Procambarus clarkii strain Jiangsu linkage group LG91, 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\nCM035563.1.\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.
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
DEP domain-containing protein 1A-like, transcript variant X3
COORDINATES: polyA evidence [ECO:0006239]
DEP domain-containing protein 1A-like, transcript variant X2
DEP domain-containing protein 1A-like, transcript variant X1
DEP domain-containing protein 1A-like isoform X3
DEP domain-containing protein 1A-like isoform X2
DEP domain-containing protein 1A-like isoform X1
DEP domain-containing protein 1A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DEP domain-containing protein 1A-like isoform X4
sodium-dependent neutral amino acid transporter B(0)AT3-like, transcript variant X1
sodium-dependent neutral amino acid transporter B(0)AT3-like, transcript variant X3
sodium-dependent neutral amino acid transporter B(0)AT3-like, transcript variant X2
sodium-dependent neutral amino acid transporter B(0)AT3-like isoform X1
sodium-dependent neutral amino acid transporter B(0)AT3-like isoform X3
sodium-dependent neutral amino acid transporter B(0)AT3-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 4 samples with support for all annotated introns
sodium-dependent neutral amino acid transporter B(0)AT3-like isoform X4
sodium-dependent neutral amino acid transporter B(0)AT3-like isoform X2
serine/threonine-protein kinase stk11-like, transcript variant X2
serine/threonine-protein kinase stk11-like, transcript variant X1
serine/threonine-protein kinase stk11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
crustacyanin-A2 subunit-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 14 samples with support for all annotated introns
crustacyanin-A2 subunit-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
crustacyanin-A2 subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
crustacyanin-A2 subunit-like, transcript variant X6
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
crustacyanin-A2 subunit-like, transcript variant X4
crustacyanin-A2 subunit-like, transcript variant X2
crustacyanin-A2 subunit-like, transcript variant X7
regulator of MON1-CCZ1 complex-like, transcript variant X2
regulator of MON1-CCZ1 complex-like, transcript variant X1
regulator of MON1-CCZ1 complex-like isoform X2
regulator of MON1-CCZ1 complex-like isoform X1
ileal sodium/bile acid cotransporter-like, transcript variant X1
ileal sodium/bile acid cotransporter-like, transcript variant X2
ileal sodium/bile acid cotransporter-like isoform X1
ileal sodium/bile acid cotransporter-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 3 samples with support for all annotated introns
uncharacterized protein LOC123746811 isoform X1
N-terminal kinase-like protein, transcript variant X2
N-terminal kinase-like protein, transcript variant X1
N-terminal kinase-like protein isoform X1
N-terminal kinase-like protein 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 8 samples with support for all annotated introns
uncharacterized LOC123746751, 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 2 samples with support for all annotated introns
uncharacterized LOC123746751, transcript variant X1
uncharacterized LOC123746816, transcript variant X1
uncharacterized LOC123746816, transcript variant X2
uncharacterized LOC123746816, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
similar to RNA sequence (same species):INSD:GARH01004253.1
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 925 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 61 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 320 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123746819, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123746819, 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 4 samples with support for all annotated introns
uncharacterized LOC123746817, transcript variant X4
uncharacterized protein LOC123746817 isoform X3
uncharacterized LOC123746817, transcript variant X2
uncharacterized LOC123746817, transcript variant X1
uncharacterized LOC123746817, transcript variant X3
uncharacterized protein LOC123746817 isoform X1
uncharacterized protein LOC123746817 isoform X2
CDK5 regulatory subunit-associated protein 3-like
uncharacterized LOC123746822, 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 1 sample with support for all annotated introns
uncharacterized protein LOC123746822 isoform X1
uncharacterized LOC123746822, 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 1 sample with support for all annotated introns
uncharacterized LOC123746822, transcript variant X2
uncharacterized protein LOC123746822 isoform X2
neuronal acetylcholine receptor subunit alpha-10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitochondrial uncoupling protein 4-like, transcript variant X2
mitochondrial uncoupling protein 4-like, transcript variant X4
mitochondrial uncoupling protein 4-like, transcript variant X3
mitochondrial uncoupling protein 4-like, transcript variant X1
mitochondrial uncoupling protein 4-like, transcript variant X6
mitochondrial uncoupling protein 4-like, transcript variant X7
mitochondrial uncoupling protein 4-like, transcript variant X5
mitochondrial uncoupling protein 4-like isoform X3
mitochondrial uncoupling protein 4-like isoform X1
mitochondrial uncoupling protein 4-like isoform X4
mitochondrial uncoupling protein 4-like isoform X5
mitochondrial uncoupling protein 4-like isoform X2
rap1 GTPase-activating protein 1-like, transcript variant X1
rap1 GTPase-activating protein 1-like, transcript variant X2
rap1 GTPase-activating protein 1-like isoform X1
rap1 GTPase-activating protein 1-like isoform X2
rap1 GTPase-activating protein 1-like, transcript variant X3
rap1 GTPase-activating protein 1-like, transcript variant X4
rap1 GTPase-activating protein 1-like isoform X3
rap1 GTPase-activating protein 1-like isoform X4
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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 169 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 39 samples with support for all annotated introns
3'-5' exoribonuclease 1-like, transcript variant X4
3'-5' exoribonuclease 1-like, transcript variant X5
3'-5' exoribonuclease 1-like, transcript variant X1
3'-5' exoribonuclease 1-like, transcript variant X2
3'-5' exoribonuclease 1-like, transcript variant X3
uncharacterized LOC123746831, transcript variant X2
uncharacterized LOC123746831, transcript variant X4
uncharacterized LOC123746831, transcript variant X1
uncharacterized protein LOC123746831 isoform X1
uncharacterized LOC123746831, transcript variant X3
uncharacterized protein LOC123746831 isoform X2
similar to RNA sequence (same species):INSD:GARH01008855.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 158 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 158 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
vicilin-like seed storage protein At2g18540
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 90 samples with support for all annotated introns
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X2
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X3
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X1
protein-cysteine N-palmitoyltransferase HHAT-like, transcript variant X4
protein-cysteine N-palmitoyltransferase HHAT-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
gametogenetin-binding protein 2-like, transcript variant X1
gametogenetin-binding protein 2-like, transcript variant X2
gametogenetin-binding protein 2-like isoform X2
gametogenetin-binding protein 2-like isoform X1
small G protein signaling modulator 3-like, transcript variant X2
small G protein signaling modulator 3-like, transcript variant X1
small G protein signaling modulator 3-like, transcript variant X3
small G protein signaling modulator 3-like isoform X1
small G protein signaling modulator 3-like isoform X2
solute carrier organic anion transporter family member 74D-like
similar to RNA sequence (same species):INSD:GARH01004287.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 354 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 188 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
growth hormone secretagogue receptor type 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% 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 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: 5 Proteins
mothers against decapentaplegic homolog 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 92 samples with support for all annotated introns
uncharacterized LOC123746753, transcript variant X1
uncharacterized LOC123746753, transcript variant X2
uncharacterized LOC123746753, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123746847, 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 3 samples with support for all annotated introns
uncharacterized LOC123746847, transcript variant X3
uncharacterized LOC123746847, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123746847, transcript variant X4
catenin delta-2-like, transcript variant X15
catenin delta-2-like, transcript variant X11
catenin delta-2-like, transcript variant X13
catenin delta-2-like, transcript variant X14
catenin delta-2-like, transcript variant X12
catenin delta-2-like, transcript variant X1
catenin delta-2-like, transcript variant X9
catenin delta-2-like, transcript variant X10
catenin delta-2-like, transcript variant X2
uncharacterized protein LOC123746850 isoform X8
uncharacterized protein LOC123746850 isoform X6
uncharacterized protein LOC123746850 isoform X2
uncharacterized protein LOC123746850 isoform X1
uncharacterized protein LOC123746850 isoform X5
catenin delta-2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
catenin delta-2-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 20 samples with support for all annotated introns
catenin delta-2-like, transcript variant X3
catenin delta-2-like, transcript variant X6
catenin delta-2-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 10 samples with support for all annotated introns
catenin delta-2-like, transcript variant X5
uncharacterized protein LOC123746850 isoform X4
uncharacterized protein LOC123746850 isoform X3
myocardin-related transcription factor B-like, transcript variant X6
myocardin-related transcription factor B-like, transcript variant X4
myocardin-related transcription factor B-like, transcript variant X2
myocardin-related transcription factor B-like, transcript variant X1
myocardin-related transcription factor B-like, transcript variant X7
myocardin-related transcription factor B-like, transcript variant X5
myocardin-related transcription factor B-like, transcript variant X3
myocardin-related transcription factor B-like, transcript variant X9
myocardin-related transcription factor B-like, transcript variant X8
uncharacterized protein LOC123746852 isoform X2
uncharacterized protein LOC123746852 isoform X1
myocardin-related transcription factor B-like isoform X3
myocardin-related transcription factor B-like isoform X4
myocardin-related transcription factor B-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC123746853, transcript variant X1
uncharacterized protein LOC123746853 isoform X1
uncharacterized LOC123746853, transcript variant X2
uncharacterized protein LOC123746853 isoform X2
small subunit processome component 20 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
small subunit processome component 20 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
small subunit processome component 20 homolog
uncharacterized LOC123746856, transcript variant X1
uncharacterized LOC123746856, transcript variant X2
uncharacterized protein LOC123746856 isoform X1
uncharacterized protein LOC123746856 isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA-dependent metalloprotease SPRTN-like, transcript variant X2
DNA-dependent metalloprotease SPRTN-like, transcript variant X1
DNA-dependent metalloprotease SPRTN-like, transcript variant X3
DNA-dependent metalloprotease SPRTN-like, transcript variant X4
DNA-dependent metalloprotease SPRTN-like isoform X1
DNA-dependent metalloprotease SPRTN-like isoform X2
fibroblast growth factor receptor substrate 2-like
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X3
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X2
ATP-binding cassette sub-family B member 10, mitochondrial-like, transcript variant X1
ATP-binding cassette sub-family B member 10, mitochondrial-like
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like, transcript variant X2
ATP-dependent (S)-NAD(P)H-hydrate dehydratase-like
myotubularin-related protein 2-like, transcript variant X1
myotubularin-related protein 2-like, transcript variant X2
myotubularin-related protein 2-like, transcript variant X3
myotubularin-related protein 2-like isoform X1
myotubularin-related protein 2-like isoform X2
myotubularin-related protein 2-like isoform X3
myotubularin-related protein 2-like, transcript variant X4
myotubularin-related protein 2-like isoform X4
ileal sodium/bile acid cotransporter-like
alpha-tocopherol transfer protein-like, transcript variant X3
alpha-tocopherol transfer protein-like, transcript variant X2
alpha-tocopherol transfer protein-like, transcript variant X4
alpha-tocopherol transfer protein-like, transcript variant X5
alpha-tocopherol transfer protein-like, transcript variant X6
alpha-tocopherol transfer protein-like, transcript variant X1
alpha-tocopherol transfer protein-like isoform X2
alpha-tocopherol transfer protein-like isoform X1
alpha-tocopherol transfer protein-like isoform X4
alpha-tocopherol transfer protein-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 59 samples with support for all annotated introns
uncharacterized LOC123746868, 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 51 samples with support for all annotated introns
uncharacterized LOC123746868, 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 62 samples with support for all annotated introns
uncharacterized LOC123746867, transcript variant X1
uncharacterized LOC123746867, transcript variant X2
adenosylhomocysteinase-like 1, transcript variant X2
adenosylhomocysteinase-like 1, transcript variant X1
adenosylhomocysteinase-like 1 isoform X2
adenosylhomocysteinase-like 1 isoform X1
repetitive proline-rich cell wall protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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 6 samples with support for all annotated introns
required for excision 1-B domain-containing protein-like
non-structural maintenance of chromosomes element 1 homolog
speckle-type POZ protein B-like, transcript variant X3
speckle-type POZ protein B-like, transcript variant X1
speckle-type POZ protein B-like, transcript variant X2
speckle-type POZ protein B-like, transcript variant X4
speckle-type POZ protein B-like isoform X3
speckle-type POZ protein B-like isoform X2
speckle-type POZ protein B-like isoform X1
speckle-type POZ protein B-like isoform X4
zinc finger protein 426-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 426-like, transcript variant X5
zinc finger protein 426-like, transcript variant X4
zinc finger protein 426-like, transcript variant X1
zinc finger protein 426-like, transcript variant X2
uncharacterized protein LOC123746876 isoform X3
uncharacterized protein LOC123746876 isoform X2
uncharacterized protein LOC123746876 isoform X1
zinc finger protein 426-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 426-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123746877, 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 12 samples with support for all annotated introns
uncharacterized LOC123746877, transcript variant X2
uncharacterized LOC123746877, transcript variant X1
uncharacterized LOC123746877, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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
DBH-like monooxygenase protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycine-rich cell wall structural protein-like
glycine-rich cell wall structural protein-like, transcript variant X3
glycine-rich cell wall structural protein-like, transcript variant X1
glycine-rich cell wall structural protein-like, transcript variant X2
glycine-rich cell wall structural protein-like isoform X1
glycine-rich cell wall structural protein-like isoform X2
arylsulfatase I-like, transcript variant X3
arylsulfatase I-like, transcript variant X4
arylsulfatase I-like, transcript variant X5
arylsulfatase I-like, transcript variant X1
arylsulfatase I-like, transcript variant X2
arylsulfatase I-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
uncharacterized LOC123746758, transcript variant X2
uncharacterized LOC123746758, transcript variant X1
uncharacterized LOC123746900, 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 13 samples with support for all annotated introns
uncharacterized LOC123746900, 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 8 samples with support for all annotated introns
uncharacterized protein LOC123746900 isoform X1
uncharacterized protein LOC123746900 isoform X2
uncharacterized LOC123746901, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X8
uncharacterized LOC123746901, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123746901, 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 14 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X10
uncharacterized LOC123746901, transcript variant X2
uncharacterized LOC123746901, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X7
uncharacterized LOC123746901, transcript variant X3
uncharacterized LOC123746901, transcript variant X5
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 12 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein LOC123746901 isoform X1
uncharacterized protein LOC123746901 isoform X3
uncharacterized protein LOC123746901 isoform X2
uncharacterized LOC123746901, transcript variant X12
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 10 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC123746901, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC123746901 isoform X4
flocculation protein FLO11-like, transcript variant X5
flocculation protein FLO11-like, transcript variant X8
flocculation protein FLO11-like, transcript variant X10
flocculation protein FLO11-like, transcript variant X11
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X9
flocculation protein FLO11-like, transcript variant X4
flocculation protein FLO11-like, transcript variant X3
flocculation protein FLO11-like, transcript variant X7
flocculation protein FLO11-like, transcript variant X6
flocculation protein FLO11-like isoform X3
uncharacterized protein LOC123746902 isoform X2
uncharacterized protein LOC123746902 isoform X1
Fanconi anemia core complex-associated protein 24-like
solute carrier organic anion transporter family member 74D-like, transcript variant X8
solute carrier organic anion transporter family member 74D-like, transcript variant X2
solute carrier organic anion transporter family member 74D-like, transcript variant X3
solute carrier organic anion transporter family member 74D-like, transcript variant X7
solute carrier organic anion transporter family member 74D-like, transcript variant X1
solute carrier organic anion transporter family member 74D-like isoform X1
solute carrier organic anion transporter family member 74D-like, transcript variant X5
solute carrier organic anion transporter family member 74D-like, transcript variant X6
solute carrier organic anion transporter family member 74D-like, transcript variant X4
solute carrier organic anion transporter family member 74D-like, transcript variant X9
solute carrier organic anion transporter family member 74D-like isoform X2
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X4
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X2
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X3
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X1
threonine--tRNA ligase 1, cytoplasmic-like isoform X3
threonine--tRNA ligase 1, cytoplasmic-like isoform X2
threonine--tRNA ligase 1, cytoplasmic-like isoform X1
coiled-coil domain-containing protein 85C-like, transcript variant X2
coiled-coil domain-containing protein 85C-like, transcript variant X1
coiled-coil domain-containing protein 85C-like, transcript variant X4
coiled-coil domain-containing protein 85C-like, transcript variant X3
coiled-coil domain-containing protein 85C-like isoform X1
coiled-coil domain-containing protein 85C-like isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X4
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G-protein coupled receptor 143-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 43 samples with support for all annotated introns
G-protein coupled receptor 143-like, transcript variant X2
thiamine transporter 2-like, transcript variant X2
thiamine transporter 2-like, transcript variant X1
thiamine transporter 2-like, transcript variant X4
thiamine transporter 2-like, transcript variant X5
thiamine transporter 2-like, transcript variant X3
6-phosphogluconate dehydrogenase, decarboxylating-like, transcript variant X2
6-phosphogluconate dehydrogenase, decarboxylating-like isoform X2
6-phosphogluconate dehydrogenase, decarboxylating-like, transcript variant X1
6-phosphogluconate dehydrogenase, decarboxylating-like isoform X1
dehydrogenase/reductase SDR family member 7-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 95 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 7-like
uncharacterized LOC123746760, transcript variant X3
uncharacterized LOC123746760, transcript variant X1
uncharacterized LOC123746760, transcript variant X2
uncharacterized protein LOC123746760 isoform X1
uncharacterized protein LOC123746760 isoform X3
uncharacterized protein LOC123746760 isoform X2
glycine-rich cell wall structural protein 1.8-like
uncharacterized LOC123746921, transcript variant X1
uncharacterized LOC123746921, transcript variant X2
dual specificity protein phosphatase 18-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
tetra-peptide repeat homeobox protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123746925, transcript variant X1
uncharacterized LOC123746925, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 53 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
uncharacterized LOC123746926, transcript variant X2
uncharacterized LOC123746926, 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 11 samples with support for all annotated introns
uncharacterized protein LOC123746926 isoform X1
uncharacterized protein LOC123746926 isoform X2
similar to RNA sequence (same species):INSD:GARH01010536.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 216 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 165 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: 97% 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: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments