Chrysemys picta bellii isolate RCT428 chromosome 10, Chrysemys_picta_BioNano-3.0.4, whole genome shotgun sequence.
Chrysemys picta bellii (western painted turtle)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Testudinoidea; Emydidae; Chrysemys.
Physical Mapping and Refinement of the Painted Turtle Genome (Chrysemys picta) Inform Amniote Genome Evolution and Challenge Turtle-Bird Chromosomal Conservation
REFSEQ INFORMATION: The reference sequence is identical to\nCM002663.2.\nOn Aug 10, 2021 this sequence version replaced NC_024226.1.\nAssembly name: Chrysemys_picta_BioNano-3.0.4\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Painted turtle genome\nsequencing consortium on 2020/08/21. The original whole-genome\nshotgun project has the accession AHGY00000000.3.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Painted turtle genome sequencing\n consortium\nAssembly Method :: Newbler v. 2.6\nAssembly Name :: Chrysemys_picta_BioNano-3.0.4\nGenome Coverage :: 19.2x\nSequencing Technology :: 454 Life Sciences\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chrysemys picta 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##
small lake 1.3 miles south of Potholes Reservoir
Derived by automated computational analysis using gene prediction method: Gnomon.
TBC1 domain family member 24, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
TBC1 domain family member 24, 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 2 samples with support for all annotated introns
TBC1 domain family member 24, transcript variant X1
TBC1 domain family member 24, transcript variant X4
V-type proton ATPase 16 kDa proteolipid subunit
uncharacterized LOC101932413, 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 19 samples with support for all annotated introns
uncharacterized LOC101932413, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC101932413, 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 32 samples with support for all annotated introns
amidohydrolase domain containing 2, transcript variant X2
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 53 samples with support for all annotated introns
amidohydrolase domain containing 2, 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 63 samples with support for all annotated introns
N-acetylglucosamine-6-phosphate deacetylase
uncharacterized LOC101951698, transcript variant X1
uncharacterized LOC101951698, transcript variant X2
uncharacterized LOC101951698, transcript variant X3
uncharacterized LOC101951698, transcript variant X4
uncharacterized protein LOC101951698 isoform X1
uncharacterized protein LOC101951698 isoform X2
uncharacterized protein LOC101951698 isoform X3
uncharacterized LOC101951066, transcript variant X1
uncharacterized LOC101951066, transcript variant X2
uncharacterized LOC101951066, transcript variant X3
uncharacterized protein LOC101951066 isoform X2
uncharacterized protein LOC101951066 isoform X1
RNA binding protein with serine rich domain 1
RNA-binding protein with serine-rich domain 1
telomere maintenance 2, transcript variant X7
telomere maintenance 2, transcript variant X8
telomere maintenance 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
telomere maintenance 2, transcript variant X10
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
telomere maintenance 2, 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 44 samples with support for all annotated introns
telomere maintenance 2, transcript variant X4
telomere maintenance 2, transcript variant X5
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 24 samples with support for all annotated introns
telomere maintenance 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
telomere maintenance 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
telomere maintenance 2, transcript variant X1
telomere maintenance 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
telomere maintenance 2, transcript variant X9
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 50 samples with support for all annotated introns
telomere length regulation protein TEL2 homolog isoform X3
telomere length regulation protein TEL2 homolog isoform X4
telomere length regulation protein TEL2 homolog isoform X1
telomere length regulation protein TEL2 homolog isoform X2
telomere length regulation protein TEL2 homolog isoform X5
telomere length regulation protein TEL2 homolog isoform X8
telomere length regulation protein TEL2 homolog isoform X7
telomere length regulation protein TEL2 homolog isoform X6
telomere length regulation protein TEL2 homolog isoform X9
telomere maintenance 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
telomere maintenance 2, transcript variant X14
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
telomere length regulation protein TEL2 homolog isoform X10
telomere length regulation protein TEL2 homolog isoform X11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: intraflagellar transport protein 140 homolog
transmembrane protein 204, 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 6 samples with support for all annotated introns
transmembrane protein 204, transcript variant X2
transmembrane protein 204, 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 18 samples with support for all annotated introns
transmembrane protein 204, 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 73 samples with support for all annotated introns
cramped chromatin regulator homolog 1, transcript variant X1
cramped chromatin regulator homolog 1, transcript variant X6
cramped chromatin regulator homolog 1, transcript variant X7
cramped chromatin regulator homolog 1, transcript variant X2
cramped chromatin regulator homolog 1, transcript variant X3
cramped chromatin regulator homolog 1, transcript variant X4
cramped chromatin regulator homolog 1, transcript variant X5
cramped chromatin regulator homolog 1, transcript variant X8
Jupiter microtubule associated homolog 2, transcript variant X1
jupiter microtubule associated homolog 2 isoform X1
Jupiter microtubule associated homolog 2, transcript variant X2
jupiter microtubule associated homolog 2 isoform X2
major facilitator superfamily domain-containing protein 1-like, transcript variant X6
major facilitator superfamily domain-containing protein 1-like, transcript variant X7
major facilitator superfamily domain-containing protein 1-like, transcript variant X3
major facilitator superfamily domain-containing protein 1-like, transcript variant X9
major facilitator superfamily domain-containing protein 1-like, transcript variant X4
major facilitator superfamily domain-containing protein 1-like, transcript variant X1
major facilitator superfamily domain-containing protein 1-like, transcript variant X10
major facilitator superfamily domain-containing protein 1-like, transcript variant X2
major facilitator superfamily domain-containing protein 1-like, transcript variant X8
major facilitator superfamily domain-containing protein 1-like isoform X8
major facilitator superfamily domain-containing protein 1-like isoform X2
major facilitator superfamily domain-containing protein 1-like isoform X4
major facilitator superfamily domain-containing protein 1-like isoform X3
major facilitator superfamily domain-containing protein 1-like isoform X1
major facilitator superfamily domain-containing protein 1-like isoform X6
major facilitator superfamily domain-containing protein 1-like isoform X7
major facilitator superfamily domain-containing protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1-like isoform X5
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X28
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X4
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X1
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X13
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X12
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X3
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X6
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X9
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X11
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X14
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X5
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X10
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X36
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X17
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X23
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X2
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X18
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X7
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X15
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X22
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X20
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X25
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X8
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X16
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X19
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X21
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X26
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X24
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X35
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X27
C-Jun-amino-terminal kinase-interacting protein 3 isoform X1
C-Jun-amino-terminal kinase-interacting protein 3 isoform X13
C-Jun-amino-terminal kinase-interacting protein 3 isoform X28
C-Jun-amino-terminal kinase-interacting protein 3 isoform X4
C-Jun-amino-terminal kinase-interacting protein 3 isoform X12
C-Jun-amino-terminal kinase-interacting protein 3 isoform X3
C-Jun-amino-terminal kinase-interacting protein 3 isoform X6
C-Jun-amino-terminal kinase-interacting protein 3 isoform X9
C-Jun-amino-terminal kinase-interacting protein 3 isoform X11
C-Jun-amino-terminal kinase-interacting protein 3 isoform X14
C-Jun-amino-terminal kinase-interacting protein 3 isoform X5
C-Jun-amino-terminal kinase-interacting protein 3 isoform X10
C-Jun-amino-terminal kinase-interacting protein 3 isoform X36
C-Jun-amino-terminal kinase-interacting protein 3 isoform X17
C-Jun-amino-terminal kinase-interacting protein 3 isoform X23
C-Jun-amino-terminal kinase-interacting protein 3 isoform X2
C-Jun-amino-terminal kinase-interacting protein 3 isoform X18
C-Jun-amino-terminal kinase-interacting protein 3 isoform X7
C-Jun-amino-terminal kinase-interacting protein 3 isoform X15
C-Jun-amino-terminal kinase-interacting protein 3 isoform X22
C-Jun-amino-terminal kinase-interacting protein 3 isoform X20
C-Jun-amino-terminal kinase-interacting protein 3 isoform X25
C-Jun-amino-terminal kinase-interacting protein 3 isoform X27
C-Jun-amino-terminal kinase-interacting protein 3 isoform X8
C-Jun-amino-terminal kinase-interacting protein 3 isoform X16
C-Jun-amino-terminal kinase-interacting protein 3 isoform X19
C-Jun-amino-terminal kinase-interacting protein 3 isoform X21
C-Jun-amino-terminal kinase-interacting protein 3 isoform X26
C-Jun-amino-terminal kinase-interacting protein 3 isoform X24
C-Jun-amino-terminal kinase-interacting protein 3 isoform X35
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X31
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X33
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X30
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X32
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X29
C-Jun-amino-terminal kinase-interacting protein 3 isoform X29
C-Jun-amino-terminal kinase-interacting protein 3 isoform X30
C-Jun-amino-terminal kinase-interacting protein 3 isoform X32
C-Jun-amino-terminal kinase-interacting protein 3 isoform X31
C-Jun-amino-terminal kinase-interacting protein 3 isoform X33
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X34
C-Jun-amino-terminal kinase-interacting protein 3 isoform X34
NME/NM23 nucleoside diphosphate kinase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
NME/NM23 nucleoside diphosphate kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
nucleoside diphosphate kinase 3 isoform X1
nucleoside diphosphate kinase 3 isoform X2
28S ribosomal protein S34, mitochondrial
essential meiotic structure-specific endonuclease subunit 2
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; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable crossover junction endonuclease EME2
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X2
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X3
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X4
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X1
SPRY domain-containing SOCS box protein 3 isoform X2
SPRY domain-containing SOCS box protein 3 isoform X1
SPRY domain-containing SOCS box protein 3 isoform X3
cytosolic Fe-S cluster assembly factor NUBP2
insulin like growth factor binding protein acid labile subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
insulin like growth factor binding protein acid labile subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
insulin-like growth factor-binding protein complex acid labile subunit isoform X2
insulin-like growth factor-binding protein complex acid labile subunit isoform X1
WW domain-binding protein 2-like, transcript variant X2
WW domain-binding protein 2-like, transcript variant X1
WW domain-binding protein 2-like, transcript variant X5
WW domain-binding protein 2-like, transcript variant X4
WW domain-binding protein 2-like, transcript variant X3
WW domain-binding protein 2-like isoform X2
WW domain-binding protein 2-like isoform X1
WW domain-binding protein 2-like isoform X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
F-box and leucine rich repeat protein 16
cholesterol side-chain cleavage enzyme, mitochondrial, transcript variant X2
cholesterol side-chain cleavage enzyme, mitochondrial, transcript variant X1
cholesterol side-chain cleavage enzyme, mitochondrial, transcript variant X3
cholesterol side-chain cleavage enzyme, mitochondrial isoform X1
cholesterol side-chain cleavage enzyme, mitochondrial isoform X2
cholesterol side-chain cleavage enzyme, mitochondrial isoform X3
coiled-coil domain containing 33, transcript variant X12
coiled-coil domain containing 33, transcript variant X3
coiled-coil domain containing 33, transcript variant X11
coiled-coil domain containing 33, transcript variant X6
coiled-coil domain containing 33, transcript variant X13
coiled-coil domain containing 33, transcript variant X4
coiled-coil domain containing 33, transcript variant X8
coiled-coil domain containing 33, transcript variant X1
coiled-coil domain containing 33, transcript variant X7
coiled-coil domain containing 33, transcript variant X2
coiled-coil domain containing 33, transcript variant X9
coiled-coil domain containing 33, transcript variant X5
coiled-coil domain containing 33, transcript variant X10
coiled-coil domain-containing protein 33 isoform X7
coiled-coil domain-containing protein 33 isoform X12
coiled-coil domain-containing protein 33 isoform X5
coiled-coil domain-containing protein 33 isoform X2
coiled-coil domain-containing protein 33 isoform X3
coiled-coil domain-containing protein 33 isoform X13
coiled-coil domain-containing protein 33 isoform X9
coiled-coil domain-containing protein 33 isoform X4
coiled-coil domain-containing protein 33 isoform X6
coiled-coil domain-containing protein 33 isoform X1
coiled-coil domain-containing protein 33 isoform X10
coiled-coil domain-containing protein 33 isoform X11
coiled-coil domain-containing protein 33 isoform X8
coiled-coil domain containing 33, transcript variant X15
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
coiled-coil domain containing 33, transcript variant X14
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
coiled-coil domain-containing protein 33 isoform X14
signaling receptor and transporter of retinol STRA6, transcript variant X2
signaling receptor and transporter of retinol STRA6, transcript variant X3
signaling receptor and transporter of retinol STRA6, transcript variant X1
signaling receptor and transporter of retinol STRA6, transcript variant X6
signaling receptor and transporter of retinol STRA6, transcript variant X5
signaling receptor and transporter of retinol STRA6, transcript variant X4
receptor for retinol uptake STRA6 isoform X1
receptor for retinol uptake STRA6 isoform X2
immunoglobulin superfamily containing leucine rich repeat, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
immunoglobulin superfamily containing leucine rich repeat, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
immunoglobulin superfamily containing leucine-rich repeat protein isoform X1
immunoglobulin superfamily containing leucine-rich repeat protein isoform X2
immunoglobulin superfamily containing leucine rich repeat 2, transcript variant X1
immunoglobulin superfamily containing leucine rich repeat 2, transcript variant X2
immunoglobulin superfamily containing leucine rich repeat 2, transcript variant X3
immunoglobulin superfamily containing leucine-rich repeat protein 2 isoform X1
immunoglobulin superfamily containing leucine-rich repeat protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
PML nuclear body scaffold, transcript variant X1
PML nuclear body scaffold, transcript variant X2
PML nuclear body scaffold, transcript variant X3
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lysyl oxidase like 1, transcript variant X2
lysyl oxidase like 1, transcript variant X1
lysyl oxidase like 1, 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 55 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC101949728, transcript variant X3
uncharacterized LOC101949728, transcript variant X2
uncharacterized LOC101949728, transcript variant X1
inhibitory synaptic factor 1, transcript variant X1
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 72 samples with support for all annotated introns
inhibitory synaptic factor 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 16 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 15-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
hyperpolarization activated cyclic nucleotide gated potassium channel 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4
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
ADP dependent glucokinase, transcript variant X3
ADP dependent glucokinase, transcript variant X1
ADP dependent glucokinase, transcript variant X2
Bardet-Biedl syndrome 4, transcript variant X11
Bardet-Biedl syndrome 4, transcript variant X1
Bardet-Biedl syndrome 4, transcript variant X15
Bardet-Biedl syndrome 4, transcript variant X22
Bardet-Biedl syndrome 4, transcript variant X7
Bardet-Biedl syndrome 4, transcript variant X4
Bardet-Biedl syndrome 4, transcript variant X6
Bardet-Biedl syndrome 4, transcript variant X8
Bardet-Biedl syndrome 4, transcript variant X2
Bardet-Biedl syndrome 4, transcript variant X9
Bardet-Biedl syndrome 4, transcript variant X21
Bardet-Biedl syndrome 4, transcript variant X12
Bardet-Biedl syndrome 4, transcript variant X17
Bardet-Biedl syndrome 4, transcript variant X20
Bardet-Biedl syndrome 4, transcript variant X13
Bardet-Biedl syndrome 4, transcript variant X18
Bardet-Biedl syndrome 4, transcript variant X14
Bardet-Biedl syndrome 4, transcript variant X19
Bardet-Biedl syndrome 4, transcript variant X5
Bardet-Biedl syndrome 4, transcript variant X3
Bardet-Biedl syndrome 4, transcript variant X23
Bardet-Biedl syndrome 4, transcript variant X16
Bardet-Biedl syndrome 4, transcript variant X10
Bardet-Biedl syndrome 4 protein isoform X5
Bardet-Biedl syndrome 4 protein isoform X1
Bardet-Biedl syndrome 4 protein isoform X3
Bardet-Biedl syndrome 4 protein isoform X2
Bardet-Biedl syndrome 4 protein isoform X4
Bardet-Biedl syndrome 4 protein isoform X6
ariadne RBR E3 ubiquitin protein ligase 1, transcript variant X1
ariadne RBR E3 ubiquitin protein ligase 1, transcript variant X2
E3 ubiquitin-protein ligase ARIH1 isoform X2
E3 ubiquitin-protein ligase ARIH1 isoform X1
hexosaminidase subunit alpha, transcript variant X2
hexosaminidase subunit alpha, transcript variant X1
beta-hexosaminidase subunit alpha isoform X1
beta-hexosaminidase subunit alpha isoform X2
hexosaminidase subunit alpha, transcript variant X3
hexosaminidase subunit alpha, transcript variant X4
beta-hexosaminidase subunit alpha isoform X3
beta-hexosaminidase subunit alpha isoform X4
CUGBP Elav-like family member 6, transcript variant X8
CUGBP Elav-like family member 6, transcript variant X12
CUGBP Elav-like family member 6, transcript variant X2
CUGBP Elav-like family member 6, transcript variant X14
CUGBP Elav-like family member 6, transcript variant X4
CUGBP Elav-like family member 6, transcript variant X15
CUGBP Elav-like family member 6, transcript variant X6
CUGBP Elav-like family member 6, transcript variant X16
CUGBP Elav-like family member 6, transcript variant X3
CUGBP Elav-like family member 6, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CUGBP Elav-like family member 6, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CUGBP Elav-like family member 6, transcript variant X7
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 7 samples with support for all annotated introns
CUGBP Elav-like family member 6, transcript variant X13
CUGBP Elav-like family member 6, transcript variant X5
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 2 samples with support for all annotated introns
CUGBP Elav-like family member 6, transcript variant X11
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 2 samples with support for all annotated introns
CUGBP Elav-like family member 6 isoform X8
CUGBP Elav-like family member 6 isoform X2
CUGBP Elav-like family member 6 isoform X4
CUGBP Elav-like family member 6 isoform X6
CUGBP Elav-like family member 6 isoform X3
CUGBP Elav-like family member 6 isoform X7
CUGBP Elav-like family member 6 isoform X5
CUGBP Elav-like family member 6 isoform X9
CUGBP Elav-like family member 6 isoform X10
CUGBP Elav-like family member 6 isoform X11
CUGBP Elav-like family member 6 isoform X12
CUGBP Elav-like family member 6, transcript variant X1
CUGBP Elav-like family member 6 isoform X1
poly(ADP-ribose) polymerase family member 6, transcript variant X9
poly(ADP-ribose) polymerase family member 6, transcript variant X8
poly(ADP-ribose) polymerase family member 6, transcript variant X7
poly(ADP-ribose) polymerase family member 6, transcript variant X6
poly(ADP-ribose) polymerase family member 6, transcript variant X5
poly(ADP-ribose) polymerase family member 6, transcript variant X4
poly(ADP-ribose) polymerase family member 6, transcript variant X3
poly(ADP-ribose) polymerase family member 6, transcript variant X2
poly(ADP-ribose) polymerase family member 6, transcript variant X1
protein mono-ADP-ribosyltransferase PARP6 isoform X9
protein mono-ADP-ribosyltransferase PARP6 isoform X7
protein mono-ADP-ribosyltransferase PARP6 isoform X6
protein mono-ADP-ribosyltransferase PARP6 isoform X5
protein mono-ADP-ribosyltransferase PARP6 isoform X8
protein mono-ADP-ribosyltransferase PARP6 isoform X4
protein mono-ADP-ribosyltransferase PARP6 isoform X3
protein mono-ADP-ribosyltransferase PARP6 isoform X2
protein mono-ADP-ribosyltransferase PARP6 isoform X1
poly(ADP-ribose) polymerase family member 6, transcript variant X10
poly(ADP-ribose) polymerase family member 6, transcript variant X12
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 11 samples with support for all annotated introns
poly(ADP-ribose) polymerase family member 6, transcript variant X11
pyruvate kinase M1/2, transcript variant X3
pyruvate kinase M1/2, transcript variant X2
pyruvate kinase M1/2, transcript variant X1
GRAM domain containing 2A, transcript variant X2
GRAM domain containing 2A, transcript variant X1
GRAM domain containing 2A, transcript variant X3
GRAM domain containing 2A, transcript variant X4
SUMO peptidase family member, NEDD8 specific, transcript variant X1
SUMO peptidase family member, NEDD8 specific, transcript variant X3
SUMO peptidase family member, NEDD8 specific, transcript variant X2
nuclear receptor subfamily 2 group E member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
paired amphipathic helix protein Sin3a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 81% coverage of the annotated genomic feature by RNAseq alignments
adaptor related protein complex 3 subunit beta 2, transcript variant X3
adaptor related protein complex 3 subunit beta 2, transcript variant X4
adaptor related protein complex 3 subunit beta 2, transcript variant X1
adaptor related protein complex 3 subunit beta 2, transcript variant X2
cytoplasmic polyadenylation element binding protein 1, transcript variant X4
cytoplasmic polyadenylation element-binding protein 1 isoform X4
cytoplasmic polyadenylation element binding protein 1, transcript variant X6
cytoplasmic polyadenylation element binding protein 1, transcript variant X3
cytoplasmic polyadenylation element binding protein 1, transcript variant X10
cytoplasmic polyadenylation element binding protein 1, transcript variant X5
cytoplasmic polyadenylation element binding protein 1, transcript variant X1
cytoplasmic polyadenylation element binding protein 1, transcript variant X2
cytoplasmic polyadenylation element-binding protein 1 isoform X1
cytoplasmic polyadenylation element-binding protein 1 isoform X5
cytoplasmic polyadenylation element-binding protein 1 isoform X2
cytoplasmic polyadenylation element binding protein 1, transcript variant X7
cytoplasmic polyadenylation element binding protein 1, transcript variant X8
cytoplasmic polyadenylation element-binding protein 1 isoform X3
cytoplasmic polyadenylation element binding protein 1, transcript variant X9
cytoplasmic polyadenylation element-binding protein 1 isoform X6
sperm axonemal maintenance protein CFAP97D1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00056
uncharacterized LOC101936663, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC101936663 isoform X5
uncharacterized LOC101936663, 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 1 sample with support for all annotated introns
uncharacterized LOC101936663, transcript variant X3
uncharacterized LOC101936663, transcript variant X2
uncharacterized LOC101936663, transcript variant X4
uncharacterized LOC101936663, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC101936663, transcript variant X7
uncharacterized LOC101936663, transcript variant X8
uncharacterized LOC101936663, transcript variant X12
uncharacterized LOC101936663, transcript variant X10
uncharacterized LOC101936663, transcript variant X9
uncharacterized LOC101936663, transcript variant X11
uncharacterized LOC101936663, transcript variant X13
uncharacterized protein LOC101936663 isoform X1
uncharacterized protein LOC101936663 isoform X3
uncharacterized protein LOC101936663 isoform X2
uncharacterized protein LOC101936663 isoform X4
uncharacterized protein LOC101936663 isoform X6
uncharacterized protein LOC101936663 isoform X7
uncharacterized protein LOC101936663 isoform X8
uncharacterized protein LOC101936663 isoform X11
uncharacterized protein LOC101936663 isoform X10
uncharacterized protein LOC101936663 isoform X9
uncharacterized protein LOC101936663 isoform X12
uncharacterized LOC122173852, transcript variant X1
uncharacterized LOC122173852, transcript variant X2
telomere repeat binding bouquet formation protein 2, transcript variant X4
telomere repeat binding bouquet formation protein 2, transcript variant X1
telomere repeat binding bouquet formation protein 2, transcript variant X3
telomere repeat binding bouquet formation protein 2, transcript variant X2
telomere repeats-binding bouquet formation protein 2 isoform X3
telomere repeats-binding bouquet formation protein 2 isoform X1
telomere repeats-binding bouquet formation protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
peptidylprolyl isomerase B, transcript variant X2
peptidylprolyl isomerase B, transcript variant X1
peptidyl-prolyl cis-trans isomerase B isoform X1
peptidyl-prolyl cis-trans isomerase B isoform X2
casein kinase 1 gamma 1, transcript variant X3
casein kinase 1 gamma 1, transcript variant X4
casein kinase 1 gamma 1, transcript variant X2
casein kinase 1 gamma 1, transcript variant X1
casein kinase 1 gamma 1, transcript variant X7
casein kinase 1 gamma 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
casein kinase 1 gamma 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thyroid hormone receptor interactor 4, transcript variant X3
thyroid hormone receptor interactor 4, transcript variant X4
thyroid hormone receptor interactor 4, transcript variant X1
activating signal cointegrator 1 isoform X1
activating signal cointegrator 1 isoform X4
activating signal cointegrator 1 isoform X3
thyroid hormone receptor interactor 4, transcript variant X2
activating signal cointegrator 1 isoform X2
zinc finger protein 609, transcript variant X1
zinc finger protein 609, transcript variant X3
zinc finger protein 609, transcript variant X2
zinc finger protein 609, transcript variant X4
ornithine decarboxylase antizyme 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
protein translation is dependent on polyamine-induced +1 ribosomal frameshift; Derived by automated computational analysis using gene prediction method: BestRefSeq.
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
RNA binding protein, mRNA processing factor 2, transcript variant X5
RNA binding protein, mRNA processing factor 2, transcript variant X4
RNA binding protein, mRNA processing factor 2, transcript variant X3
RNA binding protein, mRNA processing factor 2, transcript variant X2
RNA binding protein, mRNA processing factor 2, transcript variant X1
RNA-binding protein with multiple splicing 2 isoform X1
RNA-binding protein with multiple splicing 2 isoform X2
sorbitol dehydrogenase, transcript variant X1
sorbitol dehydrogenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
SEC11 homolog A, signal peptidase complex subunit
signal peptidase complex catalytic subunit SEC11A
zinc finger protein 592, transcript variant X4
zinc finger protein 592, transcript variant X7
zinc finger protein 592, transcript variant X6
zinc finger protein 592, transcript variant X1
zinc finger protein 592, transcript variant X5
zinc finger protein 592, transcript variant X2
zinc finger protein 592, transcript variant X3
zinc finger protein 592, transcript variant X8
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X4
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like, transcript variant X3
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like isoform X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like isoform X1
sodium/nucleoside cotransporter 1-like, 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 11 samples with support for all annotated introns
sodium/nucleoside cotransporter 1-like, transcript variant X1
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 12 samples with support for all annotated introns