Procambarus clarkii strain Jiangsu linkage group LG39, 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\nCM035511.1.\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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
protein ST7 homolog, transcript variant X6
COORDINATES: polyA evidence [ECO:0006239]
protein ST7 homolog, transcript variant X2
protein ST7 homolog, transcript variant X1
protein ST7 homolog, transcript variant X7
protein ST7 homolog, transcript variant X8
protein ST7 homolog, transcript variant X3
protein ST7 homolog, transcript variant X4
protein ST7 homolog, transcript variant X5
peptidyl-prolyl cis-trans isomerase Fkbp12-like
ATPase family AAA domain-containing protein 2-like
similar to RNA sequence (same species):INSD:GARH01013272.1
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 352 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 352 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like isoform X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like isoform X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X3
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X7
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X6
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X5
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like, transcript variant X4
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-like, transcript variant X4
ankyrin repeat domain-containing protein 10-like isoform X3
ankyrin repeat domain-containing protein 10-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 49 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-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 39 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-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 19 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-like isoform X1
uncharacterized protein LOC123764258 isoform X4
ankyrin repeat domain-containing protein 10-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 63 samples with support for all annotated introns
ankyrin repeat domain-containing protein 10-like isoform X2
vesicle-fusing ATPase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
vesicle-fusing ATPase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta chain-like, transcript variant X1
calcium/calmodulin-dependent protein kinase type II delta chain-like, transcript variant X3
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
calcium/calmodulin-dependent protein kinase type II delta chain-like isoform X3
calcium/calmodulin-dependent protein kinase type II delta chain-like isoform X2
calcium/calmodulin-dependent protein kinase type II delta chain-like isoform X1
uncharacterized LOC123764265, transcript variant X1
uncharacterized LOC123764265, transcript variant X2
uncharacterized protein LOC123764265 isoform X1
uncharacterized protein LOC123764265 isoform X2
uncharacterized LOC123764266, 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 9 samples with support for all annotated introns
uncharacterized LOC123764266, transcript variant X3
uncharacterized LOC123764266, transcript variant X1
uncharacterized protein LOC123764266 isoform X2
uncharacterized protein LOC123764266 isoform X1
ileal sodium/bile acid cotransporter-like
D-3-phosphoglycerate dehydrogenase-like, transcript variant X1
D-3-phosphoglycerate dehydrogenase-like isoform X1
D-3-phosphoglycerate dehydrogenase-like, transcript variant X2
D-3-phosphoglycerate dehydrogenase-like isoform 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: 1 Protein, and 77% 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
dynein intermediate chain 2, ciliary-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
calmodulin-interacting protein 111-like, transcript variant X1
calmodulin-interacting protein 111-like, transcript variant X4
calmodulin-interacting protein 111-like, transcript variant X3
calmodulin-interacting protein 111-like, transcript variant X2
calmodulin-interacting protein 111-like isoform X1
calmodulin-interacting protein 111-like isoform X2
aldo-keto reductase family 1 member B1-like
protein neuralized-like, transcript variant X2
protein neuralized-like, transcript variant X1
ankyrin repeat and SOCS box protein 13-like, transcript variant X1
ankyrin repeat and SOCS box protein 13-like, transcript variant X3
ankyrin repeat and SOCS box protein 13-like, transcript variant X4
ankyrin repeat and SOCS box protein 13-like, transcript variant X2
ankyrin repeat and SOCS box protein 13-like isoform X1
ankyrin repeat and SOCS box protein 13-like isoform X2
ankyrin repeat and SOCS box protein 13-like isoform 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 10 samples with support for all annotated introns
stress-activated protein kinase JNK-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: stress-activated protein kinase JNK-like
YY1-associated factor 2-like, transcript variant X1
YY1-associated factor 2-like, transcript variant X2
exosome complex component RRP41-like, transcript variant X2
exosome complex component RRP41-like, transcript variant X1
synaptic vesicle 2-related protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
synaptic vesicle 2-related protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
crossover junction endonuclease MUS81-like, transcript variant X1
crossover junction endonuclease MUS81-like, transcript variant X2
crossover junction endonuclease MUS81-like, transcript variant X3
crossover junction endonuclease MUS81-like isoform X1
crossover junction endonuclease MUS81-like isoform X2
crossover junction endonuclease MUS81-like isoform X3
uncharacterized LOC123764285, transcript variant X4
uncharacterized LOC123764285, transcript variant X6
uncharacterized protein LOC123764285 isoform X4
uncharacterized protein LOC123764285 isoform X6
uncharacterized LOC123764285, transcript variant X5
uncharacterized LOC123764285, transcript variant X1
uncharacterized LOC123764285, transcript variant X3
uncharacterized LOC123764285, transcript variant X2
uncharacterized protein LOC123764285 isoform X1
uncharacterized protein LOC123764285 isoform X3
uncharacterized protein LOC123764285 isoform X2
uncharacterized protein LOC123764285 isoform X5
Meckel syndrome type 1 protein homolog, transcript variant X2
Meckel syndrome type 1 protein homolog, transcript variant X4
Meckel syndrome type 1 protein homolog, transcript variant X3
Meckel syndrome type 1 protein homolog, transcript variant X1
Meckel syndrome type 1 protein homolog isoform X3
Meckel syndrome type 1 protein homolog isoform X2
Meckel syndrome type 1 protein homolog isoform X1
hematopoietic prostaglandin D synthase-like, transcript variant X1
hematopoietic prostaglandin D synthase-like, transcript variant X4
hematopoietic prostaglandin D synthase-like, transcript variant X5
hematopoietic prostaglandin D synthase-like, transcript variant X2
hematopoietic prostaglandin D synthase-like, transcript variant X3
hematopoietic prostaglandin D synthase-like
similar to RNA sequence (same species):INSD:GBEV01011801.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 193 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 109 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
propionyl-CoA carboxylase alpha chain, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like isoform X2
serine/arginine repetitive matrix protein 1-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 4 samples with support for all annotated introns
probable signal peptidase complex subunit 2
2-(3-amino-3-carboxypropyl)histidine synthase subunit 1
glutenin, high molecular weight subunit 12-like
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 11-like
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X5
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X4
signal peptide, CUB and EGF-like domain-containing protein 1
similar to RNA sequence (same species):INSD:GARH01007049.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 779 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 574 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 102 samples with support for all annotated introns
28S ribosomal protein S35, mitochondrial-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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123764306, transcript variant X3
uncharacterized LOC123764306, transcript variant X1
uncharacterized LOC123764306, transcript variant X2
uncharacterized LOC123764306, transcript variant X4
uncharacterized LOC123764306, transcript variant X5
FAD-dependent oxidoreductase domain-containing protein 1-like, transcript variant X1
FAD-dependent oxidoreductase domain-containing protein 1-like
FAD-dependent oxidoreductase domain-containing protein 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 68 samples with support for all annotated introns
uncharacterized LOC123764308, transcript variant X5
uncharacterized LOC123764308, transcript variant X2
uncharacterized LOC123764308, transcript variant X4
uncharacterized LOC123764308, transcript variant X1
uncharacterized LOC123764308, transcript variant X3
galactoside alpha-(1,2)-fucosyltransferase 2-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 2 samples with support for all annotated introns
uncharacterized LOC123764307, transcript variant X2
uncharacterized LOC123764307, transcript variant X1
uncharacterized protein LOC123764307 isoform X2
uncharacterized protein LOC123764307 isoform X1
H/ACA ribonucleoprotein complex subunit 2-like
chromatin assembly factor 1 subunit B-like, transcript variant X2
chromatin assembly factor 1 subunit B-like, transcript variant X1
chromatin assembly factor 1 subunit B-like
DNA-(apurinic or apyrimidinic site) endonuclease-like
LIM homeobox transcription factor 1-alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LIM homeobox transcription factor 1-alpha-like, transcript variant X1
LIM homeobox transcription factor 1-alpha-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LIM homeobox transcription factor 1-alpha-like isoform X1
LIM homeobox transcription factor 1-alpha-like isoform X3
LIM homeobox transcription factor 1-alpha-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
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
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
putative aldolase class 2 protein RP493, transcript variant X1
putative aldolase class 2 protein RP493, transcript variant X2
putative aldolase class 2 protein RP493, transcript variant X3
putative aldolase class 2 protein RP493, transcript variant X4
solute carrier family 15 member 2-like, transcript variant X2
solute carrier family 15 member 2-like isoform X2
solute carrier family 15 member 2-like, transcript variant X1
solute carrier family 15 member 2-like isoform X1
39S ribosomal protein L4, mitochondrial-like
alpha-mannosidase 2-like, transcript variant X2
alpha-mannosidase 2-like, transcript variant X1
alpha-mannosidase 2-like, transcript variant X3
myosin heavy chain, non-muscle-like, transcript variant X7
myosin heavy chain, non-muscle-like, transcript variant X6
myosin heavy chain, non-muscle-like, transcript variant X5
myosin heavy chain, non-muscle-like, transcript variant X4
myosin heavy chain, non-muscle-like, transcript variant X3
myosin heavy chain, non-muscle-like, transcript variant X2
myosin heavy chain, non-muscle-like, transcript variant X8
myosin heavy chain, non-muscle-like, transcript variant X1
myosin heavy chain, non-muscle-like, transcript variant X10
myosin heavy chain, non-muscle-like, transcript variant X9
myosin heavy chain, non-muscle-like isoform X7
myosin heavy chain, non-muscle-like isoform X6
myosin heavy chain, non-muscle-like isoform X5
myosin heavy chain, non-muscle-like isoform X4
myosin heavy chain, non-muscle-like isoform X3
myosin heavy chain, non-muscle-like isoform X2
myosin heavy chain, non-muscle-like isoform X8
myosin heavy chain, non-muscle-like isoform X1
myosin heavy chain, non-muscle-like isoform X10
myosin heavy chain, non-muscle-like isoform X9
golgin subfamily B member 1-like, transcript variant X1
golgin subfamily B member 1-like, transcript variant X2
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: 93% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein Dscam2
similar to RNA sequence (same species):INSD:GARH01008871.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 317 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 317 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
ATP-dependent RNA helicase DDX1-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 25 samples with support for all annotated introns
ATP-dependent RNA helicase DDX1-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 8 samples with support for all annotated introns
ATP-dependent RNA helicase DDX1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATP-dependent RNA helicase DDX1-like isoform X1
ATP-dependent RNA helicase DDX1-like 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 6 samples with support for all annotated introns
uncharacterized LOC123764331, transcript variant X6
uncharacterized LOC123764331, transcript variant X5
uncharacterized LOC123764331, transcript variant X4
uncharacterized LOC123764331, transcript variant X2
uncharacterized protein LOC123764331 isoform X2
uncharacterized LOC123764331, transcript variant X3
uncharacterized protein LOC123764331 isoform X3
uncharacterized LOC123764331, transcript variant X1
uncharacterized protein LOC123764331 isoform X1
uncharacterized protein LOC123764331 isoform X4
uncharacterized LOC123764331, transcript variant X7
uncharacterized protein LOC123764331 isoform X5
uncharacterized protein LOC123764331 isoform X6
macrophage mannose receptor 1-like, transcript variant X2
macrophage mannose receptor 1-like, transcript variant X1
macrophage mannose receptor 1-like isoform X2
macrophage mannose receptor 1-like isoform X1
uncharacterized LOC123764335, 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 19 samples with support for all annotated introns
uncharacterized LOC123764335, 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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X2
ras-related and estrogen-regulated growth inhibitor-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 5 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like isoform X2
ras-related and estrogen-regulated growth inhibitor-like isoform X1
transcription elongation regulator 1-like, transcript variant X7
transcription elongation regulator 1-like, transcript variant X12
transcription elongation regulator 1-like, transcript variant X11
transcription elongation regulator 1-like, transcript variant X3
transcription elongation regulator 1-like, transcript variant X8
transcription elongation regulator 1-like, transcript variant X6
transcription elongation regulator 1-like, transcript variant X10
transcription elongation regulator 1-like, transcript variant X9
transcription elongation regulator 1-like, transcript variant X4
transcription elongation regulator 1-like, transcript variant X2
transcription elongation regulator 1-like, transcript variant X5
transcription elongation regulator 1-like, transcript variant X1
transcription elongation regulator 1-like isoform X10
transcription elongation regulator 1-like isoform X9
transcription elongation regulator 1-like isoform X7
transcription elongation regulator 1-like isoform X11
transcription elongation regulator 1-like isoform X3
transcription elongation regulator 1-like isoform X4
transcription elongation regulator 1-like isoform X2
transcription elongation regulator 1-like isoform X6
transcription elongation regulator 1-like isoform X5
transcription elongation regulator 1-like isoform X1
transcription elongation regulator 1-like isoform X12
transcription elongation regulator 1-like isoform X8
protein abrupt-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 17 samples with support for all annotated introns
protein abrupt-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 14 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X1
protein abrupt-like, transcript variant X2
protein tramtrack, beta isoform-like isoform X2
39S ribosomal protein L18, mitochondrial-like
NAD(P)H-hydrate epimerase-like, transcript variant X1
NAD(P)H-hydrate epimerase-like, transcript variant X2
NAD(P)H-hydrate epimerase-like, transcript variant X5
NAD(P)H-hydrate epimerase-like, transcript variant X3
NAD(P)H-hydrate epimerase-like, transcript variant X4
NAD(P)H-hydrate epimerase-like isoform X1
NAD(P)H-hydrate epimerase-like isoform X2
glutamate receptor-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 1 sample with support for all annotated introns
glutamate receptor-like, transcript variant X2
serine/threonine-protein phosphatase PP1-like
mitochondrial-processing peptidase subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X1
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X2
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X4
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X3
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X5
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X6
B-cell CLL/lymphoma 6 member B protein-like, transcript variant X7
B-cell CLL/lymphoma 6 member B protein-like isoform X1
B-cell CLL/lymphoma 6 member B protein-like isoform X2
B-cell CLL/lymphoma 6 member B protein-like isoform X3
B-cell CLL/lymphoma 6 member B protein-like isoform X4
B-cell CLL/lymphoma 6 member B protein-like isoform X5
sulfite oxidase, mitochondrial-like, transcript variant X4
sulfite oxidase, mitochondrial-like, transcript variant X3
sulfite oxidase, mitochondrial-like, transcript variant X2
sulfite oxidase, mitochondrial-like, transcript variant X1
sulfite oxidase, mitochondrial-like isoform X2
sulfite oxidase, mitochondrial-like isoform X1
sulfite oxidase, mitochondrial-like isoform X3
paired amphipathic helix protein Sin3a-like, transcript variant X2
paired amphipathic helix protein Sin3a-like, transcript variant X3
paired amphipathic helix protein Sin3a-like, transcript variant X1
paired amphipathic helix protein Sin3a-like, transcript variant X12
paired amphipathic helix protein Sin3a-like, transcript variant X10
paired amphipathic helix protein Sin3a-like, transcript variant X4
paired amphipathic helix protein Sin3a-like, transcript variant X7
paired amphipathic helix protein Sin3a-like, transcript variant X5
paired amphipathic helix protein Sin3a-like, transcript variant X6
paired amphipathic helix protein Sin3a-like, transcript variant X8
paired amphipathic helix protein Sin3a-like, transcript variant X13
paired amphipathic helix protein Sin3a-like, transcript variant X15
paired amphipathic helix protein Sin3a-like, transcript variant X9
paired amphipathic helix protein Sin3a-like, transcript variant X11
paired amphipathic helix protein Sin3a-like, transcript variant X14
eukaryotic translation initiation factor 3 subunit A-like
paired amphipathic helix protein Sin3a-like isoform X1
paired amphipathic helix protein Sin3a-like isoform X4
paired amphipathic helix protein Sin3a-like isoform X10
paired amphipathic helix protein Sin3a-like isoform X6
paired amphipathic helix protein Sin3a-like isoform X8
paired amphipathic helix protein Sin3a-like isoform X11
paired amphipathic helix protein Sin3a-like isoform X12
paired amphipathic helix protein Sin3a-like isoform X2
paired amphipathic helix protein Sin3a-like isoform X5
paired amphipathic helix protein Sin3a-like isoform X13
paired amphipathic helix protein Sin3a-like isoform X7
paired amphipathic helix protein Sin3a-like isoform X3
paired amphipathic helix protein Sin3a-like isoform X9
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
uncharacterized LOC123764355, transcript variant X2
uncharacterized LOC123764355, transcript variant X1
uncharacterized LOC123764356, transcript variant X1
uncharacterized LOC123764356, transcript variant X2
uncharacterized protein LOC123764356 isoform X1
uncharacterized protein LOC123764356 isoform X2
neural proliferation differentiation and control 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 1 sample 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
uncharacterized protein KIAA0513-like, transcript variant X2
uncharacterized protein KIAA0513-like, transcript variant X3
uncharacterized protein KIAA0513-like, transcript variant X1
SH3 domain-containing kinase-binding protein 1-like, transcript variant X1
SH3 domain-containing kinase-binding protein 1-like, transcript variant X4
SH3 domain-containing kinase-binding protein 1-like, transcript variant X2
SH3 domain-containing kinase-binding protein 1-like isoform X1
SH3 domain-containing kinase-binding protein 1-like isoform X4
SH3 domain-containing kinase-binding protein 1-like isoform X2
SH3 domain-containing kinase-binding protein 1-like, transcript variant X3
SH3 domain-containing kinase-binding protein 1-like, transcript variant X6
SH3 domain-containing kinase-binding protein 1-like isoform X3
SH3 domain-containing kinase-binding protein 1-like isoform X6
SH3 domain-containing kinase-binding protein 1-like, transcript variant X5
SH3 domain-containing kinase-binding protein 1-like, transcript variant X10
SH3 domain-containing kinase-binding protein 1-like isoform X5
SH3 domain-containing kinase-binding protein 1-like isoform X8
SH3 domain-containing kinase-binding protein 1-like, transcript variant X8
SH3 domain-containing kinase-binding protein 1-like, transcript variant X9
SH3 domain-containing kinase-binding protein 1-like, transcript variant X7
SH3 domain-containing kinase-binding protein 1-like, transcript variant X11
SH3 domain-containing kinase-binding protein 1-like, transcript variant X12
SH3 domain-containing kinase-binding protein 1-like isoform X7
SH3 domain-containing kinase-binding protein 1-like isoform X9
SH3 domain-containing kinase-binding protein 1-like isoform X10
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X4
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X2
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X1
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X3
cytosolic 10-formyltetrahydrofolate dehydrogenase-like isoform X1
cytosolic 10-formyltetrahydrofolate dehydrogenase-like isoform X2
uncharacterized LOC123764362, transcript variant X2
uncharacterized LOC123764362, transcript variant X4
uncharacterized LOC123764362, transcript variant X1
uncharacterized LOC123764362, 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 4 samples with support for all annotated introns
uncharacterized LOC123764362, 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 9 samples with support for all annotated introns
uncharacterized protein LOC123764362 isoform X4
uncharacterized protein LOC123764362 isoform X2
uncharacterized protein LOC123764362 isoform X1
uncharacterized protein LOC123764362 isoform X3
uncharacterized protein LOC123764362 isoform X5
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-like, transcript variant X5
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 18 samples with support for all annotated introns
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-like, transcript variant X2
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-like, transcript variant X3
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-like, transcript variant X1
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-like, transcript variant X4
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial-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 41 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 46 samples with support for all annotated introns
uncharacterized LOC123764368, transcript variant X2
uncharacterized LOC123764368, transcript variant X4
uncharacterized LOC123764368, transcript variant X3
uncharacterized LOC123764368, transcript variant X1
prolyl endopeptidase FAP-like, transcript variant X2
prolyl endopeptidase FAP-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
lambda-crystallin homolog, transcript variant X4
lambda-crystallin homolog, transcript variant X3
lambda-crystallin homolog, transcript variant X1
lambda-crystallin homolog, transcript variant X2
arylalkylamine N-acetyltransferase-like 2, transcript variant X1
arylalkylamine N-acetyltransferase-like 2, transcript variant X2
arylalkylamine N-acetyltransferase-like 2
probable G-protein coupled receptor AH9.1, transcript variant X3
probable G-protein coupled receptor AH9.1, transcript variant X2
probable G-protein coupled receptor AH9.1, transcript variant X1
uncharacterized protein LOC123764371 isoform X1
probable G-protein coupled receptor AH9.1, transcript variant X4
probable G-protein coupled receptor AH9.1 isoform X2
serine/threonine-protein kinase Kist-like, transcript variant X4
serine/threonine-protein kinase Kist-like, transcript variant X3
serine/threonine-protein kinase Kist-like, transcript variant X2
serine/threonine-protein kinase Kist-like, transcript variant X5
serine/threonine-protein kinase Kist-like, transcript variant X1
serine/threonine-protein kinase Kist-like isoform X1
serine/threonine-protein kinase Kist-like isoform X2
acetyl-coenzyme A transporter 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
acetyl-coenzyme A transporter 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
acetyl-coenzyme A transporter 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
guanine nucleotide-binding protein G(s) subunit alpha isoforms XLas-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 18 samples with support for all annotated introns
uncharacterized transmembrane protein DDB_G0289901-like
probable tyrosyl-DNA phosphodiesterase, transcript variant X1
probable tyrosyl-DNA phosphodiesterase, transcript variant X2
uncharacterized LOC123764383, 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 38 samples with support for all annotated introns
uncharacterized LOC123764383, 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 22 samples with support for all annotated introns
uncharacterized LOC123764383, transcript variant X5
uncharacterized LOC123764383, 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 51 samples with support for all annotated introns
uncharacterized LOC123764383, 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 96 samples with support for all annotated introns
uncharacterized protein LOC123764383 isoform X2
uncharacterized protein LOC123764383 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 72 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 83% coverage of the annotated genomic feature by RNAseq alignments
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 49-like isoform X27
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X30
longitudinals lacking protein, isoforms H/M/V-like isoform X21
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X31
longitudinals lacking protein, isoforms H/M/V-like isoform X22
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X48
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 20 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 X32
longitudinals lacking protein, isoforms H/M/V-like isoform X23
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X49
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
longitudinals lacking protein, isoforms A/B/D/L-like isoform X36
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
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X24
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X47
longitudinals lacking protein, isoforms A/B/D/L-like isoform X34
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X7
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X50
longitudinals lacking protein, isoforms H/M/V-like isoform X37
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X25
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X6
longitudinals lacking protein, isoforms H/M/V-like isoform X4
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X10
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X25
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 56 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X18
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X15
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X44
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X41
longitudinals lacking protein, isoforms H/M/V-like isoform X32
longitudinals lacking protein, isoforms H/M/V-like isoform X30
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X21
longitudinals lacking protein, isoforms A/B/D/L-like isoform X14
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 62 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X12
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 54 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X8
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-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 76 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
longitudinals lacking protein, isoforms H/M/V-like isoform X2
longitudinals lacking protein, isoforms H/M/V-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X3
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X24
longitudinals lacking protein, isoforms H/M/V-like isoform X17
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X28
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X29
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X28
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 31 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X20
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X23
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 70 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X16
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
longitudinals lacking protein-like isoform X13
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X19
longitudinals lacking protein, isoforms H/M/V-like isoform X12
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X8
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X40
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X17
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X7
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X39
longitudinals lacking protein, isoforms H/M/V-like isoform X29
longitudinals lacking protein, isoforms A/B/D/L-like isoform X5
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: 1 Protein, 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 X10
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
longitudinals lacking protein, isoforms A/B/D/L-like isoform X6
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X16
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X15
longitudinals lacking protein, isoforms H/M/V-like isoform X11
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X46
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X45
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 49 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 X43
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 17 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X31
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X27
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X26
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 35 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X19
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X34
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X36
longitudinals lacking protein, isoforms A/B/D/L-like isoform X26
longitudinals lacking protein-like, transcript variant X4
longitudinals lacking protein-like, transcript variant X7
longitudinals lacking protein-like, transcript variant X8
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
longitudinals lacking protein-like, transcript variant X3
longitudinals lacking protein-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 37 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X6
longitudinals lacking protein-like, transcript variant X9
longitudinals lacking protein-like, transcript variant X1
longitudinals lacking protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
longitudinals lacking protein-like isoform X3
longitudinals lacking protein-like isoform X6
protein tramtrack, beta isoform-like isoform X5
broad-complex core protein isoforms 1/2/3/4/5-like isoform X7
longitudinals lacking protein-like isoform X1
F-box/LRR-repeat protein fbxl-1-like, transcript variant X6
F-box/LRR-repeat protein fbxl-1-like, transcript variant X2
F-box/LRR-repeat protein fbxl-1-like, transcript variant X1
F-box/LRR-repeat protein fbxl-1-like, transcript variant X3
F-box/LRR-repeat protein fbxl-1-like, transcript variant X4
F-box/LRR-repeat protein fbxl-1-like, transcript variant X5
F-box/LRR-repeat protein fbxl-1-like isoform X4
F-box/LRR-repeat protein fbxl-1-like isoform X2
F-box/LRR-repeat protein fbxl-1-like isoform X1
F-box/LRR-repeat protein fbxl-1-like isoform X3
zinc transporter ZIP13 homolog, transcript variant X2
zinc transporter ZIP13 homolog, transcript variant X1
zinc transporter ZIP13 homolog isoform X1
zinc transporter ZIP13 homolog, transcript variant X4
zinc transporter ZIP13 homolog isoform X3
zinc transporter ZIP13 homolog, transcript variant X3
zinc transporter ZIP13 homolog isoform X2
outer dense fiber protein 3-like, transcript variant X5
outer dense fiber protein 3-like, transcript variant X3
outer dense fiber protein 3-like, transcript variant X4
outer dense fiber protein 3-like, transcript variant X2
outer dense fiber protein 3-like, transcript variant X1
outer dense fiber protein 3-like isoform X5
outer dense fiber protein 3-like isoform X3
outer dense fiber protein 3-like isoform X4
outer dense fiber protein 3-like isoform X2
outer dense fiber protein 3-like isoform X1
uncharacterized LOC123764396, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123764396, 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 53 samples with support for all annotated introns
uncharacterized protein LOC123764396 isoform X1
uncharacterized protein LOC123764396 isoform X2
putative RNA polymerase II subunit B1 CTD phosphatase rpap2, transcript variant X3
putative RNA polymerase II subunit B1 CTD phosphatase rpap2, transcript variant X5
putative RNA polymerase II subunit B1 CTD phosphatase rpap2, transcript variant X4
putative RNA polymerase II subunit B1 CTD phosphatase rpap2, transcript variant X2
putative RNA polymerase II subunit B1 CTD phosphatase rpap2, transcript variant X1
putative RNA polymerase II subunit B1 CTD phosphatase rpap2
Y' element ATP-dependent helicase YEL077C-like
uncharacterized protein LOC123764401 isoform X2
uncharacterized protein LOC123764401 isoform X1
B9 domain-containing protein 1-like, transcript variant X3
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 54 samples with support for all annotated introns
B9 domain-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
B9 domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
B9 domain-containing protein 1-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 24 samples with support for all annotated introns
NACHT domain- and WD repeat-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
upstream activation factor subunit spp27-like, transcript variant X2
upstream activation factor subunit spp27-like, transcript variant X1
upstream activation factor subunit spp27-like isoform X2
upstream activation factor subunit spp27-like isoform X1
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X3
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X4
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X7
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X2
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X8
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X6
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X5
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X1
calcium uptake protein 1 homolog, mitochondrial-like isoform X5
calcium uptake protein 1 homolog, mitochondrial-like isoform X4
calcium uptake protein 1 homolog, mitochondrial-like isoform X1
calcium uptake protein 1 homolog, mitochondrial-like isoform X7
calcium uptake protein 1 homolog, mitochondrial-like isoform X6
calcium uptake protein 1 homolog, mitochondrial-like isoform X2
calcium uptake protein 1 homolog, mitochondrial-like isoform X3
electron transfer flavoprotein subunit beta-like
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like isoform X1
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-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 13 samples with support for all annotated introns
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like isoform X2
G-protein-signaling modulator 2-like, transcript variant X16
G-protein-signaling modulator 2-like, transcript variant X7
G-protein-signaling modulator 2-like, transcript variant X18
G-protein-signaling modulator 2-like, transcript variant X19
G-protein-signaling modulator 2-like, transcript variant X10
G-protein-signaling modulator 2-like, transcript variant X11
G-protein-signaling modulator 2-like, transcript variant X13
G-protein-signaling modulator 2-like, transcript variant X17
G-protein-signaling modulator 2-like, transcript variant X12
G-protein-signaling modulator 2-like, transcript variant X6
G-protein-signaling modulator 2-like, transcript variant X21
G-protein-signaling modulator 2-like, transcript variant X1
G-protein-signaling modulator 2-like, transcript variant X14
G-protein-signaling modulator 2-like, transcript variant X15
G-protein-signaling modulator 2-like, transcript variant X8
G-protein-signaling modulator 2-like, transcript variant X9
G-protein-signaling modulator 2-like, transcript variant X3
G-protein-signaling modulator 2-like, transcript variant X4
G-protein-signaling modulator 2-like, transcript variant X2
G-protein-signaling modulator 2-like, transcript variant X22
G-protein-signaling modulator 2-like, transcript variant X5
G-protein-signaling modulator 2-like, transcript variant X20
G-protein-signaling modulator 2-like isoform X1
G-protein-signaling modulator 2-like isoform X3
G-protein-signaling modulator 2-like isoform X8
G-protein-signaling modulator 2-like isoform X2
G-protein-signaling modulator 2-like isoform X4
G-protein-signaling modulator 2-like isoform X5
G-protein-signaling modulator 2-like isoform X7
G-protein-signaling modulator 2-like isoform X9
G-protein-signaling modulator 2-like isoform X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
multidrug resistance-associated protein 1-like, transcript variant X2
multidrug resistance-associated protein 1-like, transcript variant X1
multidrug resistance-associated protein 1-like isoform X2
multidrug resistance-associated protein 1-like isoform X1
multidrug resistance-associated protein 1-like, transcript variant X5
multidrug resistance-associated protein 1-like, transcript variant X6
multidrug resistance-associated protein 1-like, transcript variant X3
multidrug resistance-associated protein 1-like, transcript variant X4
multidrug resistance-associated protein 1-like isoform X5
multidrug resistance-associated protein 1-like isoform X6
multidrug resistance-associated protein 1-like isoform X3
multidrug resistance-associated protein 1-like isoform X4
ubiquitin-associated domain-containing protein 1-like
uncharacterized LOC123764415, transcript variant X1
uncharacterized LOC123764415, transcript variant X2
uncharacterized protein LOC123764415 isoform X1
uncharacterized protein LOC123764415 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 93 samples with support for all annotated introns
transcriptional enhancer factor TEF-1-like
similar to RNA sequence (same species):INSD:GARH01006927.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 116 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 6 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein KIAA1143 homolog
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
uncharacterized LOC123764419, transcript variant X1
uncharacterized LOC123764419, transcript variant X2
uncharacterized protein LOC123764419 isoform X1
uncharacterized protein LOC123764419 isoform X2
nuclear pore complex protein Nup205-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
ras and EF-hand domain-containing protein homolog, transcript variant X3
ras and EF-hand domain-containing protein homolog, transcript variant X2
ras and EF-hand domain-containing protein homolog, transcript variant X1
ras and EF-hand domain-containing protein homolog isoform X3
ras and EF-hand domain-containing protein-like isoform X2
ras and EF-hand domain-containing protein-like isoform X1
uncharacterized PPE family protein PPE40-like
uncharacterized LOC123764426, 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 8 samples with support for all annotated introns
uncharacterized LOC123764426, 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 15 samples with support for all annotated introns
uncharacterized protein LOC123764426 isoform X1
uncharacterized protein LOC123764426 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
endoglucanase E-4-like, transcript variant X3
endoglucanase E-4-like, transcript variant X1
endoglucanase E-4-like, transcript variant X2
putative uncharacterized protein DDB_G0285119
protein lin-52 homolog, transcript variant X1
protein lin-52 homolog, transcript variant X3
protein lin-52 homolog, transcript variant X2
N-acetylglucosamine-6-sulfatase-like, transcript variant X2
N-acetylglucosamine-6-sulfatase-like, transcript variant X3
N-acetylglucosamine-6-sulfatase-like isoform X2
N-acetylglucosamine-6-sulfatase-like, transcript variant X1
N-acetylglucosamine-6-sulfatase-like isoform X1
uncharacterized LOC123764432, transcript variant X1
uncharacterized LOC123764432, 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 50 samples with support for all annotated introns
uncharacterized LOC123764432, 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 36 samples with support for all annotated introns
uncharacterized protein LOC123764432 isoform X3
uncharacterized protein LOC123764432 isoform X2
uncharacterized protein LOC123764432 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
intraflagellar transport protein 74 homolog, transcript variant X2
intraflagellar transport protein 74 homolog, transcript variant X3
intraflagellar transport protein 74 homolog, transcript variant X1
intraflagellar transport protein 74 homolog isoform X2
intraflagellar transport protein 74 homolog isoform X1
40S ribosomal protein S11-like, transcript variant X1
40S ribosomal protein S11-like, transcript variant X2
40S ribosomal protein S11-like isoform X2
40S ribosomal protein S11-like isoform X1
uncharacterized LOC123764438, transcript variant X3
uncharacterized LOC123764438, transcript variant X2
uncharacterized LOC123764438, transcript variant X4
uncharacterized LOC123764438, transcript variant X1
uncharacterized protein LOC123764438 isoform X1
uncharacterized protein LOC123764438 isoform X2
glycine receptor subunit alpha-3-like, transcript variant X1
glycine receptor subunit alpha-3-like, transcript variant X2
glycine receptor subunit alpha-3-like isoform X1
glycine receptor subunit alpha-3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DDB_G0290685-like
similar to RNA sequence (same species):INSD:GBEV01013957.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 3 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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: 130 Proteins
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 59 samples with support for all annotated introns
general transcription factor IIF subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
coiled-coil domain-containing protein 8 homolog
golgin subfamily A member 6-like protein 2
gamete and mating-type specific protein A-like
uncharacterized protein DDB_G0288805-like