Procambarus clarkii strain Jiangsu linkage group LG20, ASM2042438v2, whole genome shotgun sequence.
Procambarus clarkii (red swamp crayfish)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Astacidea; Astacoidea; Cambaridae; Procambarus.
A chromosome-level reference genome of red swamp crayfish Procambarus clarkii provides insights into the gene families regarding growth or development in crustaceans
REFSEQ INFORMATION: The reference sequence is identical to\nCM035492.1.\nAssembly name: ASM2042438v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Freshwater Fisheries Research\nInstitute of Jiangsu Province, Nanjing 210017, China on 2021/10/12.\nThe original whole-genome shotgun project has the accession\nJAIWQB000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Freshwater Fisheries Research Institute\n of Jiangsu Province, Nanjing 210017,\n China\nAssembly Method :: LACHESIS v. may-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio RS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Procambarus clarkii Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
pyroglutamylated RF-amide peptide receptor-like
COORDINATES: polyA evidence [ECO:0006239]
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: pyroglutamylated RF-amide peptide receptor-like
hemocyte protein-glutamine gamma-glutamyltransferase-like
28S ribosomal protein S30, mitochondrial-like
apoptosis-stimulating of p53 protein 2-like
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 8 samples with support for all annotated introns
uncharacterized LOC123758238, transcript variant X6
uncharacterized LOC123758238, transcript variant X3
uncharacterized LOC123758238, transcript variant X7
uncharacterized LOC123758238, transcript variant X5
uncharacterized LOC123758238, transcript variant X8
uncharacterized LOC123758238, transcript variant X4
uncharacterized LOC123758238, transcript variant X2
uncharacterized LOC123758238, transcript variant X1
multidrug resistance-associated protein 1-like
XK-related protein 6-like, transcript variant X1
XK-related protein 6-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 12 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog, transcript variant X4
uncharacterized protein KIAA2013 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog, transcript variant X3
uncharacterized protein KIAA2013 homolog, transcript variant X5
uncharacterized protein KIAA2013 homolog, transcript variant X6
uncharacterized protein KIAA2013 homolog, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog, 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 3 samples with support for all annotated introns
uncharacterized protein KIAA2013 homolog isoform X4
uncharacterized protein KIAA2013 homolog isoform X3
uncharacterized protein KIAA2013 homolog isoform X2
uncharacterized protein KIAA2013 homolog isoform X1
uncharacterized protein KIAA2013 homolog isoform X5
LHFPL tetraspan subfamily member 3 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
isocitrate dehydrogenase [NADP], mitochondrial-like
similar to RNA sequence (same species):INSD:GARH01040907.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 64 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 55 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
SOSS complex subunit B1-B-like, transcript variant X1
SOSS complex subunit B1-B-like, transcript variant X5
SOSS complex subunit B1-B-like, transcript variant X2
SOSS complex subunit B1-B-like, transcript variant X6
SOSS complex subunit B1-B-like, transcript variant X4
SOSS complex subunit B1-B-like, transcript variant X7
SOSS complex subunit B1-B-like, transcript variant X3
SOSS complex subunit B1-B-like isoform X5
SOSS complex subunit B1-B-like isoform X1
SOSS complex subunit B1-B-like isoform X6
SOSS complex subunit B1-B-like isoform X2
SOSS complex subunit B1-B-like isoform X7
SOSS complex subunit B1-B-like isoform X4
SOSS complex subunit B1-B-like isoform X3
transcription initiation factor TFIID subunit 3-like
transport and Golgi organization protein 6 homolog, transcript variant X4
transport and Golgi organization protein 6 homolog, transcript variant X2
transport and Golgi organization protein 6 homolog, transcript variant X5
transport and Golgi organization protein 6 homolog, transcript variant X1
transport and Golgi organization protein 6 homolog, transcript variant X3
transport and Golgi organization protein 6 homolog isoform X2
transport and Golgi organization protein 6 homolog isoform X1
V-type proton ATPase 16 kDa proteolipid subunit
signal-induced proliferation-associated 1-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1, 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 62 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1, 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 23 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1 isoform X3
signal-induced proliferation-associated 1-like protein 1 isoform X2
signal-induced proliferation-associated 1-like protein 1 isoform X1
protein shifted-like, transcript variant X3
protein shifted-like, transcript variant X5
protein shifted-like, transcript variant X4
protein shifted-like, transcript variant X1
protein shifted-like, transcript variant X2
protein shifted-like, transcript variant X6
uncharacterized protein LOC123758250 isoform X2
uncharacterized protein LOC123758250 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 37 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 98% coverage of the annotated genomic feature by RNAseq alignments
ceramide-1-phosphate transfer protein-like
uncharacterized LOC123758253, 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 9 samples with support for all annotated introns
uncharacterized LOC123758253, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123758253, transcript variant X2
uncharacterized LOC123758253, 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 5 samples with support for all annotated introns
uncharacterized protein LOC123758253 isoform X2
uncharacterized LOC123758253, 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 1 sample with support for all annotated introns
uncharacterized LOC123758253, 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 4 samples with support for all annotated introns
uncharacterized protein LOC123758253 isoform X1
uncharacterized protein LOC123758253 isoform X3
uncharacterized protein LOC123758253 isoform X5
uncharacterized protein LOC123758253 isoform 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 64 samples with support for all annotated introns
isoamyl acetate-hydrolyzing esterase 1 homolog
similar to RNA sequence (same species):INSD:GBEV01012203.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 320 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 320 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 259 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
ice-structuring glycoprotein-like, transcript variant X1
ice-structuring glycoprotein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
microtubule-associated protein futsch-like isoform X1
ice-structuring glycoprotein-like isoform X2
coiled-coil domain-containing protein 93-like, transcript variant X1
coiled-coil domain-containing protein 93-like, transcript variant X2
coiled-coil domain-containing protein 93-like isoform X1
coiled-coil domain-containing protein 93-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
similar to RNA sequence (same species):INSD:GARH01038293.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 654 bases not found in genome assembly; 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 15 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 274 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
mothers against decapentaplegic homolog 4-like, transcript variant X5
mothers against decapentaplegic homolog 4-like, transcript variant X1
mothers against decapentaplegic homolog 4-like, transcript variant X2
mothers against decapentaplegic homolog 4-like, transcript variant X3
mothers against decapentaplegic homolog 4-like, transcript variant X4
mothers against decapentaplegic homolog 4-like isoform X5
mothers against decapentaplegic homolog 4-like isoform X4
mothers against decapentaplegic homolog 4-like isoform X2
mothers against decapentaplegic homolog 4-like isoform X3
mothers against decapentaplegic homolog 4-like isoform X1
microtubule-associated proteins 1A/1B light chain 3C-like, transcript variant X1
microtubule-associated proteins 1A/1B light chain 3C-like, transcript variant X3
microtubule-associated proteins 1A/1B light chain 3C-like isoform X1
microtubule-associated proteins 1A/1B light chain 3C-like isoform X3
microtubule-associated proteins 1A/1B light chain 3C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
microtubule-associated proteins 1A/1B light chain 3C-like isoform X2
alkyldihydroxyacetonephosphate synthase, peroxisomal-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 90 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123758273, 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 27 samples with support for all annotated introns
uncharacterized LOC123758273, 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 14 samples with support for all annotated introns
uncharacterized protein LOC123758273 isoform X2
uncharacterized protein LOC123758273 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
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
neuronal acetylcholine receptor subunit alpha-10-like
similar to RNA sequence (same species):INSD:GBEV01059679.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 297 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 67 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein naked cuticle homolog 1-like, transcript variant X3
protein naked cuticle homolog 1-like, transcript variant X1
protein naked cuticle homolog 1-like, transcript variant X2
protein naked cuticle homolog 1-like isoform X1
protein naked cuticle homolog 1-like isoform X2
sphingosine-1-phosphate phosphatase 2-like, transcript variant X2
sphingosine-1-phosphate phosphatase 2-like, transcript variant X1
sphingosine-1-phosphate phosphatase 2-like
mitochondrial amidoxime-reducing component 1-like, transcript variant X3
mitochondrial amidoxime-reducing component 1-like, transcript variant X1
mitochondrial amidoxime-reducing component 1-like, transcript variant X2
mitochondrial amidoxime reducing component 2-like isoform X1
mitochondrial amidoxime reducing component 2-like isoform X2
mitochondrial amidoxime-reducing component 1-like isoform X3
cleft lip and palate transmembrane protein 1-like protein
tripartite motif-containing protein 2-like, transcript variant X3
tripartite motif-containing protein 2-like, transcript variant X1
tripartite motif-containing protein 2-like, transcript variant X2
tripartite motif-containing protein 2-like, transcript variant X4
tripartite motif-containing protein 2-like isoform X1
tripartite motif-containing protein 2-like isoform X2
uncharacterized LOC123758283, transcript variant X2
uncharacterized LOC123758283, transcript variant X1
uncharacterized LOC123758283, transcript variant X3
uncharacterized protein LOC123758283 isoform X1
uncharacterized protein LOC123758283 isoform X2
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-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 19 samples with support for all annotated introns
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like, transcript variant X1
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like isoform X1
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like isoform X2
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like isoform X3
serine/threonine-protein phosphatase alpha-2 isoform
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123758286, transcript variant X1
uncharacterized protein LOC123758286 isoform X1
uncharacterized LOC123758286, transcript variant X2
uncharacterized protein LOC123758286 isoform X2
proline-, glutamic acid- and leucine-rich protein 1-like
coiled-coil domain-containing protein CG32809-like, transcript variant X1
coiled-coil domain-containing protein CG32809-like, transcript variant X4
coiled-coil domain-containing protein CG32809-like, transcript variant X2
coiled-coil domain-containing protein CG32809-like, transcript variant X3
coiled-coil domain-containing protein CG32809-like, transcript variant X8
coiled-coil domain-containing protein CG32809-like, transcript variant X6
coiled-coil domain-containing protein CG32809-like, transcript variant X5
coiled-coil domain-containing protein CG32809-like, transcript variant X7
coiled-coil domain-containing protein CG32809-like, transcript variant X10
coiled-coil domain-containing protein CG32809-like, transcript variant X9
coiled-coil domain-containing protein CG32809-like, transcript variant X11
coiled-coil domain-containing protein CG32809-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
coiled-coil domain-containing protein CG32809-like isoform X1
coiled-coil domain-containing protein CG32809-like isoform X2
coiled-coil domain-containing protein CG32809-like isoform X3
coiled-coil domain-containing protein CG32809-like isoform X5
coiled-coil domain-containing protein CG32809-like isoform X4
coiled-coil domain-containing protein CG32809-like isoform X6
coiled-coil domain-containing protein CG32809-like isoform X8
coiled-coil domain-containing protein CG32809-like isoform X7
coiled-coil domain-containing protein CG32809-like isoform X9
coiled-coil domain-containing protein CG32809-like isoform X10
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6-like, transcript variant X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6-like, transcript variant X2
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6-like isoform X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6-like isoform X2
uncharacterized LOC123758293, transcript variant X2
uncharacterized LOC123758293, transcript variant X1
uncharacterized protein LOC123758293 isoform X1
uncharacterized protein LOC123758293 isoform X2
pulmonary surfactant-associated protein D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 14-like, transcript variant X3
tyrosine-protein phosphatase non-receptor type 14-like, transcript variant X1
tyrosine-protein phosphatase non-receptor type 14-like, transcript variant X2
tyrosine-protein phosphatase non-receptor type 14-like isoform X2
tyrosine-protein phosphatase non-receptor type 14-like isoform X1
uncharacterized LOC123758303, transcript variant X2
uncharacterized LOC123758303, transcript variant X1
uncharacterized protein LOC123758303 isoform X2
uncharacterized protein LOC123758303 isoform X1
uncharacterized LOC123758303, transcript variant X4
uncharacterized LOC123758303, transcript variant X3
probable ATP-dependent RNA helicase DDX49
chromatin modification-related protein eaf-1-like, transcript variant X2
chromatin modification-related protein eaf-1-like, transcript variant X1
chromatin modification-related protein eaf-1-like isoform X2
chromatin modification-related protein eaf-1-like isoform X1
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X4
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X2
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X3
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X1
arf-GAP domain and FG repeat-containing protein 1-like isoform X4
arf-GAP domain and FG repeat-containing protein 1-like isoform X2
arf-GAP domain and FG repeat-containing protein 1-like isoform X3
arf-GAP domain and FG repeat-containing protein 1-like isoform X1
arf-GAP domain and FG repeat-containing protein 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 8 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
uncharacterized LOC123758311, transcript variant X2
uncharacterized LOC123758311, transcript variant X3
uncharacterized LOC123758311, transcript variant X5
uncharacterized LOC123758311, transcript variant X1
uncharacterized LOC123758311, transcript variant X4
uncharacterized protein LOC123758311 isoform X2
uncharacterized protein LOC123758311 isoform X3
uncharacterized protein LOC123758311 isoform X1
metal cation symporter ZIP14-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 8 samples with support for all annotated introns
metal cation symporter ZIP14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
metal cation symporter ZIP14-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein LMBR1L-like, transcript variant X2
protein LMBR1L-like, transcript variant X1
protein LMBR1L-like, transcript variant X3
uncharacterized LOC123758316, 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
uncharacterized LOC123758316, 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 5 samples with support for all annotated introns
uncharacterized LOC123758316, 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 2 samples with support for all annotated introns
uncharacterized protein LOC123758316 isoform X1
uncharacterized protein LOC123758316 isoform X3
uncharacterized protein LOC123758316 isoform X2
ras association domain-containing protein 4-like, transcript variant X2
ras association domain-containing protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras association domain-containing protein 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras association domain-containing protein 4-like isoform X2
ras association domain-containing protein 4-like isoform X1
uncharacterized protein LOC123758318 isoform X3
calsyntenin-1-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 94 samples with support for all annotated introns
calsyntenin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X14
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 32 samples with support for all annotated introns
early growth response protein 1-A-like isoform X12
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X28
longitudinals lacking protein, isoforms H/M/V-like isoform X23
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X29
longitudinals lacking protein, isoforms H/M/V-like isoform X24
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X35
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
longitudinals lacking protein, isoforms H/M/V-like isoform X27
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X10
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X11
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X24
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
zinc finger protein 358-like isoform X19
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X9
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 50 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X7
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X27
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 24 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X22
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X41
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 41 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X33
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 10-like isoform X4
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X17
protein tramtrack, beta isoform-like isoform X14
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X19
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X18
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 33 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X15
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X4
longitudinals lacking protein, isoforms H/M/V-like isoform X3
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X38
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 62 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X30
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X23
protein tramtrack, beta isoform-like isoform X18
longitudinals lacking protein, isoforms A/B/D/L-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 93 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-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 29 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X1
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X43
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 45 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X35
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X12
longitudinals lacking protein, isoforms A/B/D/L-like isoform X10
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X21
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X36
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 80 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X28
longitudinals lacking protein, isoforms H/M/V-like isoform X16
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X15
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 56 samples with support for all annotated introns
zinc finger protein 358-like isoform X13
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X11
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 51 samples with support for all annotated introns
GDNF-inducible zinc finger protein 1-like isoform X9
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X39
zinc finger and BTB domain-containing protein 7A-like isoform X31
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X25
zinc finger protein 358-like isoform X20
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
zinc finger protein 768-like isoform X17
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 5C-like isoform X5
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
B-cell CLL/lymphoma 6 member B protein-like isoform X2
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X40
longitudinals lacking protein, isoforms H/M/V-like isoform X32
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X37
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X30
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 31 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X25
longitudinals lacking protein, isoforms H/M/V-like isoform X29
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X26
longitudinals lacking protein, isoforms H/M/V-like isoform X21
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X34
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X33
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 18 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X42
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 96 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X31
longitudinals lacking protein, isoforms H/M/V-like isoform X34
longitudinals lacking protein, isoforms H/M/V-like isoform X26
aldo-keto reductase family 1 member A1-A-like
aldo-keto reductase family 1 member A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 87 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, 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 51 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, 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 55 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26 isoform X1
putative mediator of RNA polymerase II transcription subunit 26, 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 28 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26 isoform X2
ubiquitin-like modifier-activating enzyme 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 1
uncharacterized LOC123758333, transcript variant X3
uncharacterized LOC123758333, transcript variant X2
uncharacterized LOC123758333, transcript variant X1
ubiquitin-conjugating enzyme E2-17 kDa-like
serine/threonine-protein kinase Nek4-like, transcript variant X4
serine/threonine-protein kinase Nek4-like, transcript variant X5
serine/threonine-protein kinase Nek4-like, transcript variant X1
serine/threonine-protein kinase Nek4-like, transcript variant X2
serine/threonine-protein kinase Nek4-like, transcript variant X3
serine/threonine-protein kinase Nek4-like isoform X1
serine/threonine-protein kinase Nek4-like isoform X3
serine/threonine-protein kinase Nek4-like isoform X2
serine/threonine-protein kinase 17A-like
similar to RNA sequence (same species):INSD:GBEV01019687.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 202 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 202 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123758336, transcript variant X1
uncharacterized LOC123758336, transcript variant X4
uncharacterized LOC123758336, transcript variant X2
uncharacterized LOC123758336, transcript variant X3
uncharacterized protein LOC123758336 isoform X4
uncharacterized protein LOC123758336 isoform X2
uncharacterized protein LOC123758336 isoform X1
uncharacterized protein LOC123758336 isoform X3
zinc finger CCCH domain-containing protein 15 homolog
cell division cycle protein 27 homolog, transcript variant X1
cell division cycle protein 27 homolog, transcript variant X2
cell division cycle protein 27 homolog isoform X1
cell division cycle protein 27 homolog isoform X2
sperm-specific H1/protamine-like protein type 2
uncharacterized LOC123758341, 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 5 samples with support for all annotated introns
uncharacterized LOC123758341, 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 26 samples with support for all annotated introns
ATP-binding cassette sub-family C member 3-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 8 samples with support for all annotated introns
ATP-binding cassette sub-family C member 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
multidrug resistance-associated protein 1-like isoform X2
ATP-binding cassette sub-family C member 3-like isoform X1
ATP-binding cassette sub-family C member 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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
ATP-binding cassette sub-family A member 2-like
acetylcholine receptor subunit beta-like 2
nuclear cap-binding protein subunit 2-like, transcript variant X2
nuclear cap-binding protein subunit 2-like, transcript variant X1
nuclear cap-binding protein subunit 2-like isoform X2
nuclear cap-binding protein subunit 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123758347, transcript variant X1
uncharacterized LOC123758347, transcript variant X2
U1 small nuclear ribonucleoprotein C-like, transcript variant X2
U1 small nuclear ribonucleoprotein C-like, transcript variant X1
U1 small nuclear ribonucleoprotein C-like isoform X2
U1 small nuclear ribonucleoprotein C-like isoform X1
AFG3-like protein 2, transcript variant X1
AFG3-like protein 2, transcript variant X2
uncharacterized LOC123758350, transcript variant X3
uncharacterized LOC123758350, transcript variant X1
uncharacterized LOC123758350, transcript variant X2
aurora kinase-like, transcript variant X1
aurora kinase-like, transcript variant X3
aurora kinase-like, transcript variant X2
aminopeptidase O-like, transcript variant X1
aminopeptidase O-like, transcript variant X2
zinc finger protein 436-like, transcript variant X3
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant X4
zinc finger protein 436-like, transcript variant X1
zinc finger protein 436-like, transcript variant X5
zinc finger protein 436-like, transcript variant X6
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
peroxisomal membrane protein 11B-like, transcript variant X1
peroxisomal membrane protein 11B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% 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 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC123758361, transcript variant X2
uncharacterized LOC123758361, transcript variant X1
uncharacterized LOC123758361, transcript variant X3
Down syndrome cell adhesion molecule-like protein Dscam2
similar to RNA sequence (same species):INSD:GBEV01001246.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1614 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1614 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
alpha/beta hydrolase domain-containing protein 17B-like
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16-like
DDB1- and CUL4-associated factor 7, transcript variant X1
DDB1- and CUL4-associated factor 7, transcript variant X4
DDB1- and CUL4-associated factor 7, transcript variant X3
DDB1- and CUL4-associated factor 7, transcript variant X2
DDB1- and CUL4-associated factor 7, transcript variant X5
DDB1- and CUL4-associated factor 7 isoform X1
DDB1- and CUL4-associated factor 7 isoform X2
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1-like
uncharacterized LOC123758368, transcript variant X4
uncharacterized LOC123758368, transcript variant X3
uncharacterized protein LOC123758368 isoform X4
uncharacterized protein LOC123758368 isoform X3
uncharacterized LOC123758368, transcript variant X2
uncharacterized LOC123758368, transcript variant X5
uncharacterized LOC123758368, transcript variant X1
uncharacterized LOC123758368, transcript variant X9
uncharacterized LOC123758368, transcript variant X6
uncharacterized LOC123758368, transcript variant X8
uncharacterized LOC123758368, transcript variant X10
uncharacterized LOC123758368, transcript variant X7
uncharacterized LOC123758368, transcript variant X11
uncharacterized protein LOC123758368 isoform X5
uncharacterized protein LOC123758368 isoform X2
uncharacterized protein LOC123758368 isoform X1
uncharacterized protein LOC123758368 isoform X7
uncharacterized protein LOC123758368 isoform X6
uncharacterized protein LOC123758368 isoform X8
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123758540, transcript variant X1
uncharacterized LOC123758540, transcript variant X2
uncharacterized protein LOC123758540 isoform X1
uncharacterized protein LOC123758540 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
similar to RNA sequence (same species):INSD:GARH01042022.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 993 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 909 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
kelch-like protein 26, 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 75 samples with support for all annotated introns
kelch-like protein 26, 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 45 samples with support for all annotated introns
kelch-like protein 26, transcript variant X3
kelch-like protein 26, transcript variant X8
kelch-like protein 26, transcript variant X7
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 32 samples with support for all annotated introns
kelch-like protein 26, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
kelch-like protein 26, transcript variant X4
kelch-like protein 26, transcript variant X9
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
kelch-like protein 26, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123758378, transcript variant X1
uncharacterized protein LOC123758378 isoform X1
uncharacterized LOC123758378, transcript variant X7
uncharacterized LOC123758378, transcript variant X8
uncharacterized LOC123758378, transcript variant X5
uncharacterized LOC123758378, transcript variant X3
uncharacterized LOC123758378, transcript variant X4
uncharacterized LOC123758378, transcript variant X2
uncharacterized protein LOC123758378 isoform X2
uncharacterized LOC123758378, transcript variant X6
uncharacterized protein LOC123758378 isoform X3
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X7
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein 87F-like, transcript variant X8
heterogeneous nuclear ribonucleoprotein 87F-like isoform X2
heterogeneous nuclear ribonucleoprotein 87F-like isoform X6
heterogeneous nuclear ribonucleoprotein 87F-like isoform X5
heterogeneous nuclear ribonucleoprotein 87F-like isoform X3
heterogeneous nuclear ribonucleoprotein 87F-like isoform X4
heterogeneous nuclear ribonucleoprotein 87F-like isoform X1
ribonuclease P protein subunit p25-like protein, transcript variant X3
ribonuclease P protein subunit p25-like protein, transcript variant X6
ribonuclease P protein subunit p25-like protein, transcript variant X5
ribonuclease P protein subunit p25-like protein, transcript variant X4
ribonuclease P protein subunit p25-like protein, transcript variant X2
ribonuclease P protein subunit p25-like protein, transcript variant X1
ribonuclease P protein subunit p25-like protein isoform X4
ribonuclease P protein subunit p25-like protein isoform X3
uncharacterized protein LOC123758382 isoform X2
uncharacterized protein LOC123758382 isoform X1
gamma-soluble NSF attachment protein-like
putative uncharacterized protein DDB_G0282499
repetitive proline-rich cell wall protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
vicilin-like seed storage protein At2g18540
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
putative cell agglutination protein pfl3
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
putative uncharacterized protein ENSP00000383309
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% 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 66% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
uncharacterized LOC123758387, transcript variant X2
uncharacterized LOC123758387, transcript variant X1
similar to RNA sequence (same species):INSD:GBEV01246560.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 166 bases not found in genome assembly; 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 31 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 90 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
ras-like GTP-binding protein RhoL, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ras-like GTP-binding protein RhoL, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ras-like GTP-binding protein RhoL, transcript variant X1
ras-like GTP-binding protein RhoL, transcript variant X3
ras-like GTP-binding protein RhoL isoform X1
ras-like GTP-binding protein RhoL isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 4-like
uncharacterized LOC123758544, transcript variant X2
uncharacterized LOC123758544, transcript variant X1
similar to RNA sequence (same species):INSD:GBEV01014540.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123758545, transcript variant X1
uncharacterized LOC123758545, transcript variant X2
uncharacterized protein LOC123758545 isoform X1
uncharacterized protein LOC123758545 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 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: 88 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48% 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 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: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GBEV01188024.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 602 bases not found in genome assembly; 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 68 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 280 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
putative uncharacterized protein DDB_G0286901
putative uncharacterized protein DDB_G0294196
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC123758401 isoform X1
uncharacterized protein LOC123758401 isoform 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 72 samples with support for all annotated introns
uncharacterized LOC123758397, transcript variant X1
uncharacterized LOC123758397, transcript variant X2
uncharacterized LOC123758397, transcript variant X3
uncharacterized LOC123758400, transcript variant X4
uncharacterized LOC123758400, transcript variant X2
uncharacterized LOC123758400, transcript variant X3
uncharacterized LOC123758400, transcript variant X1
uncharacterized protein LOC123758400 isoform X4
uncharacterized protein LOC123758400 isoform X2
uncharacterized protein LOC123758400 isoform X3
uncharacterized protein LOC123758400 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments, including 68 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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 99% coverage of the annotated genomic feature by RNAseq alignments
probable sodium/potassium/calcium exchanger CG1090, transcript variant X2
probable sodium/potassium/calcium exchanger CG1090, transcript variant X1
probable sodium/potassium/calcium exchanger CG1090 isoform X2
probable sodium/potassium/calcium exchanger CG1090 isoform X1
transcriptional repressor p66-alpha-like, transcript variant X15
transcriptional repressor p66-alpha-like, transcript variant X5
transcriptional repressor p66-alpha-like, transcript variant X13
transcriptional repressor p66-alpha-like, transcript variant X2
transcriptional repressor p66-alpha-like, transcript variant X12
transcriptional repressor p66-alpha-like, transcript variant X6
transcriptional repressor p66-alpha-like, transcript variant X11
transcriptional repressor p66-alpha-like, transcript variant X9
transcriptional repressor p66-alpha-like, transcript variant X4
transcriptional repressor p66-alpha-like, transcript variant X21
transcriptional repressor p66-alpha-like, transcript variant X17
transcriptional repressor p66-alpha-like, transcript variant X18
transcriptional repressor p66-alpha-like, transcript variant X20
transcriptional repressor p66-alpha-like, transcript variant X19
transcriptional repressor p66-alpha-like, transcript variant X8
transcriptional repressor p66-alpha-like, transcript variant X16
transcriptional repressor p66-alpha-like, transcript variant X14
transcriptional repressor p66-alpha-like, transcript variant X1
transcriptional repressor p66-alpha-like, transcript variant X10
transcriptional repressor p66-alpha-like, transcript variant X3
transcriptional repressor p66-alpha-like, transcript variant X7
transcription factor dcp-66-like isoform X3
transcriptional repressor p66-alpha-like isoform X9
transcriptional repressor p66-alpha-like isoform X5
serine/threonine-protein kinase fray2-like isoform X6
serine/threonine-protein kinase fray2-like isoform X4
transcription factor dcp-66-like isoform X8
transcription factor dcp-66-like isoform X2
transcription factor dcp-66-like isoform X7
transcription factor dcp-66-like isoform X1
uncharacterized LOC123758410, transcript variant X2
uncharacterized LOC123758410, transcript variant X1
uncharacterized protein LOC123758410 isoform X2
uncharacterized protein LOC123758410 isoform X1
major facilitator superfamily domain-containing protein 6-A-like
similar to RNA sequence (same species):INSD:GBEV01001801.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 93 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 93 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
proline-rich protein HaeIII subfamily 1-like
uncharacterized LOC123758421, transcript variant X1
uncharacterized LOC123758421, transcript variant X2
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X4
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 80 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X6
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 78 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X9
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 19 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X8
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 58 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-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 94 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00069
tRNA N(3)-methylcytidine methyltransferase METTL6-like
ubiquitin-like modifier-activating enzyme ATG7, transcript variant X2
ubiquitin-like modifier-activating enzyme ATG7, transcript variant X1
ubiquitin-like modifier-activating enzyme ATG7
similar to RNA sequence (same species):INSD:GARH01007381.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 70 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 70 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
proton-coupled folate transporter-like, transcript variant X10
proton-coupled folate transporter-like, transcript variant X1
proton-coupled folate transporter-like, transcript variant X3
proton-coupled folate transporter-like, transcript variant X8
proton-coupled folate transporter-like, transcript variant X6
proton-coupled folate transporter-like, transcript variant X4
proton-coupled folate transporter-like, transcript variant X9
proton-coupled folate transporter-like, transcript variant X2
proton-coupled folate transporter-like, transcript variant X5
proton-coupled folate transporter-like, transcript variant X7
proton-coupled folate transporter-like isoform X1
proton-coupled folate transporter-like isoform X2
uncharacterized LOC123758426, transcript variant X1
uncharacterized LOC123758426, transcript variant X4
uncharacterized LOC123758426, transcript variant X2
uncharacterized LOC123758426, transcript variant X3
solute carrier organic anion transporter family member 3A1-like
ubiquitin-fold modifier-conjugating enzyme 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
exocyst complex component 7-like, transcript variant X2
exocyst complex component 7-like, transcript variant X1
exocyst complex component 7-like isoform X2
exocyst complex component 7-like isoform X1
kxDL motif-containing protein CG10681-like
splicing factor U2af large subunit A-like
glycine-rich cell wall structural protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
uncharacterized LOC123758435, transcript variant X2
uncharacterized LOC123758435, transcript variant X1
uncharacterized protein LOC123758435 isoform X1
uncharacterized protein LOC123758435 isoform X2
epimerase family protein SDR39U1-like, transcript variant X1
epimerase family protein SDR39U1-like, transcript variant X2
TBCC domain-containing protein 1-like, transcript variant X3
TBCC domain-containing protein 1-like, transcript variant X1
TBCC domain-containing protein 1-like, transcript variant X2
TBCC domain-containing protein 1-like isoform X2
TBCC domain-containing protein 1-like isoform X1
U3 small nucleolar RNA-associated protein 25 homolog
uncharacterized LOC123758439, transcript variant X5
uncharacterized LOC123758439, transcript variant X4
uncharacterized LOC123758439, transcript variant X1
uncharacterized LOC123758439, transcript variant X3
uncharacterized LOC123758439, transcript variant X2
uncharacterized protein LOC123758439 isoform X3
uncharacterized protein LOC123758439 isoform X2
uncharacterized protein LOC123758439 isoform X1
gamma-butyrobetaine dioxygenase-like, transcript variant X1
gamma-butyrobetaine dioxygenase-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 74 samples with support for all annotated introns
gamma-butyrobetaine dioxygenase-like, transcript variant X2
gamma-butyrobetaine dioxygenase-like isoform X1
gamma-butyrobetaine dioxygenase-like isoform X2
uncharacterized LOC123758442, transcript variant X1
uncharacterized LOC123758442, transcript variant X2
cellular tumor antigen p53-like, transcript variant X3
cellular tumor antigen p53-like, transcript variant X2
cellular tumor antigen p53-like isoform X2
cellular tumor antigen p53-like, transcript variant X1
cellular tumor antigen p53-like isoform X1
cellular tumor antigen p53-like isoform X3
cellular tumor antigen p53-like, transcript variant X4
cellular tumor antigen p53-like isoform X4
visual pigment-like receptor peropsin, 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
visual pigment-like receptor peropsin, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
visual pigment-like receptor peropsin isoform X2
visual pigment-like receptor peropsin isoform X3
visual pigment-like receptor peropsin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
visual pigment-like receptor peropsin, 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 100 samples with support for all annotated introns
UHRF1-binding protein 1-like, transcript variant X1
UHRF1-binding protein 1-like, transcript variant X2
UHRF1-binding protein 1-like, transcript variant X3
leucine-rich repeat extensin-like protein 3
torso-like protein, transcript variant X2
torso-like protein, transcript variant X1
probable ATP-dependent RNA helicase DDX31
uncharacterized LOC123758454, transcript variant X1
uncharacterized LOC123758454, transcript variant X2
uncharacterized protein LOC123758454 isoform X2
uncharacterized protein LOC123758454 isoform X1
cGMP-dependent protein kinase, isozyme 1-like
similar to RNA sequence (same species):INSD:GBEV01005879.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 352 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 306 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
chromatin-remodeling complex ATPase chain Iswi-like, transcript variant X2
chromatin-remodeling complex ATPase chain Iswi-like, transcript variant X1
chromatin-remodeling complex ATPase chain Iswi-like isoform X2
chromatin-remodeling complex ATPase chain Iswi-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 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 76% coverage of the annotated genomic feature by RNAseq alignments
lymphokine-activated killer T-cell-originated protein kinase-like
2-iminobutanoate/2-iminopropanoate deaminase-like
retinoic acid receptor RXR-alpha-B-like, transcript variant X11
retinoic acid receptor RXR-alpha-B-like, transcript variant X2
retinoic acid receptor RXR-alpha-B-like, transcript variant X8
retinoic acid receptor RXR-alpha-B-like, transcript variant X6
retinoic acid receptor RXR-alpha-B-like, transcript variant X3
retinoic acid receptor RXR-alpha-B-like, transcript variant X10
retinoic acid receptor RXR-alpha-B-like, transcript variant X9
retinoic acid receptor RXR-alpha-B-like, transcript variant X18
retinoic acid receptor RXR-alpha-B-like, transcript variant X19
retinoic acid receptor RXR-alpha-B-like, transcript variant X17
retinoic acid receptor RXR-alpha-B-like, transcript variant X15
retinoic acid receptor RXR-alpha-B-like, transcript variant X20
retinoic acid receptor RXR-alpha-B-like, transcript variant X1
retinoic acid receptor RXR-alpha-B-like, transcript variant X4
retinoic acid receptor RXR-alpha-B-like, transcript variant X5
retinoic acid receptor RXR-alpha-B-like, transcript variant X12
retinoic acid receptor RXR-alpha-B-like, transcript variant X7
retinoic acid receptor RXR-alpha-B-like, transcript variant X13
retinoic acid receptor RXR-alpha-B-like, transcript variant X14
retinoic acid receptor RXR-alpha-B-like, transcript variant X16
retinoic acid receptor RXR-alpha-B-like isoform X15
retinoic acid receptor RXR-alpha-B-like isoform X6
retinoic acid receptor RXR-alpha-B-like isoform X13
retinoic acid receptor RXR-alpha-B-like isoform X4
retinoic acid receptor RXR-alpha-B-like isoform X12
retinoic acid receptor RXR-alpha-B-like isoform X3
retinoic acid receptor RXR-alpha-B-like isoform X11
retinoic acid receptor RXR-alpha-B-like isoform X1
retinoic acid receptor RXR-alpha-B-like isoform X18
retinoic acid receptor RXR-alpha-B-like isoform X9
retinoic acid receptor RXR-alpha-B-like isoform X17
retinoic acid receptor RXR-alpha-B-like isoform X7
retinoic acid receptor RXR-alpha-B-like isoform X16
retinoic acid receptor RXR-alpha-B-like isoform X8
retinoic acid receptor RXR-alpha-B-like isoform X14
retinoic acid receptor RXR-alpha-B-like isoform X5
retinoic acid receptor RXR-alpha-B-like isoform X2
retinoic acid receptor RXR-alpha-B-like isoform X10
U1 small nuclear ribonucleoprotein 70 kDa-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 103 samples with support for all annotated introns