Procambarus clarkii strain Jiangsu linkage group LG61, 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\nCM035533.1.\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.
uncharacterized LOC123770443, 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 3 samples with support for all annotated introns
uncharacterized LOC123770443, 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 4 samples with support for all annotated introns
uncharacterized LOC123770443, transcript variant X2
uncharacterized LOC123770443, 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 LOC123770443, transcript variant X3
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
COORDINATES: polyA evidence [ECO:0006239]
similar to RNA sequence (same species):INSD:GARH01029609.1
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 813 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 813 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
heme-binding protein 1-like, transcript variant X1
heme-binding protein 1-like, transcript variant X2
uncharacterized LOC123770447, 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 19 samples with support for all annotated introns
uncharacterized LOC123770447, 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 13 samples with support for all annotated introns
uncharacterized LOC123770447, 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 9 samples with support for all annotated introns
uncharacterized LOC123770447, 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 7 samples with support for all annotated introns
uncharacterized LOC123770447, 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 8 samples with support for all annotated introns
uncharacterized LOC123770447, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123770447, 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 16 samples with support for all annotated introns
uncharacterized protein LOC123770447 isoform X1
uncharacterized protein LOC123770447 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
tectonin beta-propeller repeat-containing protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein-like, transcript variant X2
tectonin beta-propeller repeat-containing protein-like isoform X1
tectonin beta-propeller repeat-containing protein-like isoform X2
ecto-NOX disulfide-thiol exchanger 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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 5 samples with support for all annotated introns
probable 3-hydroxyisobutyrate dehydrogenase
queuine tRNA-ribosyltransferase catalytic subunit 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 22 samples with support for all annotated introns
queuine tRNA-ribosyltransferase catalytic subunit 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 6 samples with support for all annotated introns
queuine tRNA-ribosyltransferase catalytic subunit 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 5 samples with support for all annotated introns
queuine tRNA-ribosyltransferase catalytic subunit 1-like, transcript variant X1
queuine tRNA-ribosyltransferase catalytic subunit 1-like, transcript variant X5
queuine tRNA-ribosyltransferase catalytic subunit 1-like isoform X1
queuine tRNA-ribosyltransferase catalytic subunit 1-like isoform X3
queuine tRNA-ribosyltransferase catalytic subunit 1-like isoform X2
adhesion G protein-coupled receptor A3-like
similar to RNA sequence (same species):INSD:GBEV01003466.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 709 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 668 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
probable basic-leucine zipper transcription factor N
activating transcription factor 7-interacting protein 1-like, transcript variant X9
activating transcription factor 7-interacting protein 1-like, transcript variant X8
activating transcription factor 7-interacting protein 1-like isoform X5
activating transcription factor 7-interacting protein 1-like isoform X4
activating transcription factor 7-interacting protein 1-like, transcript variant X3
activating transcription factor 7-interacting protein 1-like, transcript variant X5
activating transcription factor 7-interacting protein 1-like, transcript variant X4
activating transcription factor 7-interacting protein 1-like, transcript variant X2
activating transcription factor 7-interacting protein 1-like, transcript variant X1
activating transcription factor 7-interacting protein 1-like, transcript variant X6
activating transcription factor 7-interacting protein 1-like, transcript variant X7
uncharacterized protein LOC123770459 isoform X3
uncharacterized protein LOC123770459 isoform X2
uncharacterized protein LOC123770459 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
merozoite surface protein CMZ-8-like, transcript variant X2
merozoite surface protein CMZ-8-like, transcript variant X1
merozoite surface protein CMZ-8-like isoform X2
protein TRACHEARY ELEMENT DIFFERENTIATION-RELATED 7A-like isoform X1
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: 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lisH domain-containing protein C1711.05-like
uncharacterized LOC123770462, transcript variant X1
uncharacterized LOC123770462, transcript variant X2
uncharacterized protein LOC123770462 isoform X1
uncharacterized protein LOC123770462 isoform X2
glycine-rich cell wall structural protein 1-like
probable serine/threonine-protein kinase dyrk2
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 99 samples with support for all annotated introns
transcription factor HNF-4 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription factor HNF-4 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription factor HNF-4 homolog, transcript variant X3
delta(14)-sterol reductase TM7SF2-like, transcript variant X2
delta(14)-sterol reductase TM7SF2-like, transcript variant X1
delta(14)-sterol reductase TM7SF2-like isoform X1
delta(14)-sterol reductase TM7SF2-like isoform X2
proline-rich extensin-like protein EPR1, transcript variant X3
proline-rich extensin-like protein EPR1, transcript variant X2
proline-rich extensin-like protein EPR1, transcript variant X1
proline-rich extensin-like protein EPR1 isoform X3
proline-rich extensin-like protein EPR1 isoform X2
proline-rich extensin-like protein EPR1 isoform X1
proline-rich extensin-like protein EPR1, 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 7 samples with support for all annotated introns
proline-rich extensin-like protein EPR1, 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
proline-rich extensin-like protein EPR1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
vesicle-associated membrane protein 4-like
FK506-binding protein 15-like, transcript variant X2
FK506-binding protein 15-like, transcript variant X1
FK506-binding protein 15-like, transcript variant X3
FK506-binding protein 15-like, transcript variant X5
FK506-binding protein 15-like isoform X2
FK506-binding protein 15-like isoform X1
FK506-binding protein 15-like isoform X5
FK506-binding protein 15-like isoform X3
FK506-binding protein 15-like, 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 57 samples with support for all annotated introns
FK506-binding protein 15-like isoform X4
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
tetratricopeptide repeat protein 1-like, transcript variant X4
tetratricopeptide repeat protein 1-like, transcript variant X1
tetratricopeptide repeat protein 1-like, transcript variant X3
tetratricopeptide repeat protein 1-like, transcript variant X2
tetratricopeptide repeat protein 1-like isoform X1
tetratricopeptide repeat protein 1-like isoform X2
tetratricopeptide repeat protein 1-like isoform X3
staphylococcal nuclease domain-containing protein 1-like
ATP-dependent RNA helicase DDX51-like, transcript variant X1
ATP-dependent RNA helicase DDX51-like, transcript variant X4
ATP-dependent RNA helicase DDX51-like, transcript variant X3
ATP-dependent RNA helicase DDX51-like, transcript variant X2
ATP-dependent RNA helicase DDX51-like, transcript variant X6
ATP-dependent RNA helicase DDX51-like, transcript variant X5
ATP-dependent RNA helicase DDX51-like isoform X1
ATP-dependent RNA helicase DDX51-like isoform X2
zinc finger protein 624-like, transcript variant X2
zinc finger protein 624-like, transcript variant X1
uncharacterized LOC123770470, transcript variant X3
uncharacterized LOC123770470, transcript variant X1
uncharacterized LOC123770470, transcript variant X2
transient receptor potential channel pyrexia-like, transcript variant X1
transient receptor potential channel pyrexia-like, transcript variant X2
transient receptor potential channel pyrexia-like, transcript variant X3
transient receptor potential channel pyrexia-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 85% 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 94% coverage of the annotated genomic feature by RNAseq alignments
queuine tRNA-ribosyltransferase accessory subunit 2-like, transcript variant X4
queuine tRNA-ribosyltransferase accessory subunit 2-like, transcript variant X2
queuine tRNA-ribosyltransferase accessory subunit 2-like, transcript variant X1
queuine tRNA-ribosyltransferase accessory subunit 2-like, transcript variant X5
queuine tRNA-ribosyltransferase accessory subunit 2-like, transcript variant X3
queuine tRNA-ribosyltransferase accessory subunit 2-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 63 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1 protein homolog
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
putative neutral sphingomyelinase, transcript variant X1
putative neutral sphingomyelinase, transcript variant X3
putative neutral sphingomyelinase, transcript variant X2
putative neutral sphingomyelinase, transcript variant X4
apolipoprotein D-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 3 samples with support for all annotated introns
apolipoprotein D-like, transcript variant X4
apolipoprotein D-like, transcript variant X1
apolipoprotein D-like, transcript variant X3
uncharacterized protein LOC123770484 isoform X1
uncharacterized protein LOC123770484 isoform X2
quinone oxidoreductase-like, transcript variant X5
quinone oxidoreductase-like, transcript variant X7
quinone oxidoreductase-like, transcript variant X6
quinone oxidoreductase-like, transcript variant X3
quinone oxidoreductase-like, transcript variant X2
quinone oxidoreductase-like, transcript variant X1
quinone oxidoreductase-like, transcript variant X8
quinone oxidoreductase-like, transcript variant X4
similar to RNA sequence (same species):INSD:GBEV01014094.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 233 bases not found in genome assembly
ovoinhibitor-like, transcript variant X1
ovoinhibitor-like, transcript variant X3
ovoinhibitor-like, transcript variant X4
ovoinhibitor-like, transcript variant X6
ovoinhibitor-like, transcript variant X2
ovoinhibitor-like, transcript variant X7
ovoinhibitor-like, transcript variant X5
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: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
NFX1-type zinc finger-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
SH3 domain-containing protein C23A1.17-like
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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123770493, transcript variant X2
uncharacterized LOC123770493, transcript variant X1
uncharacterized protein LOC123770493 isoform X2
uncharacterized protein LOC123770493 isoform X1
39S ribosomal protein L38, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 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: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 5A-like, transcript variant X1
von Willebrand factor A domain-containing protein 5A-like, transcript variant X5
von Willebrand factor A domain-containing protein 5A-like, transcript variant X2
von Willebrand factor A domain-containing protein 5A-like, transcript variant X4
von Willebrand factor A domain-containing protein 5A-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 10 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 5A-like, transcript variant X7
von Willebrand factor A domain-containing protein 5A-like, transcript variant X6
von Willebrand factor A domain-containing protein 5A-like isoform X1
von Willebrand factor A domain-containing protein 5A-like isoform X5
von Willebrand factor A domain-containing protein 5A-like isoform X2
von Willebrand factor A domain-containing protein 5A-like isoform X4
von Willebrand factor A domain-containing protein 5A-like isoform X6
von Willebrand factor A domain-containing protein 5A-like isoform X3
similar to RNA sequence (same species):INSD:GBEV01019103.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1106 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 421 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GBEV01044579.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 758 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% 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 669 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
F-box/LRR-repeat protein 5-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 11 samples with support for all annotated introns
F-box/LRR-repeat protein 5-like, transcript variant X2
F-box/LRR-repeat protein 5-like isoform X1
F-box/LRR-repeat protein 5-like isoform X2
MIP18 family protein galla-2-like, transcript variant X2
MIP18 family protein galla-2-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 98 samples with support for all annotated introns
EGF domain-specific O-linked N-acetylglucosamine transferase-like, transcript variant X3
EGF domain-specific O-linked N-acetylglucosamine transferase-like, transcript variant X2
EGF domain-specific O-linked N-acetylglucosamine transferase-like, transcript variant X4
EGF domain-specific O-linked N-acetylglucosamine transferase-like, transcript variant X1
EGF domain-specific O-linked N-acetylglucosamine transferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X5
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X3
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X1
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X4
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X6
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like, transcript variant X2
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like isoform X1
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like isoform X2
3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial-like isoform X3
transcriptional activator Myb-like, transcript variant X1
transcriptional activator Myb-like, transcript variant X2
transcriptional activator Myb-like, transcript variant X3
transcriptional activator Myb-like isoform X1
transcriptional activator Myb-like isoform X2
transcriptional activator Myb-like isoform X3
juvenile hormone epoxide hydrolase 1-like, transcript variant X2
juvenile hormone epoxide hydrolase 1-like, transcript variant X1
juvenile hormone epoxide hydrolase 1-like isoform X1
juvenile hormone epoxide hydrolase 1-like isoform X2
uncharacterized LOC123770508, transcript variant X2
uncharacterized LOC123770508, transcript variant X1
similar to RNA sequence (same species):INSD:GBEV01030998.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 439 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 82 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
DBIRD complex subunit ZNF326-like, transcript variant X2
DBIRD complex subunit ZNF326-like, transcript variant X1
DBIRD complex subunit ZNF326-like isoform X2
DBIRD complex subunit ZNF326-like isoform X1
glutamic acid-rich protein-like, transcript variant X1
glutamic acid-rich protein-like, transcript variant X2
glutamic acid-rich protein-like isoform X1
glutamic acid-rich protein-like isoform X2
dimethyladenosine transferase 1, mitochondrial-like, transcript variant X1
dimethyladenosine transferase 1, mitochondrial-like, transcript variant X2
dimethyladenosine transferase 1, mitochondrial-like, transcript variant X3
dimethyladenosine transferase 1, mitochondrial-like isoform X1
uncharacterized protein LOC123770515 isoform X2
receptor expression-enhancing protein 5-like, transcript variant X1
receptor expression-enhancing protein 5-like, transcript variant X3
receptor expression-enhancing protein 5-like, transcript variant X4
receptor expression-enhancing protein 5-like, transcript variant X2
receptor expression-enhancing protein 5-like isoform X1
receptor expression-enhancing protein 5-like isoform X3
receptor expression-enhancing protein 5-like isoform X4
receptor expression-enhancing protein 5-like isoform X2
uncharacterized LOC123770517, 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 42 samples with support for all annotated introns
uncharacterized LOC123770517, 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
uncharacterized LOC123770517, 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 107 samples with support for all annotated introns
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
CXXC motif containing zinc binding protein-like
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
cytochrome c oxidase assembly factor 3, mitochondrial-like, transcript variant X1
cytochrome c oxidase assembly factor 3, mitochondrial-like isoform X1
cytochrome c oxidase assembly factor 3, mitochondrial-like, transcript variant X2
cytochrome c oxidase assembly factor 3, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123770523, transcript variant X2
uncharacterized LOC123770523, transcript variant X1
uncharacterized protein LOC123770523 isoform X2
uncharacterized protein LOC123770523 isoform X1
selenoprotein N-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 65 samples with support for all annotated introns
selenoprotein N-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
selenoprotein N-like, 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 29 samples with support for all annotated introns
selenoprotein N-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 14 samples with support for all annotated introns
selenoprotein N-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 7 samples with support for all annotated introns
selenoprotein N-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 52 samples with support for all annotated introns
selenoprotein N-like, 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 17 samples with support for all annotated introns
uncharacterized protein LOC123770524 isoform X3
TBC1 domain family member 10A-like, transcript variant X7
similar to RNA sequence (same species):INSD:GARH01015070.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X6
TBC1 domain family member 10A-like, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; 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 3 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; 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, including 7 samples with support for all annotated introns
TBC1 domain family member 10A-like, transcript variant X10
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 25 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 372 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
TBC1 domain family member 10A-like isoform X1
TBC1 domain family member 10A-like isoform X3
TBC1 domain family member 10A-like, transcript variant X9
TBC1 domain family member 10A-like, transcript variant X11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 472 bases not found in genome assembly; 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, including 48 samples with support for all annotated introns
TBC1 domain family member 10A-like isoform X2
TBC1 domain family member 10A-like isoform X4
uncharacterized LOC123770526, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123770526, 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 28 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X11
uncharacterized LOC123770526, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123770526, transcript variant X6
uncharacterized LOC123770526, 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 6 samples with support for all annotated introns
uncharacterized LOC123770526, 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 11 samples with support for all annotated introns
uncharacterized protein LOC123770526 isoform X3
uncharacterized protein LOC123770526 isoform X4
uncharacterized protein LOC123770526 isoform X5
uncharacterized protein LOC123770526 isoform X1
uncharacterized protein LOC123770526 isoform X2
uncharacterized protein LOC123770526 isoform X6
uncharacterized protein DKFZp434B061-like
uncharacterized LOC123770528, 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 57 samples with support for all annotated introns
uncharacterized LOC123770528, 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 65 samples with support for all annotated introns
uncharacterized LOC123770528, 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 18 samples with support for all annotated introns
uncharacterized LOC123770528, 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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: flocculation protein FLO11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
uncharacterized LOC123770531, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
uncharacterized LOC123770531, 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 30 samples with support for all annotated introns
uncharacterized LOC123770531, transcript variant X2
uncharacterized LOC123770531, transcript variant X9
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
uncharacterized LOC123770531, transcript variant X5
uncharacterized LOC123770531, transcript variant X8
uncharacterized LOC123770531, transcript variant X7
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 LOC123770531, transcript variant X10
uncharacterized LOC123770531, transcript variant X6
uncharacterized LOC123770531, transcript variant X3
uncharacterized protein LOC123770531 isoform X1
uncharacterized LOC123770531, transcript variant X11
uncharacterized protein LOC123770531 isoform X2
uncharacterized LOC123770536, transcript variant X3
uncharacterized LOC123770536, transcript variant X2
uncharacterized LOC123770536, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC123770536, transcript variant X4
uncharacterized LOC123770536, transcript variant X5
uncharacterized protein LOC123770536 isoform X2
uncharacterized protein LOC123770536 isoform X1
UDP-glycosyltransferase UGT5-like, transcript variant X1
UDP-glycosyltransferase UGT5-like, transcript variant X3
UDP-glycosyltransferase UGT5-like, transcript variant X2
UDP-glycosyltransferase UGT5-like isoform X1
UDP-glycosyltransferase UGT5-like isoform X3
UDP-glycosyltransferase UGT5-like isoform X2
uncharacterized protein LOC123770536 isoform X3
uncharacterized LOC123770634, transcript variant X1
uncharacterized LOC123770634, transcript variant X2
SUMO-interacting motif-containing protein 1-like
demethylmenaquinone methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC123770546, transcript variant X2
uncharacterized LOC123770546, transcript variant X1
uncharacterized LOC123770546, transcript variant X3
uncharacterized LOC123770546, 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 23 samples with support for all annotated introns
uncharacterized protein LOC123770546 isoform X1
uncharacterized protein LOC123770546 isoform X2
uncharacterized protein LOC123770546 isoform X3
hyaluronan mediated motility receptor-like
methylthioribose-1-phosphate isomerase-like
uncharacterized LOC123770550, transcript variant X2
uncharacterized LOC123770550, transcript variant X1
uncharacterized LOC123770550, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 26% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 76-like, transcript variant X3
zinc finger protein 76-like, transcript variant X1
zinc finger protein 76-like, transcript variant X2
zinc finger protein 76-like, transcript variant X6
zinc finger protein 76-like, transcript variant X5
zinc finger protein 76-like, transcript variant X4
lysophospholipid acyltransferase 5-like, transcript variant X1
lysophospholipid acyltransferase 5-like, transcript variant X2
lysophospholipid acyltransferase 5-like isoform X2
lysophospholipid acyltransferase 5-like isoform X1
dentin matrix acidic phosphoprotein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
uncharacterized transmembrane protein DDB_G0289901-like
serine/threonine-protein kinase PRP4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC123770557, 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 2 samples with support for all annotated introns
uncharacterized LOC123770557, transcript variant X6
uncharacterized LOC123770557, 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 9 samples with support for all annotated introns
uncharacterized LOC123770557, 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 9 samples with support for all annotated introns
uncharacterized LOC123770557, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123770557, transcript variant X4
uncharacterized protein LOC123770557 isoform X2
uncharacterized protein LOC123770557 isoform X1
uncharacterized protein LOC123770557 isoform X3
polycystic kidney disease protein 1-like 3
armadillo repeat-containing protein 8-like, transcript variant X2
armadillo repeat-containing protein 8-like, transcript variant X1
armadillo repeat-containing protein 8-like isoform X2
armadillo repeat-containing protein 8-like isoform X1
uncharacterized LOC123770559, transcript variant X2
uncharacterized LOC123770559, 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 86 samples with support for all annotated introns
uncharacterized LOC123770559, 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 94 samples with support for all annotated introns
uncharacterized LOC123770559, 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 103 samples with support for all annotated introns
uncharacterized LOC123770560, 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 LOC123770560, 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 96 samples with support for all annotated introns
probable glucosamine 6-phosphate N-acetyltransferase
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
protein spinster-like, transcript variant X2
protein spinster-like, transcript variant X1
protein spinster-like, transcript variant X3
protein spinster-like, transcript variant X4
glutamate receptor ionotropic, kainate glr-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
uridine diphosphate glucose pyrophosphatase NUDT14-like
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1-like, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1-like, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
uncharacterized LOC123770637, transcript variant X2
uncharacterized LOC123770637, transcript variant X1
uncharacterized LOC123770570, 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 2 samples with support for all annotated introns
uncharacterized LOC123770570, transcript variant X3
uncharacterized LOC123770570, transcript variant X5
uncharacterized LOC123770570, transcript variant X2
uncharacterized LOC123770570, transcript variant X1
uncharacterized LOC123770570, transcript variant X11
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
uncharacterized LOC123770570, transcript variant X10
uncharacterized protein LOC123770570 isoform X4
uncharacterized protein LOC123770570 isoform X3
uncharacterized protein LOC123770570 isoform X5
uncharacterized protein LOC123770570 isoform X2
uncharacterized protein LOC123770570 isoform X1
uncharacterized protein LOC123770570 isoform X9
uncharacterized LOC123770570, transcript variant X6
uncharacterized protein LOC123770570 isoform X6
uncharacterized LOC123770570, transcript variant X7
uncharacterized LOC123770570, transcript variant X8
uncharacterized protein LOC123770570 isoform X7
uncharacterized LOC123770570, transcript variant X9
uncharacterized protein LOC123770570 isoform X8