylate cyclase type 2, transcript variant X3
adenylate cyclase type 2, transcript variant X2
adenylate cyclase type 2, transcript variant X6
adenylate cyclase type 2, transcript variant X4
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X4
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X5
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X2
mediator of RNA polymerase II transcription subunit 10
NPC intracellular cholesterol transporter 1 homolog 1b-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 2 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1 homolog 1b-like isoform X2
NPC intracellular cholesterol transporter 1 homolog 1b-like, transcript variant X1
NPC intracellular cholesterol transporter 1 homolog 1b-like isoform X1
NPC intracellular cholesterol transporter 1 homolog 1b-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1 homolog 1b-like isoform X3
protein still life, isoforms C/SIF type 2, transcript variant X2
protein still life, isoforms C/SIF type 2, transcript variant X4
protein still life, isoforms C/SIF type 2, transcript variant X3
protein still life, isoforms C/SIF type 2, transcript variant X6
protein still life, isoforms C/SIF type 2, transcript variant X5
protein still life, isoforms C/SIF type 2, transcript variant X7
protein still life, isoforms C/SIF type 2, transcript variant X1
protein still life, isoforms C/SIF type 2, transcript variant X8
protein still life, isoforms C/SIF type 2, transcript variant X11
protein still life, isoforms C/SIF type 2, transcript variant X9
protein still life, isoforms C/SIF type 2, transcript variant X10
protein still life, isoforms C/SIF type 2, transcript variant X12
protein still life, isoform SIF type 1 isoform X7
protein still life, isoform SIF type 1 isoform X2
protein still life, isoform SIF type 1 isoform X4
protein still life, isoform SIF type 1 isoform X3
protein still life, isoform SIF type 1 isoform X6
protein still life, isoform SIF type 1 isoform X5
protein still life, isoform SIF type 1 isoform X1
protein still life, isoform SIF type 1 isoform X8
protein still life, isoform SIF type 1 isoform X11
protein still life, isoforms C/SIF type 2 isoform X10
protein still life, isoforms C/SIF type 2 isoform X9
protein still life, isoforms C/SIF type 2 isoform X12
reticulon-4-interacting protein 1 homolog, mitochondrial-like, transcript variant X1
reticulon-4-interacting protein 1 homolog, mitochondrial-like, transcript variant X2
reticulon-4-interacting protein 1 homolog, mitochondrial-like
tryptophan--tRNA ligase, mitochondrial, transcript variant X2
tryptophan--tRNA ligase, mitochondrial, transcript variant X1
tryptophan--tRNA ligase, mitochondrial isoform X2
tryptophan--tRNA ligase, mitochondrial isoform X1
zinc finger protein 652-like, transcript variant X7
zinc finger protein 652-like, transcript variant X5
zinc finger protein 652-like, transcript variant X1
zinc finger protein 652-like, transcript variant X6
zinc finger protein 652-like, transcript variant X2
zinc finger protein 652-like, transcript variant X4
zinc finger protein 652-like, transcript variant X3
protein N-terminal asparagine amidohydrolase, transcript variant X1
protein N-terminal asparagine amidohydrolase, transcript variant X2
protein N-terminal asparagine amidohydrolase, transcript variant X3
protein N-terminal asparagine amidohydrolase
GTP-binding protein Di-Ras2, transcript variant X1
GTP-binding protein Di-Ras2, transcript variant X2
uncharacterized LOC114878390, 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 13 samples with support for all annotated introns
uncharacterized LOC114878390, transcript variant X2
uncharacterized protein LOC114878390 isoform X1
uncharacterized protein LOC114878390 isoform X2
calcium permeable stress-gated cation channel 1, transcript variant X2
calcium permeable stress-gated cation channel 1 isoform X2
calcium permeable stress-gated cation channel 1, transcript variant X1
calcium permeable stress-gated cation channel 1 isoform X1
histone-lysine N-methyltransferase NSD2, transcript variant X7
histone-lysine N-methyltransferase NSD2, transcript variant X3
histone-lysine N-methyltransferase NSD2, transcript variant X4
histone-lysine N-methyltransferase NSD2, transcript variant X1
histone-lysine N-methyltransferase NSD2, transcript variant X2
histone-lysine N-methyltransferase NSD2, transcript variant X6
histone-lysine N-methyltransferase NSD2 isoform X3
histone-lysine N-methyltransferase NSD2 isoform X2
histone-lysine N-methyltransferase NSD2 isoform X1
histone-lysine N-methyltransferase NSD2 isoform X5
histone-lysine N-methyltransferase NSD2 isoform X6
histone-lysine N-methyltransferase NSD2, 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 19 samples with support for all annotated introns
histone-lysine N-methyltransferase NSD2 isoform X4
dynein axonemal assembly factor 3, transcript variant X4
dynein axonemal assembly factor 3, transcript variant X2
dynein axonemal assembly factor 3, transcript variant X5
dynein axonemal assembly factor 3, transcript variant X3
dynein axonemal assembly factor 3, transcript variant X1
dynein axonemal assembly factor 3 isoform X1
dynein axonemal assembly factor 3 homolog isoform X2
histone deacetylase complex subunit SAP130-like, transcript variant X4
histone deacetylase complex subunit SAP130-like, transcript variant X3
histone deacetylase complex subunit SAP130-like, transcript variant X2
histone deacetylase complex subunit SAP130-like, transcript variant X1
histone deacetylase complex subunit SAP130-like
cytosolic Fe-S cluster assembly factor NUBP1 homolog
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X2
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X1
cytochrome c oxidase assembly protein COX11, mitochondrial
p21-activated protein kinase-interacting protein 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 17 samples with support for all annotated introns
p21-activated protein kinase-interacting protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
p21-activated protein kinase-interacting protein 1-like isoform X2
p21-activated protein kinase-interacting protein 1-like isoform X1
endothelin-converting enzyme 1-like, transcript variant X3
endothelin-converting enzyme 1-like, transcript variant X1
endothelin-converting enzyme 1-like, transcript variant X2
endothelin-converting enzyme 1-like isoform X2
endothelin-converting enzyme 1-like isoform X1
endothelin-converting enzyme 1-like isoform X3
endothelin-converting enzyme 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
endothelin-converting enzyme 1-like, 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 14 samples with support for all annotated introns
endothelin-converting enzyme 2-like isoform X4
endothelin-converting enzyme 2-like isoform X5
uncharacterized LOC114878319, transcript variant X1
uncharacterized LOC114878319, transcript variant X4
uncharacterized LOC114878319, transcript variant X3
uncharacterized LOC114878319, transcript variant X2
uncharacterized protein LOC114878319 isoform X1
uncharacterized protein LOC114878319 isoform X2
18S rRNA aminocarboxypropyltransferase, transcript variant X2
18S rRNA aminocarboxypropyltransferase, transcript variant X1
18S rRNA aminocarboxypropyltransferase isoform X1
18S rRNA aminocarboxypropyltransferase isoform X2
histone deacetylase HDAC1, transcript variant X1
histone deacetylase HDAC1, transcript variant X2
histone deacetylase HDAC1, transcript variant X3
putative sodium-coupled neutral amino acid transporter 10
mini-chromosome maintenance complex-binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mini-chromosome maintenance complex-binding protein, 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
mini-chromosome maintenance complex-binding protein, transcript variant X4
mini-chromosome maintenance complex-binding protein, transcript variant X1
mini-chromosome maintenance complex-binding protein
protein FAM166B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein FAM166B-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, including 1 sample with support for all annotated introns
protein FAM166B-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 5 samples with support for all annotated introns
protein FAM166B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein FAM166B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC114878329 isoform X3
uncharacterized protein LOC114878329 isoform X4
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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: xanthine dehydrogenase
bifunctional purine biosynthesis protein ATIC
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; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: egalitarian protein homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 2 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC114878384
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: la-related protein Larp4B
eukaryotic translation initiation factor eIF1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: eukaryotic translation initiation factor eIF1
ADP-ribosylation factor GTPase-activating protein 1
LOW QUALITY PROTEIN: ADP-ribosylation factor GTPase-activating protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC114878370
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 7 codons; deleted 11 bases in 9 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 7 codons; deleted 11 bases in 9 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC114878360
LOW QUALITY PROTEIN: V-type proton ATPase subunit F
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: Y+L amino acid transporter 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC114878362
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 16 bases in 13 codons; deleted 9 bases in 7 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 16 bases in 13 codons; deleted 9 bases in 7 codons; substituted 10 bases at 10 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: PHD finger protein 14
methionyl-tRNA formyltransferase, mitochondrial
LOW QUALITY PROTEIN: methionyl-tRNA formyltransferase, mitochondrial
U6 snRNA-associated Sm-like protein LSm4
LOW QUALITY PROTEIN: U6 snRNA-associated Sm-like protein LSm4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 6 codons; deleted 4 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 6 codons; deleted 4 bases in 4 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC114878364
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
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: E3 ubiquitin-protein ligase MARCHF8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC114878351, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC114878351, 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 15 samples with support for all annotated introns
uncharacterized LOC114878351, 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 6 samples with support for all annotated introns
uncharacterized protein LOC114878351 isoform X2
uncharacterized protein LOC114878351 isoform X1
vesicle transport through interaction with t-SNAREs homolog 1B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
vesicle transport through interaction with t-SNAREs homolog 1B-like isoform X2
vesicle transport through interaction with t-SNAREs homolog 1B-like, 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 5 samples with support for all annotated introns
cell division control protein 31-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CCHC-type zinc finger nucleic acid binding protein, transcript variant X1
CCHC-type zinc finger nucleic acid binding protein, transcript variant X2
CCHC-type zinc finger nucleic acid binding protein, transcript variant X3
CCHC-type zinc finger nucleic acid binding protein
protein bicaudal D, 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 16 samples with support for all annotated introns
protein bicaudal D, 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 19 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa, transcript variant X1
receptor-type tyrosine-protein phosphatase kappa, 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 6 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa isoform X1
receptor-type tyrosine-protein phosphatase kappa, 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 7 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase kappa isoform X2
uncharacterized LOC114878314, transcript variant X2
uncharacterized LOC114878314, transcript variant X1
uncharacterized LOC114878314, transcript variant X3
plasmanylethanolamine desaturase, transcript variant X5
plasmanylethanolamine desaturase, transcript variant X2
plasmanylethanolamine desaturase, transcript variant X1
plasmanylethanolamine desaturase, transcript variant X4
plasmanylethanolamine desaturase, transcript variant X3
plasmanylethanolamine desaturase isoform X1
plasmanylethanolamine desaturase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
plasmanylethanolamine desaturase isoform X2
mitochondrial ribosome-associated GTPase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mitochondrial ribosome-associated GTPase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 376 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 5 bases in 3 codons; deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: alanine--tRNA ligase, cytoplasmic
probable 28S ribosomal protein S25, mitochondrial, transcript variant X1
probable 28S ribosomal protein S25, mitochondrial, transcript variant X2
probable 28S ribosomal protein S25, mitochondrial
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
succinate--hydroxymethylglutarate CoA-transferase, transcript variant X2
succinate--hydroxymethylglutarate CoA-transferase, transcript variant X1
succinate--hydroxymethylglutarate CoA-transferase, transcript variant X3
succinate--hydroxymethylglutarate CoA-transferase isoform X1
succinate--hydroxymethylglutarate CoA-transferase isoform X2
F-box/WD repeat-containing protein 5, transcript variant X3
F-box/WD repeat-containing protein 5, transcript variant X1
F-box/WD repeat-containing protein 5, transcript variant X2
F-box/WD repeat-containing protein 5 isoform X3
F-box/WD repeat-containing protein 5 isoform X1
F-box/WD repeat-containing protein 5 isoform X2
male-specific lethal 3 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
male-specific lethal 3 homolog, 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 17 samples with support for all annotated introns
male-specific lethal 3 homolog, 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 9 samples with support for all annotated introns
male-specific lethal 3 homolog, 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 10 samples with support for all annotated introns
male-specific lethal 3 homolog isoform X2
male-specific lethal 3 homolog isoform X1
CKLF-like MARVEL transmembrane domain-containing protein 4, 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 6 samples with support for all annotated introns
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X4
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X1
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X7
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CKLF-like MARVEL transmembrane domain-containing protein 4, transcript variant X5
CKLF-like MARVEL transmembrane domain-containing protein 4 isoform X1
CKLF-like MARVEL transmembrane domain-containing protein 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycosylated lysosomal membrane protein-like, transcript variant X1
glycosylated lysosomal membrane protein-like isoform X1
glycosylated lysosomal membrane protein-like, transcript variant X2
glycosylated lysosomal membrane protein-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 8 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 89% 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 5 bases in 4 codons; deleted 8 bases in 6 codons; substituted 5 bases at 5 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium channel protein para
glycine-rich cell wall structural protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glycine-rich cell wall structural protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine-rich cell wall structural protein-like, transcript variant X2
breast cancer type 1 susceptibility protein homolog
glycine-rich cell wall structural protein-like, transcript variant X3
glycine-rich cell wall structural protein-like
ras guanine nucleotide exchange factor R-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC114874018, transcript variant X1
uncharacterized LOC114874018, transcript variant X8
uncharacterized LOC114874018, transcript variant X9
uncharacterized LOC114874018, transcript variant X10
uncharacterized LOC114874018, transcript variant X2
uncharacterized LOC114874018, transcript variant X5
uncharacterized LOC114874018, transcript variant X4
uncharacterized LOC114874018, transcript variant X7
uncharacterized LOC114874018, transcript variant X3
uncharacterized LOC114874018, transcript variant X6
uncharacterized protein LOC114874018 isoform X1
uncharacterized protein LOC114874018 isoform X2
uncharacterized protein LOC114874018 isoform X3
uncharacterized protein LOC114874018 isoform X4
myb/SANT-like DNA-binding domain-containing protein 3
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
mitochondrial potassium channel ATP-binding subunit
LOW QUALITY PROTEIN: mitochondrial potassium channel ATP-binding subunit
GPI mannosyltransferase 4, transcript variant X2
GPI mannosyltransferase 4, transcript variant X1
GPI mannosyltransferase 4, transcript variant X3
histone deacetylase 6, transcript variant X1
histone deacetylase 6, transcript variant X2
histone deacetylase 6, 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 19 samples with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X1
guanine nucleotide exchange factor DBS-like, transcript variant X2
guanine nucleotide exchange factor DBS-like, transcript variant X4
guanine nucleotide exchange factor DBS-like, transcript variant X3
guanine nucleotide exchange factor DBS-like isoform X1
guanine nucleotide exchange factor DBS-like isoform X2
guanine nucleotide exchange factor DBS-like isoform 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 11 samples with support for all annotated introns
uncharacterized protein LOC114874033 isoform X1
uncharacterized protein LOC114874033 isoform X3
uncharacterized protein LOC114874033 isoform X4
very long-chain specific acyl-CoA dehydrogenase, mitochondrial
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51, transcript variant X1
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51 isoform X1
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51 isoform X2
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X4
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 12 samples with support for all annotated introns
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X1
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X2
cAMP-dependent protein kinase type I regulatory subunit isoform X1
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X5
cAMP-dependent protein kinase type I regulatory subunit, transcript variant X6
cAMP-dependent protein kinase type I regulatory subunit isoform X3
cAMP-dependent protein kinase type I regulatory subunit isoform X2
leukocyte receptor cluster member 8 homolog, transcript variant X1
leukocyte receptor cluster member 8 homolog, transcript variant X2
leukocyte receptor cluster member 8 homolog isoform X1
leukocyte receptor cluster member 8 homolog isoform X2
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X5
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X1
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X4
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X2
zinc finger protein with KRAB and SCAN domains 5-like isoform X1
zinc finger protein with KRAB and SCAN domains 5-like, transcript variant X6
zinc finger protein with KRAB and SCAN domains 5-like isoform X2
neuroligin-4, X-linked, transcript variant X1
neuroligin-4, X-linked, transcript variant X3
neuroligin-4, X-linked, 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 3 samples with support for all annotated introns
uncharacterized LOC114874013, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC114874013, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC114874013, transcript variant X1
uncharacterized LOC114874013, 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 2 samples with support for all annotated introns
uncharacterized LOC114874013, transcript variant X5
uncharacterized LOC114874013, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC114874013 isoform X1
uncharacterized protein LOC114874013 isoform X2
ras-related protein Rab6, transcript variant X1
ras-related protein Rab6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein K, transcript variant X6
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
heterogeneous nuclear ribonucleoprotein K, transcript variant X8
heterogeneous nuclear ribonucleoprotein K, transcript variant X5
heterogeneous nuclear ribonucleoprotein K, transcript variant X7
heterogeneous nuclear ribonucleoprotein K, transcript variant X2
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
heterogeneous nuclear ribonucleoprotein K, transcript variant X4
heterogeneous nuclear ribonucleoprotein K isoform X2
heterogeneous nuclear ribonucleoprotein K isoform X1
cytochrome b5-like, transcript variant X1
cytochrome b5-like, transcript variant X3
cytochrome b5-like, transcript variant X4
cytochrome b5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 74 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
retinal-specific phospholipid-transporting ATPase ABCA4-like
uncharacterized LOC114874053, transcript variant X3
uncharacterized LOC114874053, transcript variant X2
uncharacterized LOC114874053, transcript variant X1
uncharacterized protein LOC114874053 isoform X1
uncharacterized protein LOC114874053 isoform X2
transforming acidic coiled-coil-containing protein 3
protein limb expression 1 homolog, transcript variant X2
protein limb expression 1 homolog, transcript variant X1
ATP-dependent Clp protease proteolytic subunit, transcript variant X2
ATP-dependent Clp protease proteolytic subunit, transcript variant X1
ATP-dependent Clp protease proteolytic subunit
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 15 samples with support for all annotated introns
peripheral plasma membrane protein CASK, transcript variant X7
peripheral plasma membrane protein CASK, transcript variant X8
peripheral plasma membrane protein CASK, transcript variant X4
peripheral plasma membrane protein CASK, transcript variant X6
peripheral plasma membrane protein CASK, transcript variant X2
peripheral plasma membrane protein CASK, transcript variant X3
peripheral plasma membrane protein CASK, transcript variant X5
peripheral plasma membrane protein CASK, transcript variant X1
peripheral plasma membrane protein CASK, transcript variant X9
peripheral plasma membrane protein CASK, transcript variant X11
peripheral plasma membrane protein CASK, transcript variant X10
peripheral plasma membrane protein CASK, transcript variant X12
peripheral plasma membrane protein CASK isoform X7
peripheral plasma membrane protein CASK isoform X8
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X6
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X1
peripheral plasma membrane protein CASK isoform X9
peripheral plasma membrane protein CASK isoform X12
peripheral plasma membrane protein CASK isoform X11
peripheral plasma membrane protein CASK isoform X10
autophagy-related protein 16-1, transcript variant X1
autophagy-related protein 16-1, transcript variant X2
autophagy-related protein 16-1, 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 1 sample with support for all annotated introns
autophagy-related protein 16-1 isoform X1
autophagy-related protein 16-1 isoform X2
uncharacterized LOC114881504, 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 1 sample with support for all annotated introns
uncharacterized LOC114881504, transcript variant X1
uncharacterized LOC114881465, transcript variant X1
uncharacterized LOC114881465, transcript variant X2
uncharacterized protein LOC114881465 isoform X1
uncharacterized protein LOC114881465 isoform X2
prefoldin subunit 5, transcript variant X3
prefoldin subunit 5, transcript variant X2
prefoldin subunit 5, transcript variant X1
uncharacterized LOC114881498, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
muscarinic acetylcholine receptor gar-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscarinic acetylcholine receptor gar-2, 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 1 sample with support for all annotated introns
muscarinic acetylcholine receptor gar-2 isoform X2
muscarinic acetylcholine receptor gar-2 isoform X1
uncharacterized LOC114881498, 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 2 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
zinc finger and BTB domain-containing protein 49-like
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
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: zinc finger and BTB domain-containing protein 49-like
tudor domain-containing protein 1, transcript variant X2
tudor domain-containing protein 1, transcript variant X3
tudor domain-containing protein 1, transcript variant X1
tudor domain-containing protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tudor domain-containing protein 1 isoform X1
tudor domain-containing protein 1 isoform X3
tudor domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 15 samples with support for all annotated introns
cleavage stimulation factor subunit 2, transcript variant X1
cleavage stimulation factor subunit 2, transcript variant X2
cleavage stimulation factor subunit 2 tau variant isoform X2
cleavage stimulation factor subunit 2 isoform X1
cilia- and flagella-associated protein 300-like
phospholipid-transporting ATPase IF, transcript variant X2
phospholipid-transporting ATPase IF, 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 9 samples with support for all annotated introns
phospholipid-transporting ATPase IF isoform X2
phospholipid-transporting ATPase IF isoform X1
2-oxoglutarate dehydrogenase, mitochondrial-like
mitochondrial folate transporter/carrier, transcript variant X1
mitochondrial folate transporter/carrier isoform X1
mitochondrial folate transporter/carrier, transcript variant X2
mitochondrial folate transporter/carrier isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
acetylcholine receptor subunit alpha-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 238 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC114873880, 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 2 samples with support for all annotated introns
uncharacterized LOC114873880, transcript variant X2
uncharacterized LOC114873880, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC114873880, transcript variant X1
uncharacterized protein LOC114873880 isoform X1
uncharacterized protein LOC114873880 isoform X2
uncharacterized protein LOC114873880 isoform X4
uncharacterized protein LOC114873880 isoform X3
uncharacterized LOC114873811, transcript variant X4
uncharacterized LOC114873811, 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
uncharacterized LOC114873811, transcript variant X2
uncharacterized LOC114873811, transcript variant X1
uncharacterized LOC114873811, transcript variant X5
uncharacterized protein LOC114873811 isoform X1
uncharacterized protein LOC114873811 isoform X2
ATP-dependent RNA helicase DHX30-like, transcript variant X2
ATP-dependent RNA helicase DHX30-like, transcript variant X1
ATP-dependent RNA helicase DHX30-like isoform X1
ATP-dependent RNA helicase DHX30-like, transcript variant X3
ATP-dependent RNA helicase DHX30-like isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1
putative deoxyribonuclease TATDN1, transcript variant X1
putative deoxyribonuclease TATDN1 isoform X1
putative deoxyribonuclease TATDN1, transcript variant X2
putative deoxyribonuclease TATDN1 isoform X2
spectrin beta chain, transcript variant X1
spectrin beta chain, transcript variant X3
spectrin beta chain, transcript variant X5
spectrin beta chain, transcript variant X2
spectrin beta chain, transcript variant X4
spectrin beta chain, transcript variant X6
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
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
uncharacterized LOC114872855, 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
uncharacterized LOC114872855, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
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 12 samples with support for all annotated introns
insulin-like peptide receptor, 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 3 samples with support for all annotated introns
insulin-like peptide receptor, 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 7 samples with support for all annotated introns
insulin-like peptide receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin-like peptide receptor isoform X1
insulin-like peptide receptor isoform X2
PI-PLC X domain-containing protein 1-like, transcript variant X2
PI-PLC X domain-containing protein 1-like, transcript variant X1
PI-PLC X domain-containing protein 1-like
protein lin-52 homolog, transcript variant X2
protein lin-52 homolog, transcript variant X4
protein lin-52 homolog, transcript variant X3
protein lin-52 homolog, transcript variant X1
protein lin-52 homolog, transcript variant X5
uncharacterized LOC114873330, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC114873330, 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
COPII coat assembly protein SEC16, transcript variant X3
COPII coat assembly protein SEC16, transcript variant X2
uncharacterized protein LOC114873652 isoform X2
COPII coat assembly protein SEC16, transcript variant X1
COPII coat assembly protein SEC16, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
COPII coat assembly protein SEC16, 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 6 samples with support for all annotated introns
uncharacterized protein LOC114873652 isoform X4
COPII coat assembly protein SEC16 isoform X3
uncharacterized protein LOC114873652 isoform X1
uncharacterized LOC123987629, transcript variant X2
uncharacterized LOC123987629, transcript variant X1
uncharacterized protein LOC123987629 isoform X1
uncharacterized protein LOC123987629 isoform X2
uncharacterized LOC114873964, 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
uncharacterized LOC114873964, transcript variant X1
uncharacterized protein LOC114873964 isoform X2
uncharacterized protein LOC114873964 isoform X1
kinesin light chain, transcript variant X4
kinesin light chain, transcript variant X3
kinesin light chain, transcript variant X2
kinesin light chain, transcript variant X6
kinesin light chain, transcript variant X1
kinesin light chain, transcript variant X5
eukaryotic translation initiation factor 5
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 19 samples with support for all annotated introns
arylalkylamine N-acetyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
activating transcription factor 3, transcript variant X1
activating transcription factor 3, transcript variant X2
activating transcription factor 3 isoform X1
activating transcription factor 3 isoform X2
protein transport protein Sec61 subunit gamma
calcineurin B homologous protein 1-like, transcript variant X1
calcineurin B homologous protein 1-like, transcript variant X2
calcineurin B homologous protein 1-like, transcript variant X4
calcineurin B homologous protein 1-like, transcript variant X3
calcineurin B homologous protein 1-like isoform X2
calcineurin B homologous protein 1-like isoform X1
protein transport protein Sec23A, transcript variant X3
protein transport protein Sec23A, transcript variant X1
protein transport protein Sec23A, transcript variant X2
protein transport protein Sec23A isoform X2
protein transport protein Sec23A isoform X1
mitochondrial ribonuclease P catalytic subunit, transcript variant X2
mitochondrial ribonuclease P catalytic subunit, transcript variant X1
mitochondrial ribonuclease P catalytic subunit isoform X2
mitochondrial ribonuclease P catalytic subunit isoform X1
leucine-rich repeat-containing protein 58, transcript variant X2
leucine-rich repeat-containing protein 58, transcript variant X1
leucine-rich repeat-containing protein 58
glycogen synthase kinase-3 beta-like, transcript variant X6
glycogen synthase kinase-3 beta-like, transcript variant X4
glycogen synthase kinase-3 beta-like, transcript variant X5
glycogen synthase kinase-3 beta-like, transcript variant X7
glycogen synthase kinase-3 beta-like, transcript variant X8
glycogen synthase kinase-3 beta-like, transcript variant X2
glycogen synthase kinase-3 beta-like, transcript variant X9
glycogen synthase kinase-3 beta-like, transcript variant X3
glycogen synthase kinase-3 beta-like, transcript variant X1
glycogen synthase kinase-3 beta-like, transcript variant X10
glycogen synthase kinase-3 beta-like isoform X7
glycogen synthase kinase-3 beta-like isoform X6
glycogen synthase kinase-3 beta-like isoform X4
glycogen synthase kinase-3 beta-like isoform X5
glycogen synthase kinase-3 beta-like isoform X2
glycogen synthase kinase-3 beta-like isoform X3
glycogen synthase kinase-3 beta-like isoform X10
glycogen synthase kinase-3 beta-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ammonium transporter Rh type A, transcript variant X2
ammonium transporter Rh type A, transcript variant X1
ammonium transporter Rh type A, transcript variant X3
ammonium transporter Rh type A, transcript variant X4
ammonium transporter Rh type A, transcript variant X6
ammonium transporter Rh type A isoform X1
ammonium transporter Rh type A isoform X5
ammonium transporter Rh type A isoform X3
ammonium transporter Rh type A isoform X2
ammonium transporter Rh type A, transcript variant X5
ammonium transporter Rh type A, transcript variant X7
ammonium transporter Rh type A isoform X4
ammonium transporter Rh type A isoform X6
signal recognition particle receptor subunit alpha homolog, transcript variant X2
signal recognition particle receptor subunit alpha homolog, transcript variant X1
signal recognition particle receptor subunit alpha homolog isoform X2
signal recognition particle receptor subunit alpha homolog isoform X1
uncharacterized LOC114874138, transcript variant X1
uncharacterized LOC114874138, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
calcium-transporting ATPase type 2C member 1
uncharacterized LOC114873491, transcript variant X2
uncharacterized LOC114873491, transcript variant X1
uncharacterized protein LOC114873491 isoform X2
uncharacterized protein LOC114873491 isoform X1
uncharacterized LOC114873491, transcript variant X3
uncharacterized protein LOC114873491 isoform X3
uncharacterized LOC114874228, transcript variant X1
uncharacterized protein LOC114874228 isoform X1
uncharacterized LOC114874228, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC114874228 isoform X2
biogenesis of lysosome-related organelles complex 1 subunit 5
chromatin accessibility complex 16kD protein
mitochondrial enolase superfamily member 1-like
adenosine 5'-monophosphoramidase HINT3-like
protein bric-a-brac 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 8 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein bric-a-brac 2-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 2 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X1
protein bric-a-brac 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X7
protein bric-a-brac 2-like, transcript variant X3
protein bric-a-brac 2-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X8
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
uncharacterized protein LOC114874169 isoform X6
longitudinals lacking protein-like, transcript variant X1
longitudinals lacking protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X5
longitudinals lacking protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X46
longitudinals lacking protein-like, transcript variant X7
longitudinals lacking protein-like, transcript variant X6
longitudinals lacking protein-like, transcript variant X8
longitudinals lacking protein-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X10
longitudinals lacking protein-like, transcript variant X12
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 16 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X13
longitudinals lacking protein-like, transcript variant X11
longitudinals lacking protein-like, transcript variant X9
longitudinals lacking protein-like, transcript variant X20
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 15 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X16
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 13 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X22
longitudinals lacking protein-like, transcript variant X25
longitudinals lacking protein-like, transcript variant X15
longitudinals lacking protein-like, transcript variant X17
longitudinals lacking protein-like, transcript variant X26
longitudinals lacking protein-like, transcript variant X24
longitudinals lacking protein-like, transcript variant X18
longitudinals lacking protein-like, transcript variant X19
longitudinals lacking protein-like, transcript variant X21
longitudinals lacking protein-like, transcript variant X23
longitudinals lacking protein-like, transcript variant X28
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 11 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X38
longitudinals lacking protein-like, transcript variant X32
longitudinals lacking protein-like, transcript variant X33
longitudinals lacking protein-like, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X34
longitudinals lacking protein-like, transcript variant X29
longitudinals lacking protein-like, transcript variant X36
longitudinals lacking protein-like, transcript variant X37
longitudinals lacking protein-like, transcript variant X27
longitudinals lacking protein-like, transcript variant X41
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 10 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X49
longitudinals lacking protein-like, transcript variant X40
longitudinals lacking protein-like, transcript variant X45
longitudinals lacking protein-like, transcript variant X47
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 16 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X39
longitudinals lacking protein-like, transcript variant X43
longitudinals lacking protein-like, transcript variant X31
longitudinals lacking protein-like, transcript variant X42
longitudinals lacking protein-like, transcript variant X44
longitudinals lacking protein-like, transcript variant X50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X48
longitudinals lacking protein, isoforms H/M/V-like isoform X41
longitudinals lacking protein, isoforms H/M/V-like isoform X20
longitudinals lacking protein, isoforms H/M/V-like isoform X28
longitudinals lacking protein, isoforms A/B/D/L-like isoform X49
longitudinals lacking protein-like isoform X48
longitudinals lacking protein, isoforms A/B/D/L-like isoform X8
longitudinals lacking protein, isoforms A/B/D/L-like isoform X40
longitudinals lacking protein, isoforms F/I/K/T-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X47
longitudinals lacking protein-like isoform X38
longitudinals lacking protein, isoforms A/B/D/L-like isoform X5
longitudinals lacking protein-like isoform X32
longitudinals lacking protein-like isoform X33
longitudinals lacking protein-like isoform X16
longitudinals lacking protein, isoforms H/M/V-like isoform X46
longitudinals lacking protein-like isoform X22
longitudinals lacking protein-like isoform X25
longitudinals lacking protein, isoforms A/B/D/L-like isoform X10
longitudinals lacking protein-like isoform X15
longitudinals lacking protein, isoforms A/B/D/L-like isoform X17
longitudinals lacking protein, isoforms A/B/D/L-like isoform X2
longitudinals lacking protein, isoforms A/B/D/L-like isoform X26
longitudinals lacking protein, isoforms A/B/D/L-like isoform X24
longitudinals lacking protein-like isoform X39
longitudinals lacking protein-like isoform X19
longitudinals lacking protein, isoforms A/B/D/L-like isoform X35
longitudinals lacking protein, isoforms A/B/D/L-like isoform X30
longitudinals lacking protein, isoforms A/B/D/L-like isoform X34
longitudinals lacking protein-like isoform X21
longitudinals lacking protein, isoforms A/B/D/L-like isoform X29
longitudinals lacking protein-like isoform X36
longitudinals lacking protein, isoforms A/B/D/L-like isoform X3
longitudinals lacking protein, isoforms A/B/D/L-like isoform X6
longitudinals lacking protein, isoforms H/M/V-like isoform X43
longitudinals lacking protein-like isoform X37
longitudinals lacking protein-like isoform X23
longitudinals lacking protein-like isoform X13
longitudinals lacking protein-like isoform X27
longitudinals lacking protein-like isoform X11
longitudinals lacking protein, isoforms A/B/D/L-like isoform X4
longitudinals lacking protein, isoforms H/M/V-like isoform X31
longitudinals lacking protein, isoforms A/B/D/L-like isoform X9
longitudinals lacking protein, isoforms H/M/V-like isoform X42
longitudinals lacking protein, isoforms H/M/V-like isoform X44
longitudinals lacking protein, isoforms H/M/V-like isoform X45
uncharacterized LOC114873155, transcript variant X1
uncharacterized LOC114873155, transcript variant X2
uncharacterized protein LOC114873155 isoform X2
uncharacterized protein LOC114873155 isoform X1
uncharacterized LOC114873179, transcript variant X1
uncharacterized LOC114873179, transcript variant X2
igLON family member 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
igLON family member 5-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 1 sample with support for all annotated introns
igLON family member 5-like, transcript variant X3
protein borderless-like, transcript variant X2
protein borderless-like, transcript variant X1
dopamine D2-like receptor, 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 1 sample with support for all annotated introns
dopamine D2-like receptor, transcript variant X1
dopamine D2-like receptor, transcript variant X3
dopamine D2-like receptor, transcript variant X4
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
dopamine D2-like receptor, transcript variant X5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 15% 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 78% 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
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: nuclease SbcCD subunit C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized transmembrane protein DDB_G0289901-like
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: 9 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized transmembrane protein DDB_G0289901-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC114874052
cell adhesion molecule 2-like, transcript variant X1
cell adhesion molecule 2-like, transcript variant X2
cell adhesion molecule 2-like isoform X1
cell adhesion molecule 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 4 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 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: 6 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 67a-like, transcript variant X1
odorant receptor 67a-like, transcript variant X2
uncharacterized protein LOC123987965 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable cytochrome P450 12a5, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
visual system homeobox 2-like, transcript variant X1
visual system homeobox 2-like, transcript variant X3
visual system homeobox 2-like, transcript variant X2
visual system homeobox 2-like, transcript variant X4
visual system homeobox 2-like isoform X1
visual system homeobox 2-like isoform X3
visual system homeobox 2-like isoform X2
visual system homeobox 2-like isoform X4
disheveled-associated activator of morphogenesis 1, transcript variant X4
disheveled-associated activator of morphogenesis 1, transcript variant X6
disheveled-associated activator of morphogenesis 1, transcript variant X3
disheveled-associated activator of morphogenesis 1, transcript variant X2
disheveled-associated activator of morphogenesis 1, transcript variant X5
disheveled-associated activator of morphogenesis 1, transcript variant X1
disheveled-associated activator of morphogenesis 1 isoform X2
disheveled-associated activator of morphogenesis 1 isoform X1
disheveled-associated activator of morphogenesis 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% 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 52% coverage of the annotated genomic feature by RNAseq alignments
tetra-peptide repeat homeobox protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 3 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine/tyrosine-interacting protein-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 15 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein-like isoform X1
serine/threonine/tyrosine-interacting protein-like isoform X3
serine/threonine/tyrosine-interacting protein-like isoform X2
NPC intracellular cholesterol transporter 2 homolog a-like
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X4
A disintegrin and metalloproteinase with thrombospondin motifs 9-like, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 9-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 9-like isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 9-like isoform X2
ras-related protein rab7, transcript variant X1
ras-related protein rab7, transcript variant X2
LOW QUALITY PROTEIN: DNA repair protein RAD50
RNA-binding protein 39, transcript variant X4
RNA-binding protein 39, transcript variant X3
RNA-binding protein 39, transcript variant X2
RNA-binding protein 39, transcript variant X1
RNA-binding protein 39, transcript variant X5
N-acetyltransferase ESCO1, 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
N-acetyltransferase ESCO1, transcript variant X1
N-acetyltransferase ESCO1, transcript variant X3
N-acetyltransferase ESCO1, transcript variant X4
probable ATP-dependent RNA helicase DDX43, transcript variant X4
probable ATP-dependent RNA helicase DDX43, transcript variant X3
probable ATP-dependent RNA helicase DDX43, transcript variant X2
probable ATP-dependent RNA helicase DDX43, transcript variant X1
probable ATP-dependent RNA helicase DDX43
cytochrome c oxidase subunit 6b-2-like, transcript variant X3
cytochrome c oxidase subunit 6b-2-like, transcript variant X4
cytochrome c oxidase subunit 6b-2-like, transcript variant X5
cytochrome c oxidase subunit 6b-2-like isoform X2
cytochrome c oxidase subunit 6b-2-like, transcript variant X1
cytochrome c oxidase subunit 6b-2-like, transcript variant X2
telomerase RNA component interacting RNase-like isoform X1
neuroligin-1-like, transcript variant X1
neuroligin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neuroligin-1-like, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00377
60S ribosomal protein L35a, transcript variant X1
60S ribosomal protein L35a, transcript variant X2
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X1
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 16 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X2
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 17 samples with support for all annotated introns
uncharacterized protein LOC114876942 isoform X1
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X5
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 1 isoform X3
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X4
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X2
glutaminase liver isoform, mitochondrial, transcript variant X1
glutaminase liver isoform, mitochondrial, transcript variant X2
glutaminase liver isoform, mitochondrial isoform X1
glutaminase liver isoform, mitochondrial isoform X2
glutaminase liver isoform, mitochondrial, transcript variant X3
glutaminase liver isoform, mitochondrial, transcript variant X4
glutaminase liver isoform, mitochondrial isoform X3
glutaminase liver isoform, mitochondrial isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC114876970, transcript variant X1
uncharacterized LOC114876970, transcript variant X2
uncharacterized protein LOC114876970 isoform X1
uncharacterized protein LOC114876970 isoform X2
EF-hand calcium-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier organic anion transporter family member 74D, transcript variant X2
solute carrier organic anion transporter family member 74D, transcript variant X5
solute carrier organic anion transporter family member 74D, transcript variant X1
solute carrier organic anion transporter family member 74D, transcript variant X4
solute carrier organic anion transporter family member 74D, transcript variant X6
solute carrier organic anion transporter family member 74D, transcript variant X7
solute carrier organic anion transporter family member 74D, transcript variant X3
solute carrier organic anion transporter family member 74D, transcript variant X8
solute carrier organic anion transporter family member 74D, transcript variant X9
solute carrier organic anion transporter family member 74D
uncharacterized LOC114876962, transcript variant X3
uncharacterized LOC114876962, transcript variant X1
probable elongation factor 1-delta, transcript variant X1
probable elongation factor 1-delta, transcript variant X5
probable elongation factor 1-delta, transcript variant X2
probable elongation factor 1-delta isoform X3
probable elongation factor 1-delta isoform X1
probable elongation factor 1-delta, transcript variant X4
probable elongation factor 1-delta, transcript variant X3
heparan-sulfate 6-O-sulfotransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
heparan-sulfate 6-O-sulfotransferase 2, transcript variant X1
heparan-sulfate 6-O-sulfotransferase 2 isoform X2
heparan-sulfate 6-O-sulfotransferase 2 isoform X1
uncharacterized LOC114876962, transcript variant X2
uncharacterized LOC114876975, transcript variant X2
uncharacterized LOC114876975, transcript variant X1
microtubule-associated protein futsch-like, transcript variant X2
microtubule-associated protein futsch-like, transcript variant X1
microtubule-associated protein futsch-like isoform X2
microtubule-associated protein futsch-like isoform X1
uncharacterized LOC114876967, transcript variant X2
uncharacterized LOC114876967, transcript variant X3
uncharacterized LOC114876967, transcript variant X1
circadian clock-controlled protein daywake-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor E2F2, transcript variant X2
transcription factor E2F2, transcript variant X1
transcription factor E2F2, transcript variant X4
transcription factor E2F2, transcript variant X3
mortality factor 4-like protein 1, transcript variant X1
mortality factor 4-like protein 1, transcript variant X2
mortality factor 4-like protein 1 isoform X1
mortality factor 4-like protein 1 isoform X2
mortality factor 4-like protein 1, transcript variant X4
mortality factor 4-like protein 1, transcript variant X3
mortality factor 4-like protein 1 isoform X3
mortality factor 4-like protein 1 isoform X4
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X3
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X4
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X3
uncharacterized LOC114880937, transcript variant X3
uncharacterized LOC114880937, transcript variant X1
uncharacterized LOC114880937, transcript variant X2
uncharacterized protein LOC114880937 isoform X2
uncharacterized protein LOC114880937 isoform X1
homeobox protein Nkx-2.8-like, transcript variant X1
homeobox protein Nkx-2.8-like, transcript variant X2
homeobox protein Nkx-2.8-like isoform X1
homeobox protein Nkx-2.8-like isoform X2
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X2
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X6
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X1
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X4
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X3
actin cytoskeleton-regulatory complex protein sla1-like, transcript variant X5
actin cytoskeleton-regulatory complex protein sla1-like isoform X2
uncharacterized protein LOC114875390 isoform X1
microtubule-associated protein RP/EB family member 1-like, transcript variant X1
microtubule-associated protein RP/EB family member 1-like, transcript variant X4
microtubule-associated protein RP/EB family member 1-like, transcript variant X3
microtubule-associated protein RP/EB family member 1-like, transcript variant X2
microtubule-associated protein RP/EB family member 1-like isoform X3
microtubule-associated protein RP/EB family member 1-like isoform X2
microtubule-associated protein RP/EB family member 1-like isoform X1
spermatogenesis-defective protein 39 homolog, transcript variant X3
spermatogenesis-defective protein 39 homolog, transcript variant X1
spermatogenesis-defective protein 39 homolog, transcript variant X2
spermatogenesis-defective protein 39 homolog, transcript variant X4
spermatogenesis-defective protein 39 homolog isoform X2
spermatogenesis-defective protein 39 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X3
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X5
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X1
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X2
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X4
short-chain dehydrogenase/reductase family 16C member 6-like isoform X2
short-chain dehydrogenase/reductase family 16C member 6-like isoform X1
zinc finger CCCH domain-containing protein 14, transcript variant X1
zinc finger CCCH domain-containing protein 14, transcript variant X2
zinc finger CCCH domain-containing protein 14 isoform X1
zinc finger CCCH domain-containing protein 14 isoform X2
arginine-glutamic acid dipeptide repeats protein-like, 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 4 samples with support for all annotated introns
arginine-glutamic acid dipeptide repeats protein-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
arginine-glutamic acid dipeptide repeats protein-like
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 13 samples with support for all annotated introns
tonsoku-like protein, transcript variant X1
tonsoku-like protein, transcript variant X2
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X3
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X2
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X1
guanine nucleotide exchange factor for Rab-3A-like
juvenile hormone epoxide hydrolase 1-like
trafficking protein particle complex subunit 4
translationally-controlled tumor protein homolog
retinoic acid receptor RXR-alpha-A, transcript variant X8
retinoic acid receptor RXR-alpha-A, transcript variant X7
retinoic acid receptor RXR-alpha-A, transcript variant X5
retinoic acid receptor RXR-alpha-A, transcript variant X6
retinoic acid receptor RXR-alpha-A, transcript variant X2
retinoic acid receptor RXR-alpha-A, transcript variant X1
retinoic acid receptor RXR-alpha-A, transcript variant X4
retinoic acid receptor RXR-alpha-A, transcript variant X3
retinoic acid receptor RXR-alpha-B isoform X4
retinoic acid receptor RXR-alpha-B isoform X2
retinoic acid receptor RXR-alpha-B isoform X3
retinoic acid receptor RXR-alpha-B isoform X1
retinoic acid receptor RXR-alpha-A isoform X5
ribosomal RNA-processing protein 7 homolog A
transmembrane protein 145-like, 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
transmembrane protein 145-like, transcript variant X1
transmembrane protein 145-like, transcript variant X3
transmembrane protein 145-like isoform X2
transmembrane protein 145-like isoform X1
FAD-linked sulfhydryl oxidase ALR, transcript variant X2
FAD-linked sulfhydryl oxidase ALR, 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 16 samples with support for all annotated introns
FAD-linked sulfhydryl oxidase ALR, transcript variant X1
multiple coagulation factor deficiency protein 2 homolog
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X1
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X2
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X3
MATH and LRR domain-containing protein PFE0570w-like isoform X1
MATH and LRR domain-containing protein PFE0570w-like isoform X2
MATH and LRR domain-containing protein PFE0570w-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
ufm1-specific protease 1, transcript variant X4
ufm1-specific protease 1, transcript variant X3
ufm1-specific protease 1, transcript variant X1
ufm1-specific protease 1, transcript variant X2
transmembrane protein adipocyte-associated 1 homolog, transcript variant X4
transmembrane protein adipocyte-associated 1 homolog, transcript variant X1
transmembrane protein adipocyte-associated 1 homolog, transcript variant X2
transmembrane protein adipocyte-associated 1 homolog, transcript variant X3
transmembrane protein adipocyte-associated 1 homolog isoform X2
uncharacterized protein LOC114875374 isoform X1
uncharacterized LOC114875370, 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 10 samples with support for all annotated introns
uncharacterized LOC114875370, 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 10 samples with support for all annotated introns
uncharacterized protein LOC114875370 isoform X1
uncharacterized protein LOC114875370 isoform X2
uncharacterized LOC114875370, transcript variant X3
uncharacterized protein LOC114875370 isoform X3
probable beta-hexosaminidase fdl, transcript variant X1
probable beta-hexosaminidase fdl, transcript variant X2
uncharacterized LOC114875384, transcript variant X3
uncharacterized LOC114875384, transcript variant X4
uncharacterized LOC114875384, transcript variant X1
uncharacterized LOC114875384, transcript variant X5
uncharacterized LOC114875384, transcript variant X2
probable beta-hexosaminidase fdl isoform X1
probable beta-hexosaminidase fdl isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 47% 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: 3 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
protein KRI1 homolog, 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
protein KRI1 homolog, transcript variant X1
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X2
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X3
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X6
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X4
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B isoform X3
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X1
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B, transcript variant X5
probable ubiquitin carboxyl-terminal hydrolase MINDY-4 isoform X1
probable ubiquitin carboxyl-terminal hydrolase MINDY-4 isoform X2
nicotinamidase-like, transcript variant X3
nicotinamidase-like, transcript variant X4
nicotinamidase-like, transcript variant X1
nicotinamidase-like, transcript variant X2
nicotinamidase-like, transcript variant X5
5'-deoxynucleotidase HDDC2, transcript variant X1
5'-deoxynucleotidase HDDC2, transcript variant X2
V-type proton ATPase catalytic subunit A
upstream stimulatory factor 1-like, transcript variant X1
upstream stimulatory factor 1-like, transcript variant X2
upstream stimulatory factor 1-like isoform X1
upstream stimulatory factor 1-like isoform X2
ubiquitin domain-containing protein UBFD1-like, transcript variant X1
ubiquitin domain-containing protein UBFD1-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 19 samples with support for all annotated introns
ubiquitin domain-containing protein UBFD1-like
WW domain-binding protein 2, transcript variant X2
WW domain-binding protein 2, transcript variant X1
equilibrative nucleoside transporter 4, transcript variant X2
equilibrative nucleoside transporter 4, transcript variant X1
equilibrative nucleoside transporter 4 isoform X1
equilibrative nucleoside transporter 4 isoform X2
serine/threonine-protein kinase ICK, transcript variant X1
serine/threonine-protein kinase ICK, transcript variant X9
serine/threonine-protein kinase ICK, transcript variant X7
serine/threonine-protein kinase ICK, transcript variant X8
serine/threonine-protein kinase ICK, transcript variant X6
serine/threonine-protein kinase ICK, transcript variant X3
serine/threonine-protein kinase ICK, transcript variant X4
serine/threonine-protein kinase ICK, transcript variant X2
serine/threonine-protein kinase ICK, transcript variant X5
serine/threonine-protein kinase ICK isoform X5
serine/threonine-protein kinase ICK isoform X3
serine/threonine-protein kinase ICK isoform X4
serine/threonine-protein kinase ICK isoform X2
serine/threonine-protein kinase ICK isoform X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
dynein regulatory complex protein 11-like
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 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: COP9 signalosome complex subunit 3
nicotinamide riboside kinase 1, transcript variant X1
nicotinamide riboside kinase 1 isoform X1
nicotinamide riboside kinase 1, transcript variant X2
uncharacterized LOC114875414, transcript variant X1
uncharacterized LOC114875414, transcript variant X2
COP9 signalosome complex subunit 1, transcript variant X2
COP9 signalosome complex subunit 1, transcript variant X1
COP9 signalosome complex subunit 1, transcript variant X3
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X2
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X8
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X7
aldehyde dehydrogenase, dimeric NADP-preferring isoform X2
aldehyde dehydrogenase, dimeric NADP-preferring isoform X7
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X4
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X3
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X1
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X5
aldehyde dehydrogenase, dimeric NADP-preferring, transcript variant X6
aldehyde dehydrogenase, dimeric NADP-preferring isoform X4
aldehyde dehydrogenase, dimeric NADP-preferring isoform X3
aldehyde dehydrogenase, dimeric NADP-preferring isoform X1
aldehyde dehydrogenase, dimeric NADP-preferring isoform X5
aldehyde dehydrogenase, dimeric NADP-preferring isoform X6
neuronal acetylcholine receptor subunit alpha-5-like, transcript variant X3
neuronal acetylcholine receptor subunit alpha-5-like, transcript variant X2
neuronal acetylcholine receptor subunit alpha-5-like, transcript variant X1
neuronal acetylcholine receptor subunit alpha-5-like isoform X1
neuronal acetylcholine receptor subunit alpha-5-like isoform X3
neuronal acetylcholine receptor subunit alpha-5-like isoform X2
neuronal acetylcholine receptor subunit alpha-6-like
neuronal acetylcholine receptor subunit alpha-10-like, transcript variant X2
neuronal acetylcholine receptor subunit alpha-10-like, transcript variant X1
neuronal acetylcholine receptor subunit alpha-10-like isoform X1
neuronal acetylcholine receptor subunit alpha-10-like isoform X2
acetylcholine receptor subunit beta-like
neuralized-like protein 2, transcript variant X2
neuralized-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
sperm mitochondrial-associated cysteine-rich protein-like
putative mediator of RNA polymerase II transcription subunit 12
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 4-like
RUN and FYVE domain-containing protein 2 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 9 samples with support for all annotated introns
soluble guanylate cyclase 89Da-like, transcript variant X3
soluble guanylate cyclase 89Da-like, transcript variant X1
soluble guanylate cyclase 89Da-like, transcript variant X2
soluble guanylate cyclase 89Da-like isoform X1
soluble guanylate cyclase 89Da-like isoform X2
soluble guanylate cyclase 89Da-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
soluble guanylate cyclase 89Da-like, transcript variant X4
soluble guanylate cyclase 89Da-like isoform X4
soluble guanylate cyclase 89Da-like, transcript variant X5
soluble guanylate cyclase 89Da-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
odorant receptor 4-like, transcript variant X1
odorant receptor 4-like, transcript variant X2
odorant receptor 4-like, transcript variant X4
odorant receptor 4-like, transcript variant X3
uncharacterized protein LOC114881490 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
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: 6 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123987984
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC114881151, transcript variant X2
uncharacterized LOC114881151, transcript variant X1
uncharacterized LOC114881151, transcript variant X3
uncharacterized LOC123987971, transcript variant X2
uncharacterized LOC123987971, 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
golgin subfamily A member 6-like protein 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proline-rich receptor-like protein kinase PERK2
putative mediator of RNA polymerase II transcription subunit 29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
golgin subfamily A member 6-like protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
uncharacterized LOC123988007, transcript variant X5
uncharacterized LOC123988007, transcript variant X9
uncharacterized LOC123988007, transcript variant X2
uncharacterized LOC123988007, transcript variant X3
uncharacterized LOC123988007, transcript variant X1
uncharacterized LOC123988007, transcript variant X10
uncharacterized LOC123988007, transcript variant X4
uncharacterized LOC123988007, transcript variant X7
uncharacterized LOC123988007, transcript variant X12
uncharacterized LOC123988007, transcript variant X8
uncharacterized LOC123988007, transcript variant X11
uncharacterized protein LOC123988007 isoform X1
uncharacterized LOC123988007, transcript variant X6
uncharacterized protein LOC123988007 isoform X2
uncharacterized LOC123988008, transcript variant X2
uncharacterized LOC123988008, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
uncharacterized LOC123987938, transcript variant X2
uncharacterized LOC123987938, transcript variant X1
uncharacterized protein LOC123987938 isoform X1
uncharacterized protein LOC123987938 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
general transcription factor II-I repeat domain-containing protein 2-like