Jaculus jaculus isolate mJacJac1 chromosome 21, 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\nCM036409.1.\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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized protein C5orf49-like, transcript variant X2
uncharacterized protein C5orf49-like, transcript variant X1
uncharacterized protein C5orf49-like isoform X2
uncharacterized protein C5orf49-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
FAST kinase domain-containing protein 3, mitochondrial
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X2
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X1
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X3
methionine synthase reductase isoform X1
methionine synthase reductase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 420-like
zinc finger protein 93-like, transcript variant X1
zinc finger protein 93-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
armadillo repeat-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
armadillo repeat-containing protein 1-like isoform X1
armadillo repeat-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
armadillo repeat-containing protein 1-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01156
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: 1 Protein
ATP synthase c subunit lysine N-methyltransferase, 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 7 samples with support for all annotated introns
ATP synthase c subunit lysine N-methyltransferase, 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
ATP synthase c subunit lysine N-methyltransferase, transcript variant X4
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
ATP synthase c subunit lysine N-methyltransferase, 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 14 samples with support for all annotated introns
ATP synthase subunit C lysine N-methyltransferase isoform X2
ATP synthase subunit C lysine N-methyltransferase isoform X3
ATP synthase subunit C lysine N-methyltransferase isoform X1
ATP synthase subunit C lysine N-methyltransferase isoform X4
chaperonin containing TCP1 subunit 5, transcript variant X2
T-complex protein 1 subunit epsilon isoform X2
chaperonin containing TCP1 subunit 5, transcript variant X1
T-complex protein 1 subunit epsilon isoform X1
carboxymethylenebutenolidase homolog, 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
carboxymethylenebutenolidase homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
membrane associated ring-CH-type finger 6, transcript variant X1
membrane associated ring-CH-type finger 6, transcript variant X2
E3 ubiquitin-protein ligase MARCHF6 isoform X1
E3 ubiquitin-protein ligase MARCHF6 isoform X2
rhophilin associated tail protein 1 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
programmed cell death 6, transcript variant X3
programmed cell death 6, transcript variant X2
programmed cell death 6, transcript variant X1
programmed cell death protein 6 isoform X3
programmed cell death protein 6 isoform X2
programmed cell death protein 6 isoform X1
succinate dehydrogenase complex flavoprotein subunit A, transcript variant X1
succinate dehydrogenase complex flavoprotein subunit A, transcript variant X2
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial isoform X2
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
coiled-coil domain containing 127, transcript variant X1
coiled-coil domain containing 127, transcript variant X2
coiled-coil domain containing 127, transcript variant X3
coiled-coil domain-containing protein 127
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 40% 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 22% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 14B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
epidermal growth factor receptor pathway substrate 15
epidermal growth factor receptor substrate 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 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: 54 Proteins
oxysterol binding protein like 9, transcript variant X1
oxysterol binding protein like 9, transcript variant X2
oxysterol binding protein like 9, transcript variant X4
oxysterol binding protein like 9, transcript variant X5
oxysterol binding protein like 9, transcript variant X3
oxysterol binding protein like 9, transcript variant X7
oxysterol binding protein like 9, transcript variant X6
oxysterol binding protein like 9, transcript variant X8
oxysterol binding protein like 9, transcript variant X9
oxysterol-binding protein-related protein 9 isoform X1
oxysterol-binding protein-related protein 9 isoform X2
oxysterol-binding protein-related protein 9 isoform X4
oxysterol-binding protein-related protein 9 isoform X5
oxysterol-binding protein-related protein 9 isoform X3
oxysterol-binding protein-related protein 9 isoform X7
oxysterol-binding protein-related protein 9 isoform X6
oxysterol-binding protein-related protein 9 isoform X8
oxysterol-binding protein-related protein 9 isoform X9
oxysterol binding protein like 9, transcript variant X10
oxysterol binding protein like 9, transcript variant X11
oxysterol-binding protein-related protein 9 isoform X10
oxysterol-binding protein-related protein 9 isoform X11
oxysterol binding protein like 9, transcript variant X12
oxysterol-binding protein-related protein 9 isoform X12
mediator of RNA polymerase II transcription subunit 14-like
thioredoxin domain containing 12, transcript variant X2
thioredoxin domain containing 12, transcript variant X1
thioredoxin domain-containing protein 12
basic transcription factor 3 like 4, transcript variant X2
basic transcription factor 3 like 4, transcript variant X1
coiled-coil and C2 domain-containing protein 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
zinc finger FYVE-type containing 9, transcript variant X1
zinc finger FYVE-type containing 9, 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 4 samples with support for all annotated introns
zinc finger FYVE-type containing 9, 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 1 sample with support for all annotated introns
zinc finger FYVE domain-containing protein 9 isoform X1
zinc finger FYVE domain-containing protein 9 isoform X2
zinc finger FYVE-type containing 9, transcript variant X4
zinc finger FYVE domain-containing protein 9 isoform X3
coiled-coil and C2 domain containing 1B, 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 8 samples with support for all annotated introns
coiled-coil and C2 domain-containing protein 1B
coiled-coil and C2 domain containing 1B, 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 5 samples with support for all annotated introns
origin recognition complex subunit 1, transcript variant X1
origin recognition complex subunit 1, transcript variant X2
origin recognition complex subunit 1 isoform X1
origin recognition complex subunit 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 1 sample with support for all annotated introns
origin recognition complex subunit 1 isoform X2
terminal uridylyl transferase 4, 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 3 samples with support for all annotated introns
terminal uridylyl transferase 4, transcript variant X5
terminal uridylyl transferase 4, 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 4 samples with support for all annotated introns
terminal uridylyl transferase 4, 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 5 samples with support for all annotated introns
terminal uridylyl transferase 4, transcript variant X4
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 6 samples with support for all annotated introns
terminal uridylyltransferase 4 isoform X4
terminal uridylyltransferase 4 isoform X3
terminal uridylyltransferase 4 isoform X2
terminal uridylyltransferase 4 isoform 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
enoyl-CoA hydratase domain containing 2, 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 3 samples with support for all annotated introns
enoyl-CoA hydratase domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
enoyl-CoA hydratase domain containing 2, 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 3 samples with support for all annotated introns
enoyl-CoA hydratase domain-containing protein 2, mitochondrial isoform X2
enoyl-CoA hydratase domain-containing protein 2, mitochondrial isoform 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 13 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: 21 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
carnitine palmitoyltransferase 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 4 samples with support for all annotated introns
carnitine palmitoyltransferase 2, transcript variant X1
carnitine O-palmitoyltransferase 2, mitochondrial
CXXC motif containing zinc binding protein
mago homolog, exon junction complex subunit
LDL receptor related protein 8, transcript variant X12
LDL receptor related protein 8, transcript variant X10
LDL receptor related protein 8, transcript variant X11
LDL receptor related protein 8, transcript variant X7
LDL receptor related protein 8, transcript variant X9
LDL receptor related protein 8, transcript variant X8
LDL receptor related protein 8, transcript variant X6
LDL receptor related protein 8, transcript variant X5
LDL receptor related protein 8, transcript variant X3
LDL receptor related protein 8, transcript variant X2
LDL receptor related protein 8, transcript variant X4
LDL receptor related protein 8, transcript variant X1
low-density lipoprotein receptor-related protein 8 isoform X12
low-density lipoprotein receptor-related protein 8 isoform X10
low-density lipoprotein receptor-related protein 8 isoform X11
low-density lipoprotein receptor-related protein 8 isoform X7
low-density lipoprotein receptor-related protein 8 isoform X9
low-density lipoprotein receptor-related protein 8 isoform X8
low-density lipoprotein receptor-related protein 8 isoform X6
low-density lipoprotein receptor-related protein 8 isoform X5
low-density lipoprotein receptor-related protein 8 isoform X3
low-density lipoprotein receptor-related protein 8 isoform X2
low-density lipoprotein receptor-related protein 8 isoform X4
low-density lipoprotein receptor-related protein 8 isoform X1
DMRT like family B with proline rich C-terminal 1
doublesex- and mab-3-related transcription factor B1
GLIS family zinc finger 1, transcript variant X5
GLIS family zinc finger 1, transcript variant X4
GLIS family zinc finger 1, transcript variant X3
GLIS family zinc finger 1, transcript variant X1
GLIS family zinc finger 1, transcript variant X2
NDC1 transmembrane nucleoporin, transcript variant X3
NDC1 transmembrane nucleoporin, transcript variant X2
NDC1 transmembrane nucleoporin, transcript variant X1
Yip1 domain family member 1, transcript variant X2
Yip1 domain family member 1, transcript variant X1
heat shock protein family B (small) member 11, transcript variant X2
heat shock protein family B (small) member 11, transcript variant X1
intraflagellar transport protein 25 homolog
leucine-rich repeat-containing protein 42
low density lipoprotein receptor class A domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor class A domain-containing protein 1
transmembrane protein 59, transcript variant X1
transmembrane protein 59, transcript variant X2
transcription elongation factor A N-terminal and central domain containing 2
transcription elongation factor A N-terminal and central domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 8% 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitochondrial ribosomal protein L37, transcript variant X1
mitochondrial ribosomal protein L37, 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 6 samples with support for all annotated introns
39S ribosomal protein L37, mitochondrial isoform X1
39S ribosomal protein L37, mitochondrial isoform X2
single stranded DNA binding protein 3, transcript variant X3
single stranded DNA binding protein 3, transcript variant X2
single stranded DNA binding protein 3, transcript variant X1
single-stranded DNA-binding protein 3 isoform X3
single-stranded DNA-binding protein 3 isoform X2
single-stranded DNA-binding protein 3 isoform X1
acyl-CoA thioesterase 11, transcript variant X2
acyl-CoA thioesterase 11, transcript variant X3
acyl-CoA thioesterase 11, transcript variant X1
acyl-coenzyme A thioesterase 11 isoform X1
acyl-coenzyme A thioesterase 11 isoform X2
family with sequence similarity 151 member A
maestro heat like repeat family member 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 7
tetratricopeptide repeat domain 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tetratricopeptide repeat domain 4, 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 5 samples with support for all annotated introns
tetratricopeptide repeat domain 4, transcript variant X2
tetratricopeptide repeat protein 4 isoform X1
tetratricopeptide repeat protein 4 isoform X2
tetratricopeptide repeat protein 4 isoform X3
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X4
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X5
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X7
prolyl-tRNA synthetase 2, mitochondrial, 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 4 samples with support for all annotated introns
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X1
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X2
prolyl-tRNA synthetase 2, mitochondrial, transcript variant X3
probable proline--tRNA ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 83% 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 12% coverage of the annotated genomic feature by RNAseq alignments
barttin CLCNK type accessory subunit beta
ubiquitin specific peptidase 24, transcript variant X2
ubiquitin specific peptidase 24, transcript variant X4
ubiquitin specific peptidase 24, transcript variant X3
ubiquitin specific peptidase 24, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 24 isoform X2
ubiquitin carboxyl-terminal hydrolase 24 isoform X4
ubiquitin carboxyl-terminal hydrolase 24 isoform X3
ubiquitin carboxyl-terminal hydrolase 24 isoform X1
phospholipid phosphatase 3, transcript variant X2
phospholipid phosphatase 3, transcript variant X1
protein kinase AMP-activated catalytic subunit alpha 2, transcript variant X1
protein kinase AMP-activated catalytic subunit alpha 2, transcript variant X2
5'-AMP-activated protein kinase catalytic subunit alpha-2 isoform X1
5'-AMP-activated protein kinase catalytic subunit alpha-2 isoform X2
metalloendopeptidase OMA1, mitochondrial
DAB adaptor protein 1, transcript variant X4
DAB adaptor protein 1, transcript variant X1
DAB adaptor protein 1, transcript variant X3
DAB adaptor protein 1, transcript variant X2
complement C8 beta chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
complement C8 beta chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
complement component C8 beta chain isoform X1
complement component C8 beta chain isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123456352, transcript variant X2
uncharacterized LOC123456352, transcript variant X1
zinc finger protein 84-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 84-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 84-like, transcript variant X4
zinc finger protein 84-like, transcript variant X7
zinc finger protein 84-like, transcript variant X5
zinc finger protein 84-like, transcript variant X6
zinc finger protein 84-like, transcript variant X3
zinc finger protein 84-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 33% 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.
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: 1 Protein
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 558-like
putative methyl-CpG-binding domain protein 3-like 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
zinc finger protein 317, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 317, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 317, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 317-like
zinc finger protein 420-like, transcript variant X3
zinc finger protein 420-like, transcript variant X1
zinc finger protein 420-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 4F6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytochrome P450 4F6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
leukotriene-B4 omega-hydroxylase 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leukotriene-B4 omega-hydroxylase 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leukotriene-B4 omega-hydroxylase 3-like, transcript variant X4
leukotriene-B4 omega-hydroxylase 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 97% 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: 77 Proteins, and 97% 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: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 23% 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 62% 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: N-acetylmuramoyl-L-alanine amidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123456374, 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 7 samples with support for all annotated introns
uncharacterized LOC123456374, 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 5 samples with support for all annotated introns
uncharacterized LOC123456374, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
A-kinase anchoring protein 8 like, transcript variant X1
A-kinase anchoring protein 8 like, transcript variant X2
A-kinase anchoring protein 8 like, transcript variant X3
A-kinase anchor protein 8-like isoform X1
A-kinase anchor protein 8-like isoform X2
A-kinase anchor protein 8-like isoform X3
A-kinase anchoring protein 8, transcript variant X1
A-kinase anchoring protein 8, transcript variant X3
A-kinase anchoring protein 8, transcript variant X2
bromodomain containing 4, transcript variant X1
bromodomain containing 4, 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 3 samples with support for all annotated introns
bromodomain-containing protein 4 isoform X1
bromodomain-containing protein 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
neurogenic locus notch homolog protein 3
ilvB acetolactate synthase like, transcript variant X1
ilvB acetolactate synthase like, transcript variant X2
ubiquitin-like modifier-activating enzyme 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 3 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 105
solute carrier family 1 member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 1 member 6, transcript variant X1
excitatory amino acid transporter 4 isoform X1
excitatory amino acid transporter 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
zinc finger protein OZF-like, transcript variant X4
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X3
zinc finger protein OZF-like, transcript variant X2
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; deleted 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 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 1571-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 35% 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 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor E2-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: 3 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: adhesion G protein-coupled receptor E2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 17, member A
NADH:ubiquinone oxidoreductase subunit B7
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7
DnaJ heat shock protein family (Hsp40) member B1, transcript variant X2
DnaJ heat shock protein family (Hsp40) member B1, transcript variant X1
dnaJ homolog subfamily B member 1 isoform X1
dnaJ homolog subfamily B member 1 isoform X2
GIPC PDZ domain containing family member 1
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
LOW QUALITY PROTEIN: PDZ domain-containing protein GIPC1
prostaglandin E receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
prostaglandin E receptor 1, transcript variant X1
prostaglandin E2 receptor EP1 subtype isoform X1
prostaglandin E2 receptor EP1 subtype isoform X2
adhesion G protein-coupled receptor L1, transcript variant X1
adhesion G protein-coupled receptor L1, transcript variant X2
adhesion G protein-coupled receptor L1 isoform X1
adhesion G protein-coupled receptor L1 isoform X2
anti-silencing function 1B histone chaperone
protein kinase cAMP-activated catalytic subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
cAMP-dependent protein kinase catalytic subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
MISP family member 3, transcript variant X8
MISP family member 3, transcript variant X11
MISP family member 3, transcript variant X10
MISP family member 3, transcript variant X9
MISP family member 3, transcript variant X6
MISP family member 3, transcript variant X1
MISP family member 3, transcript variant X12
MISP family member 3, transcript variant X7
MISP family member 3, transcript variant X4
MISP family member 3, transcript variant X5
MISP family member 3, transcript variant X2
MISP family member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% 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
LOW QUALITY PROTEIN: MHC class II regulatory factor RFX1
coiled-coil and C2 domain containing 1A, transcript variant X4
coiled-coil and C2 domain containing 1A, transcript variant X2
coiled-coil and C2 domain containing 1A, transcript variant X3
coiled-coil and C2 domain containing 1A, transcript variant X1
coiled-coil and C2 domain-containing protein 1A isoform X4
coiled-coil and C2 domain-containing protein 1A isoform X2
coiled-coil and C2 domain-containing protein 1A isoform X3
coiled-coil and C2 domain-containing protein 1A isoform X1
break repair meiotic recombinase recruitment factor 1
nanos C2HC-type zinc finger 3, transcript variant X2
nanos C2HC-type zinc finger 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
calcium voltage-gated channel subunit alpha1 A
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: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: voltage-dependent P/Q-type calcium channel subunit alpha-1A
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
LOW QUALITY PROTEIN: nucleus accumbens-associated protein 1
tRNA (guanine(26)-N(2))-dimethyltransferase
LYL1 basic helix-loop-helix family member, transcript variant X1
LYL1 basic helix-loop-helix family member, transcript variant X4
LYL1 basic helix-loop-helix family member, transcript variant X3
LYL1 basic helix-loop-helix family member, transcript variant X2
nuclear factor I X, transcript variant X3
nuclear factor I X, transcript variant X4
nuclear factor I X, transcript variant X1
nuclear factor I X, transcript variant X2
nuclear factor I X, transcript variant X6
nuclear factor I X, transcript variant X5
DAN domain BMP antagonist family member 5
growth arrest and DNA damage-inducible proteins-interacting protein 1
RAD23 homolog A, nucleotide excision repair protein, transcript variant X3
UV excision repair protein RAD23 homolog A isoform X3
RAD23 homolog A, nucleotide excision repair protein, transcript variant X2
RAD23 homolog A, nucleotide excision repair protein, transcript variant X1
UV excision repair protein RAD23 homolog A isoform X2
UV excision repair protein RAD23 homolog A isoform X1
RAD23 homolog A, nucleotide excision repair protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
UV excision repair protein RAD23 homolog A isoform X4
phenylalanyl-tRNA synthetase subunit alpha
phenylalanine--tRNA ligase alpha subunit
glutaryl-CoA dehydrogenase, transcript variant X2
glutaryl-CoA dehydrogenase, mitochondrial isoform X2
glutaryl-CoA dehydrogenase, transcript variant X1
glutaryl-CoA dehydrogenase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
microtubule associated serine/threonine kinase 1
microtubule-associated serine/threonine-protein kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thrombospondin type 1 domain containing 8
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
thrombospondin type-1 domain-containing protein 8
JunB proto-oncogene, AP-1 transcription factor subunit
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: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transcription factor jun-B
hook microtubule tethering protein 2, transcript variant X5
hook microtubule tethering protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hook microtubule tethering protein 2, transcript variant X2
hook microtubule tethering protein 2, transcript variant X3
hook microtubule tethering protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
guided entry of tail-anchored proteins factor 3, ATPase
telomerase RNA component interacting RNase, transcript variant X1
telomerase RNA component interacting RNase, transcript variant X2
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
telomerase RNA component interacting RNase isoform X1
telomerase RNA component interacting RNase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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 5 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 10 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00588
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
putative guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-14
WD repeat domain 83, transcript variant X2
WD repeat domain 83, transcript variant X1
WD repeat domain-containing protein 83 isoform X2
WD repeat domain-containing protein 83 isoform X1
zinc finger protein 791-like, 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 4 samples with support for all annotated introns
zinc finger protein 791-like, transcript variant X1
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 39-like, transcript variant X2
zinc finger protein 39-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 25-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 25-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
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: 3 Proteins
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; 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
zinc finger protein 14-like, transcript variant X1
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 3 samples with support for all annotated introns
zinc finger protein 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 14-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 14-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns