Cottoperca gobio chromosome 18, fCotGob3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Eupercaria; Perciformes; Notothenioidei; Bovichtidae; Cottoperca.
REFSEQ INFORMATION: The reference sequence is identical to\nLR131925.1.\nAssembly name: fCotGob3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the SC on 2019/02/06. The\noriginal whole-genome shotgun project has the accession\nCAAAFJ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cottoperca gobio Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.2\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.
sortilin related VPS10 domain containing receptor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sortilin related VPS10 domain containing receptor 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sortilin related VPS10 domain containing receptor 2, transcript variant X2
sortilin related VPS10 domain containing receptor 2, transcript variant X1
sortilin related VPS10 domain containing receptor 2, transcript variant X3
VPS10 domain-containing receptor SorCS2 isoform X5
VPS10 domain-containing receptor SorCS2 isoform X4
VPS10 domain-containing receptor SorCS2 isoform X2
VPS10 domain-containing receptor SorCS2 isoform X1
VPS10 domain-containing receptor SorCS2 isoform X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 96
tetratricopeptide repeat protein 31-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat protein 31-like, transcript variant X4
tetratricopeptide repeat protein 31-like, 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
tetratricopeptide repeat protein 31-like, transcript variant X1
tetratricopeptide repeat protein 31-like isoform X2
tetratricopeptide repeat protein 31-like isoform X4
tetratricopeptide repeat protein 31-like isoform X1
tetratricopeptide repeat protein 31-like isoform X3
major facilitator superfamily domain containing 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
major facilitator superfamily domain containing 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 8 isoform X2
major facilitator superfamily domain-containing protein 8 isoform X1
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: 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: butyrophilin subfamily 2 member A2-like
histone-lysine N-methyltransferase 2B-like
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
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X2
E3 ubiquitin-protein ligase ZFP91-like isoform X2
E3 ubiquitin-protein ligase ZFP91-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 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 81% coverage of the annotated genomic feature by RNAseq alignments
RNA binding protein, mRNA processing factor, transcript variant X1
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 4 samples with support for all annotated introns
RNA binding protein, mRNA processing factor, transcript variant X2
RNA-binding protein with multiple splicing
fatty acid-binding protein, intestinal-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
doublesex- and mab-3-related transcription factor A1
glucosidase 2 subunit beta-like, transcript variant X2
glucosidase 2 subunit beta-like, transcript variant X1
glucosidase 2 subunit beta-like isoform X1
glucosidase 2 subunit beta-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
caspase activity and apoptosis inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor L3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor L3-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G protein-coupled receptor L3-like, transcript variant X5
adhesion G protein-coupled receptor L3-like, transcript variant X4
adhesion G protein-coupled receptor L3-like, transcript variant X3
adhesion G protein-coupled receptor L3-like, transcript variant X1
adhesion G protein-coupled receptor L3-like isoform X5
adhesion G protein-coupled receptor L3-like isoform X4
adhesion G protein-coupled receptor L3-like isoform X3
adhesion G protein-coupled receptor L3-like isoform X2
adhesion G protein-coupled receptor L3-like isoform X1
adhesion G protein-coupled receptor L3-like, transcript variant X8
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
adhesion G protein-coupled receptor L3-like, transcript variant X7
adhesion G protein-coupled receptor L3-like isoform X7
adhesion G protein-coupled receptor L3-like isoform X6
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 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: multiple PDZ domain protein-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
5,6-dihydroxyindole-2-carboxylic acid oxidase
protein tyrosine phosphatase receptor type D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X6
protein tyrosine phosphatase receptor type D, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X4
protein tyrosine phosphatase receptor type D, transcript variant X14
protein tyrosine phosphatase receptor type D, transcript variant X17
protein tyrosine phosphatase receptor type D, transcript variant X7
protein tyrosine phosphatase receptor type D, transcript variant X8
protein tyrosine phosphatase receptor type D, transcript variant X20
protein tyrosine phosphatase receptor type D, transcript variant X9
protein tyrosine phosphatase receptor type D, transcript variant X11
protein tyrosine phosphatase receptor type D, transcript variant X3
protein tyrosine phosphatase receptor type D, transcript variant X37
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
protein tyrosine phosphatase receptor type D, transcript variant X5
protein tyrosine phosphatase receptor type D, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X33
protein tyrosine phosphatase receptor type D, transcript variant X10
protein tyrosine phosphatase receptor type D, transcript variant X13
protein tyrosine phosphatase receptor type D, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X15
protein tyrosine phosphatase receptor type D, transcript variant X34
protein tyrosine phosphatase receptor type D, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X21
protein tyrosine phosphatase receptor type D, transcript variant X19
protein tyrosine phosphatase receptor type D, transcript variant X41
protein tyrosine phosphatase receptor type D, transcript variant X38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tyrosine phosphatase receptor type D, transcript variant X23
protein tyrosine phosphatase receptor type D, transcript variant X25
protein tyrosine phosphatase receptor type D, transcript variant X24
protein tyrosine phosphatase receptor type D, transcript variant X39
protein tyrosine phosphatase receptor type D, transcript variant X28
protein tyrosine phosphatase receptor type D, transcript variant X26
protein tyrosine phosphatase receptor type D, transcript variant X29
protein tyrosine phosphatase receptor type D, transcript variant X40
protein tyrosine phosphatase receptor type D, transcript variant X27
protein tyrosine phosphatase receptor type D, transcript variant X30
protein tyrosine phosphatase receptor type D, transcript variant X31
protein tyrosine phosphatase receptor type D, transcript variant X32
protein tyrosine phosphatase receptor type D, transcript variant X2
receptor-type tyrosine-protein phosphatase delta isoform X1
receptor-type tyrosine-protein phosphatase delta isoform X11
receptor-type tyrosine-protein phosphatase delta isoform X5
receptor-type tyrosine-protein phosphatase delta isoform X15
receptor-type tyrosine-protein phosphatase delta isoform X3
receptor-type tyrosine-protein phosphatase delta isoform X13
receptor-type tyrosine-protein phosphatase delta isoform X16
receptor-type tyrosine-protein phosphatase delta isoform X18
receptor-type tyrosine-protein phosphatase delta isoform X21
receptor-type tyrosine-protein phosphatase delta isoform X27
receptor-type tyrosine-protein phosphatase delta isoform X22
receptor-type tyrosine-protein phosphatase delta isoform X25
receptor-type tyrosine-protein phosphatase delta isoform X28
receptor-type tyrosine-protein phosphatase delta isoform X6
receptor-type tyrosine-protein phosphatase delta isoform X7
receptor-type tyrosine-protein phosphatase delta isoform X19
receptor-type tyrosine-protein phosphatase delta isoform X24
receptor-type tyrosine-protein phosphatase delta isoform X8
receptor-type tyrosine-protein phosphatase delta isoform X10
receptor-type tyrosine-protein phosphatase delta isoform X2
receptor-type tyrosine-protein phosphatase delta isoform X36
receptor-type tyrosine-protein phosphatase delta isoform X4
receptor-type tyrosine-protein phosphatase delta isoform X17
receptor-type tyrosine-protein phosphatase delta isoform X40
receptor-type tyrosine-protein phosphatase delta isoform X39
receptor-type tyrosine-protein phosphatase delta isoform X23
receptor-type tyrosine-protein phosphatase delta isoform X26
receptor-type tyrosine-protein phosphatase delta isoform X29
receptor-type tyrosine-protein phosphatase delta isoform X32
receptor-type tyrosine-protein phosphatase delta isoform X38
receptor-type tyrosine-protein phosphatase delta isoform X9
receptor-type tyrosine-protein phosphatase delta isoform X30
receptor-type tyrosine-protein phosphatase delta isoform X12
receptor-type tyrosine-protein phosphatase delta isoform X35
receptor-type tyrosine-protein phosphatase delta isoform X14
receptor-type tyrosine-protein phosphatase delta isoform X33
receptor-type tyrosine-protein phosphatase delta isoform X34
receptor-type tyrosine-protein phosphatase delta isoform X20
receptor-type tyrosine-protein phosphatase delta isoform X37
receptor-type tyrosine-protein phosphatase delta isoform X31
inactive ubiquitin carboxyl-terminal hydrolase 53-like, 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 3 samples with support for all annotated introns
inactive ubiquitin carboxyl-terminal hydrolase 53-like, transcript variant X2
inactive ubiquitin carboxyl-terminal hydrolase 53-like
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: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: synaptopodin-2-like
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: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein transport protein Sec24D-like
potassium voltage-gated channel interacting protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel interacting protein 4, transcript variant X1
potassium voltage-gated channel interacting protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 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 interacting protein 4, transcript variant X5
potassium voltage-gated channel interacting protein 4, transcript variant X2
potassium voltage-gated channel interacting protein 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X4
Kv channel-interacting protein 4 isoform X1
Kv channel-interacting protein 4 isoform X3
Kv channel-interacting protein 4 isoform X5
Kv channel-interacting protein 4 isoform X2
Kv channel-interacting protein 4 isoform X6
adhesion G protein-coupled receptor A3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G protein-coupled receptor A3, 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 1 sample with support for all annotated introns
adhesion G protein-coupled receptor A3, 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 4 samples with support for all annotated introns
adhesion G protein-coupled receptor A3 isoform X2
adhesion G protein-coupled receptor A3 isoform X1
cytosolic beta-glucosidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytosolic beta-glucosidase-like, transcript variant X2
cytosolic beta-glucosidase-like isoform X2
cytosolic beta-glucosidase-like isoform X1
PPARG coactivator 1 alpha, transcript variant X9
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
PPARG coactivator 1 alpha, transcript variant X7
PPARG coactivator 1 alpha, transcript variant X8
PPARG coactivator 1 alpha, transcript variant X3
PPARG coactivator 1 alpha, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PPARG coactivator 1 alpha, transcript variant X5
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 1 sample with support for all annotated introns
PPARG coactivator 1 alpha, transcript variant X4
PPARG coactivator 1 alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PPARG coactivator 1 alpha, transcript variant X1
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X9
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X7
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X8
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X3
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X6
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X5
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X4
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X2
peroxisome proliferator-activated receptor gamma coactivator 1-alpha isoform X1
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15-like
coiled-coil domain-containing protein 149-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 149-like, transcript variant X1
coiled-coil domain-containing protein 149-like isoform X2
coiled-coil domain-containing protein 149-like isoform X1
leucine-rich repeat LGI family member 2-like, transcript variant X2
leucine-rich repeat LGI family member 2-like, transcript variant X3
leucine-rich repeat LGI family member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat LGI family member 2-like isoform X2
leucine-rich repeat LGI family member 2-like isoform X1
leucine-rich repeat LGI family member 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% 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 3 bases in 2 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: O-phosphoseryl-tRNA(Sec) selenium transferase
solute carrier family 24 member 2, transcript variant X3
solute carrier family 24 member 2, transcript variant X6
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
solute carrier family 24 member 2, transcript variant X2
solute carrier family 24 member 2, transcript variant X4
solute carrier family 24 member 2, transcript variant X1
solute carrier family 24 member 2, transcript variant X7
solute carrier family 24 member 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium/potassium/calcium exchanger 2 isoform X7
sodium/potassium/calcium exchanger 2 isoform X3
sodium/potassium/calcium exchanger 2 isoform X6
sodium/potassium/calcium exchanger 2 isoform X2
sodium/potassium/calcium exchanger 2 isoform X5
sodium/potassium/calcium exchanger 2 isoform X4
sodium/potassium/calcium exchanger 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
oligosaccharyltransferase complex non-catalytic subunit
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
oligosaccharyltransferase complex subunit OSTC
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen type XXV alpha 1 chain, transcript variant X4
collagen type XXV alpha 1 chain, transcript variant X5
collagen type XXV alpha 1 chain, transcript variant X2
collagen type XXV alpha 1 chain, transcript variant X1
collagen type XXV alpha 1 chain, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
collagen type XXV alpha 1 chain, transcript variant X3
stabilizer of axonemal microtubules 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
La ribonucleoprotein domain family member 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: deleted 1 base in 1 codon; 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 4 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 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 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: 1 Protein, and 100% 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: DENN domain-containing protein 4C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00286
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 4 samples with support for all annotated introns
zinc finger DHHC-type containing 21, 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 2 samples with support for all annotated introns
zinc finger DHHC-type containing 21, transcript variant X2
nuclear factor I B, 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 3 samples with support for all annotated introns
nuclear factor I B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear factor I B, transcript variant X8
nuclear factor I B, transcript variant X1
nuclear factor I B, transcript variant X6
nuclear factor I B, transcript variant X7
nuclear factor I B, transcript variant X10
nuclear factor I B, transcript variant X9
nuclear factor I B, transcript variant X4
nuclear factor I B, transcript variant X5
B cell scaffold protein with ankyrin repeats 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
B-cell scaffold protein with ankyrin repeats
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform, transcript variant X1
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform, transcript variant X2
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform isoform X1
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC115023839, 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 4 samples with support for all annotated introns
uncharacterized LOC115023839, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA damage-inducible transcript 4-like protein
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% 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: 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
sperm-associated antigen 17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sperm-associated antigen 17-like, 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 2 samples with support for all annotated introns
sperm-associated antigen 17-like, transcript variant X3
sperm-associated antigen 17-like isoform X1
sperm-associated antigen 17-like isoform X2
sperm-associated antigen 17-like isoform X3
uncharacterized LOC115023907, transcript variant X1
uncharacterized LOC115023907, 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
pyruvate carboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyruvate carboxylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyruvate carboxylase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pyruvate carboxylase, mitochondrial isoform X1
pyruvate carboxylase, mitochondrial isoform X2
pyruvate carboxylase, mitochondrial isoform X3
leucine-rich repeat and fibronectin type-III domain-containing protein 4-like
uncharacterized LOC115023750, transcript variant X2
uncharacterized LOC115023750, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC115023961, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC115023961, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 179B, transcript variant X1
transmembrane protein 179B, transcript variant X2
transmembrane protein 179B, transcript variant X3
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
BRMS1 transcriptional repressor and anoikis regulator, 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 4 samples with support for all annotated introns
BRMS1 transcriptional repressor and anoikis regulator, transcript variant X2
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 3 samples with support for all annotated introns
BRMS1 transcriptional repressor and anoikis regulator, transcript variant X3
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
protein phosphatase 1 regulatory inhibitor subunit 14B
protein phosphatase 1 regulatory subunit 14B
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: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3
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: 37 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: sodium/calcium exchanger 1-like
BCL2 associated agonist of cell death, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bcl2-associated agonist of cell death isoform X1
BCL2 associated agonist of cell death, transcript variant X2
bcl2-associated agonist of cell death isoform X2
uncharacterized oxidoreductase YtbE-like, transcript variant X2
uncharacterized oxidoreductase YtbE-like, transcript variant X1
membrane anchored junction protein, transcript variant X1
membrane anchored junction protein, transcript variant X2
membrane anchored junction protein, transcript variant X3
membrane-anchored junction protein isoform X1
membrane-anchored junction protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
glycoprotein hormone beta-5-like, transcript variant 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 2 samples with support for all annotated introns
glycoprotein hormone beta-5-like, 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
protein phosphatase 2 regulatory subunit B'beta
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: 44 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit beta isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC115023791, transcript variant X1
uncharacterized LOC115023791, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00089
COORDINATES: nucleotide motif:Rfam:12.0:RF00088
COORDINATES: nucleotide motif:Rfam:12.0:RF00070
uncharacterized LOC115023747, transcript variant X1
uncharacterized LOC115023747, transcript variant X4
uncharacterized LOC115023747, transcript variant X3
uncharacterized LOC115023747, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00099
COORDINATES: nucleotide motif:Rfam:12.0:RF00087
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3
N(alpha)-acetyltransferase 40, NatD catalytic subunit
REST corepressor 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
REST corepressor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
REST corepressor 2, transcript variant X1
REST corepressor 2, transcript variant X2
microtubule affinity regulating kinase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule affinity regulating kinase 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule affinity regulating kinase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
microtubule affinity regulating kinase 2, transcript variant X3
microtubule affinity regulating kinase 2, transcript variant X2
microtubule affinity regulating kinase 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
microtubule affinity regulating kinase 2, transcript variant X1
serine/threonine-protein kinase MARK2 isoform X4
serine/threonine-protein kinase MARK2 isoform X7
serine/threonine-protein kinase MARK2 isoform X6
serine/threonine-protein kinase MARK2 isoform X3
serine/threonine-protein kinase MARK2 isoform X2
serine/threonine-protein kinase MARK2 isoform X5
serine/threonine-protein kinase MARK2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
heat shock protein family A (Hsp70) member 12B, transcript variant X1
heat shock protein family A (Hsp70) member 12B, transcript variant X3
heat shock 70 kDa protein 12B isoform X1
heat shock 70 kDa protein 12B isoform X3
heat shock protein family A (Hsp70) member 12B, transcript variant X2
heat shock 70 kDa protein 12B isoform X2
poly(A) binding protein interacting protein 2B, transcript variant X2
poly(A) binding protein interacting protein 2B, transcript variant X1
polyadenylate-binding protein-interacting protein 2B isoform X1
polyadenylate-binding protein-interacting protein 2B isoform X2
uncharacterized LOC115023426, transcript variant X2
uncharacterized LOC115023426, transcript variant X1
N-acetylglucosamine kinase, transcript variant X3
N-acetylglucosamine kinase, transcript variant X1
N-acetylglucosamine kinase, transcript variant X2
N-acetyl-D-glucosamine kinase isoform X1
N-acetyl-D-glucosamine kinase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% 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 27% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate sulfotransferase 12-like, transcript variant X3
carbohydrate sulfotransferase 12-like, transcript variant X4
carbohydrate sulfotransferase 12-like, transcript variant X2
carbohydrate sulfotransferase 12-like, transcript variant X1
carbohydrate sulfotransferase 12-like isoform X2
carbohydrate sulfotransferase 12-like isoform X1
zinc finger protein 239-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X1
uncharacterized LOC115023825, transcript variant X3
uncharacterized LOC115023825, transcript variant X1
uncharacterized LOC115023825, transcript variant X2
uncharacterized LOC115023825, transcript variant X4
uncharacterized protein LOC115023825 isoform X3
uncharacterized protein LOC115023825 isoform X2
uncharacterized protein LOC115023825 isoform X1
uncharacterized protein LOC115023825 isoform X4
urea transporter 1-like, transcript variant X1
urea transporter 1-like, transcript variant X2
receptor-type tyrosine-protein phosphatase H-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% 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: 10 Proteins, and 22% 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 8% coverage of the annotated genomic feature by RNAseq alignments
PC-esterase domain-containing protein 1A-like, transcript variant X2
PC-esterase domain-containing protein 1A-like, transcript variant X1
PC-esterase domain-containing protein 1A-like isoform X1
PC-esterase domain-containing protein 1A-like isoform X2
dynactin subunit 1-like, transcript variant X7
dynactin subunit 1-like, transcript variant X6
dynactin subunit 1-like, transcript variant X5
dynactin subunit 1-like, transcript variant X4
dynactin subunit 1-like, transcript variant X3
dynactin subunit 1-like, transcript variant X2
dynactin subunit 1-like, transcript variant X1
dynactin subunit 1-like, transcript variant X10
dynactin subunit 1-like, transcript variant X8
dynactin subunit 1-like, transcript variant X9
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 88
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: 7 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: 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: lysine-specific demethylase 6B-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: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: dynein heavy chain 2, axonemal
WD repeat containing antisense to TP53, transcript variant X1
WD repeat containing antisense to TP53, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WD repeat containing antisense to TP53, transcript variant X2
telomerase Cajal body protein 1 isoform X2
telomerase Cajal body protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
endonuclease domain-containing 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 51% 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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 27% 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 100% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POP7 homolog, ribonuclease P/MRP subunit
up-regulator of cell proliferation-like, transcript variant X1
up-regulator of cell proliferation-like, transcript variant X3
up-regulator of cell proliferation-like, transcript variant X2
up-regulator of cell proliferation-like isoform X1
up-regulator of cell proliferation-like isoform X2
interferon-induced very large GTPase 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 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: 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
neuroligin-2-like, transcript variant X1
neuroligin-2-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 1 sample with support for all annotated introns
protein MB21D2-like, transcript variant X3
protein MB21D2-like, transcript variant X2
protein MB21D2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
cholinergic receptor nicotinic beta 1 subunit, transcript variant X2
cholinergic receptor nicotinic beta 1 subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acetylcholine receptor subunit beta isoform X1
acetylcholine receptor subunit beta isoform X2
acetylcholine receptor subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 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: 90 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G-protein coupled receptor 4-like, transcript variant X2
G-protein coupled receptor 4-like, transcript variant X1
G-protein coupled receptor 4-like isoform X1
G-protein coupled receptor 4-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: prostaglandin D2 receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 91% 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: 65 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: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115023444, transcript variant X1
uncharacterized LOC115023444, transcript variant X2
uncharacterized protein LOC115023444 isoform X1
uncharacterized protein LOC115023444 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TRAF interacting protein with forkhead associated domain
TRAF-interacting protein with FHA domain-containing protein A
RNA-binding protein 4B-like, transcript variant X4
RNA-binding protein 4B-like, transcript variant X3
RNA-binding protein 4B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RNA-binding protein 4B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fragile X mental retardation syndrome-related protein 1-like, transcript variant X2
fragile X mental retardation syndrome-related protein 1-like, transcript variant X1
fragile X mental retardation syndrome-related protein 1-like isoform X2
fragile X mental retardation syndrome-related protein 1-like isoform X1
dedicator of cytokinesis 11, transcript variant X1
dedicator of cytokinesis 11, transcript variant X2
dedicator of cytokinesis protein 11 isoform X1
dedicator of cytokinesis protein 11 isoform X2
dedicator of cytokinesis 11, transcript variant X3
dedicator of cytokinesis protein 11 isoform X3
interleukin-13 receptor subunit alpha-1-like
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NADH:ubiquinone oxidoreductase core subunit S2
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 4 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial
high affinity immunoglobulin epsilon receptor subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
OTU deubiquitinase, ubiquitin aldehyde binding 1
citrate synthase lysine methyltransferase, transcript variant X1
citrate synthase-lysine N-methyltransferase CSKMT, mitochondrial isoform X1
citrate synthase lysine methyltransferase, transcript variant X4
citrate synthase lysine methyltransferase, transcript variant X3
citrate synthase lysine methyltransferase, transcript variant X2
citrate synthase-lysine N-methyltransferase CSKMT, mitochondrial isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: alpha-protein kinase 1
RAS guanyl releasing protein 2, transcript variant X2
RAS guanyl releasing protein 2, transcript variant X1
RAS guanyl-releasing protein 2 isoform X1
RAS guanyl-releasing protein 2 isoform X2
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
mitogen-activated protein kinase kinase kinase 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor p65-like, transcript variant X2
transcription factor p65-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription factor p65-like isoform X2
transcription factor p65-like isoform X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
equilibrative nucleoside transporter 2-like
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 2 samples with support for all annotated introns
protein S100-P-like, transcript variant X2
protein S100-P-like, transcript variant X1
protein S100-P-like, transcript variant X4
uncharacterized protein LOC115023402 isoform X1
uncharacterized protein LOC115023402 isoform X2
uncharacterized protein LOC115023402 isoform X4
protein S100-P-like, transcript variant X5
protein S100-P-like, transcript variant X3
uncharacterized protein LOC115023402 isoform X3
KIAA0232 ortholog, transcript variant X1
KIAA0232 ortholog, 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 3 samples with support for all annotated introns
uncharacterized protein KIAA0232 homolog isoform X1
KIAA0232 ortholog, transcript variant X3
uncharacterized protein KIAA0232 homolog isoform X2
TBC1 domain family member 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TBC1 domain family member 14, transcript variant X1
TBC1 domain family member 14, transcript variant X3
uncharacterized LOC115023891, transcript variant X1
uncharacterized LOC115023891, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF01290
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mannose-P-dolichol utilization defect 1 protein
metallo-beta-lactamase domain containing 1
metallo-beta-lactamase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
galactose-3-O-sulfotransferase 2-like, transcript variant X1
galactose-3-O-sulfotransferase 2-like, transcript variant X2
galactose-3-O-sulfotransferase 2-like isoform X1
galactose-3-O-sulfotransferase 2-like isoform X2
microtubule-associated protein 11-like, transcript variant X1
microtubule-associated protein 11-like, transcript variant X3
microtubule-associated protein 11-like, transcript variant X2
microtubule-associated protein 11-like isoform X1
microtubule-associated protein 11-like isoform X3
microtubule-associated protein 11-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 38 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: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
small nuclear RNA activating complex polypeptide 2
snRNA-activating protein complex subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
acetylcholinesterase (Cartwright blood group)
schwannomin-interacting protein 1-like, transcript variant X2
schwannomin-interacting protein 1-like, transcript variant X1
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: 11 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: P2Y purinoceptor 3-like
chromatin complexes subunit BAP18-like, transcript variant X2
chromatin complexes subunit BAP18-like, transcript variant X1
chromatin complexes subunit BAP18-like isoform X2
chromatin complexes subunit BAP18-like isoform X1
ribonuclease kappa-A-like, transcript variant X1
ribonuclease kappa-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
proline-, glutamic acid- and leucine-rich protein 1-like
mediator of RNA polymerase II transcription subunit 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myotubularin-related protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin-related protein 1-like, transcript variant X2
myotubularin-related protein 1-like, transcript variant X3
myotubularin-related protein 1-like, transcript variant X4
myotubularin-related protein 1-like, transcript variant X6
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
myotubularin-related protein 1-like, transcript variant X5
myotubularin-related protein 1-like, transcript variant X7
myotubularin-related protein 1-like isoform X7
myotubularin-related protein 2-like isoform X4
myotubularin-related protein 2-like isoform X6
myotubularin-related protein 2-like isoform X2
myotubularin-related protein 2-like isoform X3
myotubularin-related protein 2-like isoform X5
myotubularin-related protein 2-like isoform X1
N-acetyltransferase 16 (putative), transcript variant X2
N-acetyltransferase 16 (putative), transcript variant X1
probable N-acetyltransferase 16 isoform X1
probable N-acetyltransferase 16 isoform X2
SH3 domain and tetratricopeptide repeats 1, transcript variant X2
SH3 domain and tetratricopeptide repeats 1, transcript variant X1
SH3 domain and tetratricopeptide repeat-containing protein 1
zinc finger protein 16-like, transcript variant X1
zinc finger protein 16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X3
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tyrosine-protein kinase receptor TYRO3-like, transcript variant X2
tyrosine-protein kinase receptor TYRO3-like isoform X1
tyrosine-protein kinase receptor TYRO3-like, transcript variant X1
tyrosine-protein kinase receptor TYRO3-like, transcript variant X3
ephrin type-A receptor 3-like isoform X2
EH domain-binding protein 1-like protein 1, transcript variant X2
EH domain-binding protein 1-like protein 1 isoform X2
EH domain-binding protein 1-like protein 1, transcript variant X1
uncharacterized protein LOC115023882 isoform X1
potassium channel subfamily K member 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: 4 Proteins
LOW QUALITY PROTEIN: potassium channel subfamily K member 1-like
TATA-box binding protein associated factor 6 like, transcript variant X2
TATA-box binding protein associated factor 6 like, transcript variant X1
TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L
mRNA decay activator protein ZFP36L2-like
metastasis associated 1 family member 2, transcript variant X1
metastasis associated 1 family member 2, transcript variant X2
metastasis-associated protein MTA2 isoform X2
metastasis-associated protein MTA2 isoform X1
echinoderm microtubule-associated protein-like 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 93% 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 91% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial
uncharacterized LOC115023502, transcript variant X2
uncharacterized LOC115023502, transcript variant X1
uncharacterized LOC115023502, transcript variant X3
uncharacterized protein C11orf95 homolog
reticulon-3-B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
reticulon-3-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
reticulon-3-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 2 isoform X1
mitogen-activated protein kinase kinase kinase kinase 2 isoform X2
general transcription factor II-I repeat domain-containing protein 2-like
RNA-binding protein 4.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA-binding protein 4.1-like, transcript variant X3
RNA-binding protein 4.1-like, transcript variant X1
RNA-binding protein 4.1-like, transcript variant X4
splicing factor 1, transcript variant X4
splicing factor 1, transcript variant X2
splicing factor 1, transcript variant X3
splicing factor 1, transcript variant X1
splicing factor 1, transcript variant X5
splicing factor 1, transcript variant X6
glycogen phosphorylase, muscle associated
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, 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 52% coverage of the annotated genomic feature by RNAseq alignments
structure-specific endonuclease subunit slx1-like, transcript variant X1
structure-specific endonuclease subunit slx1-like, transcript variant X2
structure-specific endonuclease subunit slx1-like isoform X2
structure-specific endonuclease subunit slx1-like isoform X1
uncharacterized LOC115023609, transcript variant X1
uncharacterized LOC115023609, transcript variant X2
uncharacterized protein LOC115023609 isoform X2
uncharacterized protein LOC115023609 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 33-like, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 33-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
disintegrin and metalloproteinase domain-containing protein 33-like isoform X1
disintegrin and metalloproteinase domain-containing protein 33-like isoform X2
PC-esterase domain-containing protein 1A-like
leucine-rich repeat and calponin homology domain-containing protein 4-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: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: leucine-rich repeat and calponin homology domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
MLLT3 super elongation complex subunit, 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 3 samples with support for all annotated introns
MLLT3 super elongation complex subunit, 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 3 samples with support for all annotated introns
3-hydroxyacyl-CoA dehydratase 4, transcript variant X1
3-hydroxyacyl-CoA dehydratase 4, transcript variant X2
3-hydroxyacyl-CoA dehydratase 4, transcript variant X3
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4 isoform X1
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4 isoform X2
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4 isoform X3
uncharacterized protein C4orf54 homolog, transcript variant X2
uncharacterized protein C4orf54 homolog, transcript variant X1
spermatogenesis associated 6-like protein, transcript variant X1
spermatogenesis associated 6-like protein, transcript variant X3
spermatogenesis associated 6-like protein, transcript variant X2
spermatogenesis associated 6-like protein isoform X1
spermatogenesis-associated protein 6-like isoform X2
uncharacterized protein LOC115023675 isoform X3
Rap1 GTPase-GDP dissociation stimulator 1, 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
Rap1 GTPase-GDP dissociation stimulator 1, transcript variant X2
rap1 GTPase-GDP dissociation stimulator 1 isoform X1
rap1 GTPase-GDP dissociation stimulator 1 isoform X2
Rap1 GTPase-GDP dissociation stimulator 1, transcript variant X3
rap1 GTPase-GDP dissociation stimulator 1 isoform X3
FRAS1 related extracellular matrix 1, transcript variant X1
FRAS1-related extracellular matrix protein 1 isoform X1
FRAS1 related extracellular matrix 1, transcript variant X2
FRAS1-related extracellular matrix protein 1 isoform X2
leucine-rich repeat-containing protein 72-like
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: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYND domain-containing protein 15
membrane progestin receptor epsilon-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC115023496 isoform X2
uncharacterized protein LOC115023496 isoform X1
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X10
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X6
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X9
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X2
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X11
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X4
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 2 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X8
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
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X5
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 2 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X1
calcium/calmodulin-dependent protein kinase type II delta chain isoform X10
calcium/calmodulin-dependent protein kinase type II delta chain isoform X6
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X3
calcium/calmodulin-dependent protein kinase type II delta chain isoform X9
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X2
calcium/calmodulin-dependent protein kinase type II delta chain isoform X11
calcium/calmodulin-dependent protein kinase type II subunit delta isoform X4
calcium/calmodulin-dependent protein kinase type II delta chain isoform X8
calcium/calmodulin-dependent protein kinase type II delta chain isoform X5
calcium/calmodulin-dependent protein kinase type II subunit delta isoform X1
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X12
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X7
calcium/calmodulin-dependent protein kinase type II delta chain, transcript variant X13
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X12
calcium/calmodulin-dependent protein kinase type II delta chain isoform X7
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X13
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: 27 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: arylsulfatase J-like
mitotic spindle assembly checkpoint protein MAD2A
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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: cGMP-specific 3',5'-cyclic phosphodiesterase
rRNA N6-adenosine-methyltransferase ZCCHC4
actin binding LIM protein family member 2, 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
actin binding LIM protein family member 2, transcript variant X1
actin binding LIM protein family member 2, transcript variant X5
actin binding LIM protein family member 2, transcript variant X3
actin binding LIM protein family member 2, transcript variant X4
actin binding LIM protein family member 2, transcript variant X6
actin binding LIM protein family member 2, transcript variant X7
actin binding LIM protein family member 2, transcript variant X10
actin binding LIM protein family member 2, transcript variant X9
actin binding LIM protein family member 2, transcript variant X8
actin filament associated protein 1, transcript variant X3
actin filament associated protein 1, transcript variant X4
actin filament associated protein 1, transcript variant X1
actin filament associated protein 1, transcript variant X2
actin filament associated protein 1, transcript variant X5
actin filament associated protein 1, transcript variant X6
actin filament-associated protein 1 isoform X1
actin filament-associated protein 1 isoform X2
actin filament-associated protein 1 isoform X4
actin filament-associated protein 1 isoform X5
actin filament-associated protein 1 isoform X3
claudin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B-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 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: oxysterol-binding protein 1-like
E3 ubiquitin-protein ligase DTX4-like, transcript variant X2
E3 ubiquitin-protein ligase DTX4-like, transcript variant X1
Myb/SANT DNA binding domain containing 1
myb/SANT-like DNA-binding domain-containing protein 1
regulator of G-protein signaling 12-like, transcript variant X2
regulator of G-protein signaling 12-like, transcript variant X1
regulator of G-protein signaling 12-like, transcript variant X3
regulator of G-protein signaling 12-like isoform X1
regulator of G-protein signaling 12-like isoform X2
regulator of G-protein signaling 12-like, transcript variant X5
regulator of G-protein signaling 12-like isoform X4
regulator of G-protein signaling 12-like, transcript variant X4
regulator of G-protein signaling 12-like isoform X3
docking protein 7, transcript variant X4
docking protein 7, transcript variant X1
docking protein 7, transcript variant X3
docking protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 8 Proteins, and 94% 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: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: carboxypeptidase Z-like
G-protein coupled receptor 26-like, transcript variant X2
G-protein coupled receptor 26-like, transcript variant X1
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: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: probable tRNA (uracil-O(2)-)-methyltransferase
non-receptor tyrosine-protein kinase TNK1
phospholipid scramblase 1-like, transcript variant X1
phospholipid scramblase 1-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 3 samples with support for all annotated introns
phospholipid scramblase 1-like, transcript variant X4
phospholipid scramblase 1-like, transcript variant X3
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 3 samples with support for all annotated introns
phospholipid scramblase 2-like isoform X1
phospholipid scramblase 1-like isoform X2
PHD finger protein 23, transcript variant X2
PHD finger protein 23, transcript variant X1
elongator acetyltransferase complex subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: elongator complex protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
gamma-aminobutyric acid receptor-associated protein
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
G protein pathway suppressor 2, transcript variant X1
G protein pathway suppressor 2, transcript variant X5
G protein pathway suppressor 2, transcript variant X2
G protein pathway suppressor 2, transcript variant X4
G protein pathway suppressor 2, transcript variant X3
G protein pathway suppressor 2 isoform X5
G protein pathway suppressor 2 isoform X1
G protein pathway suppressor 2 isoform X3
G protein pathway suppressor 2 isoform X2
G protein pathway suppressor 2 isoform X4
G protein pathway suppressor 2, transcript variant X6
G protein pathway suppressor 2 isoform X6
eukaryotic translation initiation factor 5A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
eukaryotic translation initiation factor 5A-1
Y-box binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Y-box binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase eta-like, transcript variant X1
receptor-type tyrosine-protein phosphatase eta-like, transcript variant X2
receptor-type tyrosine-protein phosphatase eta-like isoform X1
receptor-type tyrosine-protein phosphatase eta-like isoform X2
DNA-directed RNA polymerase II subunit RPB1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA-directed RNA polymerase II subunit RPB1-like
uncharacterized LOC115023859, transcript variant X3
uncharacterized LOC115023859, transcript variant X2
uncharacterized LOC115023859, transcript variant X4
uncharacterized LOC115023859, transcript variant X1
uncharacterized protein LOC115023859 isoform X1
uncharacterized protein LOC115023859 isoform X2
interphotoreceptor matrix proteoglycan 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% 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: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: neuralized-like protein 4
rho guanine nucleotide exchange factor 15-like, transcript variant X1
rho guanine nucleotide exchange factor 15-like, transcript variant X2
rho guanine nucleotide exchange factor 15-like
histone deacetylase complex subunit SAP25
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 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC115023772
uncharacterized LOC115023745, transcript variant X2
uncharacterized LOC115023745, transcript variant X1
uncharacterized LOC115023745, transcript variant X4
uncharacterized LOC115023745, transcript variant X3
uncharacterized protein LOC115023745 isoform X4
uncharacterized protein LOC115023745 isoform X3
uncharacterized protein LOC115023745 isoform X1
uncharacterized protein LOC115023745 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thyroid receptor-interacting protein 6-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: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: thyroid receptor-interacting protein 6-like
monocarboxylate transporter 13-like, transcript variant X4
monocarboxylate transporter 13-like, transcript variant X2
monocarboxylate transporter 13-like, transcript variant X1
monocarboxylate transporter 13-like, transcript variant X5
monocarboxylate transporter 13-like, transcript variant X3
monocarboxylate transporter 13-like isoform X1
monocarboxylate transporter 13-like isoform X2
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1 isoform X2
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X1
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X2
arf-GAP domain and FG repeat-containing protein 1-like isoform X1
arf-GAP domain and FG repeat-containing protein 1-like isoform X2
uncharacterized LOC115023771, transcript variant X1
uncharacterized LOC115023771, transcript variant X2
uncharacterized LOC115023771, transcript variant X3
uncharacterized protein LOC115023771 isoform X1
uncharacterized protein LOC115023771 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
segment polarity protein dishevelled homolog DVL-2
acyl-CoA dehydrogenase very long chain, transcript variant X1
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 3 samples with support for all annotated introns
acyl-CoA dehydrogenase very long chain, transcript variant X2
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 1 sample with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial
cornifelin homolog B-like, transcript variant X1
cornifelin homolog B-like, transcript variant X2
active breakpoint cluster region-related protein-like
procollagen C-endopeptidase enhancer 2-like
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: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: period circadian protein homolog 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
NACHT and WD repeat domain containing 2, transcript variant X1
NACHT and WD repeat domain containing 2, transcript variant X3
NACHT and WD repeat domain containing 2, transcript variant X2
NACHT and WD repeat domain containing 2, transcript variant X4
NACHT and WD repeat domain-containing protein 2 isoform X1
NACHT and WD repeat domain-containing protein 2 isoform X2
NACHT and WD repeat domain-containing protein 2 isoform X3
NACHT and WD repeat domain-containing protein 2 isoform X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 4 codons; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 4 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: death domain-containing protein 1
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2, transcript variant X1
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2, transcript variant X2
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2, transcript variant X3
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2 isoform X1
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2 isoform X2
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2 isoform X3
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: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: stromal interaction molecule 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
recombination signal binding protein for immunoglobulin kappa J region, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
recombination signal binding protein for immunoglobulin kappa J region, transcript variant X2
recombining binding protein suppressor of hairless isoform X1
recombining binding protein suppressor of hairless isoform X2
epididymis-specific alpha-mannosidase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: epididymis-specific alpha-mannosidase-like
low density lipoprotein receptor adapter protein 1-like, transcript variant X2
low density lipoprotein receptor adapter protein 1-like, transcript variant X1
low density lipoprotein receptor adapter protein 1-like isoform X2
low density lipoprotein receptor adapter protein 1-like isoform X1
TNF superfamily member 12, transcript variant X1
tumor necrosis factor ligand superfamily member 12 isoform X1
TNF superfamily member 12, transcript variant X2
tumor necrosis factor ligand superfamily member 12 isoform X2
chromodomain-helicase-DNA-binding protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: chromodomain-helicase-DNA-binding protein 3-like
N(alpha)-acetyltransferase 38, NatC auxiliary subunit, transcript variant X1
N(alpha)-acetyltransferase 38, NatC auxiliary subunit, transcript variant X2
N(alpha)-acetyltransferase 38, NatC auxiliary subunit, transcript variant X3
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X2
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X3
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 2 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 42% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase like 3, transcript variant X2
methyltransferase like 3, transcript variant X1
N6-adenosine-methyltransferase catalytic subunit
tetratricopeptide repeat domain 5, transcript variant X2
tetratricopeptide repeat domain 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% 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: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
OXA1L mitochondrial inner membrane protein
mitochondrial inner membrane protein OXA1L
probable E3 ubiquitin-protein ligase ARI5
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 47-like
ubiquitin carboxyl-terminal hydrolase 21-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 21-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 21-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 21-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 7-like isoform X1
ubiquitin carboxyl-terminal hydrolase 21-like isoform X2
ubiquitin carboxyl-terminal hydrolase 21-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% 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: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
39S ribosomal protein L52, mitochondrial
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: LIM domain-containing protein ajuba
apoptotic chromatin condensation inducer in the nucleus-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: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: apoptotic chromatin condensation inducer in the nucleus-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: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: embryonal Fyn-associated substrate
dehydrogenase/reductase SDR family member 4-like
TERF1 interacting nuclear factor 2, transcript variant X1
TERF1 interacting nuclear factor 2, transcript variant X2
TERF1-interacting nuclear factor 2 isoform X1
TERF1-interacting nuclear factor 2 isoform X2
cell death inducing DFFA like effector b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeobox and leucine zipper protein Homez-like, transcript variant X3
homeobox and leucine zipper protein Homez-like, transcript variant X5
homeobox and leucine zipper protein Homez-like, transcript variant X1
homeobox and leucine zipper protein Homez-like, transcript variant X2
homeobox and leucine zipper protein Homez-like, transcript variant X4
uncharacterized protein LOC115023778 isoform X1
homeobox and leucine zipper protein Homez-like isoform X2
homeobox and leucine zipper protein Homez-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
large neutral amino acids transporter small subunit 2-like
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 4 samples with support for all annotated introns
sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
prostaglandin reductase 1, transcript variant X3
prostaglandin reductase 1, transcript variant X1
prostaglandin reductase 1, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
chromosome 18 C4orf48 homolog, transcript variant X1
chromosome 18 C4orf48 homolog, transcript variant X2
neuropeptide-like protein C4orf48 homolog isoform X2
neuropeptide-like protein C4orf48 homolog isoform X1
negative elongation factor complex member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
testis associated actin remodelling kinase 1
dual specificity testis-specific protein kinase 1
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X2
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X1
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X2
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
RGP1 homolog, RAB6A GEF complex partner 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: non-lysosomal glucosylceramidase
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
chromosome 18 C20orf27 homolog, transcript variant X2
chromosome 18 C20orf27 homolog, transcript variant X1
ventral anterior homeobox 2, transcript variant X2
ventral anterior homeobox 2, transcript variant X3
ventral anterior homeobox 2, transcript variant X1
ankyrin repeat domain 53, transcript variant X2
ankyrin repeat domain 53, transcript variant X1
ankyrin repeat domain-containing protein 53 isoform X2
ankyrin repeat domain-containing protein 53 isoform X1
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: 56 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coagulation factor XIII A chain, transcript variant X1
coagulation factor XIII A chain isoform X1
coagulation factor XIII A chain, transcript variant X2
coagulation factor XIII A chain isoform X2
protein mono-ADP-ribosyltransferase PARP15-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
inturned planar cell polarity protein, transcript variant X2
inturned planar cell polarity protein, transcript variant X1
inturned planar cell polarity protein, transcript variant X3
inturned planar cell polarity protein, transcript variant X4
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
INO80 complex subunit B, transcript variant X2
INO80 complex subunit B, transcript variant X1
aminoadipate aminotransferase, transcript variant X1
aminoadipate aminotransferase, transcript variant X2
kynurenine/alpha-aminoadipate aminotransferase, mitochondrial
uncharacterized LOC115024019, transcript variant X4
uncharacterized LOC115024019, transcript variant X1
uncharacterized LOC115024019, transcript variant X3
uncharacterized LOC115024019, transcript variant X2
microfibril associated protein 3 like, transcript variant X1
microfibril associated protein 3 like, transcript variant X2
microfibrillar-associated protein 3-like isoform X2
microfibrillar-associated protein 3-like isoform X1
chloride voltage-gated channel 3, transcript variant X2
chloride voltage-gated channel 3, transcript variant X1
chloride voltage-gated channel 3, transcript variant X6
chloride voltage-gated channel 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chloride voltage-gated channel 3, transcript variant X7
chloride voltage-gated channel 3, transcript variant X3
chloride voltage-gated channel 3, transcript variant X8
H(+)/Cl(-) exchange transporter 3 isoform X2
H(+)/Cl(-) exchange transporter 3 isoform X1
H(+)/Cl(-) exchange transporter 3 isoform X3
H(+)/Cl(-) exchange transporter 3 isoform X6
chloride voltage-gated channel 3, transcript variant X5
H(+)/Cl(-) exchange transporter 3 isoform X4
H(+)/Cl(-) exchange transporter 3 isoform X7
H(+)/Cl(-) exchange transporter 3 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 328 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Ras and Rab interactor 1, transcript variant X3
Ras and Rab interactor 1, transcript variant X2
Ras and Rab interactor 1, transcript variant X1
Ras and Rab interactor 1, transcript variant X4
galactose-3-O-sulfotransferase 3, transcript variant X2
galactose-3-O-sulfotransferase 3, transcript variant X1
copper chaperone for superoxide dismutase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 76% 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: 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
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 90% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: splicing factor 3B subunit 2
calpain-1 catalytic subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
calpain-1 catalytic subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 10-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 10-like, transcript variant X4
ATP-sensitive inward rectifier potassium channel 10-like, transcript variant X2
ATP-sensitive inward rectifier potassium channel 10-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 10-like isoform X1
ATP-sensitive inward rectifier potassium channel 10-like isoform X2
signaling lymphocytic activation molecule-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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: signaling lymphocytic activation molecule-like
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: 10 Proteins, and 95% 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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: Fc receptor-like protein 5
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, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vang-like protein 2, transcript variant X3
vang-like protein 2, transcript variant X1
vang-like protein 2, transcript variant X2
Rho guanine nucleotide exchange factor 11
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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: rho guanine nucleotide exchange factor 11
myeloid-associated differentiation marker homolog
uncharacterized LOC115023694, transcript variant X1
uncharacterized LOC115023694, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC115023699, transcript variant X2
uncharacterized LOC115023699, transcript variant X1
solute carrier family 12 member 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 12 member 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 12 member 3-like isoform X1
solute carrier family 12 member 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments, 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
protein mono-ADP-ribosyltransferase PARP14-like, transcript variant X2
protein mono-ADP-ribosyltransferase PARP14-like isoform X2
protein mono-ADP-ribosyltransferase PARP14-like, transcript variant X1
protein mono-ADP-ribosyltransferase PARP14-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115023752, transcript variant X1
uncharacterized LOC115023752, transcript variant X2
uncharacterized protein LOC115023752 isoform X2
uncharacterized protein LOC115023752 isoform X1
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X7
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X14
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X13
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like isoform X1
heterogeneous nuclear ribonucleoprotein C-like isoform X5
heterogeneous nuclear ribonucleoprotein C-like isoform X2
heterogeneous nuclear ribonucleoprotein C-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein C-like isoform X3
heterogeneous nuclear ribonucleoprotein C-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 40-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 219-like, transcript variant X1
zinc finger protein 219-like, transcript variant X3
zinc finger protein 219-like, transcript variant X4
zinc finger protein 219-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 99% 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 50% 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 83% 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 29% coverage of the annotated genomic feature by RNAseq alignments
complement C1q tumor necrosis factor-related protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
calsequestrin-1-like, transcript variant X2
calsequestrin-1-like, transcript variant X1
proliferation and apoptosis adaptor protein 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 1b allele 3-like
NACHT, LRR and PYD domains-containing protein 1a-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 1a-like isoform X2
NACHT, LRR and PYD domains-containing protein 1a-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 1a-like isoform X1
39S ribosomal protein L48, mitochondrial-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: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: 39S ribosomal protein L48, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
SPT16 homolog, facilitates chromatin remodeling subunit, transcript variant X2
SPT16 homolog, facilitates chromatin remodeling subunit, transcript variant X1
SPT16 homolog, facilitates chromatin remodeling subunit, transcript variant X3
TOX high mobility group box family member 4-A-like, transcript variant X5
TOX high mobility group box family member 4-A-like, transcript variant X3
TOX high mobility group box family member 4-A-like, transcript variant X4
TOX high mobility group box family member 4-A-like, transcript variant X6
TOX high mobility group box family member 4-A-like, transcript variant X1
TOX high mobility group box family member 4-A-like, transcript variant X2
TOX high mobility group box family member 4-A-like isoform X5
TOX high mobility group box family member 4-A-like isoform X3
TOX high mobility group box family member 4-A-like isoform X6
TOX high mobility group box family member 4-A-like isoform X2
TOX high mobility group box family member 4-A-like isoform X4
TOX high mobility group box family member 4-A-like isoform X1
solute carrier family 12 member 6-like, transcript variant X3
solute carrier family 12 member 6-like, transcript variant X1
solute carrier family 12 member 6-like, transcript variant X2
solute carrier family 12 member 6-like isoform X2
solute carrier family 12 member 6-like isoform X1
H/ACA ribonucleoprotein complex subunit 3
lysophosphatidylcholine acyltransferase 4
ubiquitin carboxyl-terminal hydrolase CYLD-like
receptor-interacting serine/threonine-protein kinase 3-like, transcript variant X1
receptor-interacting serine/threonine-protein kinase 3-like, transcript variant X2
receptor-interacting serine/threonine-protein kinase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% 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: 7 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 23 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
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 1 sample with support for all annotated introns
ras-related protein Rab-38-like, transcript variant X2
ras-related protein Rab-38-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: FACT complex subunit SPT16-like
cysteine and histidine-rich domain-containing protein 1-like
diacylglycerol kinase kappa, transcript variant X2
diacylglycerol kinase kappa, transcript variant X1
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, including 1 sample with support for all annotated introns
5-hydroxytryptamine receptor 2A-like, transcript variant X1
5-hydroxytryptamine receptor 2A-like, transcript variant X2
5-hydroxytryptamine receptor 2A-like, transcript variant X3
5-hydroxytryptamine receptor 2A-like, transcript variant X4
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 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: G2/mitotic-specific cyclin-B3
tumor necrosis factor ligand superfamily member 10-like
chloride voltage-gated channel 5, transcript variant X1
chloride voltage-gated channel 5, transcript variant X2
H(+)/Cl(-) exchange transporter 5 isoform X1
H(+)/Cl(-) exchange transporter 5 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
liver-expressed antimicrobial peptide 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like, transcript variant X5
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like, transcript variant X4
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like, transcript variant X3
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like, transcript variant X2
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like, transcript variant X1
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like isoform X5
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like isoform X4
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like isoform X3
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like isoform X2
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein 6-like, transcript variant X1
rho GTPase-activating protein 6-like, transcript variant X4
rho GTPase-activating protein 6-like isoform X1
rho GTPase-activating protein 6-like, transcript variant X2
rho GTPase-activating protein 6-like, transcript variant X3
rho GTPase-activating protein 6-like isoform X2
ubiquitin carboxyl-terminal hydrolase 12-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: 36 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: retinal guanylyl cyclase 2-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; deleted 1 base in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: insulin receptor substrate 2-B-like
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: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
collagen type IV alpha 5 chain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
collagen type IV alpha 5 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen type IV alpha 5 chain, transcript variant X1
cytidine monophosphate N-acetylneuraminic acid synthetase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
circularly permutated Ras protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: circularly permutated Ras protein 1-like
triokinase and FMN cyclase, transcript variant X2
triokinase and FMN cyclase, transcript variant X4
triokinase and FMN cyclase, transcript variant X1
triokinase and FMN cyclase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% 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 2 bases in 2 codons; 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 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC115023530
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: palmitoyltransferase ZDHHC3-like
serine/threonine-protein kinase 26-like, transcript variant X2
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 2 samples with support for all annotated introns
serine/threonine-protein kinase 26-like, transcript variant X1
serine/threonine-protein kinase 26-like, transcript variant X3
serine/threonine-protein kinase 26-like isoform X1
serine/threonine-protein kinase 26-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
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 1 sample with support for all annotated introns
uncharacterized LOC115023558, transcript variant X2
uncharacterized LOC115023558, transcript variant X3
uncharacterized LOC115023558, transcript variant X1
uncharacterized protein LOC115023558 isoform X1
uncharacterized protein LOC115023558 isoform X2
GRB2-associated-binding protein 1-like, transcript variant X3
GRB2-associated-binding protein 1-like, transcript variant X2
GRB2-associated-binding protein 1-like, transcript variant X1
GRB2-associated-binding protein 1-like isoform X3
GRB2-associated-binding protein 1-like isoform X1
GRB2-associated-binding protein 1-like isoform X2
uncharacterized LOC115023566, transcript variant X2
uncharacterized LOC115023566, transcript variant X1
serine/threonine-protein kinase DCLK2-like
guanine nucleotide-binding protein subunit alpha-11-like, transcript variant X1
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 3 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-11-like, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha-like isoform X2
guanine nucleotide-binding protein subunit alpha-11-like isoform X1
endophilin-A1-like, transcript variant X2
endophilin-A1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acidic leucine-rich nuclear phosphoprotein 32 family member B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tec protein tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tec protein tyrosine kinase, transcript variant X5
tec protein tyrosine kinase, transcript variant X4
tec protein tyrosine kinase, transcript variant X3
tec protein tyrosine kinase, transcript variant X1
tec protein tyrosine kinase, transcript variant X7
tec protein tyrosine kinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family G member 2-like, transcript variant X2
ATP-binding cassette sub-family G member 2-like, transcript variant X1
ATP-binding cassette sub-family G member 2-like isoform X2
ATP-binding cassette sub-family G member 2-like isoform X1
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X4
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X1
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X3
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X2
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X5
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X4
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X3
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X1
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X2
protein phosphatase methylesterase 1-like
protein phosphatase 1K, mitochondrial-like
low affinity immunoglobulin gamma Fc region receptor II-a-like
F-box/WD repeat-containing protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 10 member 7, transcript variant X2
solute carrier family 10 member 7, transcript variant X1
sodium/bile acid cotransporter 7 isoform X1
sodium/bile acid cotransporter 7 isoform X2
tetratricopeptide repeat domain 29, transcript variant X3
tetratricopeptide repeat domain 29, transcript variant X1
tetratricopeptide repeat domain 29, transcript variant X2
tetratricopeptide repeat protein 29 isoform X2
tetratricopeptide repeat protein 29 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 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: 4 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport protein 46 homolog
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X3
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X2
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X1
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X6
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X5
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X7
high affinity immunoglobulin gamma Fc receptor I-like, transcript variant X4
high affinity immunoglobulin gamma Fc receptor I-like isoform X3
high affinity immunoglobulin gamma Fc receptor I-like isoform X2
high affinity immunoglobulin gamma Fc receptor I-like isoform X1
high affinity immunoglobulin gamma Fc receptor I-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 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: 10 Proteins, and 95% 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: 51% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
high affinity immunoglobulin gamma Fc receptor I-like
L-amino-acid oxidase-like, transcript variant X1
L-amino-acid oxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X4
tripartite motif-containing protein 2-like, transcript variant X1
tripartite motif-containing protein 2-like, transcript variant X2
tripartite motif-containing protein 2-like, transcript variant X3
tripartite motif-containing protein 2-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00016
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments