Procambarus clarkii strain Jiangsu linkage group LG03, ASM2042438v2, whole genome shotgun sequence.
Procambarus clarkii (red swamp crayfish)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Astacidea; Astacoidea; Cambaridae; Procambarus.
A chromosome-level reference genome of red swamp crayfish Procambarus clarkii provides insights into the gene families regarding growth or development in crustaceans
REFSEQ INFORMATION: The reference sequence is identical to\nCM035475.1.\nAssembly name: ASM2042438v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Freshwater Fisheries Research\nInstitute of Jiangsu Province, Nanjing 210017, China on 2021/10/12.\nThe original whole-genome shotgun project has the accession\nJAIWQB000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Freshwater Fisheries Research Institute\n of Jiangsu Province, Nanjing 210017,\n China\nAssembly Method :: LACHESIS v. may-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio RS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Procambarus clarkii Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
COORDINATES: polyA evidence [ECO:0006239]
multiple epidermal growth factor-like domains protein 6
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized PPE family protein PPE21-like
uncharacterized protein MAL13P1.304-like
TOX high mobility group box family member 3-like
FERM, ARHGEF and pleckstrin domain-containing protein 1-like
similar to RNA sequence, mRNA (same species):INSD:KY974278.1
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 1952 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 1859 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123757235, 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 39 samples with support for all annotated introns
uncharacterized LOC123757235, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized protein LOC123757235 isoform X1
uncharacterized protein LOC123757235 isoform X2
classical arabinogalactan protein 9-like
uncharacterized LOC123757258, transcript variant X2
uncharacterized LOC123757258, transcript variant X3
uncharacterized LOC123757258, transcript variant X1
uncharacterized protein LOC123757258 isoform X2
uncharacterized protein LOC123757258 isoform X1
endoribonuclease CG2145-like, transcript variant X2
endoribonuclease CG2145-like, transcript variant X1
uridylate-specific endoribonuclease-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 64 samples with support for all annotated introns
transmembrane channel-like protein 7, transcript variant X1
transmembrane channel-like protein 7, transcript variant X2
transmembrane channel-like protein 7, transcript variant X3
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
DNA-directed RNA polymerase II subunit RPB1-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GARH01009613.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 195 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 195 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
mesoderm induction early response protein 1-like, transcript variant X3
mesoderm induction early response protein 1-like, transcript variant X5
mesoderm induction early response protein 1-like, transcript variant X10
mesoderm induction early response protein 1-like, transcript variant X1
mesoderm induction early response protein 1-like, transcript variant X11
mesoderm induction early response protein 1-like, transcript variant X13
mesoderm induction early response protein 1-like, transcript variant X7
mesoderm induction early response protein 1-like, transcript variant X6
mesoderm induction early response protein 1-like, transcript variant X8
mesoderm induction early response protein 1-like, transcript variant X9
mesoderm induction early response protein 1-like, transcript variant X4
mesoderm induction early response protein 1-like, transcript variant X2
mesoderm induction early response protein 1-like, transcript variant X12
mesoderm induction early response protein 1-like isoform X8
mesoderm induction early response protein 1-like isoform X5
mesoderm induction early response protein 1-like isoform X3
mesoderm induction early response protein 1-like isoform X7
mesoderm induction early response protein 1-like isoform X1
mesoderm induction early response protein 1-like isoform X4
mesoderm induction early response protein 1-like isoform X2
mesoderm induction early response protein 1-like isoform X6
mesoderm induction early response protein 1-like isoform X9
origin recognition complex subunit 2-like
RCC1 and BTB domain-containing protein 1-like, transcript variant X2
RCC1 and BTB domain-containing protein 1-like, transcript variant X1
RCC1 and BTB domain-containing protein 1-like
PHD and RING finger domain-containing protein 1-like, transcript variant X1
PHD and RING finger domain-containing protein 1-like, transcript variant X3
PHD and RING finger domain-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
PHD and RING finger domain-containing protein 1-like, transcript variant X2
PHD and RING finger domain-containing protein 1-like isoform X1
PHD and RING finger domain-containing protein 1-like isoform X2
uncharacterized LOC123757495, 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 LOC123757495, transcript variant X1
uncharacterized protein LOC123757495 isoform X2
uncharacterized protein LOC123757495 isoform X1
uncharacterized protein DDB_G0290685-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
angiopoietin-4-like, transcript variant X2
angiopoietin-4-like, transcript variant X1
angiopoietin-4-like, transcript variant X3
fibrinogen C domain-containing protein 1-like isoform X2
similar to RNA sequence (same species):INSD:GBEV01119796.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 117 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% 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 117 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
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
paternally-expressed gene 3 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
F-BAR domain only protein 2-like, transcript variant X1
F-BAR domain only protein 2-like, transcript variant X2
F-BAR domain only protein 2-like, transcript variant X3
F-BAR domain only protein 2-like isoform X1
F-BAR domain only protein 2-like isoform X2
F-BAR domain only protein 2-like isoform X3
similar to RNA sequence (same species):INSD:GBEV01032331.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 188 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 188 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
serine/threonine-protein kinase Tao-like, transcript variant X1
serine/threonine-protein kinase Tao-like, transcript variant X2
serine/threonine-protein kinase Tao-like, transcript variant X4
serine/threonine-protein kinase Tao-like, transcript variant X3
serine/threonine-protein kinase Tao-like, transcript variant X5
serine/threonine-protein kinase Tao-like isoform X1
serine/threonine-protein kinase Tao-like isoform X3
serine/threonine-protein kinase Tao-like isoform X2
serine/threonine-protein kinase Tao-like isoform X4
protein wntless-like, transcript variant X1
protein wntless-like, transcript variant X2
protein wntless-like, transcript variant X3
uncharacterized LOC123757603, transcript variant X1
uncharacterized protein LOC123757603 isoform X1
uncharacterized LOC123757603, transcript variant X2
uncharacterized protein LOC123757603 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0282133
microfibril-associated glycoprotein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 6 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
bifunctional peptidase and arginyl-hydroxylase JMJD5-like isoform X2
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X2
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X4
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X1
bifunctional peptidase and arginyl-hydroxylase JMJD5-like, transcript variant X3
F-box/LRR-repeat protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
ceramide synthase 6-like, transcript variant X2
ceramide synthase 6-like, transcript variant X1
uncharacterized LOC123757713, 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 7 samples with support for all annotated introns
uncharacterized LOC123757713, 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 38 samples with support for all annotated introns
uncharacterized LOC123757713, 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 50 samples with support for all annotated introns
uncharacterized LOC123757713, transcript variant X4
uncharacterized protein LOC123757713 isoform X3
uncharacterized protein LOC123757713 isoform X2
uncharacterized protein LOC123757713 isoform X1
uncharacterized protein LOC123757713 isoform X4
N-acetylgalactosaminyltransferase 6-like, transcript variant X3
N-acetylgalactosaminyltransferase 6-like, transcript variant X2
N-acetylgalactosaminyltransferase 6-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase-like 6 isoform X1
N-acetylgalactosaminyltransferase 6-like isoform X2
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
dyslexia-associated protein KIAA0319-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
ubiquinol-cytochrome-c reductase complex assembly factor 1-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 90 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
protein spaetzle-like, transcript variant X2
protein spaetzle-like, transcript variant X1
protein spaetzle-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dual specificity protein phosphatase MPK-4-like, transcript variant X2
dual specificity protein phosphatase MPK-4-like, transcript variant X4
dual specificity protein phosphatase MPK-4-like, transcript variant X1
dual specificity protein phosphatase MPK-4-like isoform X1
dual specificity protein phosphatase MPK-4-like, transcript variant X3
dual specificity protein phosphatase MPK-4-like isoform X3
dual specificity protein phosphatase MPK-4-like isoform X2
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X8
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X5
tyrosine-protein phosphatase non-receptor type 11-like isoform X4
tyrosine-protein phosphatase non-receptor type 11-like isoform X7
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X6
tyrosine-protein phosphatase non-receptor type 11-like isoform X5
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X1
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X3
tyrosine-protein phosphatase non-receptor type 11-like isoform X2
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X9
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 1 sample with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X2
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X4
tyrosine-protein phosphatase non-receptor type 11-like isoform X3
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X7
tyrosine-protein phosphatase non-receptor type 11-like isoform X6
tyrosine-protein phosphatase non-receptor type 11-like isoform X1
tyrosine-protein phosphatase non-receptor type 11-like isoform X8
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X10
tyrosine-protein phosphatase corkscrew-like isoform X9
snake venom metalloprotease inhibitor 02A10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
glycine, alanine and asparagine-rich protein-like
pollen-specific leucine-rich repeat extensin-like protein 1
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cGMP-dependent protein kinase 1-like, transcript variant X1
similar to RNA sequence (same species):INSD:GARH01025651.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1155 bases not found in genome assembly
cGMP-dependent protein kinase 1-like, transcript variant X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 575 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cGMP-dependent protein kinase 1-like isoform X1
cGMP-dependent protein kinase 1-like isoform X2
oplophorus-luciferin 2-monooxygenase non-catalytic subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123757937, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123757937, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123757937, transcript variant X1
uncharacterized LOC123757937, transcript variant X4
uncharacterized LOC123757937, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123757937, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123757937, transcript variant X7
uncharacterized LOC123757937, transcript variant X2
uncharacterized protein LOC123757937 isoform X2
uncharacterized protein LOC123757937 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
DBF4-type zinc finger-containing protein 2 homolog
uncharacterized LOC123757969, transcript variant X5
uncharacterized LOC123757969, transcript variant X8
uncharacterized LOC123757969, transcript variant X4
uncharacterized LOC123757969, transcript variant X6
uncharacterized LOC123757969, transcript variant X1
uncharacterized LOC123757969, transcript variant X10
uncharacterized LOC123757969, transcript variant X16
uncharacterized LOC123757969, transcript variant X14
uncharacterized LOC123757969, transcript variant X18
uncharacterized LOC123757969, transcript variant X19
uncharacterized LOC123757969, transcript variant X15
uncharacterized LOC123757969, transcript variant X11
uncharacterized LOC123757969, transcript variant X12
uncharacterized LOC123757969, transcript variant X9
uncharacterized LOC123757969, transcript variant X13
uncharacterized LOC123757969, transcript variant X17
uncharacterized LOC123757969, transcript variant X2
uncharacterized LOC123757969, transcript variant X3
uncharacterized LOC123757969, transcript variant X7
uncharacterized protein LOC123757969 isoform X1
uncharacterized protein LOC123757969 isoform X3
uncharacterized protein LOC123757969 isoform X9
uncharacterized protein LOC123757969 isoform X7
uncharacterized protein LOC123757969 isoform X11
uncharacterized protein LOC123757969 isoform X12
uncharacterized protein LOC123757969 isoform X8
uncharacterized protein LOC123757969 isoform X4
uncharacterized protein LOC123757969 isoform X5
uncharacterized protein LOC123757969 isoform X2
uncharacterized protein LOC123757969 isoform X6
uncharacterized protein LOC123757969 isoform X10
uncharacterized LOC123758020, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123758020, 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 13 samples with support for all annotated introns
uncharacterized protein LOC123758020 isoform X2
uncharacterized protein LOC123758020 isoform X1
repetitive proline-rich cell wall protein 2-like
basic salivary proline-rich protein 1-like
receptor-like tyrosine-protein kinase kin-16
G patch domain-containing protein 11-like, transcript variant X1
G patch domain-containing protein 11-like, transcript variant X2
G patch domain-containing protein 11-like isoform X2
G patch domain-containing protein 11-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase synoviolin B-like
similar to RNA sequence (same species):INSD:GBEV01005236.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 318 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 318 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase MARK2-like, transcript variant X7
serine/threonine-protein kinase MARK2-like, transcript variant X6
serine/threonine-protein kinase MARK2-like, transcript variant X10
serine/threonine-protein kinase MARK2-like, transcript variant X13
serine/threonine-protein kinase MARK2-like, transcript variant X8
serine/threonine-protein kinase MARK2-like, transcript variant X12
serine/threonine-protein kinase MARK2-like, transcript variant X14
serine/threonine-protein kinase MARK2-like, transcript variant X9
serine/threonine-protein kinase MARK2-like, transcript variant X5
serine/threonine-protein kinase MARK2-like, transcript variant X22
serine/threonine-protein kinase MARK2-like, transcript variant X21
serine/threonine-protein kinase MARK2-like, transcript variant X2
serine/threonine-protein kinase MARK2-like, transcript variant X20
serine/threonine-protein kinase MARK2-like, transcript variant X23
serine/threonine-protein kinase MARK2-like, transcript variant X19
serine/threonine-protein kinase MARK2-like, transcript variant X17
serine/threonine-protein kinase MARK2-like, transcript variant X3
serine/threonine-protein kinase MARK2-like, transcript variant X16
serine/threonine-protein kinase MARK2-like, transcript variant X11
serine/threonine-protein kinase MARK2-like, transcript variant X4
serine/threonine-protein kinase MARK2-like, transcript variant X1
serine/threonine-protein kinase MARK2-like, transcript variant X15
serine/threonine-protein kinase MARK2-like isoform X11
serine/threonine-protein kinase MARK2-like isoform X8
serine/threonine-protein kinase MARK2-like isoform X6
serine/threonine-protein kinase MARK2-like isoform X12
serine/threonine-protein kinase MARK2-like isoform X10
serine/threonine-protein kinase MARK2-like isoform X7
serine/threonine-protein kinase MARK2-like isoform X5
serine/threonine-protein kinase MARK2-like isoform X19
serine/threonine-protein kinase MARK2-like isoform X18
serine/threonine-protein kinase MARK2-like isoform X2
serine/threonine-protein kinase MARK2-like isoform X17
MAP/microtubule affinity-regulating kinase 3-like isoform X20
MAP/microtubule affinity-regulating kinase 3-like isoform X16
MAP/microtubule affinity-regulating kinase 3-like isoform X15
serine/threonine-protein kinase MARK2-like isoform X3
MAP/microtubule affinity-regulating kinase 3-like isoform X14
MAP/microtubule affinity-regulating kinase 3-like isoform X9
serine/threonine-protein kinase MARK2-like isoform X4
serine/threonine-protein kinase MARK2-like isoform X1
serine/threonine-protein kinase MARK2-like isoform X13
serine/threonine-protein kinase MARK2-like, transcript variant X25
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 38 samples with support for all annotated introns
serine/threonine-protein kinase MARK2-like, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine/threonine-protein kinase MARK2-like, transcript variant X18
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 7 samples with support for all annotated introns
GATOR complex protein MIOS-like, transcript variant X2
GATOR complex protein MIOS-like, transcript variant X3
GATOR complex protein MIOS-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
U-scoloptoxin(01)-Er1a-like, transcript variant X1
U-scoloptoxin(01)-Er1a-like, transcript variant X3
U-scoloptoxin(01)-Er1a-like, transcript variant X2
U-scoloptoxin(01)-Cw1a-like, transcript variant X2
U-scoloptoxin(01)-Cw1a-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
isocitrate dehydrogenase [NADP] cytoplasmic-like
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X3
organic cation transporter protein-like, transcript variant X1
organic cation transporter protein-like isoform X1
organic cation transporter protein-like isoform X2
uncharacterized LOC123758324, transcript variant X8
uncharacterized LOC123758324, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123758324, transcript variant X4
uncharacterized LOC123758324, transcript variant X3
uncharacterized LOC123758324, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123758324, transcript variant X6
uncharacterized LOC123758324, transcript variant X5
uncharacterized LOC123758324, 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 LOC123758324, transcript variant X2
uncharacterized protein LOC123758324 isoform X2
uncharacterized protein LOC123758324 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor 7, ovary-like, transcript variant X2
nuclear factor 7, ovary-like, transcript variant X1
nuclear factor 7, ovary-like, transcript variant X3
nuclear factor 7, ovary-like, transcript variant X4
DBH-like monooxygenase protein 1, transcript variant X2
DBH-like monooxygenase protein 1, transcript variant X1
DBH-like monooxygenase protein 1 isoform X1
DBH-like monooxygenase protein 1 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 52 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC123758409, transcript variant X1
uncharacterized LOC123758409, 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 111 samples with support for all annotated introns
tubulointerstitial nephritis antigen-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized zinc finger CCHC domain-containing protein At4g19190-like
serine/arginine repetitive matrix protein 4-like
uncharacterized LOC123758433, 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 38 samples with support for all annotated introns
uncharacterized LOC123758433, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 93 samples with support for all annotated introns
uncharacterized LOC123758424, transcript variant X2
uncharacterized LOC123758424, transcript variant X1
uncharacterized protein LOC123758424 isoform X1
uncharacterized protein LOC123758424 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
uncharacterized LOC123758464, transcript variant X4
uncharacterized LOC123758464, transcript variant X2
uncharacterized LOC123758464, transcript variant X1
uncharacterized LOC123758464, transcript variant X3
uncharacterized protein LOC123758464 isoform X4
uncharacterized protein LOC123758464 isoform X3
uncharacterized protein LOC123758464 isoform X2
uncharacterized protein LOC123758464 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123758482, transcript variant X3
uncharacterized LOC123758482, transcript variant X5
uncharacterized LOC123758482, transcript variant X2
uncharacterized protein LOC123758482 isoform X2
uncharacterized LOC123758482, transcript variant X4
uncharacterized LOC123758482, transcript variant X1
uncharacterized protein LOC123758482 isoform X1
uncharacterized protein LOC123758482 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
iodotyrosine deiodinase 1-like, transcript variant X2
iodotyrosine deiodinase 1-like, transcript variant X1
iodotyrosine deiodinase 1-like, transcript variant X3
iodotyrosine deiodinase 1-like isoform X1
iodotyrosine deiodinase 1-like isoform 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 5 samples with support for all annotated introns
proclotting enzyme-like, transcript variant X1
proclotting enzyme-like, transcript variant X2
uncharacterized LOC123758598, transcript variant X1
uncharacterized LOC123758598, transcript variant X2
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X2
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X4
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X1
phytanoyl-CoA dioxygenase, peroxisomal-like, transcript variant X3
phytanoyl-CoA dioxygenase, peroxisomal-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
lysyl oxidase homolog 2-like, transcript variant X3
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 23 samples with support for all annotated introns
lysyl oxidase homolog 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
lysyl oxidase homolog 2-like, transcript variant X5
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 12 samples with support for all annotated introns
lysyl oxidase homolog 2-like, transcript variant X4
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
lysyl oxidase homolog 2-like, transcript variant X2
uncharacterized LOC123758649, transcript variant X1
uncharacterized LOC123758649, transcript variant X3
uncharacterized LOC123758649, transcript variant X2
uncharacterized LOC123758649, 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 51 samples with support for all annotated introns
uncharacterized LOC123758649, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized LOC123758649, 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 49 samples with support for all annotated introns
uncharacterized LOC123758649, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized protein LOC123758649 isoform X1
uncharacterized protein LOC123758649 isoform X3
uncharacterized protein LOC123758649 isoform X2
uncharacterized protein LOC123758649 isoform X4
uncharacterized protein LOC123758649 isoform X5
transcription initiation factor IIA subunit 1-like
similar to RNA sequence (same species):INSD:GBEV01021641.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 205 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 205 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GARH01033133.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 47 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 88 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 47 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein FAM135A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein FAM135A-like, transcript variant X2
uncharacterized protein LOC123758709 isoform X2
protein HGH1 homolog, transcript variant X2
protein HGH1 homolog, transcript variant X3
protein HGH1 homolog, transcript variant X1
similar to RNA sequence (same species):INSD:GBEV01017346.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 148 bases not found in genome assembly
sarcoplasmic reticulum histidine-rich calcium-binding protein-like
tetra-peptide repeat homeobox protein 1-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 1 sample with support for all annotated introns
venom protease-like, transcript variant X1
venom protease-like, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B-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 82 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123758810, 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 6 samples with support for all annotated introns
uncharacterized LOC123758810, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Friend leukemia integration 1 transcription factor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
transcriptional regulator Erg-like, transcript variant X1
transcriptional regulator Erg-like, transcript variant X2
transcriptional regulator Erg-like, transcript variant X4
transcriptional regulator Erg-like, transcript variant X5
transcriptional regulator Erg-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 20 samples with support for all annotated introns
protein trapped in endoderm-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein trapped in endoderm-1-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 8 samples with support for all annotated introns
protein trapped in endoderm-1-like, transcript variant X3
protein trapped in endoderm-1-like isoform X2
protein trapped in endoderm-1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
phosphorylated adapter RNA export protein-like
GLABROUS1 enhancer-binding protein-like 3
protein suppressor of hairy wing-like, transcript variant X2
protein suppressor of hairy wing-like, transcript variant X1
protein suppressor of hairy wing-like, transcript variant X3
protein suppressor of hairy wing-like isoform X1
protein suppressor of hairy wing-like isoform X2
uncharacterized protein LOC123758915 isoform X3
ferric-chelate reductase 1-like, transcript variant X1
ferric-chelate reductase 1-like, transcript variant X2
ubiquitin-fold modifier 1, transcript variant X5
ubiquitin-fold modifier 1, 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 102 samples with support for all annotated introns
ubiquitin-fold modifier 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 94 samples with support for all annotated introns
ubiquitin-fold modifier 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
ubiquitin-fold modifier 1, transcript variant X3
uncharacterized protein LOC123758990 isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member A-like
RNA-binding motif, single-stranded-interacting protein 1-like
transforming growth factor-beta-induced protein ig-h3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein wntless-like, transcript variant X4
vitamin K-dependent gamma-carboxylase-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 2 samples with support for all annotated introns
uncharacterized LOC123759080, transcript variant X2
uncharacterized LOC123759080, transcript variant X1
uncharacterized protein LOC123759080 isoform X1
uncharacterized protein LOC123759080 isoform X2
uncharacterized LOC123759087, transcript variant X2
uncharacterized LOC123759087, transcript variant X1
uncharacterized LOC123759087, transcript variant X4
uncharacterized LOC123759087, transcript variant X3
uncharacterized protein LOC123759087 isoform X2
uncharacterized protein LOC123759087 isoform X1
receptor-type tyrosine-protein phosphatase T-like, transcript variant X1
receptor-type tyrosine-protein phosphatase T-like, transcript variant X2
receptor-type tyrosine-protein phosphatase T-like, transcript variant X4
receptor-type tyrosine-protein phosphatase delta-like isoform X1
receptor-type tyrosine-protein phosphatase T-like isoform X3
receptor-type tyrosine-protein phosphatase T-like, transcript variant X3
receptor-type tyrosine-protein phosphatase mu-like isoform X2
protein polybromo-1-like, transcript variant X7
protein polybromo-1-like, transcript variant X6
protein polybromo-1-like, transcript variant X4
protein polybromo-1-like, transcript variant X3
protein polybromo-1-like, transcript variant X2
protein polybromo-1-like, transcript variant X1
protein polybromo-1-like, transcript variant X10
protein polybromo-1-like, transcript variant X9
protein polybromo-1-like, transcript variant X8
protein polybromo-1-like, transcript variant X11
protein polybromo-1-like, transcript variant X5
dolichol kinase-like, transcript variant X3
dolichol kinase-like, transcript variant X1
dolichol kinase-like, transcript variant X4
dolichol kinase-like, transcript variant X2
AMP deaminase 2-like, transcript variant X1
AMP deaminase 2-like, transcript variant X4
AMP deaminase 2-like, transcript variant X3
AMP deaminase 2-like, transcript variant X5
AMP deaminase 2-like, transcript variant X6
AMP deaminase 2-like, transcript variant X2
AMP deaminase 2-like, transcript variant X7
AMP deaminase 2-like, transcript variant X8
AMP deaminase 2-like, transcript variant X9
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
general transcription factor IIH subunit 1-like, transcript variant X1
general transcription factor IIH subunit 1-like, transcript variant X2
general transcription factor IIH subunit 1-like
uncharacterized LOC123759343, transcript variant X1
uncharacterized LOC123759343, transcript variant X4
uncharacterized LOC123759343, transcript variant X6
uncharacterized LOC123759343, transcript variant X7
uncharacterized LOC123759343, transcript variant X5
uncharacterized LOC123759343, transcript variant X2
uncharacterized LOC123759343, transcript variant X9
uncharacterized LOC123759343, transcript variant X8
uncharacterized LOC123759343, transcript variant X3
uncharacterized protein LOC123759343 isoform X1
uncharacterized protein LOC123759343 isoform X4
uncharacterized protein LOC123759343 isoform X6
uncharacterized protein LOC123759343 isoform X7
uncharacterized protein LOC123759343 isoform X5
uncharacterized protein LOC123759343 isoform X9
uncharacterized protein LOC123759343 isoform X8
uncharacterized protein LOC123759343 isoform X3
uncharacterized protein LOC123759343 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein trapped in endoderm-1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
protein trapped in endoderm-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein trapped in endoderm-1-like isoform X3
G-protein coupled receptor moody-like isoform X1
AP-1 complex subunit sigma-2-like, transcript variant X4
AP-1 complex subunit sigma-2-like, transcript variant X3
AP-1 complex subunit sigma-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
AP-1 complex subunit sigma-2-like, transcript variant X2
AP-1 complex subunit sigma-2-like isoform X4
AP-1 complex subunit sigma-2-like isoform X3
AP-1 complex subunit sigma-2-like isoform X1
AP-1 complex subunit sigma-2-like isoform X2
mediator of RNA polymerase II transcription subunit 4-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 4-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 4-like isoform X2
mediator of RNA polymerase II transcription subunit 4-like isoform X1
mediator of RNA polymerase II transcription subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 104 samples with support for all annotated introns
histone deacetylase 6-like, transcript variant X1
histone deacetylase 6-like, transcript variant X3
histone deacetylase 6-like, transcript variant X2
histone deacetylase 6-like, transcript variant X4
arginine/serine-rich protein PNISR-like, transcript variant X4
arginine/serine-rich protein PNISR-like, transcript variant X2
arginine/serine-rich protein PNISR-like, transcript variant X1
arginine/serine-rich protein PNISR-like, transcript variant X3
arginine/serine-rich protein PNISR-like isoform X2
arginine/serine-rich protein PNISR-like isoform X1
diphthine methyltransferase-like, transcript variant X1
diphthine methyltransferase-like, transcript variant X2
G2/mitotic-specific cyclin-B3-like, transcript variant X2
G2/mitotic-specific cyclin-B3-like, transcript variant X1
G2/mitotic-specific cyclin-B3-like, transcript variant X7
G2/mitotic-specific cyclin-B3-like, transcript variant X6
G2/mitotic-specific cyclin-B3-like, transcript variant X3
G2/mitotic-specific cyclin-B3-like, transcript variant X4
G2/mitotic-specific cyclin-B3-like, transcript variant X5
G2/mitotic-specific cyclin-B3-like isoform X2
G2/mitotic-specific cyclin-B3-like isoform X1
26S proteasome regulatory subunit 4, transcript variant X1
26S proteasome regulatory subunit 4, transcript variant X2
26S proteasome regulatory subunit 4 isoform X1
26S proteasome regulatory subunit 4 isoform X2
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X5
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X1
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X3
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X4
serine/threonine-protein phosphatase 4 catalytic subunit isoform X3
serine/threonine-protein phosphatase 4 catalytic subunit isoform X1
serine/threonine-protein phosphatase 4 catalytic subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
GATA zinc finger domain-containing protein 14-like, transcript variant X6
GATA zinc finger domain-containing protein 14-like isoform X4
GATA zinc finger domain-containing protein 14-like, transcript variant X3
GATA zinc finger domain-containing protein 14-like, transcript variant X4
GATA zinc finger domain-containing protein 14-like, transcript variant X7
GATA zinc finger domain-containing protein 14-like isoform X5
GATA zinc finger domain-containing protein 14-like, transcript variant X5
GATA zinc finger domain-containing protein 14-like, transcript variant X2
GATA zinc finger domain-containing protein 14-like, transcript variant X1
GATA zinc finger domain-containing protein 14-like isoform X3
GATA zinc finger domain-containing protein 14-like isoform X1
GATA zinc finger domain-containing protein 14-like isoform X2
zinc finger protein 37-like, transcript variant X1
zinc finger protein 37-like, transcript variant X2
cysteine-rich secretory protein LCCL domain-containing 2-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 46 samples with support for all annotated introns
cysteine-rich secretory protein LCCL domain-containing 2-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 48 samples with support for all annotated introns
cysteine-rich secretory protein LCCL domain-containing 2-like isoform X1
cysteine-rich secretory protein LCCL domain-containing 2-like isoform X2
receptor-type tyrosine-protein phosphatase epsilon-like
RRP15-like protein, transcript variant X2
RRP15-like protein, transcript variant X1
receptor-type tyrosine-protein phosphatase mu-like
probable myosin light chain kinase DDB_G0282429
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin-like
sodium/bile acid cotransporter-like, transcript variant X2
sodium/bile acid cotransporter-like, transcript variant X1
DNA-dependent metalloprotease SPRTN-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA-dependent metalloprotease SPRTN-like, transcript variant X3
DNA-dependent metalloprotease SPRTN-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 13 samples with support for all annotated introns
DNA-dependent metalloprotease SPRTN-like, transcript variant X2
DNA-dependent metalloprotease SPRTN-like isoform X1
DNA-dependent metalloprotease SPRTN-like isoform X2
peroxisomal membrane protein PEX14-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 86 samples with support for all annotated introns
peroxisomal membrane protein PEX14-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 101 samples with support for all annotated introns
peroxisomal membrane protein PEX14-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 87 samples with support for all annotated introns
peroxisomal membrane protein PEX14-like isoform X1
peroxisomal membrane protein PEX14-like isoform X2
uncharacterized LOC123759742, 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 17 samples with support for all annotated introns
uncharacterized protein LOC123759742 isoform X2
uncharacterized LOC123759742, transcript variant X1
uncharacterized protein LOC123759742 isoform X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial-like
uncharacterized LOC123759760, transcript variant X2
uncharacterized LOC123759760, transcript variant X3
uncharacterized LOC123759760, transcript variant X1
uncharacterized LOC123759760, transcript variant X6
uncharacterized LOC123759760, transcript variant X5
uncharacterized LOC123759760, transcript variant X4
uncharacterized LOC123759760, transcript variant X7
uncharacterized protein LOC123759760 isoform X2
uncharacterized protein LOC123759760 isoform X1
uncharacterized protein LOC123759760 isoform X4
uncharacterized protein LOC123759760 isoform X3
uncharacterized protein LOC123759760 isoform X5
uncharacterized LOC123759823, transcript variant X1
uncharacterized LOC123759823, transcript variant X2
vesicle-associated membrane protein 2-like, transcript variant X4
vesicle-associated membrane protein 2-like, transcript variant X3
vesicle-associated membrane protein 2-like, transcript variant X1
vesicle-associated membrane protein 2-like, transcript variant X2
vesicle-associated membrane protein 2-like, transcript variant X5
vesicle-associated membrane protein 2-like isoform X1
vesicle-associated membrane protein 2-like isoform X2
vesicle-associated membrane protein 2-like isoform X3
vesicle-associated membrane protein 2-like isoform X4
ankyrin repeat and SOCS box protein 12-like, transcript variant X1
ankyrin repeat and SOCS box protein 12-like, transcript variant X2
ankyrin repeat and SOCS box protein 12-like
dedicator of cytokinesis protein 7-like, transcript variant X5
dedicator of cytokinesis protein 7-like, transcript variant X2
dedicator of cytokinesis protein 7-like, transcript variant X4
dedicator of cytokinesis protein 7-like, transcript variant X3
dedicator of cytokinesis protein 7-like, transcript variant X7
dedicator of cytokinesis protein 7-like, transcript variant X9
dedicator of cytokinesis protein 7-like, transcript variant X6
dedicator of cytokinesis protein 7-like, transcript variant X8
dedicator of cytokinesis protein 7-like, transcript variant X1
dedicator of cytokinesis protein 7-like isoform X9
dedicator of cytokinesis protein 7-like isoform X8
dedicator of cytokinesis protein 7-like isoform X5
dedicator of cytokinesis protein 7-like isoform X2
dedicator of cytokinesis protein 7-like isoform X4
dedicator of cytokinesis protein 7-like isoform X3
dedicator of cytokinesis protein 7-like isoform X7
dedicator of cytokinesis protein 7-like isoform X6
dedicator of cytokinesis protein 7-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
out at first protein-like, transcript variant X1
out at first protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat domain-containing protein 12-like
epidermal retinol dehydrogenase 2-like, transcript variant X3
epidermal retinol dehydrogenase 2-like, transcript variant X2
epidermal retinol dehydrogenase 2-like isoform X2
epidermal retinol dehydrogenase 2-like, transcript variant X1
epidermal retinol dehydrogenase 2-like isoform X1
vacuolar-sorting protein SNF8-like, transcript variant X3
vacuolar-sorting protein SNF8-like, transcript variant X2
vacuolar-sorting protein SNF8-like, transcript variant X1
uncharacterized LOC123759991, transcript variant X2
uncharacterized LOC123759991, transcript variant X1
uncharacterized protein LOC123759991 isoform X1
uncharacterized protein LOC123759991 isoform X2
protein Spindly-like, transcript variant X3
protein Spindly-like, transcript variant X4
protein Spindly-like, transcript variant X2
protein Spindly-like, transcript variant X1
protein Spindly-like, transcript variant X6
protein Spindly-like, transcript variant X5
uncharacterized LOC123760046, transcript variant X1
uncharacterized LOC123760046, transcript variant X3
uncharacterized LOC123760046, transcript variant X2
uncharacterized protein LOC123760046 isoform X1
uncharacterized protein LOC123760046 isoform X2
uncharacterized protein LOC123760046 isoform X3
protein quiver-like, transcript variant X1
protein quiver-like, transcript variant X3
protein quiver-like, transcript variant X2
protein quiver-like, transcript variant X4
uncharacterized protein LOC123760060 isoform X3
uncharacterized protein LOC123760060 isoform X2
tRNA-specific adenosine deaminase 1-like
anaphase-promoting complex subunit 15-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 108 samples with support for all annotated introns
cyanocobalamin reductase / alkylcobalamin dealkylase-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 98 samples with support for all annotated introns
cyanocobalamin reductase / alkylcobalamin dealkylase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cyanocobalamin reductase / alkylcobalamin dealkylase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
cyanocobalamin reductase / alkylcobalamin dealkylase-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 49 samples with support for all annotated introns
cyanocobalamin reductase / alkylcobalamin dealkylase-like, transcript variant X5
cyanocobalamin reductase / alkylcobalamin dealkylase-like isoform X2
putative uncharacterized protein ENSP00000383309
abnormal spindle-like microcephaly-associated protein homolog
protein VAPYRIN-like, transcript variant X2
protein VAPYRIN-like, transcript variant X4
protein VAPYRIN-like, transcript variant X1
protein VAPYRIN-like, transcript variant X3
zinc finger MYND domain-containing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123760147, transcript variant X2
uncharacterized LOC123760147, transcript variant X1
uncharacterized protein LOC123760147 isoform X1
uncharacterized protein LOC123760147 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 22 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 26 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 10 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 67% coverage of the annotated genomic feature by RNAseq alignments
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1-like
immunoglobulin domain-containing protein oig-4-like
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 6 samples with support for all annotated introns
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like, transcript variant X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like, transcript variant X3
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like, transcript variant X2
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like, transcript variant X4
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like isoform X2
eukaryotic translation initiation factor 2A-like
rhodanese domain-containing protein CG4456-like
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell wall protein RBR3-like, transcript variant X2
cell wall protein RBR3-like, transcript variant X1
alpha-aminoadipic semialdehyde dehydrogenase-like, transcript variant X1
alpha-aminoadipic semialdehyde dehydrogenase-like, transcript variant X2
alpha-aminoadipic semialdehyde dehydrogenase-like isoform X1
alpha-aminoadipic semialdehyde dehydrogenase-like isoform X2
3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase FUT3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NEDD8-activating enzyme E1 regulatory subunit-like
protein sidekick-like, transcript variant X1
protein sidekick-like, transcript variant X3
protein sidekick-like, transcript variant X5
protein sidekick-like, transcript variant X2
protein sidekick-like, transcript variant X4
protein sidekick-like, transcript variant X7
protein sidekick-like, transcript variant X6
protein sidekick-like, transcript variant X8
parathyroid hormone/parathyroid hormone-related peptide receptor-like, transcript variant X2
parathyroid hormone/parathyroid hormone-related peptide receptor-like, transcript variant X1
parathyroid hormone/parathyroid hormone-related peptide receptor-like isoform X2
parathyroid hormone/parathyroid hormone-related peptide receptor-like isoform X1
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily KQT member 1-like isoform X2
potassium voltage-gated channel subfamily KQT member 1-like isoform X1
RNA-binding protein fusilli-like, transcript variant X8
similar to RNA sequence (same species):INSD:GARH01009118.1
RNA-binding protein fusilli-like, transcript variant X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 750 bases not found in genome assembly
RNA-binding protein fusilli-like, transcript variant X5
RNA-binding protein fusilli-like, transcript variant X7
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 574 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
RNA-binding protein fusilli-like isoform X5
RNA-binding protein fusilli-like isoform X7
RNA-binding protein fusilli-like isoform X6
RNA-binding protein fusilli-like, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 750 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 18 samples with support for all annotated introns
RNA-binding protein fusilli-like isoform X4
RNA-binding protein fusilli-like, transcript variant X1
RNA-binding protein fusilli-like, transcript variant X2
RNA-binding protein fusilli-like, transcript variant X3
epithelial splicing regulatory protein 1-like isoform X1
epithelial splicing regulatory protein 1-like isoform X2
epithelial splicing regulatory protein 1-like isoform 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 15 samples with support for all annotated introns
amino acid transporter AVT1D-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 40 samples with support for all annotated introns
amino acid transporter AVT1D-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 14 samples with support for all annotated introns
amino acid transporter AVT1D-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
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