Procambarus clarkii strain Jiangsu linkage group LG65, 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\nCM035537.1.\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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate glr-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DKFZp434B061-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, delta-1-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 1 sample with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
probable GPI-anchored adhesin-like protein PGA55
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: 1 Protein, and 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: 3 Proteins, and 36% 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 55% 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 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 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 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, NMDA 2A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
WD repeat-containing protein 47-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 3 samples with support for all annotated introns
WD repeat-containing protein 47-like, 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 36 samples with support for all annotated introns
WD repeat-containing protein 47-like, transcript variant X2
WD repeat-containing protein 47-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat-containing protein 47-like isoform X1
WD repeat-containing protein 47-like isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
WD repeat-containing protein 47-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
transcription initiation factor TFIID subunit 5-like isoform X3
tigger transposable element-derived protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like
28S ribosomal protein S27, mitochondrial-like
uncharacterized protein DDB_G0290685-like
dynein axonemal intermediate chain 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123771430, transcript variant X1
uncharacterized LOC123771430, transcript variant X2
uncharacterized protein LOC123771430 isoform X1
uncharacterized protein LOC123771430 isoform X2
uncharacterized LOC123771433, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123771433, transcript variant X3
uncharacterized LOC123771433, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
repetitive proline-rich cell wall protein 2-like
galactose-specific cell agglutination protein gsf2-like
uncharacterized protein LOC123771433 isoform X1
uncharacterized protein LOC123771433 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 102 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 300-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
choline transporter-like protein 4, transcript variant X2
choline transporter-like protein 4, transcript variant X1
choline transporter-like protein 4, transcript variant X6
choline transporter-like protein 4 isoform X1
choline transporter-like protein 4 isoform X4
choline transporter-like protein 4, transcript variant X4
choline transporter-like protein 4, transcript variant X3
choline transporter-like protein 4 isoform X2
choline transporter-like protein 4, transcript variant X5
choline transporter-like protein 4 isoform X3
protein LSM14 homolog A-like, transcript variant X7
protein LSM14 homolog A-like, transcript variant X5
protein LSM14 homolog A-like, transcript variant X3
protein LSM14 homolog A-like, transcript variant X1
protein LSM14 homolog A-like, transcript variant X6
protein LSM14 homolog A-like, transcript variant X2
protein LSM14 homolog A-like, transcript variant X4
protein LSM14 homolog B-A-like isoform X4
cytochrome c1, heme protein, mitochondrial-like
V-type proton ATPase catalytic subunit A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
serine-aspartate repeat-containing protein I-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
splicing factor U2af large subunit A-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 49 samples with support for all annotated introns
muscle M-line assembly protein unc-89-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 7-like
uncharacterized PE-PGRS family protein PE_PGRS46-like
interference hedgehog-like, transcript variant X1
similar to RNA sequence (same species):INSD:GBEV01015278.1
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 503 bases not found in genome assembly
interference hedgehog-like, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 378 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123771446, transcript variant X4
uncharacterized LOC123771446, transcript variant X1
uncharacterized LOC123771446, transcript variant X3
uncharacterized LOC123771446, transcript variant X2
uncharacterized LOC123771446, transcript variant X7
uncharacterized LOC123771446, transcript variant X8
uncharacterized LOC123771446, transcript variant X5
uncharacterized LOC123771446, transcript variant X9
uncharacterized LOC123771446, transcript variant X6
uncharacterized LOC123771446, transcript variant X10
uncharacterized LOC123771446, transcript variant X12
uncharacterized protein LOC123771446 isoform X4
uncharacterized protein LOC123771446 isoform X1
uncharacterized protein LOC123771446 isoform X3
uncharacterized protein LOC123771446 isoform X2
uncharacterized protein LOC123771446 isoform X7
uncharacterized protein LOC123771446 isoform X8
uncharacterized protein LOC123771446 isoform X5
uncharacterized protein LOC123771446 isoform X9
uncharacterized protein LOC123771446 isoform X6
uncharacterized protein LOC123771446 isoform X10
uncharacterized protein LOC123771446 isoform X12
uncharacterized LOC123771446, transcript variant X11
uncharacterized protein LOC123771446 isoform X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable rhodanese domain-containing dual specificity protein phosphatase, 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
probable rhodanese domain-containing dual specificity protein phosphatase, 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 18 samples with support for all annotated introns
probable rhodanese domain-containing dual specificity protein phosphatase
BTB/POZ domain-containing protein 6-B-like, transcript variant X1
BTB/POZ domain-containing protein 6-B-like, transcript variant X2
BTB/POZ domain-containing protein 6-B-like
uncharacterized LOC123771459, transcript variant X5
uncharacterized LOC123771459, transcript variant X4
uncharacterized LOC123771459, transcript variant X2
uncharacterized LOC123771459, transcript variant X3
uncharacterized LOC123771459, transcript variant X1
uncharacterized LOC123771459, transcript variant X6
retinol dehydrogenase 13-like, transcript variant X3
retinol dehydrogenase 13-like, transcript variant X1
retinol dehydrogenase 13-like isoform X1
retinol dehydrogenase 13-like, transcript variant X2
retinol dehydrogenase 13-like isoform X3
retinol dehydrogenase 13-like isoform X2
fasciclin-2-like, transcript variant X11
fasciclin-2-like, transcript variant X10
fasciclin-2-like, transcript variant X15
fasciclin-2-like, transcript variant X13
fasciclin-2-like, transcript variant X12
fasciclin-2-like, transcript variant X14
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
probable serine/threonine-protein kinase clkA
DNA-directed RNA polymerase II subunit RPB1-like
U1 small nuclear ribonucleoprotein 70 kDa-like
uncharacterized LOC123771462, 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 3 samples with support for all annotated introns
uncharacterized LOC123771462, 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 3 samples with support for all annotated introns
uncharacterized LOC123771462, 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
uncharacterized protein LOC123771462 isoform X2
uncharacterized protein LOC123771462 isoform X1
uncharacterized protein LOC123771462 isoform X3
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X4
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X3
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X5
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X3
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X2
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like, transcript variant X2
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like, transcript variant X3
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like, transcript variant X1
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like isoform X2
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like isoform X1
radical S-adenosyl methionine domain-containing protein 1, mitochondrial-like isoform X3
uncharacterized LOC123771469, transcript variant X2
uncharacterized LOC123771469, transcript variant X3
uncharacterized LOC123771469, transcript variant X1
macrophage migration inhibitory factor-like
corticotropin-releasing factor-binding protein-like
uncharacterized LOC123771473, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123771473, 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 24 samples with support for all annotated introns
uncharacterized protein LOC123771473 isoform X2
uncharacterized protein LOC123771473 isoform X1
uncharacterized LOC123771474, 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 6 samples with support for all annotated introns
uncharacterized LOC123771474, 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 5 samples with support for all annotated introns
uncharacterized LOC123771474, 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 9 samples with support for all annotated introns
uncharacterized LOC123771474, transcript variant X3
uncharacterized LOC123771474, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC123771474 isoform X1
uncharacterized protein LOC123771474 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
calcium-binding mitochondrial carrier protein Aralar1-like
similar to RNA sequence (same species):INSD:GARH01020610.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 57 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% 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 57 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123771477, transcript variant X3
uncharacterized LOC123771477, transcript variant X6
uncharacterized LOC123771477, transcript variant X5
uncharacterized LOC123771477, transcript variant X4
uncharacterized LOC123771477, transcript variant X1
uncharacterized LOC123771477, transcript variant X2
similar to RNA sequence (same species):INSD:GBEV01003262.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1734 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 106 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 917 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
10 kDa heat shock protein, mitochondrial-like
ER membrane protein complex subunit 4-like
nuclear apoptosis-inducing factor 1-like, transcript variant X1
nuclear apoptosis-inducing factor 1-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 11 samples with support for all annotated introns
nuclear apoptosis-inducing factor 1-like isoform X2
nuclear apoptosis-inducing factor 1-like isoform 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
solute carrier family 41 member 1-like, transcript variant X3
solute carrier family 41 member 1-like, transcript variant X1
solute carrier family 41 member 1-like, transcript variant X2
solute carrier family 41 member 1-like, transcript variant X5
solute carrier family 41 member 1-like, transcript variant X4
solute carrier family 41 member 1-like isoform X2
solute carrier family 41 member 1-like isoform X1
solute carrier family 41 member 1-like isoform X4
solute carrier family 41 member 1-like isoform X3
uncharacterized LOC123771491, transcript variant X2
uncharacterized LOC123771491, transcript variant X1
uncharacterized LOC123771491, transcript variant X3
acetylcholine receptor subunit alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acetylcholine receptor subunit alpha-like isoform X2
acetylcholine receptor subunit alpha-like isoform X1
similar to RNA sequence (same species):INSD:GARH01011685.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1015 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 930 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
single-stranded nucleic acid-binding protein-like
probable acyl-CoA dehydrogenase 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6, 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 12 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6, 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 37 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6 isoform X2
probable acyl-CoA dehydrogenase 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 96 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6, 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 22 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
probable acyl-CoA dehydrogenase 6 isoform X1
germinal-center associated nuclear protein-like, transcript variant X12
germinal-center associated nuclear protein-like, transcript variant X9
germinal-center associated nuclear protein-like, transcript variant X8
germinal-center associated nuclear protein-like, transcript variant X10
germinal-center associated nuclear protein-like, transcript variant X7
germinal-center associated nuclear protein-like, transcript variant X11
germinal-center associated nuclear protein-like, transcript variant X4
germinal-center associated nuclear protein-like, transcript variant X3
germinal-center associated nuclear protein-like, transcript variant X5
germinal-center associated nuclear protein-like, transcript variant X6
germinal-center associated nuclear protein-like, transcript variant X1
germinal-center associated nuclear protein-like, transcript variant X2
germinal-center associated nuclear protein-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 2 samples with support for all annotated introns
PTB domain-containing engulfment adapter protein 1-like, transcript variant X1
PTB domain-containing engulfment adapter protein 1-like, transcript variant X6
PTB domain-containing engulfment adapter protein 1-like, transcript variant X3
PTB domain-containing engulfment adapter protein 1-like, transcript variant X4
PTB domain-containing engulfment adapter protein 1-like, transcript variant X2
PTB domain-containing engulfment adapter protein 1-like, transcript variant X5
PTB domain-containing engulfment adapter protein 1-like isoform X1
PTB domain-containing engulfment adapter protein 1-like isoform X2
PTB domain-containing engulfment adapter protein 1-like isoform X3
uncharacterized LOC123771500, transcript variant X2
uncharacterized LOC123771500, transcript variant X1
uncharacterized LOC123771500, transcript variant X4
uncharacterized LOC123771500, transcript variant X6
uncharacterized LOC123771500, transcript variant X5
uncharacterized LOC123771500, transcript variant X3
uncharacterized protein LOC123771500 isoform X1
uncharacterized protein LOC123771500 isoform X3
uncharacterized protein LOC123771500 isoform X4
uncharacterized protein LOC123771500 isoform X6
uncharacterized protein LOC123771500 isoform X2
uncharacterized protein LOC123771500 isoform X5
uncharacterized LOC123771500, transcript variant X7
uncharacterized protein LOC123771500 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
protein Churchill-like, transcript variant X1
protein Churchill-like, transcript variant X2
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like, transcript variant X1
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like, transcript variant X4
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like, transcript variant X3
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like isoform X1
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like isoform X4
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like isoform X3
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase P-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cysteine protease ATG4D-like, transcript variant X1
cysteine protease ATG4D-like, transcript variant X5
cysteine protease ATG4D-like, transcript variant X2
cysteine protease ATG4D-like, transcript variant X4
cysteine protease ATG4D-like, transcript variant X3
carbonic anhydrase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
carbonic anhydrase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DBH-like monooxygenase protein 1, transcript variant X1
DBH-like monooxygenase protein 1, transcript variant X2
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polycystic kidney disease protein 1-like 3
serine/threonine-protein kinase PRP4 homolog
mediator of DNA damage checkpoint protein 1-like
toll-like receptor Tollo, transcript variant X2
toll-like receptor Tollo, transcript variant X1
golgin subfamily A member 6-like protein 22