Chelonia mydas isolate rCheMyd1 chromosome 28, rCheMyd1.pri.v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Americhelydia; Chelonioidea; Cheloniidae; Chelonia.
REFSEQ INFORMATION: The reference sequence is identical to\nCM026925.2.\nOn Sep 23, 2021 this sequence version replaced NC_051268.1.\nAssembly name: rCheMyd1.pri.v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/07/15. The original whole-genome shotgun project has the\naccession JADCQM000000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 28-MAY-2021\nAssembly Method :: FALCON 1.3.0 v. 2018.31.08-03.06;\n FALCON-Unzip v. 1.2.0 6.0.0.47841;\n purge_dups v. github\n ca23030ccf4254dfd2d3a5ea90d0eed41c24f88b\n ca23030ccf4254dfd2d3a5ea90d0eed41c24f88b;\n Scaff10x v. 4.1.0; Bionano Solve v.\n 3.2.1_04122018; Salsa2 HiC v. 2.2; Arrow\n polishing and gap filling v.\n SMRTLink7.0.1; Longranger Align v. 2.2.2;\n freebayes v. 1.3.1; gEVAL manual curation\n v. 2021-05-28; VGP assembly pipeline v.\n 1.6\nAssembly Name :: rCheMyd1.pri.v2\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 60.0x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chelonia mydas Annotation Release\n 103\nAnnotation Version :: 103\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: 2 long SRA reads, and 81% 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: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC122463944, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC122463944, 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 LOC122463941, transcript variant X1
uncharacterized LOC122463941, transcript variant X2
zinc finger protein 3, transcript variant X3
zinc finger protein 3, transcript variant X6
zinc finger protein 3, transcript variant X4
zinc finger protein 3, transcript variant X1
zinc finger protein 3, transcript variant X5
zinc finger protein 3, transcript variant X2
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: zinc finger protein 436
flavin-containing monooxygenase FMO GS-OX4, transcript variant X1
flavin-containing monooxygenase FMO GS-OX4, transcript variant X4
flavin-containing monooxygenase FMO GS-OX4, transcript variant X2
flavin-containing monooxygenase FMO GS-OX4, transcript variant X3
flavin-containing monooxygenase FMO GS-OX4 isoform X1
flavin-containing monooxygenase FMO GS-OX4, transcript variant X5
flavin-containing monooxygenase FMO GS-OX4 isoform X2
fibroin heavy chain, transcript variant X8
fibroin heavy chain, transcript variant X9
fibroin heavy chain, transcript variant X3
fibroin heavy chain, transcript variant X5
fibroin heavy chain, transcript variant X4
fibroin heavy chain, transcript variant X2
fibroin heavy chain, transcript variant X1
fibroin heavy chain, transcript variant X7
fibroin heavy chain, transcript variant X6
lysophosphatidic acid receptor 6, 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 39 samples with support for all annotated introns
lysophosphatidic acid receptor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lysophosphatidic acid receptor 6, 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 7 samples with support for all annotated introns
lysophosphatidic acid receptor 6, 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
beta-galactoside alpha-2,6-sialyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
minichromosome maintenance complex component 7, transcript variant X2
minichromosome maintenance complex component 7, transcript variant X1
adaptor related protein complex 4 subunit mu 1, transcript variant X1
adaptor related protein complex 4 subunit mu 1, transcript variant X2
stromal antigen 3, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stromal antigen 3, 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 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stromal antigen 3, 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 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X1
stromal antigen 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X11
stromal antigen 3, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X4
stromal antigen 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stromal antigen 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
stromal antigen 3, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
stromal antigen 3, transcript variant X13
stromal antigen 3, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactose-3-O-sulfotransferase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
galactose-3-O-sulfotransferase 4 isoform X2
galactose-3-O-sulfotransferase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactose-3-O-sulfotransferase 4 isoform X1
trafficking protein particle complex subunit 14, transcript variant X2
trafficking protein particle complex subunit 14, transcript variant X1
trafficking protein particle complex subunit 14 isoform X1
trafficking protein particle complex subunit 14 isoform X2
trafficking protein particle complex subunit 14, transcript variant X3
trafficking protein particle complex subunit 14 isoform X3
late endosomal/lysosomal adaptor, MAPK and MTOR activator 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% 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 2 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
acetylcholinesterase (Cartwright blood group), transcript variant X2
acetylcholinesterase (Cartwright blood group), transcript variant X1
histidine-rich protein PFHRP-II-like, transcript variant X2
histidine-rich protein PFHRP-II-like, transcript variant X1
histidine-rich protein PFHRP-II-like, transcript variant X3
histidine-rich protein PFHRP-II-like, transcript variant X4
histidine-rich protein PFHRP-II-like isoform X1
histidine-rich protein PFHRP-II-like isoform X3
uncharacterized protein LOC122463938 isoform X2
uncharacterized protein LOC122463938 isoform X4
similar to RNA sequence (same species):INSD:GGMX01219109.1
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: deleted 2 bases in 2 codons; added 91 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; added 91 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger MYND domain-containing protein 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vitelline membrane outer layer protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vitelline membrane outer layer protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Ig heavy chain Mem5, 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
vitelline membrane outer layer protein 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 23 samples with support for all annotated introns
Ig heavy chain Mem5, 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 19 samples with support for all annotated introns
Ig heavy chain Mem5, 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 8 samples with support for all annotated introns
Ig heavy chain Mem5, 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 10 samples with support for all annotated introns
Ig heavy chain Mem5, 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 2 samples with support for all annotated introns
Ig heavy chain Mem5, transcript variant X3
Ig heavy chain Mem5, 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 13 samples with support for all annotated introns
glycolipid transfer protein domain containing 2, transcript variant X1
glycolipid transfer protein domain containing 2, transcript variant X2
glycolipid transfer protein domain-containing protein 2 isoform X1
glycolipid transfer protein domain containing 2, transcript variant X4
glycolipid transfer protein domain containing 2, transcript variant X3
glycolipid transfer protein domain-containing protein 2 isoform X2
glycolipid transfer protein domain-containing protein 2 isoform X3
leucine-rich repeat extensin-like protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
misshapen like kinase 1, transcript variant X2
similar to RNA sequence (same species):INSD:GGMX01185595.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 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, including 27 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 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, including 29 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 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, including 28 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
misshapen like kinase 1, transcript variant X7
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 2039 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 53 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 1638 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cholinergic receptor nicotinic epsilon subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 11, transcript variant X1
solute carrier family 25 member 11, transcript variant X2
mitochondrial 2-oxoglutarate/malate carrier protein isoform X1
mitochondrial 2-oxoglutarate/malate carrier protein isoform X2
ring finger protein 167, transcript variant X1
ring finger protein 167, transcript variant X2
calmodulin binding transcription activator 2, transcript variant X6
calmodulin binding transcription activator 2, transcript variant X2
calmodulin binding transcription activator 2, transcript variant X7
calmodulin binding transcription activator 2, transcript variant X4
calmodulin binding transcription activator 2, transcript variant X3
calmodulin binding transcription activator 2, transcript variant X1
calmodulin binding transcription activator 2, transcript variant X5
calmodulin-binding transcription activator 2 isoform X5
calmodulin-binding transcription activator 2 isoform X3
calmodulin-binding transcription activator 2 isoform X2
calmodulin-binding transcription activator 2 isoform X1
calmodulin-binding transcription activator 2 isoform X4
inhibitor of CDK, cyclin A1 interacting protein 1
histone-lysine N-methyltransferase 2B-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 17 samples with support for all annotated introns
procollagen C-endopeptidase enhancer, transcript variant X1
procollagen C-endopeptidase enhancer, transcript variant X2
procollagen C-endopeptidase enhancer 1 isoform X1
procollagen C-endopeptidase enhancer 1 isoform X2
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: F-box only protein 24
leucine rich repeats and calponin homology domain containing 4, 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 9 samples with support for all annotated introns
leucine rich repeats and calponin homology domain containing 4, transcript variant X4
leucine rich repeats and calponin homology domain containing 4, transcript variant X1
leucine rich repeats and calponin homology domain containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
rhomboid-related protein 4-like, transcript variant X1
rhomboid-related protein 4-like, transcript variant X2
rhomboid-related protein 4-like isoform X1
rhomboid-related protein 4-like isoform X2
arf-GAP domain and FG repeat-containing protein 2, transcript variant X4
similar to RNA sequence (same species):INSD:GGMX01162359.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1021 bases not found in genome assembly
arf-GAP domain and FG repeat-containing protein 2, transcript variant X3
arf-GAP domain and FG repeat-containing protein 2, transcript variant X2
arf-GAP domain and FG repeat-containing protein 2, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 679 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
arf-GAP domain and FG repeat-containing protein 2 isoform X4
arf-GAP domain and FG repeat-containing protein 2 isoform X3
arf-GAP domain and FG repeat-containing protein 2 isoform X2
arf-GAP domain and FG repeat-containing protein 2 isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 16 member 13, transcript variant X1
solute carrier family 16 member 13, transcript variant X3
solute carrier family 16 member 13, transcript variant X2
solute carrier family 16 member 13, transcript variant X6
solute carrier family 16 member 13, transcript variant X4
solute carrier family 16 member 13, transcript variant X5
monocarboxylate transporter 13 isoform X2
monocarboxylate transporter 13 isoform X1
LOW QUALITY PROTEIN: B-cell CLL/lymphoma 6 member B protein
thyroid hormone receptor interactor 6, transcript variant X1
thyroid hormone receptor interactor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 4, transcript variant X1
zinc finger and BTB domain containing 4, transcript variant X2
zinc finger and BTB domain-containing protein 4
similar to RNA sequence (same species):INSD:GGMX01012542.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 357 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 204 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
WD repeat containing antisense to TP53, transcript variant X2
WD repeat containing antisense to TP53, transcript variant X1
telomerase Cajal body protein 1 isoform X1
telomerase Cajal body protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
dynein axonemal heavy chain 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 2 isoform X1
dynein axonemal heavy chain 2 isoform X2
dynein axonemal heavy chain 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal heavy chain 2 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lysine-specific demethylase 6B
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 41 samples with support for all annotated introns
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit
cytochrome b5 domain-containing protein 1, transcript variant X1
cytochrome b5 domain-containing protein 1, transcript variant X3
cytochrome b5 domain-containing protein 1, transcript variant X4
cytochrome b5 domain-containing protein 1, transcript variant X2
cytochrome b5 domain-containing protein 1
chromodomain helicase DNA binding protein 3, transcript variant X1
chromodomain helicase DNA binding protein 3, transcript variant X14
chromodomain helicase DNA binding protein 3, transcript variant X7
chromodomain helicase DNA binding protein 3, transcript variant X12
chromodomain helicase DNA binding protein 3, transcript variant X16
chromodomain helicase DNA binding protein 3, transcript variant X11
chromodomain helicase DNA binding protein 3, transcript variant X15
chromodomain helicase DNA binding protein 3, transcript variant X9
chromodomain helicase DNA binding protein 3, transcript variant X2
chromodomain helicase DNA binding protein 3, transcript variant X5
chromodomain helicase DNA binding protein 3, transcript variant X6
chromodomain helicase DNA binding protein 3, transcript variant X10
chromodomain helicase DNA binding protein 3, transcript variant X20
chromodomain helicase DNA binding protein 3, transcript variant X21
chromodomain helicase DNA binding protein 3, transcript variant X3
chromodomain helicase DNA binding protein 3, transcript variant X4
chromodomain helicase DNA binding protein 3, transcript variant X19
chromodomain helicase DNA binding protein 3, transcript variant X8
chromodomain helicase DNA binding protein 3, transcript variant X13
chromodomain helicase DNA binding protein 3, transcript variant X22
chromodomain-helicase-DNA-binding protein 3 isoform X1
chromodomain-helicase-DNA-binding protein 3 isoform X2
chromodomain-helicase-DNA-binding protein 3 isoform X5
chromodomain-helicase-DNA-binding protein 3 isoform X7
chromodomain-helicase-DNA-binding protein 3 isoform X6
chromodomain-helicase-DNA-binding protein 3 isoform X9
chromodomain-helicase-DNA-binding protein 3 isoform X10
chromodomain-helicase-DNA-binding protein 3 isoform X3
chromodomain-helicase-DNA-binding protein 3 isoform X8
chromodomain-helicase-DNA-binding protein 3 isoform X12
chromodomain-helicase-DNA-binding protein 3 isoform X4
chromodomain-helicase-DNA-binding protein 3 isoform X14
chromodomain-helicase-DNA-binding protein 3 isoform X16
chromodomain-helicase-DNA-binding protein 3 isoform X13
chromodomain-helicase-DNA-binding protein 3 isoform X11
chromodomain-helicase-DNA-binding protein 3 isoform X15
chromodomain-helicase-DNA-binding protein 3 isoform X20
chromodomain-helicase-DNA-binding protein 3 isoform X21
chromodomain-helicase-DNA-binding protein 3 isoform X22
chromodomain-helicase-DNA-binding protein 3 isoform X19
chromodomain helicase DNA binding protein 3, transcript variant X18
chromodomain helicase DNA binding protein 3, transcript variant X23
chromodomain helicase DNA binding protein 3, transcript variant X17
chromodomain helicase DNA binding protein 3, transcript variant X24
chromodomain-helicase-DNA-binding protein 3 isoform X17
chromodomain-helicase-DNA-binding protein 3 isoform X18
chromodomain-helicase-DNA-binding protein 3 isoform X23
chromodomain-helicase-DNA-binding protein 3 isoform X24
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X2
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X9
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X8
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X6
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X5
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X4
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X7
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X3
protein mono-ADP-ribosyltransferase TIPARP, transcript variant X1
protein mono-ADP-ribosyltransferase TIPARP isoform X2
protein mono-ADP-ribosyltransferase TIPARP isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A regulatory beta subunit 3, 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 10 samples with support for all annotated introns
potassium voltage-gated channel subfamily A regulatory beta subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
voltage-gated potassium channel subunit beta-3 isoform X2
voltage-gated potassium channel subunit beta-3 isoform X1
trafficking protein particle complex subunit 1
centrobin, centriole duplication and spindle assembly protein, transcript variant X1
centrobin, centriole duplication and spindle assembly protein, transcript variant X6
centrobin, centriole duplication and spindle assembly protein, transcript variant X8
centrobin, centriole duplication and spindle assembly protein, transcript variant X7
centrobin, centriole duplication and spindle assembly protein, transcript variant X9
centrobin, centriole duplication and spindle assembly protein, transcript variant X4
centrobin, centriole duplication and spindle assembly protein, transcript variant X3
centrobin, centriole duplication and spindle assembly protein, transcript variant X5
centrobin, centriole duplication and spindle assembly protein, transcript variant X10
centrobin, centriole duplication and spindle assembly protein, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transmembrane protein 107, transcript variant X5
transmembrane protein 107, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
transmembrane protein 107, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
transmembrane protein 107, 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 9 samples with support for all annotated introns
transmembrane protein 107, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
transmembrane protein 107, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
vesicle associated membrane protein 2, transcript variant X1
vesicle associated membrane protein 2, transcript variant X2
LOW QUALITY PROTEIN: period circadian protein homolog 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 99% 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.
transcription factor HES-7.1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription factor HES-7.1, 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 4 samples with support for all annotated introns
transfer RNA glutamine (anticodon UUG); 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.
transfer RNA lysine (anticodon UUU); 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: 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 436, transcript variant X1
zinc finger protein 436, transcript variant X3
zinc finger protein 436, transcript variant X2
zinc finger protein 436, transcript variant X10
zinc finger protein 436, transcript variant X5
zinc finger protein 436, transcript variant X8
zinc finger protein 436, transcript variant X9
zinc finger protein 436, transcript variant X6
zinc finger protein 436, transcript variant X4
zinc finger protein 436, transcript variant X7
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon UCC); 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 9 samples with support for all annotated introns
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 883, transcript variant X1
zinc finger protein 883, transcript variant X2
zinc finger protein 883, transcript variant X3
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
hydroperoxide isomerase ALOXE3, transcript variant X1
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 4 samples with support for all annotated introns
hydroperoxide isomerase ALOXE3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hydroperoxide isomerase ALOXE3 isoform X1
hydroperoxide isomerase ALOXE3 isoform X2
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
cytosolic Fe-S cluster assembly factor nubp1, transcript variant X1
cytosolic Fe-S cluster assembly factor nubp1, transcript variant X2
cytosolic Fe-S cluster assembly factor NUBP1 isoform X1
cytosolic Fe-S cluster assembly factor nubp1 isoform X2
uncharacterized LOC119564619, transcript variant X1
uncharacterized LOC119564619, transcript variant X2
zinc finger protein OZF, 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 2 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X2
zinc finger protein OZF, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 135, transcript variant X1
zinc finger protein 135, transcript variant X2
uncharacterized LOC119564619, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 384 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 501, transcript variant X25
zinc finger protein 28 homolog isoform X13
zinc finger protein 501, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 501, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 501, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 501, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 106 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 501, transcript variant X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 501, transcript variant X20
zinc finger protein 501, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 501, transcript variant X23
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 501-like, transcript variant X2
zinc finger protein 501-like, transcript variant X1
zinc finger protein 883, transcript variant X38
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein OZF, transcript variant X6
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 501, transcript variant X28
zinc finger protein 501, transcript variant X26
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
zinc finger protein 28 homolog isoform X14
zinc finger protein 28 homolog isoform X16
tripartite motif-containing protein 10-like, transcript variant X2
tripartite motif-containing protein 10-like isoform X2
tripartite motif-containing protein 10-like, transcript variant X3
tripartite motif-containing protein 10-like isoform X3
tripartite motif-containing protein 10-like, transcript variant X1
tripartite motif-containing protein 10-like isoform X1
tripartite motif-containing protein 10-like, transcript variant X4
zinc finger protein RFP, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein RFP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger protein RFP, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein RFP, transcript variant X6
zinc finger protein RFP, 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 22 samples with support for all annotated introns
zinc finger protein RFP, 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 25 samples with support for all annotated introns
zinc finger protein 501, transcript variant X29
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
zinc finger protein 501, transcript variant X15
zinc finger protein 501, transcript variant X14
zinc finger protein 501, transcript variant X5
zinc finger protein 501, transcript variant X4
zinc finger protein 501, transcript variant X9
zinc finger protein 501, transcript variant X13
zinc finger protein 501, transcript variant X8
zinc finger protein 501, transcript variant X10
zinc finger protein 501, transcript variant X16
zinc finger protein 501, transcript variant X18
zinc finger protein 501, transcript variant X27
zinc finger protein 501, transcript variant X12
zinc finger protein 501, transcript variant X11
zinc finger protein 501, transcript variant X6
zinc finger protein 501, transcript variant X3
zinc finger protein 501, transcript variant X2
zinc finger protein 501, transcript variant X1
zinc finger protein 883, transcript variant X21
zinc finger protein 883, transcript variant X48
zinc finger protein 883, transcript variant X33
zinc finger protein 883, transcript variant X35
zinc finger protein 883, transcript variant X34
zinc finger protein 883, transcript variant X49
zinc finger protein 883, transcript variant X36
zinc finger protein 883, transcript variant X37
zinc finger protein 883, transcript variant X39
zinc finger protein 883, transcript variant X14
zinc finger protein 883, transcript variant X26
zinc finger protein 883, transcript variant X27
zinc finger protein 883, transcript variant X25
zinc finger protein 883, transcript variant X42
zinc finger protein 883, transcript variant X43
zinc finger protein 883, transcript variant X24
zinc finger protein 883, transcript variant X28
zinc finger protein 883, transcript variant X4
zinc finger protein 883, transcript variant X13
zinc finger protein 883, transcript variant X29
zinc finger protein 883, transcript variant X44
zinc finger protein 883, transcript variant X12
zinc finger protein 883, transcript variant X10
zinc finger protein 883, transcript variant X9
zinc finger protein 883, transcript variant X41
zinc finger protein 883, transcript variant X40
zinc finger protein 883, transcript variant X16
zinc finger protein 883, transcript variant X15
zinc finger protein 883, transcript variant X45
zinc finger protein 883, transcript variant X22
zinc finger protein 883, transcript variant X23
zinc finger protein 79, transcript variant X8
zinc finger protein 79, transcript variant X1
zinc finger protein 79, transcript variant X7
zinc finger protein 79, transcript variant X4
zinc finger protein 79, transcript variant X6
zinc finger protein 79, transcript variant X3
zinc finger protein 79, transcript variant X2
zinc finger protein 79, transcript variant X5
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 883, transcript variant X47
zinc finger protein 883, transcript variant X31
zinc finger protein 883, transcript variant X32
zinc finger protein 883, transcript variant X30
zinc finger protein 883, transcript variant X50
zinc finger protein 883, transcript variant X46
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 883, transcript variant X18
zinc finger protein 883, transcript variant X5
zinc finger protein 883, transcript variant X6
zinc finger protein 883, transcript variant X7
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
zinc finger protein 883, transcript variant X20
zinc finger protein 883, transcript variant X11
zinc finger protein 879, transcript variant X1
zinc finger protein 879, transcript variant X2
zinc finger protein 879, 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 14 samples with support for all annotated introns
myb/SANT-like DNA-binding domain-containing protein 2
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 72 samples with support for all annotated introns
zinc finger protein 879, 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 41 samples with support for all annotated introns
putative KRAB domain-containing protein ZNF788 isoform X3
zinc finger protein 420, transcript variant X11
uncharacterized protein LOC102929296 isoform X8
zinc finger protein 420, transcript variant X1
zinc finger protein 420, transcript variant X2
zinc finger protein 420, transcript variant X6
zinc finger protein 420, transcript variant X3
zinc finger protein 420, transcript variant X7
zinc finger protein 420, transcript variant X9
zinc finger protein with KRAB and SCAN domains 3 isoform X4
uncharacterized protein LOC102929296 isoform X6
zinc finger protein 420, transcript variant X8
uncharacterized protein LOC102929296 isoform X5
zinc finger protein 420, transcript variant X10
uncharacterized protein LOC102929296 isoform X7
zinc finger protein 420, transcript variant X5
zinc finger protein 420, transcript variant X4
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X3
zinc finger protein 250-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 250-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X3
zinc finger protein 501-like, transcript variant X4
zinc finger protein 883-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 221 Proteins, and 98% 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 long SRA reads, 64 Proteins, and 99% 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: 9 long SRA reads, 64 Proteins, and 99% 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: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X4
zinc finger protein 883-like, transcript variant X4
zinc finger protein 883-like, transcript variant X7
zinc finger protein 883-like, transcript variant X2
zinc finger protein 883-like, transcript variant X3
zinc finger protein 883-like, transcript variant X5
zinc finger protein 883-like, transcript variant X6
zinc finger protein 883, transcript variant X8
zinc finger protein 883, transcript variant X19
zinc finger protein 883, transcript variant X17
gastrula zinc finger protein XlCGF57.1 isoform X15
gastrula zinc finger protein XlCGF57.1 isoform X16
gastrula zinc finger protein XlCGF57.1 isoform X24
putative KRAB domain-containing protein ZNF788
uncharacterized LOC114018488, transcript variant X1
uncharacterized protein LOC114018488 isoform X1
uncharacterized LOC114018488, transcript variant X6
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, including 1 sample with support for all annotated introns
uncharacterized protein LOC114018488 isoform X2
butyrophilin subfamily 1 member A1, transcript variant X1
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 1 sample with support for all annotated introns
butyrophilin subfamily 1 member A1, 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 5 samples with support for all annotated introns
butyrophilin subfamily 1 member A1 isoform X1
butyrophilin subfamily 1 member A1 isoform X2
uncharacterized LOC114018488, transcript variant X5
uncharacterized LOC114018488, transcript variant X4
uncharacterized LOC114018488, transcript variant X3
uncharacterized LOC114018488, transcript variant X2
zinc finger protein 418, transcript variant X2
zinc finger protein 418, transcript variant X4
zinc finger protein 418, transcript variant X7
zinc finger protein 418, transcript variant X8
zinc finger protein 418, transcript variant X10
zinc finger protein 418, transcript variant X9
zinc finger protein 418, transcript variant X1
zinc finger protein 418, transcript variant X5
zinc finger protein 418, transcript variant X3
zinc finger protein 418, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 86 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 214 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: 25 long SRA reads, 221 Proteins, and 99% 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: 3 long SRA reads, 214 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable inactive tRNA-specific adenosine deaminase-like protein 3
alpha-2,8-sialyltransferase 8F, transcript variant X4
alpha-2,8-sialyltransferase 8F, transcript variant X2
alpha-2,8-sialyltransferase 8F, transcript variant X1
alpha-2,8-sialyltransferase 8F, transcript variant X3
alpha-2,8-sialyltransferase 8F isoform X1
alpha-2,8-sialyltransferase 8F isoform X3
alpha-2,8-sialyltransferase 8F isoform X2
phosphoribosylformylglycinamidine synthase, transcript variant X1
phosphoribosylformylglycinamidine synthase, transcript variant X2
phosphoribosylformylglycinamidine synthase, transcript variant X3
phosphoribosylformylglycinamidine synthase, transcript variant X9
phosphoribosylformylglycinamidine synthase, transcript variant X4
phosphoribosylformylglycinamidine synthase, transcript variant X5
phosphoribosylformylglycinamidine synthase, transcript variant X8
phosphoribosylformylglycinamidine synthase isoform X4
phosphoribosylformylglycinamidine synthase isoform X5
phosphoribosylformylglycinamidine synthase isoform X8
phosphoribosylformylglycinamidine synthase isoform X1
phosphoribosylformylglycinamidine synthase isoform X2
phosphoribosylformylglycinamidine synthase isoform X3
phosphoribosylformylglycinamidine synthase, transcript variant X6
phosphoribosylformylglycinamidine synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
phosphoribosylformylglycinamidine synthase-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 12 samples with support for all annotated introns
phosphoribosylformylglycinamidine synthase-like
phosphoribosylformylglycinamidine synthase isoform X6
phosphoribosylformylglycinamidine synthase, transcript variant X7
phosphoribosylformylglycinamidine synthase isoform X7
phosphoribosylformylglycinamidine synthase, transcript variant X10
phosphoribosylformylglycinamidine synthase isoform X9
anomalous homeobox protein, transcript variant X7
anomalous homeobox protein, transcript variant X5
anomalous homeobox protein, transcript variant X16
anomalous homeobox protein, transcript variant X11
anomalous homeobox protein, transcript variant X4
anomalous homeobox protein, transcript variant X3
anomalous homeobox protein, transcript variant X15
anomalous homeobox protein, transcript variant X1
anomalous homeobox protein, transcript variant X14
anomalous homeobox protein, transcript variant X18
anomalous homeobox protein, transcript variant X2
anomalous homeobox protein, transcript variant X12
anomalous homeobox protein, transcript variant X13
anomalous homeobox protein, transcript variant X10
anomalous homeobox protein, transcript variant X9
anomalous homeobox protein, transcript variant X8
anomalous homeobox protein, transcript variant X6
anomalous homeobox protein, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphoribosylformylglycinamidine synthase, transcript variant X13
phosphoribosylformylglycinamidine synthase, transcript variant X12
phosphoribosylformylglycinamidine synthase, transcript variant X15
phosphoribosylformylglycinamidine synthase, transcript variant X14
phosphoribosylformylglycinamidine synthase, transcript variant X16
phosphoribosylformylglycinamidine synthase, transcript variant X11
zinc finger protein with KRAB and SCAN domains 8-like
zinc finger and SCAN domain-containing protein 29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 91 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 91 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X38
zinc finger protein OZF, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 190 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 255 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 255 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 98% 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 long SRA read, 214 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 214 Proteins, and 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 transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 883
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 214 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, transcript variant X15
zinc finger protein OZF, transcript variant X7
gastrula zinc finger protein XlCGF57.1 isoform X7
zinc finger protein OZF, transcript variant X17
zinc finger protein OZF, transcript variant X12
zinc finger protein OZF, transcript variant X14
zinc finger protein OZF, transcript variant X16
zinc finger protein OZF, transcript variant X10
zinc finger protein OZF, transcript variant X11
zinc finger protein OZF, transcript variant X9
gastrula zinc finger protein XlCGF57.1 isoform X9
gastrula zinc finger protein XlCGF57.1 isoform X10
gastrula zinc finger protein XlCGF57.1 isoform X11
zinc finger protein OZF, transcript variant X8
gastrula zinc finger protein XlCGF57.1 isoform X5
gastrula zinc finger protein XlCGF57.1 isoform X8
gastrula zinc finger protein XlCGF57.1 isoform X6
zinc finger protein OZF, transcript variant X13
gastrula zinc finger protein XlCGF57.1, 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 1 sample with support for all annotated introns
zinc finger protein 300, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 300, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 300, transcript variant X2
gastrula zinc finger protein XlCGF57.1, transcript variant X8
gastrula zinc finger protein XlCGF57.1, transcript variant X10
gastrula zinc finger protein XlCGF57.1, transcript variant X5
gastrula zinc finger protein XlCGF57.1, transcript variant X4
gastrula zinc finger protein XlCGF57.1, transcript variant X7
gastrula zinc finger protein XlCGF57.1, transcript variant X3
gastrula zinc finger protein XlCGF57.1, transcript variant X2
gastrula zinc finger protein XlCGF57.1, transcript variant X1
gastrula zinc finger protein XlCGF57.1, transcript variant X9
gastrula zinc finger protein XlCGF57.1, transcript variant X12
gastrula zinc finger protein XlCGF57.1, transcript variant X11
gastrula zinc finger protein XlCGF57.1 isoform X1
gastrula zinc finger protein XlCGF57.1 isoform X3
zinc finger protein OZF, transcript variant X26
zinc finger protein OZF, transcript variant X25
zinc finger protein OZF, transcript variant X18
zinc finger protein OZF, transcript variant X23
zinc finger protein OZF, transcript variant X39
zinc finger protein OZF, transcript variant X40
uncharacterized LOC122463960, transcript variant X2
uncharacterized LOC122463960, transcript variant X1
zinc finger protein OZF, transcript variant X31
zinc finger protein OZF, transcript variant X28
zinc finger protein OZF, transcript variant X44
zinc finger protein OZF, transcript variant X43
zinc finger protein OZF, transcript variant X36
zinc finger protein OZF, transcript variant X35
zinc finger protein OZF, transcript variant X32
zinc finger protein OZF, transcript variant X34
zinc finger protein OZF, transcript variant X33
zinc finger protein OZF, transcript variant X49
zinc finger protein OZF, transcript variant X19
zinc finger protein OZF, transcript variant X50
zinc finger protein OZF, transcript variant X42
zinc finger protein OZF, transcript variant X45
zinc finger protein OZF, transcript variant X37
zinc finger protein OZF, transcript variant X48
zinc finger protein OZF, transcript variant X47
zinc finger protein OZF, transcript variant X29
zinc finger protein OZF, transcript variant X46
gastrula zinc finger protein XlCGF57.1 isoform X21
gastrula zinc finger protein XlCGF57.1 isoform X18
gastrula zinc finger protein XlCGF57.1 isoform X19
gastrula zinc finger protein XlCGF57.1 isoform X13
zinc finger protein OZF, transcript variant X22
zinc finger protein OZF, transcript variant X20
zinc finger protein OZF, transcript variant X21
zinc finger protein OZF, transcript variant X41
uncharacterized LOC122463953, transcript variant X3
uncharacterized LOC122463953, transcript variant X2
uncharacterized LOC122463953, transcript variant X1
uncharacterized protein LOC122463953 isoform X1
uncharacterized protein LOC122463953 isoform X3
uncharacterized protein LOC122463953 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 99% 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: 15 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 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 34 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 27 samples with support for all annotated introns
zinc finger protein 132-like, transcript variant X4
zinc finger protein 132-like, transcript variant X3
zinc finger protein 132-like, transcript variant X1
zinc finger protein 132-like, transcript variant X2
zinc finger protein 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 19-like, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 154, transcript variant X2
zinc finger protein 154, transcript variant X3
zinc finger protein 154, transcript variant X1
zinc finger protein 154, transcript variant X4
zinc finger protein 154, transcript variant X5
uncharacterized LOC119564616, transcript variant X2
uncharacterized LOC119564616, 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 24 samples with support for all annotated introns
KRAB domain-containing protein 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 214 Proteins, and 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, 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 214 Proteins, and 95% 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: 2 long SRA reads, 214 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: 1 long SRA read, 214 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 214 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: 1 long SRA read, 214 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: 1 long SRA read, 214 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: 3 long SRA reads, 214 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 214 Proteins, and 99% 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: 2 long SRA reads, 217 Proteins, and 99% 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 long SRA reads, 217 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 217 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 214 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns