Procambarus clarkii strain Jiangsu linkage group LG87, 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\nCM035559.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123745992, 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 7 samples with support for all annotated introns
uncharacterized LOC123745992, transcript variant X3
uncharacterized LOC123745992, transcript variant X1
uncharacterized LOC123745991, transcript variant X3
uncharacterized LOC123745991, transcript variant X1
uncharacterized LOC123745991, transcript variant X4
uncharacterized LOC123745991, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 60% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X5
trichohyalin-like, transcript variant X1
trichohyalin-like, transcript variant X3
trichohyalin-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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC123746001, transcript variant X3
uncharacterized LOC123746001, transcript variant X4
uncharacterized LOC123746001, transcript variant X1
uncharacterized LOC123746001, transcript variant X2
CCR4-NOT transcription complex subunit 3-like, transcript variant X1
CCR4-NOT transcription complex subunit 3-like, transcript variant X3
CCR4-NOT transcription complex subunit 3-like, transcript variant X2
CCR4-NOT transcription complex subunit 3-like
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.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
chloride intracellular channel exc-4-like
NADPH oxidase 5-like, transcript variant X3
NADPH oxidase 5-like, transcript variant X2
NADPH oxidase 5-like, transcript variant X1
sorting nexin-5-like, transcript variant X2
sorting nexin-5-like, transcript variant X1
sorting nexin-5-like, transcript variant X3
sorting nexin-5-like, transcript variant X4
transmembrane protein 41A-A-like, transcript variant X1
transmembrane protein 41A-A-like, transcript variant X2
transmembrane protein 41A-A-like, transcript variant X6
transmembrane protein 41A-A-like, transcript variant X3
transmembrane protein 41A-A-like, transcript variant X5
transmembrane protein 41A-A-like, transcript variant X4
transmembrane protein 41A-like isoform X1
transmembrane protein 41A-A-like isoform X3
transmembrane protein 41A-A-like isoform X2
SH3 domain-containing protein 19-like, transcript variant X3
SH3 domain-containing protein 19-like isoform X2
SH3 domain-containing protein 19-like, transcript variant X1
SH3 domain-containing protein 19-like, transcript variant X5
SH3 domain-containing protein 19-like, transcript variant X4
SH3 domain-containing protein 19-like, transcript variant X2
SH3 domain-containing protein 19-like isoform X1
SH3 domain-containing protein 19-like, transcript variant X6
SH3 domain-containing protein 19-like isoform X3
SH3 domain-containing protein 19-like, transcript variant X7
SH3 domain-containing protein 19-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GARH01003166.1
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 177 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% 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 69 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 36% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S31, mitochondrial-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
uncharacterized LOC123746012, 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 LOC123746012, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
anaphase-promoting complex subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transcription elongation factor S-II-like
putative E3 ubiquitin-protein ligase UBR7
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X4
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X2
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X1
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X3
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
exocyst complex component 3-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 45 samples with support for all annotated introns
exocyst complex component 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
exocyst complex component 3-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 52 samples with support for all annotated introns
exocyst complex component 3-like isoform X2
exocyst complex component 3-like isoform X1
exocyst complex component 3-like isoform X3
uncharacterized LOC123746023, transcript variant X1
uncharacterized LOC123746023, transcript variant X2
uncharacterized protein LOC123746023 isoform X1
uncharacterized protein LOC123746023 isoform X2
equilibrative nucleoside transporter 1-like, transcript variant X2
equilibrative nucleoside transporter 1-like, transcript variant X1
equilibrative nucleoside transporter 1-like, transcript variant X3
equilibrative nucleoside transporter 1-like, transcript variant X4
equilibrative nucleoside transporter 1-like isoform X1
equilibrative nucleoside transporter 1-like isoform X2
equilibrative nucleoside transporter 1-like isoform X3
uncharacterized LOC123746027, transcript variant X2
uncharacterized LOC123746027, transcript variant X1
uncharacterized LOC123746027, transcript variant X3
uncharacterized protein LOC123746027 isoform X1
uncharacterized protein LOC123746027 isoform X2
nicotinamide phosphoribosyltransferase-like
zinc finger protein 184-like, transcript variant X1
zinc finger protein 184-like, transcript variant X2
zinc finger protein 184-like, transcript variant X3
translocon-associated protein subunit gamma-like
glucose-6-phosphatase 3-like, transcript variant X1
glucose-6-phosphatase 3-like, transcript variant X2
glucose-6-phosphatase 3-like, transcript variant X3
uncharacterized LOC123746032, transcript variant X6
uncharacterized LOC123746032, transcript variant X1
uncharacterized LOC123746032, transcript variant X7
uncharacterized LOC123746032, transcript variant X4
uncharacterized LOC123746032, transcript variant X2
uncharacterized LOC123746032, transcript variant X3
uncharacterized LOC123746032, transcript variant X5
uncharacterized protein LOC123746032 isoform X1
uncharacterized protein LOC123746032 isoform X3
uncharacterized protein LOC123746032 isoform X2
zinc finger protein 771-like, transcript variant X10
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 55 samples with support for all annotated introns
zinc finger protein 771-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 33 samples with support for all annotated introns
zinc finger protein 771-like, transcript variant X7
zinc finger protein 771-like, transcript variant X8
zinc finger protein 771-like, 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 23 samples with support for all annotated introns
zinc finger protein 771-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 6 samples with support for all annotated introns
zinc finger protein 771-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 35 samples with support for all annotated introns
zinc finger protein 771-like, transcript variant X11
zinc finger protein 771-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 771-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 39 samples with support for all annotated introns
zinc finger protein 771-like, transcript variant X2
zinc finger and BTB domain-containing protein 17-like isoform X6
zinc finger and BTB domain-containing protein 17-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 36 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X3
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X2
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X1
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X3
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X2
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X1
protein sel-1 homolog 1-like, transcript variant X1
protein sel-1 homolog 1-like, transcript variant X2
E3 SUMO-protein ligase PIAS1-like, transcript variant X1
E3 SUMO-protein ligase PIAS1-like, transcript variant X3
E3 SUMO-protein ligase PIAS1-like, transcript variant X2
E3 SUMO-protein ligase PIAS1-like, transcript variant X4
E3 SUMO-protein ligase PIAS1-like, transcript variant X5
E3 SUMO-protein ligase PIAS1-like isoform X1
E3 SUMO-protein ligase PIAS1-like isoform X3
E3 SUMO-protein ligase PIAS1-like isoform X2
E3 SUMO-protein ligase PIAS1-like isoform X4
E3 SUMO-protein ligase PIAS1-like isoform X5
60S ribosome subunit biogenesis protein NIP7 homolog
beta,beta-carotene 15,15'-dioxygenase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
beta,beta-carotene 15,15'-dioxygenase-like, transcript variant X2
beta,beta-carotene 15,15'-dioxygenase-like
leucine-rich repeat-containing protein 58-like
uncharacterized LOC123746054, transcript variant X1
uncharacterized protein LOC123746054 isoform X1
uncharacterized LOC123746054, transcript variant X2
uncharacterized protein LOC123746054 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
regulator of chromosome condensation-like
TATA box-binding protein-like 1, transcript variant X4
TATA box-binding protein-like 1, transcript variant X1
TATA box-binding protein-like 1, transcript variant X2
TATA box-binding protein-like 1, transcript variant X3
TATA box-binding protein-like 1 isoform X1
TATA box-binding protein-like 1 isoform X2
TATA box-binding protein-like 1 isoform X3
translocon-associated protein subunit alpha-like
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 27 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X5
longitudinals lacking protein-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 14 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X11
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
longitudinals lacking protein-like, transcript variant X14
longitudinals lacking protein-like, transcript variant X16
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 41 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X3
longitudinals lacking protein-like, transcript variant X15
longitudinals lacking protein-like, transcript variant X8
longitudinals lacking protein-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X12
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-like, transcript variant X13
longitudinals lacking protein-like, transcript variant X7
longitudinals lacking protein-like, transcript variant X22
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 48 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X40
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 44 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X33
longitudinals lacking protein-like, transcript variant X26
longitudinals lacking protein-like, transcript variant X27
longitudinals lacking protein-like, transcript variant X29
longitudinals lacking protein-like, transcript variant X28
longitudinals lacking protein-like, transcript variant X30
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 46 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X39
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
longitudinals lacking protein-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X31
longitudinals lacking protein-like, transcript variant X20
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 17 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X19
longitudinals lacking protein-like, transcript variant X32
longitudinals lacking protein-like, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X34
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 50 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X41
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
longitudinals lacking protein-like, transcript variant X24
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
longitudinals lacking protein-like, transcript variant X37
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 X25
longitudinals lacking protein-like, transcript variant X36
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 30 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X38
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
longitudinals lacking protein-like, transcript variant X17
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 18 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X23
longitudinals lacking protein-like, transcript variant X21
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 64 samples with support for all annotated introns
longitudinals lacking protein-like, transcript variant X42
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 28 samples with support for all annotated introns
longitudinals lacking protein-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 1 sample with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X19
longitudinals lacking protein, isoforms H/M/V-like isoform X36
longitudinals lacking protein, isoforms A/B/D/L-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X2
longitudinals lacking protein, isoforms H/M/V-like isoform X5
longitudinals lacking protein, isoforms H/M/V-like isoform X6
longitudinals lacking protein, isoforms H/M/V-like isoform X10
longitudinals lacking protein, isoforms H/M/V-like isoform X30
longitudinals lacking protein, isoforms H/M/V-like isoform X13
longitudinals lacking protein, isoforms H/M/V-like isoform X23
longitudinals lacking protein, isoforms H/M/V-like isoform X24
longitudinals lacking protein, isoforms H/M/V-like isoform X26
longitudinals lacking protein, isoforms H/M/V-like isoform X25
longitudinals lacking protein, isoforms H/M/V-like isoform X27
longitudinals lacking protein, isoforms H/M/V-like isoform X35
longitudinals lacking protein, isoforms H/M/V-like isoform X16
longitudinals lacking protein, isoforms H/M/V-like isoform X28
longitudinals lacking protein, isoforms H/M/V-like isoform X15
longitudinals lacking protein, isoforms H/M/V-like isoform X17
longitudinals lacking protein, isoforms H/M/V-like isoform X3
longitudinals lacking protein, isoforms H/M/V-like isoform X14
longitudinals lacking protein, isoforms H/M/V-like isoform X8
longitudinals lacking protein, isoforms H/M/V-like isoform X29
longitudinals lacking protein-like isoform X32
longitudinals lacking protein, isoforms H/M/V-like isoform X31
longitudinals lacking protein, isoforms H/M/V-like isoform X37
longitudinals lacking protein, isoforms H/M/V-like isoform X9
longitudinals lacking protein, isoforms H/M/V-like isoform X11
longitudinals lacking protein, isoforms H/M/V-like isoform X21
longitudinals lacking protein, isoforms H/M/V-like isoform X33
longitudinals lacking protein, isoforms H/M/V-like isoform X22
longitudinals lacking protein, isoforms H/M/V-like isoform X12
longitudinals lacking protein, isoforms H/M/V-like isoform X34
longitudinals lacking protein, isoforms H/M/V-like isoform X7
longitudinals lacking protein, isoforms A/B/D/L-like isoform X20
longitudinals lacking protein, isoforms H/M/V-like isoform X18
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X3
longitudinals lacking protein, isoforms H/M/V-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 58 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X7
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X11
longitudinals lacking protein, isoforms H/M/V-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 38 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X8
longitudinals lacking protein, isoforms H/M/V-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 22 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X6
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 94 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like, transcript variant X2
longitudinals lacking protein, isoforms H/M/V-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X4
zinc finger and BTB domain-containing protein 14-like, transcript variant X2
zinc finger and BTB domain-containing protein 14-like, transcript variant X3
zinc finger and BTB domain-containing protein 14-like, transcript variant X1
zinc finger and BTB domain-containing protein 14-like
GTP-binding protein ypt1-like, transcript variant X2
GTP-binding protein ypt1-like, transcript variant X1
NAD-dependent protein deacetylase sirtuin-1-like, transcript variant X1
NAD-dependent protein deacetylase sirtuin-1-like, transcript variant X2
NAD-dependent protein deacetylase sirtuin-1-like isoform X1
NAD-dependent protein deacetylase sirtuin-1-like isoform X2
replication stress response regulator SDE2-like
uncharacterized LOC123746068, 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 25 samples with support for all annotated introns
uncharacterized LOC123746068, 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 20 samples with support for all annotated introns
uncharacterized protein LOC123746068 isoform X1
uncharacterized protein LOC123746068 isoform X2
vascular endothelial growth factor A-like, transcript variant X3
vascular endothelial growth factor A-like, transcript variant X2
vascular endothelial growth factor A-like, transcript variant X1
vascular endothelial growth factor A-like, transcript variant X4
vascular endothelial growth factor D-like isoform X2
vascular endothelial growth factor A-like isoform X3
vascular endothelial growth factor D-like isoform X1
uncharacterized LOC123746070, transcript variant X1
uncharacterized LOC123746070, transcript variant X3
uncharacterized LOC123746070, transcript variant X2
uncharacterized protein LOC123746070 isoform X1
uncharacterized protein LOC123746070 isoform X2
ubiquitin carboxyl-terminal hydrolase isozyme L5-like
D-arabinose dehydrogenase [NAD(P)+] heavy chain-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 44 samples with support for all annotated introns
1,4-alpha-glucan-branching enzyme-like, transcript variant X1
1,4-alpha-glucan-branching enzyme-like, transcript variant X2
1,4-alpha-glucan-branching enzyme-like, transcript variant X3
1,4-alpha-glucan-branching enzyme-like isoform X2
1,4-alpha-glucan-branching enzyme-like isoform X1
1,4-alpha-glucan-branching enzyme-like isoform X3
phosphoethanolamine N-methyltransferase-like, transcript variant X3
phosphoethanolamine N-methyltransferase-like, transcript variant X2
phosphoethanolamine N-methyltransferase-like, transcript variant X1
phosphoethanolamine N-methyltransferase-like
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-like, transcript variant X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-like, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-like, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-like isoform X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-like isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit-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 51 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
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 LOC123746086, transcript variant X4
uncharacterized LOC123746086, transcript variant X5
uncharacterized LOC123746086, transcript variant X6
uncharacterized LOC123746086, transcript variant X8
uncharacterized LOC123746086, transcript variant X7
uncharacterized LOC123746086, transcript variant X1
uncharacterized LOC123746086, transcript variant X2
uncharacterized protein LOC123746086 isoform X4
uncharacterized protein LOC123746086 isoform X1
uncharacterized LOC123746086, transcript variant X3
uncharacterized protein LOC123746086 isoform X2
uncharacterized LOC123746086, transcript variant X9
uncharacterized protein LOC123746086 isoform X3
uncharacterized protein LOC123746086 isoform X5
VPS35 endosomal protein-sorting factor-like, transcript variant X2
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 62 samples with support for all annotated introns
VPS35 endosomal protein-sorting factor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
VPS35 endosomal protein-sorting factor-like isoform X2
VPS35 endosomal protein-sorting factor-like isoform X1
TLC domain-containing protein 2-like, transcript variant X1
TLC domain-containing protein 2-like, transcript variant X2
TLC domain-containing protein 2-like isoform X1
TLC domain-containing protein 2-like isoform X2
TLC domain-containing protein 2-like, transcript variant X3
TLC domain-containing protein 2-like isoform X3
glutamate [NMDA] receptor subunit 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1-like, transcript variant X2
glutamate [NMDA] receptor subunit 1-like
Bardet-Biedl syndrome 2 protein homolog, transcript variant X2
Bardet-Biedl syndrome 2 protein homolog, transcript variant X4
Bardet-Biedl syndrome 2 protein homolog, transcript variant X3
Bardet-Biedl syndrome 2 protein homolog isoform X2
Bardet-Biedl syndrome 2 protein homolog, transcript variant X1
Bardet-Biedl syndrome 2 protein homolog 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123746099, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123746099, transcript variant X2
polyamine-transporting ATPase 13A3-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 1 sample with support for all annotated introns
polyamine-transporting ATPase 13A3-like isoform X5
polyamine-transporting ATPase 13A3-like, transcript variant X2
polyamine-transporting ATPase 13A3-like, transcript variant X1
polyamine-transporting ATPase 13A3-like, transcript variant X4
polyamine-transporting ATPase 13A3-like, transcript variant X3
polyamine-transporting ATPase 13A3-like isoform X2
polyamine-transporting ATPase 13A3-like isoform X1
polyamine-transporting ATPase 13A3-like isoform X4
polyamine-transporting ATPase 13A3-like isoform X3
palmitoyltransferase ZDHHC23-like, transcript variant X1
palmitoyltransferase ZDHHC23-like isoform X1
zinc finger and SCAN domain-containing protein 12-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 29 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 12-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 52 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 12-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 45 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 12-like isoform X3
palmitoyltransferase ZDHHC23-like, transcript variant X2
palmitoyltransferase ZDHHC23-like isoform X2
palmitoyltransferase ZDHHC23-like, transcript variant X3
palmitoyltransferase ZDHHC23-like, transcript variant X4
palmitoyltransferase ZDHHC23-like isoform X3
lipopolysaccharide-induced tumor necrosis factor-alpha factor-like, transcript variant X1
lipopolysaccharide-induced tumor necrosis factor-alpha factor-like, transcript variant X2
uncharacterized protein LOC123746101 isoform X1
lipopolysaccharide-induced tumor necrosis factor-alpha factor-like isoform X2
uncharacterized LOC123746105, transcript variant X4
uncharacterized LOC123746105, transcript variant X1
uncharacterized LOC123746105, transcript variant X2
uncharacterized LOC123746105, transcript variant X3
protein Mo25-like, transcript variant X1
protein Mo25-like, transcript variant X3
protein Mo25-like, transcript variant X2
putative L-aspartate dehydrogenase, transcript variant X1
putative L-aspartate dehydrogenase isoform X1
putative L-aspartate dehydrogenase, transcript variant X2
putative L-aspartate dehydrogenase isoform X2
uncharacterized LOC123746106, 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 76 samples with support for all annotated introns
uncharacterized LOC123746106, 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 31 samples with support for all annotated introns
uncharacterized LOC123746106, 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 95 samples with support for all annotated introns
uncharacterized LOC123746107, transcript variant X1
uncharacterized LOC123746107, transcript variant X2
uncharacterized protein LOC123746107 isoform X1
uncharacterized protein LOC123746107 isoform X2
discoidin domain-containing receptor 2-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 14 samples with support for all annotated introns
discoidin domain-containing receptor 2-like, 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 23 samples with support for all annotated introns
discoidin domain-containing receptor 2-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 19 samples with support for all annotated introns
discoidin domain-containing receptor 2-like isoform X1
discoidin domain-containing receptor 2-like isoform X3
discoidin domain-containing receptor 2-like isoform X2
similar to RNA sequence (same species):INSD:GBEV01011646.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 362 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 362 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
nuclear pore complex protein DDB_G0274915-like
keratin-3, type I cytoskeletal 51 kDa-like
claw keratin-like, transcript variant X1
claw keratin-like, transcript variant X2
glycine-rich cell wall structural protein 1.8-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 3 samples with support for all annotated introns
glycine-rich cell wall structural protein 1.8-like, transcript variant X3
glycine-rich cell wall structural protein 1.8-like isoform X1
glycine-rich cell wall structural protein-like
glycine-rich cell wall structural protein 1.8-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 21 samples with support for all annotated introns
glycine-rich cell wall structural protein 1.8-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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 8 samples with support for all annotated introns
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 4 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 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
octopamine receptor-like, transcript variant X6
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
octopamine receptor-like, transcript variant X4
octopamine receptor-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 8 samples with support for all annotated introns
octopamine receptor-like, transcript variant X1
octopamine receptor-like, transcript variant X3
tyramine/octopamine receptor-like isoform X1
octopamine receptor-like, transcript variant X8
octopamine receptor-like, transcript variant X7
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 3 samples with support for all annotated introns
probable G-protein coupled receptor No18 isoform X3
probable G-protein coupled receptor No18 isoform X4
octopamine receptor-like, transcript variant X11
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 3 samples with support for all annotated introns
probable G-protein coupled receptor No18
octopamine receptor-like, transcript variant X5
octopamine receptor-like, transcript variant X9
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 9 samples with support for all annotated introns
probable G-protein coupled receptor No18 isoform X2
probable G-protein coupled receptor No18 isoform X5
octopamine receptor-like, transcript variant X10
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 23 samples with support for all annotated introns
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 27 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 79 samples with support for all annotated introns
basic salivary proline-rich protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative uncharacterized protein ENSP00000383309
repetitive proline-rich cell wall protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
AP-4 complex subunit mu-1-like, transcript variant X1
AP-4 complex subunit mu-1-like, transcript variant X3
AP-4 complex subunit mu-1-like, transcript variant X2
AP-4 complex subunit mu-1-like, transcript variant X4
AP-4 complex subunit mu-1-like isoform X1
AP-4 complex subunit mu-1-like isoform X3
AP-4 complex subunit mu-1-like isoform X2
AP-4 complex subunit mu-1-like isoform X4
probable cation-transporting ATPase 13A4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
centrosomal protein of 76 kDa-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 9 samples with support for all annotated introns
centrosomal protein of 76 kDa-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 23 samples with support for all annotated introns
ras GTPase-activating protein raskol-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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
chorion peroxidase-like, transcript variant X1
chorion peroxidase-like, transcript variant X2
mitochondrial enolase superfamily member 1-like, transcript variant X3
mitochondrial enolase superfamily member 1-like, transcript variant X4
mitochondrial enolase superfamily member 1-like, transcript variant X1
mitochondrial enolase superfamily member 1-like, transcript variant X2
mitochondrial enolase superfamily member 1-like
probable cyclin-dependent serine/threonine-protein kinase DDB_G0292550
golgin subfamily A member 6-like protein 2
uncharacterized protein DKFZp434B061-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 34 samples with support for all annotated introns
protein draper-like, transcript variant X2
protein draper-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein draper-like, transcript variant X9
protein draper-like, transcript variant X12
protein draper-like, transcript variant X10
protein draper-like, transcript variant X3
protein draper-like, transcript variant X13
protein draper-like, transcript variant X1
protein draper-like, transcript variant X5
protein draper-like, transcript variant X8
protein draper-like, transcript variant X4
protein draper-like, transcript variant X7
protein draper-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
nuclear transcription factor Y subunit alpha-like, transcript variant X10
nuclear transcription factor Y subunit alpha-like, transcript variant X6
nuclear transcription factor Y subunit alpha-like, transcript variant X4
nuclear transcription factor Y subunit alpha-like, transcript variant X5
nuclear transcription factor Y subunit alpha-like, transcript variant X1
nuclear transcription factor Y subunit alpha-like, transcript variant X2
nuclear transcription factor Y subunit alpha-like, transcript variant X7
nuclear transcription factor Y subunit alpha-like, transcript variant X3
nuclear transcription factor Y subunit alpha-like, transcript variant X8
nuclear transcription factor Y subunit alpha-like, transcript variant X9
nuclear transcription factor Y subunit alpha-like isoform X5
nuclear transcription factor Y subunit alpha-like isoform X4
nuclear transcription factor Y subunit alpha-like isoform X2
nuclear transcription factor Y subunit alpha-like isoform X3
nuclear transcription factor Y subunit alpha-like isoform X1
BTB/POZ domain-containing protein KCTD5-like, transcript variant X2
BTB/POZ domain-containing protein KCTD5-like isoform X2
BTB/POZ domain-containing protein KCTD5-like, transcript variant X1
BTB/POZ domain-containing protein KCTD5-like isoform X1
YTH domain-containing family protein 2-like, transcript variant X1
YTH domain-containing family protein 2-like, transcript variant X5
YTH domain-containing family protein 2-like, transcript variant X2
YTH domain-containing family protein 2-like, transcript variant X3
YTH domain-containing family protein 2-like, transcript variant X6
YTH domain-containing family protein 2-like, transcript variant X4
YTH domain-containing family protein 2-like isoform X1
YTH domain-containing family protein 2-like isoform X4
YTH domain-containing family protein 2-like isoform X2
YTH domain-containing family protein 3-like isoform X3
YTH domain-containing family protein 3-like isoform X5
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X1
methylated-DNA--protein-cysteine methyltransferase-like
protein phosphatase 1 regulatory subunit 7-like, transcript variant X1
protein phosphatase 1 regulatory subunit 7-like, transcript variant X2
protein phosphatase 1 regulatory subunit 7-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 101 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 7-like isoform X1
protein phosphatase 1 regulatory subunit 7-like isoform X2
leucine-rich repeat-containing protein 15-like
class E basic helix-loop-helix protein 23-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like
uncharacterized transmembrane protein DDB_G0289901-like
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: 16 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF01268
putative uncharacterized protein DDB_G0281733