Penaeus chinensis breed Huanghai No. 1 chromosome 38, 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\nCM032963.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
baculoviral IAP repeat-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, 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: 2 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
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: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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 19 samples with support for all annotated introns
transient receptor potential cation channel subfamily V member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily V member 3-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
uncharacterized protein C10orf82 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like isoform X1
CCR4-NOT transcription complex subunit 7-like isoform X2
ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1-like, transcript variant X1
ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1-like, transcript variant X2
ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1-like isoform X1
ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
probable tyrosyl-DNA phosphodiesterase, transcript variant X1
probable tyrosyl-DNA phosphodiesterase, transcript variant X2
probable tyrosyl-DNA phosphodiesterase, transcript variant X3
probable tyrosyl-DNA phosphodiesterase, 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 10 samples with support for all annotated introns
probable tyrosyl-DNA phosphodiesterase isoform X1
probable tyrosyl-DNA phosphodiesterase isoform X2
probable tyrosyl-DNA phosphodiesterase isoform X3
probable tyrosyl-DNA phosphodiesterase isoform X4
uncharacterized LOC125046013, 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 14 samples with support for all annotated introns
uncharacterized LOC125046013, transcript variant X2
uncharacterized LOC125046013, 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 11 samples with support for all annotated introns
uncharacterized protein LOC125046013 isoform X2
uncharacterized protein LOC125046013 isoform X1
uncharacterized protein LOC125046013 isoform X3
long chain acyl-CoA synthetase 9, chloroplastic-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
glycine-rich cell wall structural protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein arginine N-methyltransferase 6-like
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X2
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X9
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X7
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X6
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X4
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X5
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X3
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X1
E3 ubiquitin-protein ligase MGRN1-like isoform X2
probable E3 ubiquitin-protein ligase MGRN1 isoform X8
probable E3 ubiquitin-protein ligase MGRN1 isoform X7
probable E3 ubiquitin-protein ligase MGRN1 isoform X6
probable E3 ubiquitin-protein ligase MGRN1 isoform X4
probable E3 ubiquitin-protein ligase MGRN1 isoform X5
probable E3 ubiquitin-protein ligase MGRN1 isoform X3
E3 ubiquitin-protein ligase MGRN1-like isoform X1
probable E3 ubiquitin-protein ligase MGRN1, transcript variant X8
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 13 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 5-like, transcript variant X2
conserved oligomeric Golgi complex subunit 5-like, transcript variant X1
conserved oligomeric Golgi complex subunit 5-like
uncharacterized LOC125046109, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC125046109, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125046109, 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 LOC125046109, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125046109, 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 3 samples with support for all annotated introns
uncharacterized protein LOC125046109 isoform X3
uncharacterized protein LOC125046109 isoform X2
uncharacterized protein LOC125046109 isoform X5
uncharacterized protein LOC125046109 isoform X1
uncharacterized protein LOC125046109 isoform X4
acetylcholinesterase-like, transcript variant X2
acetylcholinesterase-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 4 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitochondrial uncoupling protein Bmcp-like
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial-like, transcript variant X2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial-like, transcript variant X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized protein KIAA1522-like isoform X1
uncharacterized protein KIAA1522-like isoform X4
zinc finger protein 112-like, transcript variant X1
zinc finger protein 112-like, transcript variant X2
glutamate receptor ionotropic, kainate glr-3-like
glycine receptor subunit alpha-3-like, transcript variant X1
glycine receptor subunit alpha-3-like, transcript variant X2
glycine receptor subunit alpha-3-like isoform X1
glycine receptor subunit alpha-3-like isoform X2
probable serine/threonine-protein kinase clkA
zwei Ig domain protein zig-8-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 17 samples with support for all annotated introns
zwei Ig domain protein zig-8-like, transcript variant X1
zwei Ig domain protein zig-8-like isoform X2
zwei Ig domain protein zig-8-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GHUY01009077.1
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 1229 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 872 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Krueppel-like factor 10, 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 7 samples with support for all annotated introns
Krueppel-like factor 10, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
tripartite motif-containing protein 55-like, transcript variant X3
tripartite motif-containing protein 55-like, transcript variant X1
tripartite motif-containing protein 55-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 1 sample with support for all annotated introns
uncharacterized protein LOC125046158 isoform X1
tripartite motif-containing protein 55-like isoform X2
uncharacterized protein LOC125046158 isoform X3
uncharacterized LOC125046088, transcript variant X1
uncharacterized LOC125046088, transcript variant X2
uncharacterized protein LOC125046088 isoform X1
uncharacterized protein LOC125046088 isoform X2
uncharacterized LOC125046132, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC125046132, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125046132, transcript variant X1
uncharacterized LOC125046132, transcript variant X4
uncharacterized LOC125046132, transcript variant X7
uncharacterized LOC125046132, transcript variant X5
uncharacterized protein LOC125046132 isoform X3
uncharacterized protein LOC125046132 isoform X1
uncharacterized protein LOC125046132 isoform X2
uncharacterized protein LOC125046132 isoform X4
uncharacterized protein LOC125046132 isoform X6
uncharacterized LOC125046132, transcript variant X6
uncharacterized protein LOC125046132 isoform X5
receptor-type tyrosine-protein phosphatase S-like
uncharacterized LOC125046200, transcript variant X5
uncharacterized LOC125046200, transcript variant X2
uncharacterized LOC125046200, transcript variant X1
uncharacterized LOC125046200, transcript variant X3
uncharacterized LOC125046200, transcript variant X4
N-acetylglucosamine-6-sulfatase-like, transcript variant X1
N-acetylglucosamine-6-sulfatase-like, transcript variant X2
polycomb group RING finger protein 3-like
nucleolar protein 56-like, transcript variant X2
nucleolar protein 56-like, transcript variant X1
putative transferase CAF17 homolog, mitochondrial, transcript variant X1
putative transferase CAF17 homolog, mitochondrial, transcript variant X2
putative transferase CAF17 homolog, mitochondrial, transcript variant X3
putative transferase CAF17 homolog, mitochondrial
isoleucine--tRNA ligase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC125046248, transcript variant X4
uncharacterized LOC125046248, transcript variant X5
uncharacterized LOC125046248, transcript variant X2
uncharacterized LOC125046248, transcript variant X1
uncharacterized LOC125046248, transcript variant X6
uncharacterized LOC125046248, transcript variant X3
probable serine/threonine-protein kinase MARK-A
probable serine/threonine-protein kinase DDB_G0272282
GATA zinc finger domain-containing protein 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable serine/threonine-protein kinase DDB_G0267686
zinc transporter ZIP13-like, transcript variant X2
zinc transporter ZIP13-like, transcript variant X1
zinc transporter ZIP13-like, transcript variant X4
zinc transporter ZIP13-like, transcript variant X3
zinc transporter ZIP13-like, transcript variant X5
zinc transporter ZIP13-like, transcript variant X6
F-box/LRR-repeat protein 7-like, transcript variant X3
F-box/LRR-repeat protein 7-like isoform X2
F-box/LRR-repeat protein 7-like, transcript variant X1
F-box/LRR-repeat protein 7-like, transcript variant X2
F-box/LRR-repeat protein 7-like isoform X1
F-box/LRR-repeat protein 7-like, transcript variant X4
F-box/LRR-repeat protein 7-like, transcript variant X5
F-box/LRR-repeat protein 7-like isoform X3
F-box/LRR-repeat protein 7-like, transcript variant X6
F-box/LRR-repeat protein 7-like isoform X4
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X4
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X19
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X15
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X13
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X24
longitudinals lacking protein, isoforms H/M/V-like isoform X23
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X22
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
protein tramtrack, beta isoform-like isoform X3
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X6
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
longitudinals lacking protein, isoforms H/M/V-like isoform X18
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
broad-complex core protein-like isoform X9
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X11
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X15
longitudinals lacking protein, isoforms H/M/V-like isoform X14
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X8
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X21
longitudinals lacking protein, isoforms H/M/V-like isoform X20
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X12
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X5
longitudinals lacking protein, isoforms A/B/D/L-like isoform X5
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X22
longitudinals lacking protein, isoforms H/M/V-like isoform X21
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X7
protein tramtrack, beta isoform-like isoform X7
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X18
longitudinals lacking protein, isoforms H/M/V-like isoform X17
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
broad-complex core protein isoforms 1/2/3/4/5-like isoform X2
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X17
longitudinals lacking protein, isoforms H/M/V-like isoform X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X41
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 34 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X31
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X30
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 26 samples with support for all annotated introns
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 23 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
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 27 samples with support for all annotated introns
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X39
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X40
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
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 39 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X33
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X26
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X28
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
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 14 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 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X36
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X38
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X27
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
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X37
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X34
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 25 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X32
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 11 samples with support for all annotated introns
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
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 5 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like, transcript variant X29
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 34 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like isoform X8
longitudinals lacking protein, isoforms H/M/V-like isoform X36
longitudinals lacking protein, isoforms H/M/V-like isoform X12
longitudinals lacking protein, isoforms A/B/D/L-like isoform X28
longitudinals lacking protein, isoforms H/M/V-like isoform X27
longitudinals lacking protein, isoforms H/M/V-like isoform X2
longitudinals lacking protein, isoforms H/M/V-like isoform X37
longitudinals lacking protein, isoforms H/M/V-like isoform X31
longitudinals lacking protein, isoforms H/M/V-like isoform X4
longitudinals lacking protein, isoforms A/B/D/L-like isoform X6
longitudinals lacking protein, isoforms A/B/D/L-like isoform X16
zinc finger protein 768-like isoform X17
longitudinals lacking protein, isoforms H/M/V-like isoform X34
longitudinals lacking protein, isoforms H/M/V-like isoform X35
longitudinals lacking protein, isoforms A/B/D/L-like isoform X13
longitudinals lacking protein, isoforms A/B/D/L-like isoform X18
longitudinals lacking protein, isoforms H/M/V-like isoform X11
longitudinals lacking protein, isoforms H/M/V-like isoform X3
longitudinals lacking protein, isoforms A/B/D/L-like isoform X30
longitudinals lacking protein, isoforms H/M/V-like isoform X25
longitudinals lacking protein, isoforms A/B/D/L-like isoform X22
longitudinals lacking protein, isoforms A/B/D/L-like isoform X7
longitudinals lacking protein-like isoform X19
longitudinals lacking protein, isoforms H/M/V-like isoform X10
longitudinals lacking protein-like isoform X32
longitudinals lacking protein, isoforms H/M/V-like isoform X24
longitudinals lacking protein, isoforms H/M/V-like isoform X33
longitudinals lacking protein, isoforms H/M/V-like isoform X9
longitudinals lacking protein, isoforms H/M/V-like isoform X29
zinc finger and BTB domain-containing protein 17-like isoform X20
zinc finger and BTB domain-containing protein 17-like isoform X1
longitudinals lacking protein, isoforms H/M/V-like isoform X26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125046114, 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 1 sample with support for all annotated introns
uncharacterized LOC125046114, transcript variant X1
WAS/WASL-interacting protein family member 1-like
similar to RNA sequence (same species):INSD:GIYE01035308.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 138 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 138 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Meckel syndrome type 1 protein-like, transcript variant X1
Meckel syndrome type 1 protein-like, transcript variant X2
Meckel syndrome type 1 protein-like, transcript variant X3
organic cation transporter protein-like, transcript variant X4
organic cation transporter protein-like, transcript variant X6
organic cation transporter protein-like, transcript variant X7
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 15 samples with support for all annotated introns
organic cation transporter protein-like, transcript variant X1
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X5
organic cation transporter protein-like, transcript variant X3
organic cation transporter protein-like isoform X1
organic cation transporter protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
crossover junction endonuclease MUS81-like, transcript variant X3
crossover junction endonuclease MUS81-like, transcript variant X5
crossover junction endonuclease MUS81-like, transcript variant X4
crossover junction endonuclease MUS81-like, transcript variant X6
crossover junction endonuclease MUS81-like, transcript variant X2
crossover junction endonuclease MUS81-like, transcript variant X1
crossover junction endonuclease MUS81-like isoform X4
crossover junction endonuclease MUS81-like isoform X2
crossover junction endonuclease MUS81-like isoform X1
crossover junction endonuclease MUS81-like isoform X3
suppressor of fused homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
suppressor of fused homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125045871, transcript variant X4
uncharacterized LOC125045871, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125045871, transcript variant X6
uncharacterized LOC125045871, transcript variant X2
uncharacterized LOC125045871, 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
uncharacterized LOC125045871, transcript variant X3
uncharacterized protein LOC125045871 isoform X4
uncharacterized protein LOC125045871 isoform X5
uncharacterized protein LOC125045871 isoform X2
uncharacterized protein LOC125045871 isoform X1
uncharacterized protein LOC125045871 isoform X3
40S ribosomal protein S11-like, transcript variant X1
40S ribosomal protein S11-like, transcript variant X2
40S ribosomal protein S11-like isoform X2
40S ribosomal protein S11-like isoform X1
uncharacterized LOC125045890, transcript variant X2
uncharacterized LOC125045890, transcript variant X1
uncharacterized protein LOC125045890 isoform X2
uncharacterized protein LOC125045890 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC125045908, transcript variant X1
uncharacterized LOC125045908, transcript variant X2
protein jim lovell-like, transcript variant X2
protein jim lovell-like, transcript variant X1
L-galactose dehydrogenase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
L-galactose dehydrogenase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
L-galactose dehydrogenase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
muscle M-line assembly protein unc-89-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
glycine-rich cell wall structural protein 1.0-like
glycine-rich cell wall structural protein 1-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: iodotyrosine deiodinase 1-like
glycosyltransferase 8 domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125046063, transcript variant X3
uncharacterized LOC125046063, transcript variant X1
uncharacterized LOC125046063, transcript variant X2
uncharacterized LOC125046063, transcript variant X4
uncharacterized protein LOC125046063 isoform X1
uncharacterized protein LOC125046063 isoform X2
BAG family molecular chaperone regulator 1-like, transcript variant X2
BAG family molecular chaperone regulator 1-like, transcript variant X1
BAG family molecular chaperone regulator 1-like isoform X1
BAG family molecular chaperone regulator 1-like, transcript variant X6
BAG family molecular chaperone regulator 1-like, transcript variant X3
BAG family molecular chaperone regulator 1-like, transcript variant X7
BAG family molecular chaperone regulator 1-like, transcript variant X5
BAG family molecular chaperone regulator 1-like, transcript variant X4
BAG family molecular chaperone regulator 1-like isoform X2
BAG family molecular chaperone regulator 1-like isoform X3
intraflagellar transport protein 74 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase pim-1-like
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
vegetative cell wall protein gp1-like, transcript variant X1
vegetative cell wall protein gp1-like, transcript variant X3
vegetative cell wall protein gp1-like, transcript variant X4
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 17 samples with support for all annotated introns
vegetative cell wall protein gp1-like, transcript variant X2
vegetative cell wall protein gp1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X1
vegetative cell wall protein gp1-like isoform X2
uncharacterized LOC125045883, transcript variant X1
uncharacterized LOC125045883, transcript variant X2
hematopoietic prostaglandin D synthase-like
hematopoietic prostaglandin D synthase-like, transcript variant X1
hematopoietic prostaglandin D synthase-like, transcript variant X3
hematopoietic prostaglandin D synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 55% 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: xanthine dehydrogenase/oxidase-like
protein lin-52 homolog, transcript variant X1
protein lin-52 homolog, transcript variant X2
protein lin-52 homolog, transcript variant X4
protein lin-52 homolog, 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 20 samples with support for all annotated introns
39S ribosomal protein L15, mitochondrial-like
zinc finger protein OZF-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB7
major facilitator superfamily domain-containing protein 6-like
ketosamine-3-kinase-like, transcript variant X1
ketosamine-3-kinase-like, transcript variant X2
pancreas transcription factor 1 subunit alpha-like
similar to RNA sequence (same species):INSD:GHUY01007931.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 512 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 88 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
coiled-coil domain-containing protein 40-like
ubiquitin-like modifier-activating enzyme ATG7
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X1
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X2
tRNA N(3)-methylcytidine methyltransferase METTL6-like isoform X1
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X4
tRNA N(3)-methylcytidine methyltransferase METTL6-like, transcript variant X3
uncharacterized protein LOC125046238 isoform X2
uncharacterized LOC125045857, transcript variant X5
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 3 samples with support for all annotated introns
uncharacterized LOC125045857, 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 30 samples with support for all annotated introns
uncharacterized protein LOC125045857 isoform X2
uncharacterized LOC125045857, 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 20 samples with support for all annotated introns
uncharacterized LOC125045857, transcript variant X4
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 26 samples with support for all annotated introns
uncharacterized LOC125045857, 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 35 samples with support for all annotated introns
uncharacterized protein LOC125045857 isoform X1
uncharacterized LOC125045857, transcript variant X6
uncharacterized protein LOC125045857 isoform X3
solute carrier organic anion transporter family member 3A1-like
nuclear speckle splicing regulatory protein 1-like
protein bric-a-brac 1-like, transcript variant X2
protein bric-a-brac 1-like, transcript variant X3
protein bric-a-brac 1-like, transcript variant X4
protein bric-a-brac 1-like, transcript variant X1
longitudinals lacking protein, isoforms H/M/V-like isoform X1
guanine nucleotide exchange factor subunit RIC1-like, transcript variant X1
guanine nucleotide exchange factor subunit RIC1-like, transcript variant X2
guanine nucleotide exchange factor subunit RIC1-like, transcript variant X3
guanine nucleotide exchange factor subunit RIC1-like isoform X1
guanine nucleotide exchange factor subunit RIC1-like isoform X2
guanine nucleotide exchange factor subunit RIC1-like isoform X3
serine-rich adhesin for platelets-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
serine-rich adhesin for platelets-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 18 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X9
serine-rich adhesin for platelets-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 26 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X8
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 32 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X6
serine-rich adhesin for platelets-like, transcript variant X5
serine-rich adhesin for platelets-like, transcript variant X7
uncharacterized protein LOC125045823 isoform X3
serine-rich adhesin for platelets-like isoform X1
serine-rich adhesin for platelets-like isoform X2
transcription factor dcp-66-like, transcript variant X1
transcription factor dcp-66-like, transcript variant X9
transcription factor dcp-66-like, transcript variant X8
transcription factor dcp-66-like, transcript variant X10
transcription factor dcp-66-like, transcript variant X7
transcription factor dcp-66-like, transcript variant X11
transcription factor dcp-66-like, transcript variant X12
transcription factor dcp-66-like, transcript variant X3
transcription factor dcp-66-like, transcript variant X5
transcription factor dcp-66-like, transcript variant X4
transcription factor dcp-66-like, transcript variant X2
transcription factor dcp-66-like, transcript variant X6
transcription factor dcp-66-like isoform X1
transcription factor dcp-66-like isoform X4
transcription factor dcp-66-like isoform X3
transcription factor dcp-66-like isoform X5
transcription factor dcp-66-like isoform X2
transcription factor dcp-66-like isoform X6
transcription factor dcp-66-like isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized histidine-rich protein DDB_G0274557-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
equilibrative nucleobase transporter 1-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 21 samples with support for all annotated introns
equilibrative nucleobase transporter 1-like, transcript variant X2
equilibrative nucleobase transporter 1-like
uncharacterized LOC125046106, 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 12 samples with support for all annotated introns
uncharacterized LOC125046106, 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 16 samples with support for all annotated introns
adenomatous polyposis coli protein-like, transcript variant X2
adenomatous polyposis coli protein-like, transcript variant X1
adenomatous polyposis coli protein-like, transcript variant X4
adenomatous polyposis coli protein-like, transcript variant X3
adenomatous polyposis coli protein-like, transcript variant X6
adenomatous polyposis coli protein-like, transcript variant X5
adenomatous polyposis coli protein-like isoform X1
adenomatous polyposis coli protein-like isoform X3
adenomatous polyposis coli protein-like isoform X2
adenomatous polyposis coli protein-like isoform X5
adenomatous polyposis coli protein-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
prolyl 4-hydroxylase subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 EST, and 53% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding protein 34-like, transcript variant X1
RNA-binding protein 34-like, transcript variant X4
RNA-binding protein 34-like, transcript variant X2
RNA-binding protein 34-like, transcript variant X3
ADP-ribosylation factor-like protein 6-interacting protein 4
PHD finger protein rhinoceros-like isoform X2
PHD finger protein rhinoceros-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X1
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X2
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X3
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X7
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X6
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X9
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X8
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X4
wiskott-Aldrich syndrome protein family member 2-like, transcript variant X5
wiskott-Aldrich syndrome protein family member 2-like isoform X5
wiskott-Aldrich syndrome protein family member 2-like isoform X4
wiskott-Aldrich syndrome protein family member 2-like isoform X7
wiskott-Aldrich syndrome protein family member 2-like isoform X6
wiskott-Aldrich syndrome protein family member 2-like isoform X2
wiskott-Aldrich syndrome protein family member 2-like isoform X3
wiskott-Aldrich syndrome protein family member 2-like isoform X1
histone-lysine N-methyltransferase 2D-like, transcript variant X1
histone-lysine N-methyltransferase 2D-like, transcript variant X2
uncharacterized protein LOC125046034 isoform X1
histone-lysine N-methyltransferase 2D-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 15 samples with support for all annotated introns
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 X4
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 X8
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 X6
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X2
flocculation protein FLO11-like isoform X1
flocculation protein FLO11-like isoform X2
PDZ domain-containing protein 7-like isoform X7
flocculation protein FLO11-like isoform X3
ras-associated and pleckstrin homology domains-containing protein 1-like, transcript variant X7
ras-associated and pleckstrin homology domains-containing protein 1-like isoform X6
histone-lysine N-methyltransferase Suv4-20-like, transcript variant X2
histone-lysine N-methyltransferase Suv4-20-like, transcript variant X1
histone-lysine N-methyltransferase Suv4-20-like
AN1-type zinc finger protein 4-like, transcript variant X1
AN1-type zinc finger protein 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
AN1-type zinc finger protein 4-like, transcript variant X2
AN1-type zinc finger protein 4-like isoform X1
AN1-type zinc finger protein 4-like isoform X2
mitochondrial basic amino acids transporter-like
CD2-associated protein-like, transcript variant X2
CD2-associated protein-like, transcript variant X3
CD2-associated protein-like, transcript variant X1
CD2-associated protein-like, transcript variant X21
CD2-associated protein-like, transcript variant X17
CD2-associated protein-like, transcript variant X4
CD2-associated protein-like, transcript variant X5
CD2-associated protein-like, transcript variant X16
CD2-associated protein-like, transcript variant X8
CD2-associated protein-like, transcript variant X10
CD2-associated protein-like, transcript variant X6
CD2-associated protein-like, transcript variant X18
CD2-associated protein-like, transcript variant X9
CD2-associated protein-like, transcript variant X20
CD2-associated protein-like, transcript variant X12
CD2-associated protein-like, transcript variant X14
CD2-associated protein-like, transcript variant X13
CD2-associated protein-like, transcript variant X15
CD2-associated protein-like, transcript variant X7
CD2-associated protein-like, transcript variant X19
CD2-associated protein-like, transcript variant X11
SH3 domain-containing kinase-binding protein 1-like isoform X3
SH3 domain-containing kinase-binding protein 1-like isoform X15
SH3 domain-containing kinase-binding protein 1-like isoform X4
SH3 domain-containing kinase-binding protein 1-like isoform X8
SH3 domain-containing kinase-binding protein 1-like isoform X6
SH3 domain-containing kinase-binding protein 1-like isoform X9
SH3 domain-containing kinase-binding protein 1-like isoform X12
SH3 domain-containing kinase-binding protein 1-like isoform X7
SH3 domain-containing kinase-binding protein 1-like isoform X11
uncharacterized protein KIAA0513-like, transcript variant X1
uncharacterized protein KIAA0513-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 231 Proteins
glucose-6-phosphate exchanger SLC37A2-like, transcript variant X2
glucose-6-phosphate exchanger SLC37A2-like, transcript variant X1
glucose-6-phosphate exchanger SLC37A2-like isoform X1
glucose-6-phosphate exchanger SLC37A2-like isoform X2
transcriptional repressor CTCF-like, transcript variant X3
transcriptional repressor CTCF-like, transcript variant X4
transcriptional repressor CTCF-like, transcript variant X1
transcriptional repressor CTCF-like, transcript variant X2
transcriptional repressor CTCF-like isoform X2
transcriptional repressor CTCF-like isoform X3
transcriptional repressor CTCF-like isoform X1
uncharacterized LOC125045876, transcript variant X2
uncharacterized LOC125045876, transcript variant X1
uncharacterized protein LOC125045876 isoform X2
uncharacterized protein LOC125045876 isoform X1
uncharacterized LOC125045783, transcript variant X1
uncharacterized LOC125045783, transcript variant X3
uncharacterized LOC125045783, transcript variant X2
uncharacterized LOC125045783, transcript variant X4
uncharacterized protein LOC125045783 isoform X1
uncharacterized protein LOC125045783 isoform X3
uncharacterized protein LOC125045783 isoform X2
uncharacterized protein LOC125045783 isoform X4
angiopoietin-related protein 7-like, transcript variant X1
angiopoietin-related protein 7-like, transcript variant X2
angiopoietin-related protein 7-like isoform X2
uncharacterized LOC125046160, transcript variant X1
uncharacterized LOC125046160, transcript variant X2
uncharacterized protein LOC125046160 isoform X1
uncharacterized protein LOC125046160 isoform X2
transcription initiation factor IIB-like, transcript variant X1
transcription initiation factor IIB-like isoform X1
transcription initiation factor IIB-like, transcript variant X2
transcription initiation factor IIB-like isoform X2
arylalkylamine N-acetyltransferase-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-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
pneumococcal serine-rich repeat 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 6 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 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% 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, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative uncharacterized protein DDB_G0286901
uncharacterized protein DDB_G0271670-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
facilitated trehalose transporter Tret1-like, transcript variant X4
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like
uncharacterized LOC125045887, transcript variant X2
uncharacterized LOC125045887, transcript variant X1
uncharacterized protein LOC125045887 isoform X1
uncharacterized protein LOC125045887 isoform X2
relaxin receptor 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 2 samples with support for all annotated introns
relaxin receptor 2-like, transcript variant X2
relaxin receptor 2-like, transcript variant X3
beta-1,3-galactosyltransferase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
beta-1,3-galactosyltransferase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GIYE01019689.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 343 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 297 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
forkhead box protein F1-A-like, transcript variant X3
forkhead box protein F1-A-like, transcript variant X1
forkhead box protein F1-A-like isoform X1
forkhead box protein F1-A-like, transcript variant X2
forkhead box protein F1-A-like isoform X2
phosphatidylserine synthase-like, transcript variant X2
phosphatidylserine synthase-like, transcript variant X1
phosphatidylserine synthase-like isoform X1
phosphatidylserine synthase-like isoform X2
outer dense fiber protein 3-like, transcript variant X2
outer dense fiber protein 3-like, transcript variant X3
outer dense fiber protein 3-like, transcript variant X1
outer dense fiber protein 3-like isoform X2
outer dense fiber protein 3-like isoform X3
outer dense fiber protein 3-like isoform X1
aldo-keto reductase family 1 member B1-like, transcript variant X1
aldo-keto reductase family 1 member B1-like isoform X1
aldo-keto reductase family 1 member B1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
aldo-keto reductase family 1 member B1-like isoform X2
ankyrin repeat and SOCS box protein 13-like, transcript variant X3
ankyrin repeat and SOCS box protein 13-like, transcript variant X2
ankyrin repeat and SOCS box protein 13-like, transcript variant X1
ankyrin repeat and SOCS box protein 13-like isoform X1
ankyrin repeat and SOCS box protein 13-like isoform X2
protein neuralized-like, transcript variant X2
protein neuralized-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X2
cytosolic 10-formyltetrahydrofolate dehydrogenase-like, transcript variant X1
cytosolic 10-formyltetrahydrofolate dehydrogenase-like isoform X1
cytosolic 10-formyltetrahydrofolate dehydrogenase-like isoform X2
uncharacterized LOC125046143, 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 31 samples with support for all annotated introns
uncharacterized LOC125046143, transcript variant X3
uncharacterized LOC125046143, transcript variant X2
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 3 samples with support for all annotated introns
inactive dipeptidyl peptidase 10-like, transcript variant X1
inactive dipeptidyl peptidase 10-like, transcript variant X2
inactive dipeptidyl peptidase 10-like isoform X2
inactive dipeptidyl peptidase 10-like isoform X1
sulfite oxidase-like, transcript variant X2
sulfite oxidase-like, transcript variant X1
cysteine sulfinic acid decarboxylase-like
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 3 samples with support for all annotated introns
galactose mutarotase-like, transcript variant X2
galactose mutarotase-like, transcript variant 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
growth hormone secretagogue receptor type 1-like
glutamyl aminopeptidase-like, transcript variant X2
glutamyl aminopeptidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
hemocyanin subunit-like, transcript variant X2
hemocyanin subunit-like, transcript variant X1
hemocyanin subunit-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase PP1-like, transcript variant X2
serine/threonine-protein phosphatase PP1-like, transcript variant X1
serine/threonine-protein phosphatase alpha-3 isoform-like isoform X1
serine/threonine-protein phosphatase PP1-like isoform X2
mitochondrial-processing peptidase subunit alpha-like
probable G-protein coupled receptor AH9.1, transcript variant X1
probable G-protein coupled receptor AH9.1, transcript variant X3
probable G-protein coupled receptor AH9.1, transcript variant X5
probable G-protein coupled receptor AH9.1, transcript variant X4
probable G-protein coupled receptor AH9.1 isoform X1
probable G-protein coupled receptor AH9.1 isoform X3
probable G-protein coupled receptor AH9.1 isoform X4
probable G-protein coupled receptor AH9.1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable G-protein coupled receptor AH9.1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 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
uncharacterized LOC125046197, transcript variant X1
uncharacterized LOC125046197, transcript variant X2
uncharacterized protein LOC125046197 isoform X1
uncharacterized protein LOC125046197 isoform X2
RNA/RNP complex-1-interacting phosphatase-like
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X3
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X2
heparan sulfate glucosamine 3-O-sulfotransferase 6-like, transcript variant X1
heparan sulfate glucosamine 3-O-sulfotransferase 6-like
trafficking protein particle complex subunit 3-like
RAC-alpha serine/threonine-protein kinase-like, transcript variant X1
RAC-alpha serine/threonine-protein kinase-like, transcript variant X2
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 20 samples with support for all annotated introns
RAC-alpha serine/threonine-protein kinase-like isoform X1
RAC-alpha serine/threonine-protein kinase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
RAC-alpha serine/threonine-protein kinase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
RAC-alpha serine/threonine-protein kinase-like, transcript variant X6
RAC-alpha serine/threonine-protein kinase-like isoform X2
RAC-alpha serine/threonine-protein kinase-like, transcript variant X3
RAC-alpha serine/threonine-protein kinase-like, transcript variant X7
RAC-alpha serine/threonine-protein kinase-like isoform X3
RAC-alpha serine/threonine-protein kinase-like isoform X4
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WAS/WASL-interacting protein family member 2-like
uncharacterized LOC125046105, transcript variant X2
uncharacterized LOC125046105, transcript variant X1
ARF GTPase-activating protein GIT2-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 31 samples with support for all annotated introns
ARF GTPase-activating protein GIT2-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 32 samples with support for all annotated introns
ARF GTPase-activating protein GIT2-like, transcript variant X4
ARF GTPase-activating protein GIT2-like, transcript variant X1
ARF GTPase-activating protein GIT2-like isoform X1
ARF GTPase-activating protein GIT2-like isoform X4
uncharacterized protein LOC125045784 isoform X2
uncharacterized protein LOC125045784 isoform X3
tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6-like, transcript variant X1
tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6-like, transcript variant X2
tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6-like
U3 small nucleolar RNA-associated protein 6 homolog
acetyl-coenzyme A transporter 1-like, transcript variant X1
acetyl-coenzyme A transporter 1-like, transcript variant X2
acetyl-coenzyme A transporter 1-like isoform X1
acetyl-coenzyme A transporter 1-like isoform X2
brain protein I3-like, transcript variant X1
brain protein I3-like, transcript variant X2
probable ATP-dependent RNA helicase DDX52
uncharacterized LOC125046199, 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 15 samples with support for all annotated introns
uncharacterized LOC125046199, transcript variant X2
paired amphipathic helix protein Sin3a-like, transcript variant X2
paired amphipathic helix protein Sin3a-like, transcript variant X1
paired amphipathic helix protein Sin3a-like, transcript variant X3
paired amphipathic helix protein Sin3a-like, transcript variant X5
paired amphipathic helix protein Sin3a-like, transcript variant X6
paired amphipathic helix protein Sin3a-like, transcript variant X4
paired amphipathic helix protein Sin3a-like, transcript variant X7
paired amphipathic helix protein Sin3a-like isoform X1
paired amphipathic helix protein Sin3a-like isoform X2
paired amphipathic helix protein Sin3a-like isoform X4
paired amphipathic helix protein Sin3a-like isoform X5
paired amphipathic helix protein Sin3a-like isoform X3
paired amphipathic helix protein Sin3a-like isoform X6
astacin-like metalloendopeptidase, transcript variant X3
astacin-like metalloendopeptidase, transcript variant X1
astacin-like metalloendopeptidase, transcript variant X2
astacin-like metalloendopeptidase isoform X2
astacin-like metalloendopeptidase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125046113, transcript variant X1
uncharacterized protein LOC125046113 isoform X1
uncharacterized LOC125046113, transcript variant X2
uncharacterized protein LOC125046113 isoform X2
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X2
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X1
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X5
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X4
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X6
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X3
1-phosphatidylinositol 3-phosphate 5-kinase-like isoform X1
1-phosphatidylinositol 3-phosphate 5-kinase-like isoform X3
1-phosphatidylinositol 3-phosphate 5-kinase-like isoform X2
1-phosphatidylinositol 3-phosphate 5-kinase-like isoform X4
1-phosphatidylinositol 3-phosphate 5-kinase-like, transcript variant X7
1-phosphatidylinositol 3-phosphate 5-kinase-like isoform X5
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase TPTE2-like
similar to RNA sequence (same species):INSD:GHUY01000880.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 212 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% 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 141 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
transcriptional regulator ovo-like, transcript variant X1
transcriptional regulator ovo-like, transcript variant X2
transcriptional regulator ovo-like isoform X1
transcriptional regulator ovo-like isoform X2
phosphoinositide 3-kinase regulatory subunit 4-like, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 4-like, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 4-like, transcript variant X3
phosphoinositide 3-kinase regulatory subunit 4-like
uncharacterized LOC125046115, transcript variant X2
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 32 samples with support for all annotated introns
uncharacterized LOC125046115, transcript variant X1
uncharacterized protein LOC125046115 isoform X1
uncharacterized protein LOC125046115 isoform X2
uncharacterized LOC125045817, transcript variant X4
uncharacterized protein LOC125045817 isoform X4
uncharacterized LOC125045817, transcript variant X1
uncharacterized LOC125045817, transcript variant X5
uncharacterized LOC125045817, transcript variant X3
uncharacterized LOC125045817, transcript variant X2
uncharacterized protein LOC125045817 isoform X1
uncharacterized protein LOC125045817 isoform X5
uncharacterized protein LOC125045817 isoform X3
uncharacterized protein LOC125045817 isoform X2
trafficking protein particle complex subunit 4-like
gastrula zinc finger protein XlCGF8.2DB-like
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like, transcript variant X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial-like isoform X2
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
xanthine dehydrogenase/oxidase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
xanthine dehydrogenase/oxidase-like, transcript variant X1
xanthine dehydrogenase/oxidase-like isoform X1
xanthine dehydrogenase/oxidase-like, transcript variant X2
xanthine dehydrogenase/oxidase-like isoform X2
uncharacterized LOC125046250, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
uncharacterized LOC125046250, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125046250, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized protein LOC125046250 isoform X3
uncharacterized protein LOC125046250 isoform X2
uncharacterized protein LOC125046250 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex subunit pan3-like, transcript variant X5
PAN2-PAN3 deadenylation complex subunit pan3-like, transcript variant X3
PAN2-PAN3 deadenylation complex subunit pan3-like, transcript variant X2
PAN2-PAN3 deadenylation complex subunit pan3-like, transcript variant X4
PAN2-PAN3 deadenylation complex subunit pan3-like, transcript variant X1
PAN2-PAN3 deadenylation complex subunit pan3-like
uncharacterized LOC125046031, transcript variant X3
uncharacterized LOC125046031, transcript variant X1
uncharacterized LOC125046031, transcript variant X2
uncharacterized LOC125046031, transcript variant X5
uncharacterized LOC125046031, transcript variant X4
protein cab-1-like, transcript variant X1
protein cab-1-like, transcript variant X2
protein fuzzy homolog, transcript variant X1
protein fuzzy homolog, transcript variant X2
dihydropyrimidinase-like, transcript variant X3
dihydropyrimidinase-like, transcript variant X5
dihydropyrimidinase-like, transcript variant X2
dihydropyrimidinase-like, transcript variant X4
dihydropyrimidinase-like, transcript variant X1
dihydropyrimidinase-like, transcript variant X6
dihydropyrimidinase-like, transcript variant X7
ketosamine-3-kinase-like, transcript variant X3
uncharacterized LOC125045879, transcript variant X6
uncharacterized protein LOC125045879 isoform X6
uncharacterized LOC125045879, transcript variant X7
uncharacterized protein LOC125045879 isoform X7
uncharacterized LOC125045879, transcript variant X1
uncharacterized LOC125045879, transcript variant X2
uncharacterized LOC125045879, transcript variant X3
uncharacterized LOC125045879, transcript variant X4
uncharacterized LOC125045879, transcript variant X5
uncharacterized LOC125045879, transcript variant X9
uncharacterized LOC125045879, transcript variant X8
uncharacterized LOC125045879, transcript variant X10
uncharacterized LOC125045879, transcript variant X11
uncharacterized LOC125045879, transcript variant X12
uncharacterized protein LOC125045879 isoform X1
uncharacterized protein LOC125045879 isoform X2
uncharacterized protein LOC125045879 isoform X3
uncharacterized protein LOC125045879 isoform X4
uncharacterized protein LOC125045879 isoform X8
uncharacterized protein LOC125045879 isoform X5
uncharacterized protein LOC125045879 isoform X9
uncharacterized protein LOC125045879 isoform X10
uncharacterized protein LOC125045879 isoform X11
uncharacterized protein LOC125045879 isoform X12
uncharacterized LOC125045877, transcript variant X5
uncharacterized LOC125045877, transcript variant X3
uncharacterized LOC125045877, transcript variant X4
uncharacterized LOC125045877, transcript variant X1
uncharacterized LOC125045877, transcript variant X2
uncharacterized protein LOC125045877 isoform X4
uncharacterized protein LOC125045877 isoform X2
uncharacterized protein LOC125045877 isoform X3
uncharacterized protein LOC125045877 isoform X1
zinc transporter ZIP11-like, transcript variant X4
zinc transporter ZIP11-like, transcript variant X1
zinc transporter ZIP11-like, transcript variant X2
zinc transporter ZIP11-like, transcript variant X3
PAX-interacting protein 1-like, transcript variant X2
PAX-interacting protein 1-like, transcript variant X1
PAX-interacting protein 1-like isoform X2
PAX-interacting protein 1-like isoform X1
uncharacterized LOC125046155, transcript variant X7
uncharacterized LOC125046155, transcript variant X8
uncharacterized LOC125046155, transcript variant X10
uncharacterized LOC125046155, transcript variant X6
uncharacterized LOC125046155, transcript variant X3
uncharacterized LOC125046155, transcript variant X1
uncharacterized LOC125046155, transcript variant X2
uncharacterized LOC125046155, transcript variant X11
uncharacterized LOC125046155, transcript variant X12
uncharacterized LOC125046155, transcript variant X5
uncharacterized LOC125046155, transcript variant X4
uncharacterized LOC125046155, transcript variant X9
uncharacterized protein LOC125046155 isoform X3
uncharacterized protein LOC125046155 isoform X1
uncharacterized protein LOC125046155 isoform X2
uncharacterized protein LOC125046155 isoform X4
uncharacterized protein LOC125046155 isoform X5
hormone receptor 4-like, transcript variant X7
hormone receptor 4-like, transcript variant X10
hormone receptor 4-like, transcript variant X9
hormone receptor 4-like, transcript variant X11
hormone receptor 4-like, transcript variant X8
hormone receptor 4-like, transcript variant X2
hormone receptor 4-like, transcript variant X4
hormone receptor 4-like, transcript variant X1
hormone receptor 4-like, transcript variant X3
hormone receptor 4-like, transcript variant X6
hormone receptor 4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 6% 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 84% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor Mth-like 1, transcript variant X2
probable G-protein coupled receptor Mth-like 1, transcript variant X1
probable G-protein coupled receptor Mth-like 1 isoform X2
probable G-protein coupled receptor Mth-like 1 isoform X1
similar to RNA sequence (same species):INSD:GIYE01005583.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 440 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 310 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: 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
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 20 samples with support for all annotated introns
cysteine sulfinic acid decarboxylase-like, transcript variant X2
cysteine sulfinic acid decarboxylase-like, transcript variant X1
cysteine sulfinic acid decarboxylase-like, transcript variant X3
cysteine sulfinic acid decarboxylase-like isoform X1
cysteine sulfinic acid decarboxylase-like isoform X2
acidic amino acid decarboxylase GADL1-like
uncharacterized LOC125046043, transcript variant X1
uncharacterized LOC125046043, transcript variant X2
C-type lectin domain family 17, member A-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 6 samples with support for all annotated introns
transcriptional enhancer factor TEF-1-like
similar to RNA sequence (same species):INSD:GHUY01009081.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 190 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 190 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
transfer RNA serine (anticodon AGA); 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: 56% 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
zinc finger and BTB domain-containing protein 14-like, transcript variant X14
zinc finger and BTB domain-containing protein 14-like, transcript variant X8
zinc finger and BTB domain-containing protein 14-like, transcript variant X11
zinc finger and BTB domain-containing protein 14-like, transcript variant X4
zinc finger and BTB domain-containing protein 14-like, transcript variant X6
zinc finger and BTB domain-containing protein 14-like, transcript variant X15
zinc finger and BTB domain-containing protein 14-like, transcript variant X13
zinc finger and BTB domain-containing protein 14-like, transcript variant X12
zinc finger and BTB domain-containing protein 14-like, transcript variant X7
zinc finger and BTB domain-containing protein 14-like, transcript variant X9
zinc finger and BTB domain-containing protein 14-like, transcript variant X5
zinc finger and BTB domain-containing protein 14-like, transcript variant X16
zinc finger and BTB domain-containing protein 14-like, transcript variant X2
zinc finger and BTB domain-containing protein 14-like, transcript variant X1
zinc finger and BTB domain-containing protein 14-like, transcript variant X3
zinc finger and BTB domain-containing protein 14-like, transcript variant X10
E3 SUMO-protein ligase EGR2-like isoform X7
E3 SUMO-protein ligase EGR2-like isoform X5
E3 SUMO-protein ligase EGR2-like isoform X4
E3 SUMO-protein ligase EGR2-like isoform X9
E3 SUMO-protein ligase EGR2-like isoform X6
E3 SUMO-protein ligase EGR2-like isoform X10
zinc finger and BTB domain-containing protein 14-like isoform X3
E3 SUMO-protein ligase EGR2-like isoform X2
E3 SUMO-protein ligase EGR2-like isoform X1
E3 SUMO-protein ligase EGR2-like isoform X8
E3 SUMO-protein ligase EGR2-like isoform X11
colorectal mutant cancer protein-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 21 samples with support for all annotated introns
colorectal mutant cancer protein-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 7 samples with support for all annotated introns
colorectal mutant cancer protein-like isoform X2
colorectal mutant cancer protein-like isoform X1