Aythya fuligula isolate bAytFul2 chromosome 21, bAytFul2.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Anseriformes; Anatidae; Aythyinae; Aythya.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020320.1.\nAssembly name: bAytFul2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2019/12/31. The original whole-genome shotgun project has the\naccession WNMM00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 20-SEP-2019\nAssembly Method :: FALCON v. 2018.31.08-03.06; FALCON-Unzip\n v. 6.0.0.47841; purge_haplotigs v.\n v1.0.3+ 1.Nov.2018; scaff10x v. 4.1.0;\n Bionano Solve DLS v. 3.2.1; Salsa HiC v.\n 2.2; Arrow smrtanalysis Pacbio polishing\n & gap filling v. 6.0.0.47841; longranger\n align v. 2.2.2; freebayes Illumina\n polishing v. 1.3; gEVAL manual curation\n v. 2019-09-20; VGP assembly pipeline\n individual v. 1.5\nAssembly Name :: bAytFul2.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 64.03x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Aythya fuligula Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.3\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Patrik Ellstrom, Mahmoud Naguib, Josef Jarhult
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Wnt family member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Wnt family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
cell division cycle 42, 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
cell division control protein 42 homolog isoform X1
cell division cycle 42, 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 3 samples with support for all annotated introns
cell division control protein 42 homolog isoform X2
cell division cycle 42, transcript variant 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 3 samples with support for all annotated introns
cell division control protein 42 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% 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: 7 Proteins, and 90% 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: 10 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: 7 Proteins
Y-box binding protein 1, 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 3 samples with support for all annotated introns
Y-box binding protein 1, 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
peptidylprolyl isomerase H, transcript variant X2
peptidylprolyl isomerase H, transcript variant X1
peptidylprolyl isomerase H, transcript variant X3
coiled-coil domain-containing protein 30
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYND domain-containing protein 12
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
solute carrier family 2, facilitated glucose transporter member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 362, 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
zinc finger protein 362, 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 1 sample with support for all annotated introns
zinc finger protein 362, transcript variant X1
zinc finger protein 362, transcript variant X8
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
zinc finger protein 362, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 362, transcript variant X6
zinc finger protein 362, transcript variant X4
zinc finger protein 362, transcript variant X5
zinc finger protein 362, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 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: 17 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
chymotrypsin-like elastase family member 3B
heparan sulfate proteoglycan 2, transcript variant X1
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
heparan sulfate proteoglycan 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 3 samples with support for all annotated introns
heparan sulfate proteoglycan 2, transcript variant X2
heparan sulfate proteoglycan 2, transcript variant X5
heparan sulfate proteoglycan 2, transcript variant X6
heparan sulfate proteoglycan 2, transcript variant X7
heparan sulfate proteoglycan 2, transcript variant X3
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 3 samples with support for all annotated introns
heparan sulfate proteoglycan 2, transcript variant X8
basement membrane-specific heparan sulfate proteoglycan core protein isoform X1
basement membrane-specific heparan sulfate proteoglycan core protein isoform X4
basement membrane-specific heparan sulfate proteoglycan core protein isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein isoform X5
basement membrane-specific heparan sulfate proteoglycan core protein isoform X6
basement membrane-specific heparan sulfate proteoglycan core protein isoform X7
basement membrane-specific heparan sulfate proteoglycan core protein isoform X3
basement membrane-specific heparan sulfate proteoglycan core protein isoform X8
ubiquitin specific peptidase 48, transcript variant X1
ubiquitin specific peptidase 48, transcript variant X2
ubiquitin specific peptidase 48, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 48 isoform X1
ubiquitin carboxyl-terminal hydrolase 48 isoform X2
ubiquitin carboxyl-terminal hydrolase 48 isoform X3
ubiquitin specific peptidase 48, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 48 isoform X4
ubiquitin specific peptidase 48, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 48 isoform X5
ubiquitin specific peptidase 48, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 48 isoform X6
ubiquitin specific peptidase 48, transcript variant X7
ubiquitin carboxyl-terminal hydrolase 48 isoform X7
RAP1 GTPase activating protein, transcript variant X1
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 3 samples with support for all annotated introns
RAP1 GTPase activating protein, 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 2 samples with support for all annotated introns
RAP1 GTPase activating protein, 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 3 samples with support for all annotated introns
rap1 GTPase-activating protein 1 isoform X1
rap1 GTPase-activating protein 1 isoform X2
alkaline phosphatase, biomineralization associated, transcript variant X2
alkaline phosphatase, biomineralization associated, transcript variant X1
alkaline phosphatase, tissue-nonspecific isozyme
endothelin converting enzyme 1, 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 1 sample with support for all annotated introns
endothelin-converting enzyme 1 isoform X2
endothelin converting enzyme 1, transcript variant X1
endothelin-converting enzyme 1 isoform X1
endothelin converting enzyme 1, transcript variant X3
endothelin converting enzyme 1, transcript variant X4
endothelin-converting enzyme 1 isoform X3
eukaryotic translation initiation factor 4 gamma 3, transcript variant X1
eukaryotic translation initiation factor 4 gamma 3, transcript variant X9
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
eukaryotic translation initiation factor 4 gamma 3, transcript variant X11
eukaryotic translation initiation factor 4 gamma 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eukaryotic translation initiation factor 4 gamma 3, transcript variant X4
eukaryotic translation initiation factor 4 gamma 3, transcript variant X2
eukaryotic translation initiation factor 4 gamma 3, transcript variant X3
eukaryotic translation initiation factor 4 gamma 3, transcript variant X5
eukaryotic translation initiation factor 4 gamma 3, transcript variant X6
eukaryotic translation initiation factor 4 gamma 3, transcript variant X7
eukaryotic translation initiation factor 4 gamma 3, transcript variant X12
eukaryotic translation initiation factor 4 gamma 3, transcript variant X8
eukaryotic translation initiation factor 4 gamma 3 isoform X1
eukaryotic translation initiation factor 4 gamma 3 isoform X4
eukaryotic translation initiation factor 4 gamma 3 isoform X2
eukaryotic translation initiation factor 4 gamma 3 isoform X9
eukaryotic translation initiation factor 4 gamma 3 isoform X3
eukaryotic translation initiation factor 4 gamma 3 isoform X5
eukaryotic translation initiation factor 4 gamma 3 isoform X6
eukaryotic translation initiation factor 4 gamma 3 isoform X7
eukaryotic translation initiation factor 4 gamma 3 isoform X10
eukaryotic translation initiation factor 4 gamma 3 isoform X8
heterochromatin protein 1 binding protein 3, transcript variant X1
heterochromatin protein 1 binding protein 3, transcript variant X2
heterochromatin protein 1-binding protein 3 isoform X1
heterochromatin protein 1-binding protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit
regulatory solute carrier protein family 1 member 1
pleckstrin homology and RUN domain containing M2, transcript variant X1
pleckstrin homology and RUN domain containing M2, transcript variant X2
pleckstrin homology and RUN domain containing M2, transcript variant X3
pleckstrin homology domain-containing family M member 2 isoform X1
pleckstrin homology domain-containing family M member 2 isoform X2
pleckstrin homology domain-containing family M member 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 77% 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 76% coverage of the annotated genomic feature by RNAseq alignments
filamin binding LIM protein 1, transcript variant X2
filamin binding LIM protein 1, transcript variant X1
filamin-binding LIM protein 1 isoform X1
filamin-binding LIM protein 1 isoform X2
spen family transcriptional repressor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
spen family transcriptional repressor, transcript variant X1
spen family transcriptional repressor, transcript variant X2
zinc finger and BTB domain containing 17
zinc finger and BTB domain-containing protein 17
heat shock protein family B (small) member 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
heat shock protein family B (small) member 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
heat shock protein family B (small) member 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
heat shock protein family B (small) member 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
ciliogenesis and planar polarity effector 2
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, including 3 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 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SUZ RNA binding domain containing 1, transcript variant X2
SUZ RNA binding domain containing 1, transcript variant X1
SUZ domain-containing protein 1 isoform X1
SUZ domain-containing protein 1 isoform X2
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 3 samples with support for all annotated introns
adaptin ear-binding coat-associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% 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 94% coverage of the annotated genomic feature by RNAseq alignments
succinate dehydrogenase complex iron sulfur subunit B
succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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
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 3 samples with support for all annotated introns
Rho guanine nucleotide exchange factor 10 like, transcript variant X6
Rho guanine nucleotide exchange factor 10 like, transcript variant X1
Rho guanine nucleotide exchange factor 10 like, transcript variant X2
Rho guanine nucleotide exchange factor 10 like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor 10 like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 10-like protein isoform X1
rho guanine nucleotide exchange factor 10-like protein isoform X2
rho guanine nucleotide exchange factor 10-like protein isoform X4
rho guanine nucleotide exchange factor 10-like protein isoform X5
Rho guanine nucleotide exchange factor 10 like, transcript variant X3
rho guanine nucleotide exchange factor 10-like protein isoform X6
rho guanine nucleotide exchange factor 10-like protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 8 Proteins, and 30% 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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
aldehyde dehydrogenase 4 family member A1
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 3 samples with support for all annotated introns
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
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
ubiquitin protein ligase E3 component n-recognin 4
ER membrane protein complex subunit 1, transcript variant X2
ER membrane protein complex subunit 1, transcript variant X1
ER membrane protein complex subunit 1 isoform X2
ER membrane protein complex subunit 1 isoform X1
MRT4 homolog, ribosome maturation factor
aflatoxin B1 aldehyde reductase member 2-like
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
lysosomal amino acid transporter 1 homolog
capping actin protein of muscle Z-line subunit beta, 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 3 samples with support for all annotated introns
F-actin-capping protein subunit beta isoform X2
capping actin protein of muscle Z-line subunit beta, transcript variant X1
F-actin-capping protein subunit beta isoform X1
mitochondrial contact site and cristae organizing system subunit 10
neuroblastoma suppressor of tumorigenicity 1
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
complement C1q B chain, transcript variant X1
complement C1q B chain, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 40
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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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 2 bases in 2 codons; substituted 4 bases at 4 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger and BTB domain-containing protein 40
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and coiled-coil domains 4, transcript variant X1
transmembrane and coiled-coil domains 4, transcript variant X3
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
transmembrane and coiled-coil domains 4, transcript variant X2
transmembrane and coiled-coil domain-containing protein 4
group IIE secretory phospholipase A2-like
phospholipase A2, membrane associated-like
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
von Willebrand factor A domain containing 5B1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 29% 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: von Willebrand factor A domain-containing protein 5B1
calcium/calmodulin dependent protein kinase II inhibitor 1
calcium/calmodulin-dependent protein kinase II inhibitor 1
mitochondrial E3 ubiquitin protein ligase 1
mitochondrial ubiquitin ligase activator of NFKB 1
family with sequence similarity 43 member B
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase PINK1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member C16
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
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
EF-hand domain family member D2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
EF-hand domain family member D2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EF-hand domain-containing protein D2 isoform X1
EF-hand domain-containing protein D2 isoform X2
forkhead associated phosphopeptide binding domain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
forkhead-associated domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kazrin, periplakin interacting protein, transcript variant X1
kazrin, periplakin interacting protein, 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
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 3 samples with support for all annotated introns
PR domain zinc finger protein 2 isoform X2
PR domain zinc finger protein 2 isoform X1
PR domain zinc finger protein 2 isoform X5
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
PR domain zinc finger protein 2 isoform X4
PR domain zinc finger protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 38
uncharacterized protein C1orf158 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 78% 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 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vacuolar protein sorting 13 homolog D, transcript variant X4
vacuolar protein sorting 13 homolog D, transcript variant X2
vacuolar protein sorting 13 homolog D, transcript variant X3
vacuolar protein sorting 13 homolog D, transcript variant X1
vacuolar protein sorting-associated protein 13D isoform X4
vacuolar protein sorting-associated protein 13D isoform X2
vacuolar protein sorting-associated protein 13D isoform X3
vacuolar protein sorting-associated protein 13D isoform X1
tumor necrosis factor receptor superfamily member 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 8
migration and invasion inhibitory protein
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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: migration and invasion-inhibitory protein
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
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1
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
uncharacterized protein KIAA2013 homolog
chymotrypsin-like elastase family member 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% 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 38% coverage of the annotated genomic feature by RNAseq alignments
methylenetetrahydrofolate reductase, 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 2 samples with support for all annotated introns
methylenetetrahydrofolate reductase, transcript variant X2
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
angiotensin II receptor associated protein
type-1 angiotensin II receptor-associated protein
mitotic arrest deficient 2 like 2, transcript variant X1
mitotic arrest deficient 2 like 2, transcript variant X2
mitotic spindle assembly checkpoint protein MAD2B
dispatched RND transporter family member 3, transcript variant X2
dispatched RND transporter family member 3, transcript variant X1
UbiA prenyltransferase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UbiA prenyltransferase domain containing 1, transcript variant X1
ubiA prenyltransferase domain-containing protein 1
mechanistic target of rapamycin kinase, transcript variant 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, including 3 samples with support for all annotated introns
mechanistic target of rapamycin kinase, transcript variant X3
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
mechanistic target of rapamycin kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
exosome component 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
exosome component 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mannan binding lectin serine peptidase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
TAR DNA binding protein, transcript variant X2
TAR DNA binding protein, transcript variant X1
castor zinc finger 1, transcript variant X4
castor zinc finger 1, transcript variant X3
zinc finger protein castor homolog 1 isoform X3
castor zinc finger 1, transcript variant X1
castor zinc finger 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein castor homolog 1 isoform X1
zinc finger protein castor homolog 1 isoform X4
castor zinc finger 1, transcript variant X2
zinc finger protein castor homolog 1 isoform X2
6-phosphogluconate dehydrogenase, decarboxylating
kinesin family member 1B, transcript variant X2
kinesin family member 1B, transcript variant X9
kinesin family member 1B, transcript variant X6
kinesin family member 1B, transcript variant X3
kinesin family member 1B, transcript variant X8
kinesin family member 1B, transcript variant X5
kinesin family member 1B, transcript variant X4
kinesin family member 1B, transcript variant X7
kinesin family member 1B, transcript variant X1
kinesin family member 1B, transcript variant X10
ubiquitination factor E4B, transcript variant X1
ubiquitination factor E4B, transcript variant X2
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
ubiquitin conjugation factor E4 B isoform X1
ubiquitin conjugation factor E4 B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
nicotinamide nucleotide adenylyltransferase 1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1
leucine zipper and CTNNBIP1 domain containing, 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 2 samples with support for all annotated introns
leucine zipper and CTNNBIP1 domain containing, transcript variant X2
leucine zipper and CTNNBIP1 domain containing, transcript variant X1
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
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
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
splA/ryanodine receptor domain and SOCS box containing 1
SPRY domain-containing SOCS box protein 1
hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase
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, including 1 sample with support for all annotated introns
GDH/6PGL endoplasmic bifunctional protein
solute carrier family 2, facilitated glucose transporter member 5-like, 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 2 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 5-like isoform X2
solute carrier family 2, facilitated glucose transporter member 5-like, 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
solute carrier family 2, facilitated glucose transporter member 5-like isoform X1
mindbomb E3 ubiquitin protein ligase 2, transcript variant X1
mindbomb E3 ubiquitin protein ligase 2, transcript variant X2
E3 ubiquitin-protein ligase MIB2 isoform X2
E3 ubiquitin-protein ligase MIB2 isoform X1
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
fibronectin type III domain containing 10
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
fibronectin type III domain-containing protein 10
SSU72 homolog, RNA polymerase II CTD phosphatase
RNA polymerase II subunit A C-terminal domain phosphatase SSU72
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
ATPase family AAA domain-containing protein 3A
von Willebrand factor A domain containing 1
von Willebrand factor A domain-containing protein 1
39S ribosomal protein L20, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aurora kinase A interacting protein 1, transcript variant X4
aurora kinase A interacting protein 1, transcript variant X2
aurora kinase A interacting protein 1, transcript variant X5
aurora kinase A interacting protein 1, transcript variant X3
aurora kinase A interacting protein 1, transcript variant X1
dishevelled segment polarity protein 1, transcript variant X1
dishevelled segment polarity protein 1, transcript variant X2
dishevelled segment polarity protein 1, transcript variant X3
segment polarity protein dishevelled homolog DVL-1 isoform X1
segment polarity protein dishevelled homolog DVL-1 isoform X2
segment polarity protein dishevelled homolog DVL-1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3, transcript variant X5
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3, transcript variant X1
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3, transcript variant X3
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3, transcript variant X4
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X3
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X4
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 3 isoform X5
sodium channel epithelial 1 subunit delta
amiloride-sensitive sodium channel subunit delta
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
C1q and TNF related 12, transcript variant X1
C1q and TNF related 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
stromal cell derived factor 4, transcript variant X2
stromal cell derived factor 4, transcript variant X1
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
tumor necrosis factor receptor superfamily member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 18
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: 10 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: inactive polyglycylase TTLL10
chromosome 21 C1orf159 homolog, transcript variant X1
chromosome 21 C1orf159 homolog, transcript variant X3
chromosome 21 C1orf159 homolog, transcript variant X2
uncharacterized protein C1orf159 homolog
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X2
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X1
tyrosine-protein phosphatase non-receptor type 11-like, transcript variant X3
tyrosine-protein phosphatase non-receptor type 11-like isoform X1
tyrosine-protein phosphatase non-receptor type 11-like isoform X2
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
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: 6 Proteins, and 93% 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor HES-4
PPARGC1 and ESRR induced regulator, muscle 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
PGC-1 and ERR-induced regulator in muscle protein 1
pleckstrin homology domain containing N1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family N member 1
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
NOC2 like nucleolar associated transcriptional repressor
sterile alpha motif domain containing 11
sterile alpha motif domain-containing protein 11
arginine-glutamic acid dipeptide repeats, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arginine-glutamic acid dipeptide repeats, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arginine-glutamic acid dipeptide repeats, transcript variant X2
arginine-glutamic acid dipeptide repeats, transcript variant X4
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 3 samples with support for all annotated introns
arginine-glutamic acid dipeptide repeats protein isoform X2
arginine-glutamic acid dipeptide repeats protein isoform X1
arginine-glutamic acid dipeptide repeats protein isoform X3
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, including 1 sample with support for all annotated introns
tumor necrosis factor receptor superfamily member 9
solute carrier family 45 member 1, transcript variant X1
solute carrier family 45 member 1, transcript variant X3
proton-associated sugar transporter A isoform X1
solute carrier family 45 member 1, transcript variant X4
solute carrier family 45 member 1, transcript variant X2
proton-associated sugar transporter A isoform X2
28S ribosomal protein S16, mitochondrial
period circadian regulator 3, 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
period circadian regulator 3, transcript variant X1
period circadian protein homolog 3 isoform X2
period circadian protein homolog 3 isoform X1
calmodulin binding transcription activator 1, transcript variant X4
calmodulin binding transcription activator 1, transcript variant X3
calmodulin binding transcription activator 1, transcript variant X2
calmodulin binding transcription activator 1, transcript variant X1
calmodulin binding transcription activator 1, transcript variant X5
calmodulin binding transcription activator 1, transcript variant X6
calmodulin binding transcription activator 1, transcript variant X7
calmodulin-binding transcription activator 1 isoform X4
calmodulin-binding transcription activator 1 isoform X2
calmodulin-binding transcription activator 1 isoform X3
calmodulin-binding transcription activator 1 isoform X1
calmodulin-binding transcription activator 1 isoform X5
calmodulin-binding transcription activator 1 isoform X6
DnaJ heat shock protein family (Hsp40) member C11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain containing 48
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pleckstrin homology and RhoGEF domain containing G5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pleckstrin homology domain-containing family G member 5 isoform X2
pleckstrin homology and RhoGEF domain containing G5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pleckstrin homology domain-containing family G member 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
cytosolic acyl coenzyme A thioester hydrolase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
isoprenylcysteine carboxyl methyltransferase
protein-S-isoprenylcysteine O-methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
chromodomain helicase DNA binding protein 5, transcript variant X1
chromodomain helicase DNA binding protein 5, transcript variant X2
chromodomain helicase DNA binding protein 5, transcript variant X5
chromodomain helicase DNA binding protein 5, transcript variant X4
chromodomain helicase DNA binding protein 5, transcript variant X3
chromodomain-helicase-DNA-binding protein 5 isoform X1
chromodomain-helicase-DNA-binding protein 5 isoform X4
chromodomain-helicase-DNA-binding protein 5 isoform X3
chromodomain-helicase-DNA-binding protein 5 isoform X2
chromodomain helicase DNA binding protein 5, transcript variant X6
chromodomain-helicase-DNA-binding protein 5 isoform X5
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X8
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X5
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X9
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X6
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X7
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X1
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X2
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X3
potassium voltage-gated channel subfamily A regulatory beta subunit 2, transcript variant X4
voltage-gated potassium channel subunit beta-2 isoform X6
voltage-gated potassium channel subunit beta-2 isoform X5
voltage-gated potassium channel subunit beta-2 isoform X2
voltage-gated potassium channel subunit beta-2 isoform X1
voltage-gated potassium channel subunit beta-2 isoform X4
voltage-gated potassium channel subunit beta-2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% 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: 6 Proteins, and 97% 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: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 47
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, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 27
tumor protein p73, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
tumor protein p73, transcript variant X3
tumor protein p73, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
tumor protein p73, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 6% 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 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 6
Rho guanine nucleotide exchange factor 16
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
histone-lysine N-methyltransferase PRDM16 isoform X3
histone-lysine N-methyltransferase PRDM16 isoform X2
histone-lysine N-methyltransferase PRDM16 isoform X1
uncharacterized LOC116497540, transcript variant X2
uncharacterized LOC116497540, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 681 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 701 Proteins
LOW QUALITY PROTEIN: tetratricopeptide repeat protein 34
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor HES-5-like
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
probable glutamate receptor, transcript variant X5
probable glutamate receptor, transcript variant X2
probable glutamate receptor, transcript variant X3
probable glutamate receptor, transcript variant X1
probable glutamate receptor, transcript variant X4
phospholipase C eta 2, transcript variant X2
phospholipase C eta 2, transcript variant X1
phospholipase C eta 2, transcript variant X3
phospholipase C eta 2, transcript variant X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 isoform X3
phospholipase C eta 2, transcript variant X5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 isoform X4
phospholipase C eta 2, transcript variant X6
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 isoform X5
peroxisomal biogenesis factor 10, transcript variant X1
peroxisome biogenesis factor 10 isoform X1
peroxisomal biogenesis factor 10, transcript variant X2
peroxisome biogenesis factor 10 isoform X2
retention in endoplasmic reticulum sorting receptor 1, transcript variant X1
retention in endoplasmic reticulum sorting receptor 1, transcript variant X2
SKI proto-oncogene, transcript variant X1
SKI proto-oncogene, transcript variant X2
Fanconi anemia core complex-associated protein 20
protein kinase C zeta, transcript variant X1
protein kinase C zeta, transcript variant X2
gamma-aminobutyric acid type A receptor subunit delta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit delta
cilia and flagella associated protein 74
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: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: cilia- and flagella-associated protein 74
G protein subunit beta 1, transcript variant X5
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 3 samples with support for all annotated introns
G protein subunit beta 1, transcript variant X1
G protein subunit beta 1, transcript variant X3
G protein subunit beta 1, transcript variant X2
G protein subunit beta 1, transcript variant X4
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
solute carrier family 35 member E2A-like, transcript variant X2
solute carrier family 35 member E2A-like, transcript variant X1
solute carrier family 35 member E2A-like, transcript variant X3
solute carrier family 35 member E2A-like
cyclin dependent kinase 11A, transcript variant X2
cyclin dependent kinase 11A, transcript variant X1
cyclin dependent kinase 11A, transcript variant X3
matrix metallopeptidase 23B, transcript variant X2
matrix metallopeptidase 23B, transcript variant X1
matrix metallopeptidase 23B, transcript variant X4
matrix metallopeptidase 23B, transcript variant X3