Penaeus chinensis breed Huanghai No. 1 chromosome 42, ASM1920278v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Dendrobranchiata; Penaeoidea; Penaeidae; Penaeus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032967.1.\nAssembly name: ASM1920278v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2021/07/13. The\noriginal whole-genome shotgun project has the accession\nJAGKSU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Date :: 2020\nAssembly Method :: FALCON-Unzip v. MAY-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 150.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Penaeus chinensis Annotation Release\n 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##
conservation base of Haifeng Aquaculture Co., Ltd.
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC125047877, transcript variant X2
uncharacterized LOC125047877, transcript variant X1
small integral membrane protein 8-like, transcript variant X1
small integral membrane protein 8-like, transcript variant X2
TATA-binding protein-associated factor 172-like, transcript variant X1
TATA-binding protein-associated factor 172-like isoform X1
TATA-binding protein-associated factor 172-like, transcript variant X2
TATA-binding protein-associated factor 172-like isoform X2
U3 small nucleolar ribonucleoprotein protein IMP4-like, transcript variant X1
U3 small nucleolar ribonucleoprotein protein IMP4-like isoform X1
U3 small nucleolar ribonucleoprotein protein IMP4-like, transcript variant X2
U3 small nucleolar ribonucleoprotein protein IMP4-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
acyl-CoA-binding domain-containing protein 5-like, transcript variant X3
acyl-CoA-binding domain-containing protein 5-like, transcript variant X2
acyl-CoA-binding domain-containing protein 5-like, transcript variant X1
acyl-CoA-binding domain-containing protein 5-like isoform X3
acyl-CoA-binding domain-containing protein 5-like isoform X2
acyl-CoA-binding domain-containing protein 5-like isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial-like, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial-like, transcript variant X2
glutamyl-tRNA(Gln) amidotransferase subunit A, 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, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% 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: 100% 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: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); 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: 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
AT-rich interactive domain-containing protein 3A-like
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like, transcript variant X3
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like, transcript variant X5
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like, transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like, transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like, transcript variant X4
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
non-classical arabinogalactan protein 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
beta-1,4-galactosyltransferase galt-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
beta-1,4-galactosyltransferase galt-1-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
beta-1,4-galactosyltransferase galt-1-like isoform X1
beta-1,4-galactosyltransferase galt-1-like isoform X2
uncharacterized LOC125047999, transcript variant X2
uncharacterized LOC125047999, transcript variant X1
uncharacterized protein LOC125047999 isoform X1
uncharacterized protein LOC125047999 isoform X2
protein kinase shaggy-like, transcript variant X2
protein kinase shaggy-like, transcript variant X1
protein kinase shaggy-like, transcript variant X3
glycogen synthase kinase-3 beta-like isoform X3
lymphocyte activation gene 3 protein-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 1 sample with support for all annotated introns
anamorsin homolog, transcript variant X1
anamorsin homolog, transcript variant X3
anamorsin homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 68-like, transcript variant X4
transmembrane protein 68-like, transcript variant X1
transmembrane protein 68-like, transcript variant X3
transmembrane protein 68-like, transcript variant X2
SET domain-containing protein SmydA-8-like
SET and MYND domain-containing protein 4-like
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 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 96% coverage of the annotated genomic feature by RNAseq alignments
L-asparaginase 1-like, transcript variant X2
L-asparaginase 1-like, transcript variant X3
L-asparaginase 1-like, transcript variant X1
L-asparaginase 1-like, transcript variant X4
L-asparaginase 1-like, transcript variant X5
anoctamin-10-like, transcript variant X2
anoctamin-10-like, transcript variant X4
anoctamin-10-like, transcript variant X1
anoctamin-10-like, transcript variant X3
uncharacterized LOC125047866, 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 35 samples with support for all annotated introns
uncharacterized LOC125047866, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S35, mitochondrial-like
tropomyosin-1, isoforms 9A/A/B isoform X25
mortality factor 4-like protein 1, transcript variant X3
mortality factor 4-like protein 1, transcript variant X2
mortality factor 4-like protein 1, transcript variant X1
mortality factor 4-like protein 1 isoform X3
mortality factor 4-like protein 1 isoform X2
mortality factor 4-like protein 1 isoform X1
similar to RNA sequence (same species):INSD:GIYE01019856.1
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 1237 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1182 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
tRNA-splicing endonuclease subunit Sen2-like, transcript variant X1
tRNA-splicing endonuclease subunit Sen2-like, transcript variant X2
tRNA-splicing endonuclease subunit Sen2-like, transcript variant X3
tRNA-splicing endonuclease subunit Sen2-like isoform X1
tRNA-splicing endonuclease subunit Sen2-like isoform X2
uncharacterized LOC125047751, transcript variant X1
uncharacterized LOC125047751, transcript variant X5
uncharacterized LOC125047751, transcript variant X3
uncharacterized LOC125047751, transcript variant X4
uncharacterized LOC125047751, transcript variant X2
uncharacterized protein LOC125047751 isoform X1
uncharacterized protein LOC125047751 isoform X5
uncharacterized protein LOC125047751 isoform X3
uncharacterized protein LOC125047751 isoform X4
uncharacterized protein LOC125047751 isoform X2
uncharacterized LOC125047751, transcript variant X7
uncharacterized LOC125047751, transcript variant X6
uncharacterized protein LOC125047751 isoform X6
pleckstrin homology domain-containing family M member 1-like
yrdC domain-containing protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC10-like
vacuolar protein-sorting-associated protein 36-like
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 14 samples with support for all annotated introns
retinoblastoma-binding protein 5 homolog
b(0,+)-type amino acid transporter 1-like
probable peroxisomal acyl-coenzyme A oxidase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125047958, 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 13 samples with support for all annotated introns
uncharacterized LOC125047958, 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 23 samples with support for all annotated introns
heparan sulfate 2-O-sulfotransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HECTD2, 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
probable E3 ubiquitin-protein ligase HECTD2, transcript variant X2
probable E3 ubiquitin-protein ligase HECTD2
serine/threonine-protein kinase PknL-like
uncharacterized LOC125047870, transcript variant X1
uncharacterized LOC125047870, transcript variant X2
uncharacterized protein LOC125047870 isoform X1
uncharacterized protein LOC125047870 isoform X2
dipeptidyl peptidase 1-like, transcript variant X1
dipeptidyl peptidase 1-like, transcript variant X2
general transcriptional corepressor trfA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 70% 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
U5 small nuclear ribonucleoprotein 200 kDa helicase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: U5 small nuclear ribonucleoprotein 200 kDa helicase-like
uncharacterized LOC125047859, transcript variant X1
uncharacterized LOC125047859, transcript variant X2
uncharacterized LOC125047859, transcript variant X4
uncharacterized LOC125047859, transcript variant X3
uncharacterized protein LOC125047859 isoform X1
uncharacterized protein LOC125047859 isoform X2
microtubule-associated protein futsch-like, transcript variant X1
microtubule-associated protein futsch-like, transcript variant X2
microtubule-associated protein futsch-like isoform X1
microtubule-associated protein futsch-like isoform X2
microtubule-associated protein futsch-like, transcript variant X4
microtubule-associated protein futsch-like, transcript variant X3
microtubule-associated protein futsch-like, transcript variant X5
microtubule-associated protein futsch-like, transcript variant X6
microtubule-associated protein futsch-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 6-like
uncharacterized LOC125047879, transcript variant X4
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 3 samples with support for all annotated introns
uncharacterized LOC125047879, 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 14 samples with support for all annotated introns
uncharacterized LOC125047879, 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 18 samples with support for all annotated introns
uncharacterized LOC125047879, transcript variant X5
uncharacterized LOC125047879, 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 24 samples with support for all annotated introns
uncharacterized protein LOC125047879 isoform X4
uncharacterized protein LOC125047879 isoform X5
uncharacterized protein LOC125047879 isoform X2
uncharacterized protein LOC125047879 isoform X1
uncharacterized protein LOC125047879 isoform X3
dynein assembly factor with WDR repeat domains 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
PRKR-interacting protein 1 homolog, transcript variant X2
PRKR-interacting protein 1 homolog, transcript variant X1
PRKR-interacting protein 1 homolog isoform X2
PRKR-interacting protein 1 homolog isoform X1
probable flavin-containing monoamine oxidase A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01041209.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 121 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 73 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
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 22 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cell division cycle and apoptosis regulator 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
protein obstructor-E-like, transcript variant X1
protein obstructor-E-like, transcript variant X3
protein obstructor-E-like, transcript variant X2
proprotein convertase subtilisin/kexin type 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
proprotein convertase subtilisin/kexin type 4-like, transcript variant X2
proprotein convertase subtilisin/kexin type 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
proprotein convertase subtilisin/kexin type 4-like
transforming growth factor-beta-induced protein ig-h3-like
similar to RNA sequence (same species):INSD:GHUY01007179.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 557 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 527 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: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 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: 29 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
enoyl-CoA delta isomerase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
enoyl-CoA delta isomerase 2-like, transcript variant X2
enoyl-CoA delta isomerase 2-like isoform X1
enoyl-CoA delta isomerase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
arginine/serine-rich coiled-coil protein 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
neural cell adhesion molecule L1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125048061, transcript variant X2
uncharacterized LOC125048061, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
sporulation-specific protein 15-like, transcript variant X1
sporulation-specific protein 15-like, transcript variant X2
sporulation-specific protein 15-like, transcript variant X3
golgin subfamily B member 1-like isoform X1
golgin subfamily B member 1-like isoform X2
sporulation-specific protein 15-like isoform X3
diacylglycerol kinase epsilon-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
diacylglycerol kinase epsilon-like, transcript variant X1
MARVEL domain-containing protein 1-like, transcript variant X1
MARVEL domain-containing protein 1-like, transcript variant X2
MARVEL domain-containing protein 1-like isoform X2
uncharacterized protein LOC125047817 isoform X1
serine palmitoyltransferase 2-like, transcript variant X3
serine palmitoyltransferase 2-like, transcript variant X4
serine palmitoyltransferase 2-like, transcript variant X1
serine palmitoyltransferase 2-like, transcript variant X2
serine palmitoyltransferase 2-like, transcript variant X5
serine palmitoyltransferase 2-like isoform X3
serine palmitoyltransferase 2-like isoform X4
serine palmitoyltransferase 2-like isoform X1
serine palmitoyltransferase 2-like isoform X2
serine palmitoyltransferase 2-like isoform X5
uncharacterized LOC125047816, 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 27 samples with support for all annotated introns
uncharacterized LOC125047816, 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 4 samples with support for all annotated introns
uncharacterized protein LOC125047816 isoform X2
uncharacterized LOC125047816, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized protein LOC125047816 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01003537.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 279 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 279 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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: 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermidine/spermine N(1)-acetyltransferase-like protein 1, transcript variant X2
spermidine/spermine N(1)-acetyltransferase-like protein 1, transcript variant X1
SR-related and CTD-associated factor 4-like isoform X2
spermidine/spermine N(1)-acetyltransferase-like protein 1 isoform 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 21 samples with support for all annotated introns
gamma-aminobutyric acid receptor-associated protein-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
PR domain zinc finger protein 15-like, 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 19 samples with support for all annotated introns
PR domain zinc finger protein 15-like isoform X1
PR domain zinc finger protein 15-like, transcript variant X2
PR domain zinc finger protein 15-like isoform X2
LOW QUALITY PROTEIN: neuroendocrine convertase 1-like
vacuolar protein sorting-associated protein 62-like, transcript variant X1
vacuolar protein sorting-associated protein 62-like, transcript variant X2
vacuolar protein sorting-associated protein 62-like
inter-alpha-trypsin inhibitor heavy chain H5-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 27 samples with support for all annotated introns
inter-alpha-trypsin inhibitor heavy chain H5-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 7 samples with support for all annotated introns
inter-alpha-trypsin inhibitor heavy chain H5-like isoform X1
uncharacterized protein LOC125048012 isoform X2
peptidyl-prolyl cis-trans isomerase D-like
GTP-binding protein SAR1-like, transcript variant X1
GTP-binding protein SAR1-like, transcript variant X2
transient receptor potential cation channel subfamily A member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
netrin receptor DCC-like, transcript variant X1
netrin receptor DCC-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
cilia- and flagella-associated protein 251-like
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
hydroxymethylglutaryl-CoA lyase, mitochondrial-like, transcript variant X1
hydroxymethylglutaryl-CoA lyase, mitochondrial-like, transcript variant X2
hydroxymethylglutaryl-CoA lyase, mitochondrial-like isoform X2
hydroxymethylglutaryl-CoA lyase, mitochondrial-like isoform X1
transfer RNA arginine (anticodon CCG); 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: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125047875, 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 28 samples with support for all annotated introns
uncharacterized LOC125047875, transcript variant X1
uncharacterized protein LOC125047875 isoform X2
uncharacterized protein LOC125047875 isoform X1
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 31 samples with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-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 20 samples with support for all annotated introns
COP9 signalosome complex subunit 3-like, transcript variant X2
COP9 signalosome complex subunit 3-like, transcript variant X1
COP9 signalosome complex subunit 3-like isoform X2
COP9 signalosome complex subunit 3-like isoform X1
C-type lectin domain family 4 member M-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
39S ribosomal protein L47, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
death-inducer obliterator 1-like, transcript variant X1
death-inducer obliterator 1-like, transcript variant X5
death-inducer obliterator 1-like, transcript variant X6
death-inducer obliterator 1-like, transcript variant X7
death-inducer obliterator 1-like, transcript variant X2
death-inducer obliterator 1-like, transcript variant X3
death-inducer obliterator 1-like, transcript variant X4
uncharacterized protein LOC125048013 isoform X1
death-inducer obliterator 1-like isoform X2
death-inducer obliterator 1-like isoform X3
death-inducer obliterator 1-like isoform X4
lysM and putative peptidoglycan-binding domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
trichohyalin-like, transcript variant X5
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X4
trichohyalin-like, transcript variant X3
trichohyalin-like, transcript variant X11
trichohyalin-like, transcript variant X19
trichohyalin-like, transcript variant X1
trichohyalin-like, transcript variant X9
trichohyalin-like, transcript variant X13
trichohyalin-like, transcript variant X21
trichohyalin-like, transcript variant X30
trichohyalin-like, transcript variant X7
trichohyalin-like, transcript variant X18
trichohyalin-like, transcript variant X26
trichohyalin-like, transcript variant X33
trichohyalin-like, transcript variant X8
trichohyalin-like, transcript variant X17
trichohyalin-like, transcript variant X25
trichohyalin-like, transcript variant X27
trichohyalin-like, transcript variant X29
trichohyalin-like, transcript variant X32
trichohyalin-like, transcript variant X34
trichohyalin-like, transcript variant X35
trichohyalin-like, transcript variant X36
trichohyalin-like, transcript variant X37
trichohyalin-like, transcript variant X14
trichohyalin-like, transcript variant X12
trichohyalin-like, transcript variant X15
trichohyalin-like, transcript variant X22
trichohyalin-like, transcript variant X10
trichohyalin-like, transcript variant X6
trichohyalin-like, transcript variant X20
trichohyalin-like, transcript variant X16
trichohyalin-like, transcript variant X24
trichohyalin-like, transcript variant X31
FK506-binding protein 5-like isoform X17
FK506-binding protein 5-like isoform X11
FK506-binding protein 5-like isoform X19
FK506-binding protein 5-like isoform X16
FK506-binding protein 5-like isoform X24
FK506-binding protein 5-like isoform X31
FK506-binding protein 5-like isoform X15
FK506-binding protein 5-like isoform X23
FK506-binding protein 5-like isoform X25
FK506-binding protein 5-like isoform X27
FK506-binding protein 5-like isoform X30
FK506-binding protein 5-like isoform X32
FK506-binding protein 5-like isoform X34
FK506-binding protein 5-like isoform X35
FK506-binding protein 5-like isoform X12
FK506-binding protein 5-like isoform X10
FK506-binding protein 5-like isoform X13
FK506-binding protein 5-like isoform X20
FK506-binding protein 5-like isoform X18
FK506-binding protein 5-like isoform X14
FK506-binding protein 5-like isoform X22
FK506-binding protein 5-like isoform X29
trichohyalin-like, transcript variant X23
trichohyalin-like, transcript variant X28
trichohyalin-like, transcript variant X38
trichohyalin-like, transcript variant X39
FK506-binding protein 5-like isoform X36
amyloid-beta-like protein, transcript variant X2
similar to RNA sequence (same species):INSD:GIYE01008125.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 283 bases not found in genome assembly
amyloid-beta-like protein, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 255 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
golgin subfamily A member 6-like protein 22
similar to RNA sequence (same species):INSD:GHUY01000069.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1246 bases not found in genome assembly
anion exchange protein 3-like, transcript variant X3
anion exchange protein 3-like, 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 5 samples with support for all annotated introns
anion exchange protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
anion exchange protein 3-like, transcript variant X4
anion exchange protein 3-like isoform X2
anion exchange protein 3-like isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 253 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
prothoracicostatic peptides-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
prothoracicostatic peptides-like, transcript variant X1
prothoracicostatic peptides-like isoform X2
prothoracicostatic peptides-like isoform X1
ER membrane protein complex subunit 1-like
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
serine/threonine-protein phosphatase 6 catalytic subunit-like
39S ribosomal protein L4, mitochondrial-like, transcript variant X1
39S ribosomal protein L4, mitochondrial-like isoform X1
39S ribosomal protein L4, mitochondrial-like, transcript variant X2
39S ribosomal protein L4, mitochondrial-like isoform X2
squamous cell carcinoma antigen recognized by T-cells 3-like
uncharacterized LOC125047764, 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 2 samples with support for all annotated introns
uncharacterized LOC125047764, transcript variant X3
uncharacterized LOC125047764, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC125047764 isoform X2
uncharacterized protein LOC125047764 isoform X3
uncharacterized protein LOC125047764 isoform X1
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X1
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X3
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X4
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X5
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X2
ras-associated and pleckstrin homology domains-containing protein 1-like isoform X1
ras-associated and pleckstrin homology domains-containing protein 1-like isoform X3
ras-associated and pleckstrin homology domains-containing protein 1-like isoform X2
ras-associated and pleckstrin homology domains-containing protein 1-like isoform X4
protein adenylyltransferase SelO, mitochondrial-like, transcript variant X1
protein adenylyltransferase SelO, mitochondrial-like, transcript variant X2
protein adenylyltransferase SelO-like isoform X1
protein adenylyltransferase SelO, mitochondrial-like isoform X2
eukaryotic translation initiation factor 3 subunit L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding protein cabeza-like, transcript variant X2
RNA-binding protein cabeza-like, transcript variant X3
RNA-binding protein cabeza-like, transcript variant X1
RNA-binding protein cabeza-like isoform X2
RNA-binding protein cabeza-like isoform X3
RNA-binding protein cabeza-like isoform X1
feline leukemia virus subgroup C receptor-related protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-like, transcript variant X2
feline leukemia virus subgroup C receptor-related protein 2-like
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X2
similar to RNA sequence (same species):INSD:GIYE01010769.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 369 bases not found in genome assembly; 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 13 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 369 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 369 bases not found in genome assembly; 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 20 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 369 bases not found in genome assembly; 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 15 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like isoform X2
ATP-dependent translocase ABCB1-like isoform X1
baculoviral IAP repeat-containing protein 5-like
transcription activator MSS11-like, transcript variant X3
transcription activator MSS11-like, transcript variant X2
transcription activator MSS11-like, transcript variant X1
uncharacterized protein LOC125047853 isoform X3
transcription activator MSS11-like isoform X2
transcription activator MSS11-like isoform X1
uncharacterized LOC125048016, transcript variant X1
uncharacterized LOC125048016, 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 21 samples with support for all annotated introns
uncharacterized protein LOC125048016 isoform X1
uncharacterized protein LOC125048016 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
cell wall protein IFF6-like, transcript variant X2
cell wall protein IFF6-like, transcript variant X1
neuronal acetylcholine receptor subunit alpha-7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor II-I repeat domain-containing protein 2B-like
CBY1-interacting BAR domain-containing protein 1-like
LOW QUALITY PROTEIN: CBY1-interacting BAR domain-containing protein 1-like
piggyBac transposable element-derived protein 4-like, transcript variant X1
piggyBac transposable element-derived protein 4-like, transcript variant X3
piggyBac transposable element-derived protein 4-like, transcript variant X2
piggyBac transposable element-derived protein 4-like, transcript variant X4
piggyBac transposable element-derived protein 4-like
gastrula zinc finger protein XlCGF52.1-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 24 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-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 20 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-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 9 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-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 4 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-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 17 samples with support for all annotated introns
gastrula zinc finger protein XlCGF52.1-like, transcript variant X7
gastrula zinc finger protein XlCGF52.1-like, transcript variant X8
gastrula zinc finger protein XlCGF52.1-like isoform X2
gastrula zinc finger protein XlCGF52.1-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X2
alpha-(1,3)-fucosyltransferase fut-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
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
zinc finger protein 883-like, transcript variant X1
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 35 samples with support for all annotated introns
zinc finger protein 883-like, transcript variant X2
angiopoietin-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 16 samples with support for all annotated introns
angiopoietin-2-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 22 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: 12 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GHUY01005141.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1249 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1080 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: 75% coverage of the annotated genomic feature by RNAseq alignments
pollen-specific leucine-rich repeat extensin-like protein 1
probable nuclear transport factor 2, transcript variant X1
probable nuclear transport factor 2, transcript variant X2
glucose-induced degradation protein 4 homolog
tetratricopeptide repeat protein 28-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 10 samples with support for all annotated introns
tetratricopeptide repeat protein 28-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 14 samples with support for all annotated introns
tetratricopeptide repeat protein 28-like isoform X2
tetratricopeptide repeat protein 28-like isoform X1
tetratricopeptide repeat protein 28-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tetratricopeptide repeat protein 28-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 1 sample with support for all annotated introns
irregular chiasm C-roughest protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
methyltransferase-like 26, transcript variant X2
methyltransferase-like 26, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
eukaryotic translation initiation factor 2-alpha kinase 1-like
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 25-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 25-like
endoglucanase E-4-like, transcript variant X2
endoglucanase E-4-like, transcript variant X1