Jaculus jaculus isolate mJacJac1 chromosome 23, mJacJac1.mat.Y.cur, whole genome shotgun sequence.
Jaculus jaculus (lesser Egyptian jerboa)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Dipodoidea; Dipodidae; Dipodinae; Jaculus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM036411.1.\nAssembly name: mJacJac1.mat.Y.cur\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/11/04. The original whole-genome shotgun project has the\naccession JAJGSA000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 2021\nAssembly Method :: Trio HiCanu v. 2.1; purge_dups v. 1.2.3;\n Scaff10x v. 4.2; Bionano Solve v. 3.5.1;\n bwa v. 0.7.17; gcpp v. 1.9.0; Longranger\n Align v. 2.2.2; Freebayes v. 1.3.2; gEVAL\n manual curation v. 2021-05--07\nAssembly Name :: mJacJac1.mat.Y.cur\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 61.0x\nSequencing Technology :: PacBio Sequel II CLR 101X; 10X Gemonics\n linked reads 78X; Bionano Genomics DLS\n 182X; Arima Genomics Hi-C v1 60X\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Jaculus jaculus Annotation Release\n 102\nAnnotation Version :: 102\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.
glutamate ionotropic receptor NMDA type subunit 2B, transcript variant X4
COORDINATES: polyA evidence [ECO:0006239]
glutamate ionotropic receptor NMDA type subunit 2B, transcript variant X3
glutamate ionotropic receptor NMDA type subunit 2B, transcript variant X2
glutamate ionotropic receptor NMDA type subunit 2B, transcript variant X1
glutamate ionotropic receptor NMDA type subunit 2B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins
activating transcription factor 7 interacting protein, transcript variant X4
activating transcription factor 7 interacting protein, transcript variant X5
activating transcription factor 7 interacting protein, transcript variant X3
activating transcription factor 7 interacting protein, transcript variant X2
activating transcription factor 7 interacting protein, transcript variant X1
activating transcription factor 7-interacting protein 1 isoform X1
activating transcription factor 7-interacting protein 1 isoform X3
activating transcription factor 7-interacting protein 1 isoform X2
activating transcription factor 7 interacting protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
activating transcription factor 7-interacting protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 39% 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 28% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
cAMP responsive element binding protein like 2
cAMP-responsive element-binding protein-like 2
BLOC-1 related complex subunit 5, transcript variant X2
BLOC-1 related complex subunit 5, transcript variant X1
BLOC-1-related complex subunit 5 isoform X2
BLOC-1-related complex subunit 5 isoform 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 14 samples with support for all annotated introns
low-density lipoprotein receptor-related protein 6
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
apoptosis facilitator Bcl-2-like protein 14 isoform X2
apoptosis facilitator Bcl-2-like protein 14 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
kidney androgen-regulated protein-like, transcript variant X2
kidney androgen-regulated protein-like, transcript variant X1
kidney androgen-regulated protein-like isoform X1
kidney androgen-regulated protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
small integral membrane protein 10 like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small integral membrane protein 10-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 155 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
double homeobox protein 4-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 173 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 34% 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 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: vomeronasal type-2 receptor 116-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 260-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ubiquitin-protein ligase E3C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
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: 6 Proteins
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: taste receptor type 2 member 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
basic salivary proline-rich protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
serine/threonine/tyrosine kinase 1, transcript variant X1
serine/threonine/tyrosine kinase 1, transcript variant X2
killer cell lectin-like receptor 2, transcript variant X1
killer cell lectin-like receptor 2, transcript variant X4
killer cell lectin-like receptor 2, transcript variant X2
killer cell lectin-like receptor 2, transcript variant X3
killer cell lectin-like receptor 2 isoform X1
killer cell lectin-like receptor 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
NKG2-D type II integral membrane protein
GABA type A receptor associated protein like 1
gamma-aminobutyric acid receptor-associated protein-like 1
oxidized low density lipoprotein receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oxidized low-density lipoprotein receptor 1
C-type lectin domain family 7 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 7 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 7 member A isoform X1
C-type lectin domain family 7 member A isoform 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 4 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 2 member F-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
C-type lectin domain family 2 member E-like
killer cell lectin-like receptor subfamily B member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase FKBP4
integrin alpha FG-GAP repeat containing 2, transcript variant X1
integrin alpha FG-GAP repeat containing 2, transcript variant X2
integrin alpha FG-GAP repeat containing 2, transcript variant X3
KICSTOR complex protein ITFG2 isoform X1
KICSTOR complex protein ITFG2 isoform X2
KICSTOR complex protein ITFG2 isoform X3
nuclear receptor interacting protein 2, transcript variant X1
nuclear receptor interacting protein 2, transcript variant X2
nuclear receptor-interacting protein 2 isoform X1
nuclear receptor-interacting protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 23% 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 88% 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: 7 Proteins, and 88% 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: 11 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein arginine methyltransferase 8, transcript variant X3
protein arginine methyltransferase 8, transcript variant X1
protein arginine methyltransferase 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein arginine N-methyltransferase 8 isoform X1
protein arginine N-methyltransferase 8 isoform X2
protein arginine N-methyltransferase 8 isoform X3
calcium release activated channel regulator 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding domain-containing protein 4B
poly(ADP-ribose) polymerase family member 11, transcript variant X2
poly(ADP-ribose) polymerase family member 11, transcript variant X1
protein mono-ADP-ribosyltransferase PARP11
TP53 induced glycolysis regulatory phosphatase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TP53 induced glycolysis regulatory phosphatase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
fructose-2,6-bisphosphatase TIGAR isoform X1
fructose-2,6-bisphosphatase TIGAR isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00420
chromosome 23 C12orf4 homolog, transcript variant X1
chromosome 23 C12orf4 homolog, transcript variant X3
chromosome 23 C12orf4 homolog, transcript variant X2
RAD51 associated protein 1, transcript variant X1
RAD51 associated protein 1, transcript variant X2
dual specificity tyrosine phosphorylation regulated kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
dual specificity tyrosine-phosphorylation-regulated kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit A9
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
polypeptide N-acetylgalactosaminyltransferase 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
probable polypeptide N-acetylgalactosaminyltransferase 8
potassium voltage-gated channel subfamily A member 6, transcript variant X1
potassium voltage-gated channel subfamily A member 6, transcript variant X2
potassium voltage-gated channel subfamily A member 6
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
potassium voltage-gated channel subfamily A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily A member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00438
pleckstrin homology and RhoGEF domain containing G6, transcript variant X1
pleckstrin homology domain-containing family G member 6 isoform X1
pleckstrin homology and RhoGEF domain containing G6, transcript variant X2
pleckstrin homology domain-containing family G member 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 1A
sodium channel epithelial 1 subunit alpha, transcript variant X5
sodium channel epithelial 1 subunit alpha, transcript variant X2
sodium channel epithelial 1 subunit alpha, transcript variant X3
sodium channel epithelial 1 subunit alpha, transcript variant X4
sodium channel epithelial 1 subunit alpha, transcript variant X1
amiloride-sensitive sodium channel subunit alpha
lymphotoxin beta receptor, transcript variant X2
tumor necrosis factor receptor superfamily member 3 isoform X2
lymphotoxin beta receptor, transcript variant X1
tumor necrosis factor receptor superfamily member 3 isoform X1
TAP binding protein like, transcript variant X2
TAP binding protein like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TAP binding protein like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
39S ribosomal protein L51, mitochondrial
non-SMC condensin I complex subunit D2, transcript variant X1
non-SMC condensin I complex subunit D2, transcript variant X3
non-SMC condensin I complex subunit D2, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01296
glyceraldehyde-3-phosphate dehydrogenase, transcript variant X1
glyceraldehyde-3-phosphate dehydrogenase isoform X1
glyceraldehyde-3-phosphate dehydrogenase, transcript variant X2
glyceraldehyde-3-phosphate dehydrogenase isoform X2
intermediate filament family orphan 1, transcript variant X7
intermediate filament family orphan 1, transcript variant X6
intermediate filament family orphan 1, transcript variant X5
intermediate filament family orphan 1, transcript variant X3
intermediate filament family orphan 1, transcript variant X2
intermediate filament family orphan 1, transcript variant X4
intermediate filament family orphan 1, transcript variant X1
non-homologous end joining factor IFFO1 isoform X7
non-homologous end joining factor IFFO1 isoform X6
non-homologous end joining factor IFFO1 isoform X5
non-homologous end joining factor IFFO1 isoform X3
non-homologous end joining factor IFFO1 isoform X2
non-homologous end joining factor IFFO1 isoform X1
non-homologous end joining factor IFFO1 isoform X4
probable 28S rRNA (cytosine(4447)-C(5))-methyltransferase
chromodomain helicase DNA binding protein 4, transcript variant X6
chromodomain helicase DNA binding protein 4, transcript variant X5
chromodomain helicase DNA binding protein 4, transcript variant X7
chromodomain helicase DNA binding protein 4, transcript variant X4
chromodomain helicase DNA binding protein 4, transcript variant X3
chromodomain helicase DNA binding protein 4, transcript variant X2
chromodomain helicase DNA binding protein 4, transcript variant X1
chromodomain-helicase-DNA-binding protein 4 isoform X6
chromodomain-helicase-DNA-binding protein 4 isoform X5
chromodomain-helicase-DNA-binding protein 4 isoform X7
chromodomain-helicase-DNA-binding protein 4 isoform X4
chromodomain-helicase-DNA-binding protein 4 isoform X3
chromodomain-helicase-DNA-binding protein 4 isoform X2
chromodomain-helicase-DNA-binding protein 4 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00564
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inhibitor of growth family member 4, transcript variant X4
inhibitor of growth family member 4, transcript variant X3
inhibitor of growth family member 4, transcript variant X2
inhibitor of growth family member 4, transcript variant X1
inhibitor of growth family member 4, transcript variant X5
inhibitor of growth protein 4 isoform X4
inhibitor of growth protein 4 isoform X3
inhibitor of growth protein 4 isoform X2
inhibitor of growth protein 4 isoform X1
inhibitor of growth protein 4 isoform X5
zinc finger protein 384, transcript variant X2
zinc finger protein 384, transcript variant X9
zinc finger protein 384, transcript variant X5
zinc finger protein 384, transcript variant X8
zinc finger protein 384, transcript variant X12
zinc finger protein 384, transcript variant X3
zinc finger protein 384, transcript variant X1
zinc finger protein 384, transcript variant X4
zinc finger protein 384, transcript variant X7
zinc finger protein 384, transcript variant X10
zinc finger protein 384, transcript variant X6
zinc finger protein 384, transcript variant X11
PILR alpha associated neural protein, transcript variant X3
PILR alpha associated neural protein, transcript variant X4
PILR alpha associated neural protein, transcript variant X2
PILR alpha associated neural protein, transcript variant X1
PILR alpha-associated neural protein isoform X1
PILR alpha associated neural protein, 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 4 samples with support for all annotated introns
PILR alpha-associated neural protein isoform X2
myeloid leukemia factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
myeloid leukemia factor 2, 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
G protein-coupled receptor 162, transcript variant X2
G protein-coupled receptor 162, transcript variant X1
G protein subunit beta 3, 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 4 samples with support for all annotated introns
G protein subunit beta 3, transcript variant X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-3
cell division cycle associated 3, transcript variant X3
cell division cycle associated 3, transcript variant X2
cell division cycle associated 3, transcript variant X1
cell division cycle-associated protein 3
ubiquitin specific peptidase 5, transcript variant X1
ubiquitin specific peptidase 5, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 5 isoform X1
ubiquitin carboxyl-terminal hydrolase 5 isoform X2
splA/ryanodine receptor domain and SOCS box containing 2
SPRY domain-containing SOCS box protein 2
leucine rich repeat containing 23, transcript variant X2
leucine rich repeat containing 23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 23, 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 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 23 isoform X1
leucine-rich repeat-containing protein 23 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
protein tyrosine phosphatase non-receptor type 6, transcript variant X1
protein tyrosine phosphatase non-receptor type 6, transcript variant X2
tyrosine-protein phosphatase non-receptor type 6 isoform X1
protein tyrosine phosphatase non-receptor type 6, transcript variant X3
tyrosine-protein phosphatase non-receptor type 6 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01294
EMG1 N1-specific pseudouridine methyltransferase
ribosomal RNA small subunit methyltransferase NEP1
lysophosphatidylcholine acyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
complement C1r subcomponent-like protein
retinol binding protein 5, transcript variant X1
retinol binding protein 5, transcript variant X2
retinol binding protein 5, transcript variant X3
peroxisomal biogenesis factor 5, transcript variant X2
peroxisomal biogenesis factor 5 isoform X2
peroxisomal biogenesis factor 5, transcript variant X1
peroxisomal biogenesis factor 5 isoform X1
peroxisomal biogenesis factor 5, transcript variant X4
peroxisomal biogenesis factor 5, transcript variant X5
peroxisomal biogenesis factor 5, transcript variant X3
peroxisomal biogenesis factor 5, transcript variant X6
peroxisomal biogenesis factor 5 isoform X3
peroxisomal biogenesis factor 5 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor cysteine-rich type 1 protein M130
tripartite motif-containing protein 26-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 80% 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tripartite motif-containing protein 26-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: C-type lectin domain family 4 member D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase makorin-1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 91% 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase makorin-1-like
solute carrier family 2 member 3, transcript variant X1
solute carrier family 2 member 3, transcript variant X2
solute carrier family 2, facilitated glucose transporter member 3 isoform X1
solute carrier family 2, facilitated glucose transporter member 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: forkhead box protein J2
adaptin ear-binding coat-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 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: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 50 Proteins, and 11% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
protein tyrosine phosphatase type IVA 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments